Cardiomyopathy Herceptin administration can result in sub - clinical and clinical cardiac failure. The incidence and severity was highest in patients receiving Herceptin with anthracycline - containing chemotherapy regimens. Evaluate left ventricular function in all patients prior to and during treatment with Herceptin. Discontinue Herceptin treatment in patients receiving adjuvant therapy and withhold Herceptin i...
Herceptin is indicated in adults for adjuvant treatment of HER2 overexpressing node positive or node negative (ER/PR negative or with one high risk feature [see Clinical Studies (14.1) ] ) breast cancer as part of a treatment regimen consisting of doxorubicin, cyclophosphamide, and either paclitaxel or docetaxel as part of a treatment regimen with docetaxel and carboplatin as a single agent following multi-modalit...
Assess left ventricular ejection fraction (LVEF) prior to initiation of Herceptin and at regular intervals during treatment. [see Boxed Warning , Dosage and Administration (2.5) , Warnings and Precautions (5.1) ]. Verify the pregnancy status of females of reproductive potential prior to the initiation of Herceptin [see Warnings and Precautions (5.3) , Use in Specific Populations (8.1 , 8.3) ] . Select patients bas...
150 mg Single-dose vial Herceptin (trastuzumab) for injection 150 mg/vial is supplied in a single-dose vial as a preservative-free, white to pale yellow lyophilized sterile powder, under vacuum. Available in a carton containing one single-dose vial (NDC 50242-132-01) and a carton containing 10 single-dose vials (NDC 50242-132-10). Store Herceptin vials in the refrigerator at 2°C to 8°C (36°F to 46°F) until time of...
www.fda.gov/CompanionDiagnosticswww.fda.gov/medwatchCardiomyopathy
Herceptin administration can result in sub-clinical and clinical cardiac failure. The incidence and severity was highest in patients receiving Herceptin with anthracycline-containing chemotherapy regimens.
Evaluate left ventricular function in all patients prior to and during treatment with Herceptin. Discontinue Herceptin treatment in patients receiving adjuvant therapy and withhold Herceptin in patients with metastatic disease for clinically significant decrease in left ventricular function [see Dosage and Administration (2.5) and Warnings and Precautions (5.1)].
Infusion Reactions; Pulmonary Toxicity
Herceptin administration can result in serious and fatal infusion reactions and pulmonary toxicity. Symptoms usually occur during or within 24 hours of Herceptin administration. Interrupt Herceptin infusion for dyspnea or clinically significant hypotension. Monitor patients until symptoms completely resolve. Discontinue Herceptin for anaphylaxis, angioedema, interstitial pneumonitis, or acute respiratory distress syndrome [see Warnings and Precautions (5.2, 5.4)].
Embryo-Fetal Toxicity
Exposure to Herceptin during pregnancy can result in oligohydramnios and oligohydramnios sequence manifesting as pulmonary hypoplasia, skeletal abnormalities, and neonatal death. Advise patients of these risks and the need for effective contraception [see Warnings and Precautions (5.3) and Use in Specific Populations (8.1, 8.3)].
Herceptin is indicated in adults for adjuvant treatment of HER2 overexpressing node positive or node negative (ER/PR negative or with one high risk feature [see Clinical Studies (14.1)]) breast cancer
Select patients for therapy based on an FDA-authorized companion diagnostic for Herceptin [see Dosage and Administration (2.2)].
Herceptin is indicated in adults:
Select patients for therapy based on an FDA-authorized companion diagnostic for Herceptin [see Dosage and Administration (2.2)].
Herceptin is indicated in adults, in combination with cisplatin and capecitabine or 5-fluorouracil, for the treatment of patients with HER2-overexpressing metastatic gastric or gastroesophageal junction adenocarcinoma who have not received prior treatment for metastatic disease.
Select patients for therapy based on an FDA-authorized companion diagnostic for Herceptin [see Dosage and Administration (2.2)].
Assess left ventricular ejection fraction (LVEF) prior to initiation of Herceptin and at regular intervals during treatment. [see Boxed Warning, Dosage and Administration (2.5), Warnings and Precautions (5.1)].
Verify the pregnancy status of females of reproductive potential prior to the initiation of Herceptin [see Warnings and Precautions (5.3), Use in Specific Populations (8.1, 8.3)].
Select patients based on HER2 protein overexpression or HER2 gene amplification in tumor specimens [see Indications and Usage (1) and Clinical Studies (14)]. Assessment of HER2 protein overexpression and HER2 gene amplification should be performed using FDA-authorized tests specific for breast or gastric cancers by laboratories with demonstrated proficiency. Information on the FDA-authorized tests for the detection of HER2 protein overexpression and HER2 gene amplification is available at: www.fda.gov/CompanionDiagnostics.
Assessment of HER2 protein overexpression and HER2 gene amplification in metastatic gastric cancer should be performed using FDA-authorized tests specifically for gastric cancers due to differences in gastric vs. breast histopathology, including incomplete membrane staining and more frequent heterogeneous expression of HER2 seen in gastric cancers.
Improper assay performance, including use of suboptimally fixed tissue, failure to utilize specified reagents, deviation from specific assay instructions, and failure to include appropriate controls for assay validation, can lead to unreliable results.
Adjuvant Treatment of Breast Cancer
Administer according to one of the following doses and schedules for a total of 52 weeks of Herceptin therapy:
During and following paclitaxel, docetaxel, or docetaxel/carboplatin:
As a single agent within three weeks following completion of multi-modality, anthracycline-based chemotherapy regimens:
Metastatic Breast Cancer
Metastatic Gastric Cancer
Missed Dose
If the patient has missed a dose of Herceptin by one week or less, then the usual maintenance dose (weekly schedule: 2 mg/kg; once every three weeks schedule: 6 mg/kg) should be administered as soon as possible. Do not wait until the next planned cycle. Subsequent Herceptin maintenance doses should be administered 7 days or 21 days later according to the weekly or once every three week schedules, respectively.
If the patient has missed a dose of Herceptin by more than one week, a re-loading dose of Herceptin should be administered over approximately 90 minutes (weekly schedule: 4 mg/kg; once every three week schedule: 8 mg/kg) as soon as possible. Subsequent Herceptin maintenance doses (weekly schedule: 2 mg/kg; three-weekly schedule 6 mg/kg) should be administered 7 days or 21 days later according to the weekly or once every three week schedules, respectively.
Infusion Reactions
[See Boxed Warning, Warnings and Precautions (5.2)]
Cardiomyopathy
[See Boxed Warning, Warnings and Precautions (5.1)]
Assess left ventricular ejection fraction (LVEF) prior to initiation of Herceptin and at regular intervals during treatment. Withhold Herceptin dosing for at least 4 weeks for either of the following:
Herceptin may be resumed if, within 4–8 weeks, the LVEF returns to normal limits and the absolute decrease from baseline is ≤ 15%.
Permanently discontinue Herceptin for a persistent (> 8 weeks) LVEF decline or for suspension of Herceptin dosing on more than 3 occasions for cardiomyopathy.
To prevent medication errors, it is important to check the vial labels to ensure that the drug being prepared and administered is Herceptin (trastuzumab) and not ado-trastuzumab emtansine or fam-trastuzumab deruxtecan.
150 mg Single-dose vial
Reconstitution
Reconstitute each 150 mg vial of Herceptin with 7.4 mL of Sterile Water for Injection (SWFI) (not supplied) to yield a single-dose solution containing 21 mg/mL trastuzumab that delivers 7.15 mL (150 mg trastuzumab).
Use appropriate aseptic technique when performing the following reconstitution steps:
Dilution
For injection: 150 mg white to pale yellow lyophilized powder in a single-dose vial
None.
Herceptin can cause left ventricular cardiac dysfunction, arrhythmias, hypertension, disabling cardiac failure, cardiomyopathy, and cardiac death [see Boxed Warning: Cardiomyopathy]. Herceptin can also cause asymptomatic decline in left ventricular ejection fraction (LVEF).
There is a 4–6 fold increase in the incidence of symptomatic myocardial dysfunction among patients receiving Herceptin as a single agent or in combination therapy compared with those not receiving Herceptin. The highest absolute incidence occurs when Herceptin is administered with an anthracycline.
Withhold Herceptin for ≥ 16% absolute decrease in LVEF from pre-treatment values or an LVEF value below institutional limits of normal and ≥ 10% absolute decrease in LVEF from pretreatment values [see Dosage and Administration (2.5)]. The safety of continuation or resumption of Herceptin in patients with Herceptin-induced left ventricular cardiac dysfunction has not been studied. Patients who receive anthracycline after stopping Herceptin may also be at increased risk of cardiac dysfunction [see Drug Interactions (7) and Clinical Pharmacology (12.3)].
Cardiac Monitoring
Conduct thorough cardiac assessment, including history, physical examination, and determination of LVEF by echocardiogram or MUGA scan. The following schedule is recommended:
In NSABP B31, 15% (158/1031) of patients discontinued Herceptin due to clinical evidence of myocardial dysfunction or significant decline in LVEF after a median follow-up duration of 8.7 years in the AC-TH arm. In HERA (one-year Herceptin treatment), the number of patients who discontinued Herceptin due to cardiac toxicity at 12.6 months median duration of follow-up was 2.6% (44/1678). In BCIRG006, a total of 2.9% (31/1056) of patients in the TCH arm (1.5% during the chemotherapy phase and 1.4% during the monotherapy phase) and 5.7% (61/1068) of patients in the AC-TH arm (1.5% during the chemotherapy phase and 4.2% during the monotherapy phase) discontinued Herceptin due to cardiac toxicity.
Among 64 patients receiving adjuvant chemotherapy (NSABP B31 and NCCTG N9831) who developed congestive heart failure, one patient died of cardiomyopathy, one patient died suddenly without documented etiology, and 33 patients were receiving cardiac medication at last follow-up. Approximately 24% of the surviving patients had recovery to a normal LVEF (defined as ≥ 50%) and no symptoms on continuing medical management at the time of last follow-up. Incidence of congestive heart failure (CHF) is presented in Table 1. The safety of continuation or resumption of Herceptin in patients with Herceptin-induced left ventricular cardiac dysfunction has not been studied.
| Incidence of Congestive Heart Failure % (n) | |||
|---|---|---|---|
| Study | Regimen | Herceptin | Control |
| NSABP B31 & NCCTG N9831* | AC†→Paclitaxel+Herceptin | 3.2% (64/2000)‡ | 1.3% (21/1655) |
| HERA§ | Chemotherapy → Herceptin | 2% (30/1678) | 0.3% (5/1708) |
| BCIRG006 | AC†→Docetaxel+Herceptin | 2% (20/1068) | 0.3% (3/1050) |
| BCIRG006 | Docetaxel+Carboplatin+Herceptin | 0.4% (4/1056) | 0.3% (3/1050) |
* Median follow-up duration for NSABP B31 & NCCTG N9831 combined was 8.3 years in the AC→paclitaxel+Herceptin arm.
† Anthracycline (doxorubicin) and cyclophosphamide.
‡ Includes 1 patient with fatal cardiomyopathy and 1 patient with sudden death without documented etiology.
§ Includes NYHA II-IV and cardiac death at 12.6 months median duration of follow-up in the one-year Herceptin arm.
In HERA (one-year Herceptin treatment), at a median follow-up duration of 8 years, the incidence of severe CHF (NYHA III & IV) was 0.8%, and the rate of mild symptomatic and asymptomatic left ventricular dysfunction was 4.6%.
| Incidence | |||||
|---|---|---|---|---|---|
| NYHA I–IV | NYHA III–IV | ||||
| Study | Event | Herceptin | Control | Herceptin | Control |
| H0648g (AC)† | Cardiac Dysfunction | 28% | 7% | 19% | 3% |
| H0648g (paclitaxel) | Cardiac Dysfunction | 11% | 1% | 4% | 1% |
| H0649g | Cardiac Dysfunction‡ | 7% | N/A | 5% | N/A |
* Congestive heart failure or significant asymptomatic decrease in LVEF.
† Anthracycline (doxorubicin or epirubicin) and cyclophosphamide.
‡ Includes 1 patient with fatal cardiomyopathy.
In BCIRG006, the incidence of NCI-CTC Grade 3/4 cardiac ischemia/infarction was higher in the Herceptin containing regimens (AC-TH: 0.3% (3/1068) and TCH: 0.2% (2/1056)) as compared to none in AC-T.
Infusion reactions consist of a symptom complex characterized by fever and chills, and on occasion included nausea, vomiting, pain (in some cases at tumor sites), headache, dizziness, dyspnea, hypotension, rash, and asthenia [see Adverse Reactions (6.1)].
In post-marketing reports, serious and fatal infusion reactions have been reported. Severe reactions, which include bronchospasm, anaphylaxis, angioedema, hypoxia, and severe hypotension, were usually reported during or immediately following the initial infusion. However, the onset and clinical course were variable, including progressive worsening, initial improvement followed by clinical deterioration, or delayed post-infusion events with rapid clinical deterioration. For fatal events, death occurred within hours to days following a serious infusion reaction.
Interrupt Herceptin infusion in all patients experiencing dyspnea, clinically significant hypotension, and intervention of medical therapy administered (which may include epinephrine, corticosteroids, diphenhydramine, bronchodilators, and oxygen). Patients should be evaluated and carefully monitored until complete resolution of signs and symptoms. Permanent discontinuation should be strongly considered in all patients with severe infusion reactions.
There are no data regarding the most appropriate method of identification of patients who may safely be retreated with Herceptin after experiencing a severe infusion reaction. Prior to resumption of Herceptin infusion, the majority of patients who experienced a severe infusion reaction were pre-medicated with antihistamines and/or corticosteroids. While some patients tolerated Herceptin infusions, others had recurrent severe infusion reactions despite pre-medications.
Herceptin can cause fetal harm when administered to a pregnant woman. In post-marketing reports, use of Herceptin during pregnancy resulted in cases of oligohydramnios and oligohydramnios sequence manifesting as pulmonary hypoplasia, skeletal abnormalities, and neonatal death.
Verify the pregnancy status of females of reproductive potential prior to the initiation of Herceptin. Advise pregnant women and females of reproductive potential that exposure to Herceptin during pregnancy or within 7 months prior to conception can result in fetal harm. Advise females of reproductive potential to use effective contraception during treatment and for 7 months following the last dose of Herceptin [see Use in Specific Populations (8.1, 8.3) and Clinical Pharmacology (12.3)].
Herceptin use can result in serious and fatal pulmonary toxicity. Pulmonary toxicity includes dyspnea, interstitial pneumonitis, pulmonary infiltrates, pleural effusions, non-cardiogenic pulmonary edema, pulmonary insufficiency and hypoxia, acute respiratory distress syndrome, and pulmonary fibrosis. Such events can occur as sequelae of infusion reactions [see Warnings and Precautions (5.2)]. Patients with symptomatic intrinsic lung disease or with extensive tumor involvement of the lungs, resulting in dyspnea at rest, appear to have more severe toxicity.
In randomized, controlled clinical trials, the per-patient incidences of NCI-CTC Grade 3–4 neutropenia and of febrile neutropenia were higher in patients receiving Herceptin in combination with myelosuppressive chemotherapy as compared to those who received chemotherapy alone. The incidence of septic death was similar among patients who received Herceptin and those who did not [see Adverse Reactions (6.1)].
The following adverse reactions are discussed in greater detail in other sections of the label:
Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.
The most common adverse reactions in patients receiving Herceptin in the adjuvant and metastatic breast cancer setting are fever, nausea, vomiting, infusion reactions, diarrhea, infections, increased cough, headache, fatigue, dyspnea, rash, neutropenia, anemia, and myalgia. Adverse reactions requiring interruption or discontinuation of Herceptin treatment include CHF, significant decline in left ventricular cardiac function, severe infusion reactions, and pulmonary toxicity [see Dosage and Administration (2.5)].
In the metastatic gastric cancer setting, the most common adverse reactions (≥ 10%) that were increased (≥ 5% difference) in the Herceptin arm as compared to the chemotherapy alone arm were neutropenia, diarrhea, fatigue, anemia, stomatitis, weight loss, upper respiratory tract infections, fever, thrombocytopenia, mucosal inflammation, nasopharyngitis, and dysgeusia.
The most common adverse reactions which resulted in discontinuation of treatment on the Herceptin-containing arm in the absence of disease progression were infection, diarrhea, and febrile neutropenia.
Adjuvant Breast Cancer
The information below reflects exposure to one-year Herceptin therapy across three randomized, open-label studies, Studies 1, 2, and 3, with (n = 3678) or without (n = 3363) trastuzumab in the adjuvant treatment of breast cancer.
HERA
Table 3 reflects exposure to Herceptin in 1678 patients in HERA; the median treatment duration was 51 weeks and median number of infusions was 18 [see Clinical Studies (14.1)].
| Adverse Reactions | Herceptin (n = 1678) % | Observation (n = 1708) % |
|---|---|---|
| Nervous System | ||
| Headache | 10 | 3 |
| Paresthesia | 2 | 0.6 |
| Musculoskeletal | ||
| Arthralgia | 8 | 6 |
| Back pain | 5 | 3 |
| Myalgia | 4 | 1 |
| Bone pain | 3 | 2 |
| Muscle spasm | 3 | 0.2 |
| Infections | ||
| Nasopharyngitis | 8 | 3 |
| Urinary tract infection | 3 | 0.8 |
| Gastrointestinal | ||
| Diarrhea | 7 | 1 |
| Nausea | 6 | 1 |
| Vomiting | 3.5 | 0.6 |
| Constipation | 2 | 1 |
| Dyspepsia | 2 | 0.5 |
| Upper abdominal pain | 2 | 1 |
| General | ||
| Pyrexia | 6 | 0.4 |
| Peripheral edema | 5 | 2 |
| Chills | 5 | 0 |
| Asthenia | 4.5 | 2 |
| Influenza-like illness | 2 | 0.2 |
| Respiratory Thoracic Mediastinal | ||
| Cough | 5 | 2 |
| Influenza | 4 | 0.5 |
| Dyspnea | 3 | 2 |
| URI | 3 | 1 |
| Rhinitis | 2 | 0.4 |
| Pharyngolaryngeal pain | 2 | 0.5 |
| Sinusitis | 2 | 0.3 |
| Epistaxis | 2 | 0.06 |
| Cardiac | ||
| Hypertension | 4 | 2 |
| Dizziness | 4 | 2 |
| Ejection fraction decreased | 3.5 | 0.6 |
| Palpitations | 3 | 0.7 |
| Cardiac arrhythmias† | 3 | 1 |
| Cardiac failure (congestive) | 2 | 0.3 |
| Skin & Subcutaneous Tissue | ||
| Rash | 4 | 0.6 |
| Nail disorders | 2 | 0 |
| Pruritus | 2 | 0.6 |
* The incidence of Grade 3 or higher adverse reactions was <1% in both arms for each listed term.
† Higher level grouping term.
Clinically relevant adverse reactions in < 1% of patients who received Herceptin in HERA included hypersensitivity (0.6%), cardiac failure (0.5%), cardiac disorder (0.3%), interstitial pneumonitis (0.2%), pulmonary hypertension (0.2%), ventricular disorder (0.2%), autoimmune thyroiditis (0.3%), and sudden death (0.06%).
Adjuvant Treatment of Breast Cancer with Herceptin Beyond One Year
Extending adjuvant treatment beyond one year is not recommended [see Dosage and Administration (2.2)]. In HERA, a comparison of Herceptin administered once every 3 weeks for two years versus one year was performed. The rate of asymptomatic cardiac dysfunction was increased in the 2-year Herceptin compared to the 1-year Herceptin treatment arm (8.1% versus 4.6%, respectively). More patients experienced at least one adverse reaction of Grade 3 or higher in the 2-year Herceptin treatment arm (20.4%) compared with the one-year Herceptin treatment arm (16.3%).
NSABP B31 and NCCTG N9831
The safety data from NSABP B31 and NCCTG N9831 were obtained from 3655 patients, of whom 2000 received Herceptin; the median treatment duration was 51 weeks [see Clinical Studies (14.1)].
In NSABP B31, only Grade 3–5 adverse events, treatment-related Grade 2 events, and Grade 2–5 dyspnea were collected during and for up to 3 months following protocol-specified treatment. The following non-cardiac adverse reactions of Grade 2–5 occurred at an incidence of at least 2% greater among patients receiving Herceptin plus chemotherapy as compared to chemotherapy alone: fatigue (29.5% vs. 22.4%), infection (24.0% vs. 12.8%), hot flashes (17.1% vs. 15%), anemia (12.3% vs. 6.7%), dyspnea (11.8% vs. 4.6%), rash/desquamation (10.9% vs. 7.6%), leukopenia (10.5% vs. 8.4%), neutropenia (6.4% vs. 4.3%), headache (6.2% vs. 3.8%), pain (5.5% vs. 3%), edema (4.7% vs. 2.7%), and insomnia (4.3% vs. 1.5%). The majority of these events were Grade 2 in severity.
In NCCTG N9831, data collection was limited to the following investigator-attributed treatment-related adverse reactions: NCI-CTC Grade 4 and 5 hematologic toxicities, Grade 3–5 non-hematologic toxicities, selected Grade 2–5 toxicities associated with taxanes (myalgia, arthralgias, nail changes, motor neuropathy, and sensory neuropathy) and Grade 1–5 cardiac toxicities occurring during chemotherapy and/or Herceptin treatment. The following non-cardiac adverse reactions of Grade 2–5 occurred at an incidence of at least 2% greater among patients receiving Herceptin plus chemotherapy as compared to chemotherapy alone: arthralgia (12.2% vs. 9.1%), nail changes (11.5% vs. 6.8%), dyspnea (2.4% vs. 0.2%), and diarrhea (2.2% vs. 0%). The majority of these events were Grade 2 in severity.
BCIRG006
Safety data from BCIRG006 reflect exposure to Herceptin as part of an adjuvant treatment regimen from 2124 patients receiving at least one dose of study treatment [AC-TH: n = 1068; TCH: n = 1056]. The overall median treatment duration was 54 weeks in both the AC-TH and TCH arms. The median number of infusions was 26 in the AC-TH arm and 30 in the TCH arm, including weekly infusions during the chemotherapy phase and once every three week dosing in the monotherapy period [see Clinical Studies (14.1)]. In BCIRG006, the toxicity profile was similar to that reported in Studies NSABP B31, NCCTG N9831, and HERA with the exception of a lower incidence of CHF in the TCH arm.
Metastatic Breast Cancer Studies
The safety of Herceptin was evaluated in one randomized, open-label study (H0648g) of chemotherapy with (n = 235) or without (n = 234) intravenous trastuzumab in patients with metastatic breast cancerand in one single-arm study (H0649g); in patients with metastatic breast cancer (n=222) [see Clinical Studies (14.1)]. Patients received 4 mg/kg initial dose of Herceptin followed by 2 mg/kg weekly. In H0648g, 58% of patients received Herceptin for ≥ 6 months and 9% received Herceptin ≥ 12 months, respectively. In H0649g, 31% of patients received Herceptin for ≥ 6 months and 16% received Herceptin for ≥ 12 months, respectively.
Table 4 shows the adverse reactions (≥ 5%) in patients from H0648g and H0649g.
| Herceptin*
n = 352 % | Herceptin + Paclitaxel n = 91 % | Paclitaxel n = 95 % | Herceptin + AC†
n = 143 % | AC†
n = 135 % | |
|---|---|---|---|---|---|
| General | |||||
| Pain | 47 | 61 | 62 | 57 | 42 |
| Asthenia | 42 | 62 | 57 | 54 | 55 |
| Fever | 36 | 49 | 23 | 56 | 34 |
| Chills | 32 | 41 | 4 | 35 | 11 |
| Headache | 26 | 36 | 28 | 44 | 31 |
| Abdominal pain | 22 | 34 | 22 | 23 | 18 |
| Back pain | 22 | 34 | 30 | 27 | 15 |
| Infection | 20 | 47 | 27 | 47 | 31 |
| Flu syndrome | 10 | 12 | 5 | 12 | 6 |
| Accidental injury | 6 | 13 | 3 | 9 | 4 |
| Allergic reaction | 3 | 8 | 2 | 4 | 2 |
| Gastrointestinal | |||||
| Nausea | 33 | 51 | 9 | 76 | 77 |
| Diarrhea | 25 | 45 | 29 | 45 | 26 |
| Vomiting | 23 | 37 | 28 | 53 | 49 |
| Anorexia | 14 | 24 | 16 | 31 | 26 |
| Nausea and vomiting | 8 | 14 | 11 | 18 | 9 |
| Respiratory | |||||
| Cough increased | 26 | 41 | 22 | 43 | 29 |
| Dyspnea | 22 | 27 | 26 | 42 | 25 |
| Rhinitis | 14 | 22 | 5 | 22 | 16 |
| Pharyngitis | 12 | 22 | 14 | 30 | 18 |
| Sinusitis | 9 | 21 | 7 | 13 | 6 |
| Skin | |||||
| Rash | 18 | 38 | 18 | 27 | 17 |
| Herpes simplex | 2 | 12 | 3 | 7 | 9 |
| Acne | 2 | 11 | 3 | 3 | < 1 |
| Nervous | |||||
| Insomnia | 14 | 25 | 13 | 29 | 15 |
| Dizziness | 13 | 22 | 24 | 24 | 18 |
| Paresthesia | 9 | 48 | 39 | 17 | 11 |
| Depression | 6 | 12 | 13 | 20 | 12 |
| Peripheral neuritis | 2 | 23 | 16 | 2 | 2 |
| Neuropathy | 1 | 13 | 5 | 4 | 4 |
| Metabolic | |||||
| Peripheral edema | 10 | 22 | 20 | 20 | 17 |
| Edema | 8 | 10 | 8 | 11 | 5 |
| Cardiovascular | |||||
| Congestive heart failure | 7 | 11 | 1 | 28 | 7 |
| Tachycardia | 5 | 12 | 4 | 10 | 5 |
| Musculoskeletal | |||||
| Bone pain | 7 | 24 | 18 | 7 | 7 |
| Arthralgia | 6 | 37 | 21 | 8 | 9 |
| Urogenital | |||||
| Urinary tract infection | 5 | 18 | 14 | 13 | 7 |
| Blood and Lymphatic | |||||
| Anemia | 4 | 14 | 9 | 36 | 26 |
| Leukopenia | 3 | 24 | 17 | 52 | 34 |
Metastatic Gastric Cancer
The safety of Herceptin was evaluated in patients with previously untreated for metastatic gastric or gastroesophageal junction adenocarcinoma in an open label, multi-center trial (ToGA) [see Clinical Studies (14.3)]. Patients were randomized (1:1) to receive Herceptin in combination with cisplatin and a fluoropyrimidine (FC+H) (n=294) or chemotherapy alone (FC) (n=290) Patients in the Herceptin plus chemotherapy arm received Herceptin 8 mg/kg administered on Day 1 (prior to chemotherapy) followed by 6 mg/kg every 21 days until disease progression. Cisplatin was administered at 80 mg/m2 on Day 1 and the fluoropyrimidine was administered as either capecitabine 1000 mg/m2 orally twice a day on Days 1–14 or 5-fluorouracil 800 mg/m2/day as a continuous intravenous infusion Days 1 through 5. Chemotherapy was administered for six 21-day cycles. Median duration of Herceptin treatment was 21 weeks and the median number of Herceptin infusions administered was eight.
| Adverse Reactions | Herceptin +FC (N = 294) % | FC (N = 290) % | ||
|---|---|---|---|---|
| All Grades | Grades 3-4 | All Grades | Grades 3-4 | |
| Investigations | ||||
| Neutropenia | 78 | 34 | 73 | 29 |
| Hypokalemia | 28 | 10 | 24 | 6 |
| Anemia | 28 | 12 | 21 | 10 |
| Thrombocytopenia | 16 | 5 | 11 | 3 |
| Blood and Lymphatic System Disorders | ||||
| Febrile Neutropenia | — | 5 | — | 3 |
| Gastrointestinal Disorders | ||||
| Diarrhea | 37 | 9 | 28 | 4 |
| Stomatitis | 24 | 1 | 15 | 2 |
| Dysphagia | 6 | 2 | 3 | < 1 |
| General | ||||
| Fatigue | 35 | 4 | 28 | 2 |
| Fever | 18 | 1 | 12 | 0 |
| Mucosal Inflammation | 13 | 2 | 6 | 1 |
| Chills | 8 | < 1 | 0 | 0 |
| Metabolism and Nutrition Disorders | ||||
| Weight Decrease | 23 | 2 | 14 | 2 |
| Infections and Infestations | ||||
| Upper Respiratory Tract Infections | 19 | 0 | 10 | 0 |
| Nasopharyngitis | 13 | 0 | 6 | 0 |
| Renal and Urinary Disorders | ||||
| Renal Failure and Impairment | 18 | 3 | 15 | 2 |
| Nervous System Disorders | ||||
| Dysgeusia | 10 | 0 | 5 | 0 |
The following subsections provide additional detail regarding adverse reactions observed in clinical trials of adjuvant breast cancer, metastatic breast cancer, metastatic gastric cancer, or post-marketing experience.
Cardiomyopathy
Serial measurement of cardiac function (LVEF) was obtained in clinical trials in the adjuvant treatment of breast cancer. In HERA, the median duration of follow-up was 12.6 months (12.4 months in the observation arm; 12.6 months in the 1-year Herceptin arm); and in NSABP B31 and NCCTG N9831, 7.9 years in the AC-T arm, 8.3 years in the AC-TH arm. Following initiation of Herceptin therapy, the incidence of new-onset dose-limiting myocardial dysfunction was higher among patients receiving Herceptin and paclitaxel as compared to those receiving paclitaxel alone in NSABP B31 and NCCTG N9831, and in patients receiving one-year Herceptin monotherapy compared to observation in HERA (see Table 6, Figures 1 and 2). The incidence of new-onset cardiac dysfunction, as measured by LVEF, remained similar when compared to the analysis performed at a median follow-up of 2.0 years in the AC-TH arm. This analysis showed evidence of reversibility of left ventricular dysfunction, with 64.5% of patients who experienced symptomatic CHF in the AC-TH group being asymptomatic at latest follow-up, and 90.3% having full or partial LVEF recovery.
| Study and Arm | LVEF < 50% and Decrease from Baseline | LVEF Decrease | |||
|---|---|---|---|---|---|
| LVEF < 50% | ≥ 10% decrease | ≥ 16% decrease | < 20% and ≥ 10% | ≥ 20% | |
| Studies 1 & 2† , ‡ | |||||
| AC→TH (n = 1856) | 23.1% (428) | 18.5% (344) | 11.2% (208) | 37.9% (703) | 8.9% (166) |
| AC→T (n = 1170) | 11.7% (137) | 7.0% (82) | 3.0% (35) | 22.1% (259) | 3.4% (40) |
| HERA§ | |||||
| Herceptin (n = 1678) | 8.6% (144) | 7.0% (118) | 3.8% (64) | 22.4% (376) | 3.5% (59) |
| Observation (n = 1708) | 2.7% (46) | 2.0% (35) | 1.2% (20) | 11.9% (204) | 1.2% (21) |
| BCIRG006¶ | |||||
| TCH (n = 1056) | 8.5% (90) | 5.9% (62) | 3.3% (35) | 34.5% (364) | 6.3% (67) |
| AC→TH (n = 1068) | 17% (182) | 13.3% (142) | 9.8% (105) | 44.3% (473) | 13.2% (141) |
| AC→T (n = 1050) | 9.5% (100) | 6.6% (69) | 3.3% (35) | 34% (357) | 5.5% (58) |
* For Studies 1, 2 and 3, events are counted from the beginning of Herceptin treatment. For BCIRG006, events are counted from the date of randomization.
† NSABP B31 and NCCTG N9831 regimens: doxorubicin and cyclophosphamide followed by paclitaxel (AC→T) or paclitaxel plus Herceptin (AC→TH).
‡ Median duration of follow-up for NSABP B31 and NCCTG N9831 combined was 8.3 years in the AC→TH arm.
§ Median follow-up duration of 12.6 months in the one-year Herceptin treatment arm.
¶ BCIRG006 regimens: doxorubicin and cyclophosphamide followed by docetaxel (AC→T) or docetaxel plus Herceptin (AC→TH); docetaxel and carboplatin plus Herceptin (TCH).
| Figure 1 NSABP B31 and NCCTG N9831: Cumulative Incidence of Time to First LVEF Decline of ≥ 10 Percentage Points from Baseline and to Below 50% with Death as a Competing Risk Event |
|
Time 0 is initiation of paclitaxel or Herceptin + paclitaxel therapy.
| Figure 2 HERA: Cumulative Incidence of Time to First LVEF Decline of ≥ 10 Percentage Points from Baseline and to Below 50% with Death as a Competing Risk Event |
|
Time 0 is the date of randomization.
| Figure 3 BCIRG006: Cumulative Incidence of Time to First LVEF Decline of ≥ 10 Percentage Points from Baseline and to Below 50% with Death as a Competing Risk Event |
|
Time 0 is the date of randomization.
The incidence of congestive heart failure among patients in the metastatic breast cancer trials was classified for severity using the New York Heart Association classification system (I–IV, where IV is the most severe level of cardiac failure) (see Table 2). In the metastatic breast cancer trials, the probability of cardiac dysfunction was highest in patients who received Herceptin concurrently with anthracyclines.
In ToGA, 5% of patients in the Herceptin plus chemotherapy arm compared to 1.1% of patients in the chemotherapy alone arm had LVEF value below 50% with a ≥ 10% absolute decrease in LVEF from pretreatment values.
Infusion Reactions
During the first infusion with Herceptin, the symptoms most commonly reported were chills and fever, occurring in approximately 40% of patients in clinical trials. Symptoms were treated with acetaminophen, diphenhydramine, and meperidine (with or without reduction in the rate of Herceptin infusion); permanent discontinuation of Herceptin for infusion reactions was required in < 1% of patients. Other signs and/or symptoms may include nausea, vomiting, pain (in some cases at tumor sites), rigors, headache, dizziness, dyspnea, hypotension, elevated blood pressure, rash, and asthenia. Infusion reactions occurred in 21% and 35% of patients, and were severe in 1.4% and 9% of patients, on second or subsequent Herceptin infusions administered as monotherapy or in combination with chemotherapy, respectively. In the post-marketing setting, severe infusion reactions, including hypersensitivity, anaphylaxis, and angioedema have been reported.
Anemia
In randomized controlled clinical trials, the overall incidence of anemia (30% vs. 21% [H0648g]), of selected NCI-CTC Grade 2–5 anemia (12.3% vs. 6.7% [NSABP B31]), and of anemia requiring transfusions (0.1% vs. 0 patients [NCCTG N9831]) were increased in patients receiving Herceptin and chemotherapy compared with those receiving chemotherapy alone. Following the administration of Herceptin as a single agent (H0649g), the incidence of NCI-CTC Grade 3 anemia was < 1%. In ToGA (metastatic gastric cancer), on the Herceptin containing arm as compared to the chemotherapy alone arm, the overall incidence of anemia was 28% compared to 21% and of NCI- CTC Grade 3/4 anemia was 12.2% compared to 10.3%.
Neutropenia
In randomized controlled clinical trials in the adjuvant setting, the incidence of selected NCI-CTC Grade 4–5 neutropenia (1.7% vs. 0.8% [NCCTG N9831]) and of selected Grade 2–5 neutropenia (6.4% vs. 4.3% [NSABP B31]) were increased in patients receiving Herceptin and chemotherapy compared with those receiving chemotherapy alone. In a randomized, controlled trial in patients with metastatic breast cancer, the incidences of NCI-CTC Grade 3/4 neutropenia (32% vs. 22%) and of febrile neutropenia (23% vs. 17%) were also increased in patients randomized to Herceptin in combination with myelosuppressive chemotherapy as compared to chemotherapy alone. In ToGA (metastatic gastric cancer) on the Herceptin containing arm as compared to the chemotherapy alone arm, the incidence of NCI-CTC Grade 3/4 neutropenia was 36.8% compared to 28.9%; febrile neutropenia 5.1% compared to 2.8%.
Infection
The overall incidences of infection (46% vs. 30% [H0648g]), of selected NCI-CTC Grade 2–5 infection/febrile neutropenia (24.3% vs. 13.4% [NSABP B31]) and of selected Grade 3–5 infection/febrile neutropenia (2.9% vs. 1.4% [NCCTG N9831]) were higher in patients receiving Herceptin and chemotherapy compared with those receiving chemotherapy alone. The most common site of infections in the adjuvant setting involved the upper respiratory tract, skin, and urinary tract.
In BCIRG006, the overall incidence of infection was higher with the addition of Herceptin to AC-T but not to TCH [44% (AC-TH), 37% (TCH), 38% (AC-T)]. The incidences of NCI-CTC Grade 3–4 infection were similar [25% (AC-TH), 21% (TCH), 23% (AC-T)] across the three arms.
In a randomized, controlled trial in treatment of metastatic breast cancer, the reported incidence of febrile neutropenia was higher (23% vs. 17%) in patients receiving Herceptin in combination with myelosuppressive chemotherapy as compared to chemotherapy alone.
Pulmonary Toxicity
Adjuvant Breast Cancer
Among women receiving adjuvant therapy for breast cancer, the incidence of selected NCI-CTC Grade 2–5 pulmonary toxicity (14.3% vs. 5.4% [NSABP B31]) and of selected NCI-CTC Grade 3–5 pulmonary toxicity and spontaneous reported Grade 2 dyspnea (3.4% vs. 0.9% [NCCTG N9831]) was higher in patients receiving Herceptin and chemotherapy compared with chemotherapy alone. The most common pulmonary toxicity was dyspnea (NCI-CTC Grade 2–5: 11.8% vs. 4.6% [NSABP B31]; NCI-CTC Grade 2–5: 2.4% vs. 0.2% [NCCTG N9831]).
Pneumonitis/pulmonary infiltrates occurred in 0.7% of patients receiving Herceptin compared with 0.3% of those receiving chemotherapy alone. Fatal respiratory failure occurred in 3 patients receiving Herceptin, one as a component of multi-organ system failure, as compared to 1 patient receiving chemotherapy alone.
In HERA, there were 4 cases of interstitial pneumonitis in the one-year Herceptin treatment arm compared to none in the observation arm at a median follow-up duration of 12.6 months.
Metastatic Breast Cancer
Among women receiving Herceptin for treatment of metastatic breast cancer, the incidence of pulmonary toxicity was also increased. Pulmonary adverse events have been reported in the post-marketing experience as part of the symptom complex of infusion reactions. Pulmonary events include bronchospasm, hypoxia, dyspnea, pulmonary infiltrates, pleural effusions, non-cardiogenic pulmonary edema, and acute respiratory distress syndrome. For a detailed description, see Warnings and Precautions (5.4).
Thrombosis/Embolism
In 4 randomized, controlled clinical trials, the incidence of thrombotic adverse events was higher in patients receiving Herceptin and chemotherapy compared to chemotherapy alone in three studies (2.6% vs. 1.5% [NSABP B31], 2.5% and 3.7% vs. 2.2% [BCIRG006] and 2.1% vs. 0% [H0648g]).
Diarrhea
Among women receiving adjuvant therapy for breast cancer, the incidence of NCI-CTC Grade 2–5 diarrhea (6.7% vs. 5.4% [NSABP B31]) and of NCI-CTC Grade 3–5 diarrhea (2.2% vs. 0% [NCCTG N9831]), and of Grade 1–4 diarrhea (7% vs. 1% [HERA; one-year Herceptin treatment at 12.6 months median duration of follow-up]) were higher in patients receiving Herceptin as compared to controls. In BCIRG006, the incidence of Grade 3–4 diarrhea was higher [5.7% AC-TH, 5.5% TCH vs. 3.0% AC-T] and of Grade 1–4 was higher [51% AC-TH, 63% TCH vs. 43% AC-T] among women receiving Herceptin. Of patients receiving Herceptin as a single agent for the treatment of metastatic breast cancer, 25% experienced diarrhea. An increased incidence of diarrhea was observed in patients receiving Herceptin in combination with chemotherapy for treatment of metastatic breast cancer.
Renal Toxicity
In ToGA (metastatic gastric cancer) on the Herceptin-containing arm as compared to the chemotherapy alone arm the incidence of renal impairment was 18% compared to 14.5%. Severe (Grade 3/4) renal failure was 2.7% on the Herceptin-containing arm compared to 1.7% on the chemotherapy only arm. Treatment discontinuation for renal insufficiency/failure was 2% on the Herceptin-containing arm and 0.3% on the chemotherapy only arm.
In the post-marketing setting, rare cases of nephrotic syndrome with pathologic evidence of glomerulopathy have been reported. The time to onset ranged from 4 months to approximately 18 months from initiation of Herceptin therapy. Pathologic findings included membranous glomerulonephritis, focal glomerulosclerosis, and fibrillary glomerulonephritis. Complications included volume overload and congestive heart failure.
The following adverse reactions have been identified during post-approval use of Herceptin. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.
Anthracyclines
Patients who receive anthracycline after stopping Herceptin may be at increased risk of cardiac dysfunction because of trastuzumab's estimated long washout period [see Clinical Pharmacology (12.3)]. If possible, avoid anthracycline-based therapy for up to 7 months after stopping Herceptin. If anthracyclines are used, closely monitor the patient's cardiac function.
If Herceptin is administered during pregnancy, or if a patient becomes pregnant while receiving Herceptin or within 7 months following the last dose of Herceptin, health care providers and patients should immediately report Herceptin exposure to Genentech at 1-888-835-2555.
Risk Summary
Herceptin can cause fetal harm when administered to a pregnant woman. In post-marketing reports and published literature, use of Herceptin during pregnancy resulted in cases of oligohydramnios and of oligohydramnios sequence, manifesting as pulmonary hypoplasia, skeletal abnormalities, and neonatal death [see Data]. Apprise the patient of the potential risks to a fetus. There are clinical considerations if Herceptin is used in a pregnant woman or if a patient becomes pregnant within 7 months following the last dose of Herceptin [see Clinical Considerations].
The background risk of major birth defects and miscarriage for the indicated population is unknown. In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2% to 4% and 15% to 20%, respectively.
Clinical Considerations
Fetal/Neonatal Adverse Reactions
Monitor women who received Herceptin during pregnancy or within 7 months prior to conception for oligohydramnios. If oligohydramnios occurs, perform fetal/neonatal testing that is appropriate for gestational age and consistent with community standards of care.
Data
Human Data
In post-marketing reports and published literature, use of Herceptin during pregnancy resulted in cases of oligohydramnios and of oligohydramnios sequence. Fetal manifestations included pulmonary hypoplasia, skeletal abnormalities, and neonatal death. These case reports described oligohydramnios in pregnant women who received Herceptin either alone or in combination with chemotherapy. In most reported cases, amniotic fluid index increased after Herceptin was stopped. In reported cases where Herceptin therapy was resumed after amniotic index improved, oligohydramnios recurred.
Animal Data
In studies where trastuzumab was administered to pregnant Cynomolgus monkeys during the period of organogenesis at doses up to 25 mg/kg given twice weekly (up to 25 times the recommended weekly human dose of 2 mg/kg), trastuzumab crossed the placental barrier during the early (Gestation Days 20 to 50) and late (Gestation Days 120 to 150) phases of gestation. The resulting concentrations of trastuzumab in fetal serum and amniotic fluid were approximately 33% and 25%, respectively, of those present in the maternal serum but were not associated with adverse developmental effects.
Risk Summary
There is no information regarding the presence of trastuzumab in human milk, the effects on the breastfed infant, or the effects on milk production. Published data suggest human IgG is present in human milk but does not enter the neonatal and infant circulation in substantial amounts. Trastuzumab was present in the milk of lactating Cynomolgus monkeys but not associated with neonatal toxicity [see Data]. Consider the developmental and health benefits of breastfeeding along with the mother's clinical need for Herceptin treatment and any potential adverse effects on the breastfed child from Herceptin or from the underlying maternal condition. This consideration should also take into account the trastuzumab wash out period of 7 months [see Clinical Pharmacology (12.3)].
Data
In lactating Cynomolgus monkeys, trastuzumab was present in breast milk at about 0.3% of maternal serum concentrations after pre- (beginning Gestation Day 120) and post-partum (through Post-partum Day 28) doses of 25 mg/kg administered twice weekly (25 times the recommended weekly human dose of 2 mg/kg of Herceptin). Infant monkeys with detectable serum levels of trastuzumab did not exhibit any adverse effects on growth or development from birth to 1 month of age.
Pregnancy Testing
Verify the pregnancy status of females of reproductive potential prior to the initiation of Herceptin.
Contraception
Females
Herceptin can cause embryo-fetal harm when administered during pregnancy. Advise females of reproductive potential to use effective contraception during treatment with Herceptin and for 7 months following the last dose of Herceptin [see Use in Specific Populations (8.1) and Clinical Pharmacology (12.3)].
The safety and effectiveness of Herceptin in pediatric patients have not been established.
Herceptin has been administered to 386 patients who were 65 years of age or over (253 in the adjuvant treatment and 133 in metastatic breast cancer treatment settings). The risk of cardiac dysfunction was increased in geriatric patients as compared to younger patients in both those receiving treatment for metastatic disease in H0648g and H0649g, or adjuvant therapy in NSABP B31 and NCCTG N9831. Limitations in data collection and differences in study design of the 4 studies of Herceptin in adjuvant treatment of breast cancer preclude a determination of whether the toxicity profile of Herceptin in older patients is different from younger patients. The reported clinical experience is not adequate to determine whether the efficacy improvements (ORR, TTP, OS, DFS) of Herceptin treatment in older patients is different from that observed in patients < 65 years of age for metastatic disease and adjuvant treatment.
In ToGA (metastatic gastric cancer), of the 294 patients treated with Herceptin, 108 (37%) were 65 years of age or older, while 13 (4.4%) were 75 and over. No overall differences in safety or effectiveness were observed.
Trastuzumab is a humanized IgG1 kappa monoclonal antibody that selectively binds with high affinity to the extracellular domain of the human epidermal growth factor receptor 2 protein, HER2. Trastuzumab is produced by recombinant DNA technology in a mammalian cell (Chinese Hamster Ovary) culture.
Herceptin (trastuzumab) for injection is a sterile, white to pale yellow, preservative-free lyophilized powder with a cake-like appearance, for intravenous administration.
Each single-dose vial of Herceptin delivers 150 mg trastuzumab, 136.2 mg α,α-trehalose dihydrate, 3.4 mg L-histidine HCl monohydrate, 2.2 mg L-histidine, and 0.6 mg polysorbate 20. Reconstitution with 7.4 mL of sterile water for injection (SWFI) yields a solution containing 21 mg/mL trastuzumab that delivers 7.15 mL (150 mg trastuzumab), at a pH of approximately 6.
The HER2 (or c-erbB2) proto-oncogene encodes a transmembrane receptor protein of 185 kDa, which is structurally related to the epidermal growth factor receptor. Herceptin has been shown, in both in vitro assays and in animals, to inhibit the proliferation of human tumor cells that overexpress HER2.
Herceptin is a mediator of antibody-dependent cellular cytotoxicity (ADCC). In vitro, Herceptin-mediated ADCC has been shown to be preferentially exerted on HER2 overexpressing cancer cells compared with cancer cells that do not overexpress HER2.
Herceptin exposure-response relationships and the time course of pharmacodynamic responses are not fully characterized.
Cardiac Electrophysiology
The effects of trastuzumab on electrocardiographic (ECG) endpoints, including QTc interval duration, were evaluated in patients with HER2 positive solid tumors. Trastuzumab had no clinically relevant effect on the QTc interval duration and there was no apparent relationship between serum trastuzumab concentrations and change in QTcF interval duration in patients with HER2 positive solid tumors.
The pharmacokinetics of trastuzumab was evaluated in a pooled population pharmacokinetic (PK) model analysis of 1,582 subjects with primarily breast cancer and metastatic gastric cancer (MGC) receiving intravenous Herceptin. Total trastuzumab clearance increases with decreasing concentrations due to parallel linear and non-linear elimination pathways.
Although the average trastuzumab exposure was higher following the first cycle in breast cancer patients receiving the once every three week schedule compared to the weekly schedule of Herceptin, the average steady-state exposure was essentially the same at both dosages. The average trastuzumab exposure following the first cycle and at steady state as well as the time to steady state was higher in breast cancer patients compared to MGC patients at the same dosage; however, the reason for this exposure difference is unknown. Additional predicted trastuzumab exposure and PK parameters following the first Herceptin cycle and at steady state exposure are described in Tables 7 and 8, respectively.
Population PK based simulations indicate that following discontinuation of Herceptin, concentrations in at least 95% of breast cancer and MGC patients will decrease to approximately 3% of the population predicted steady-state trough serum concentration (approximately 97% washout) by 7 months [see Warnings and Precautions (5.1) and Use in Specific Populations (8.1, 8.3)].
| Schedule | Primary tumor type | N | Cmin
(µg/mL) | Cmax
(µg/mL) | AUC0-21days
(µg.day/mL) |
|---|---|---|---|---|---|
| 8 mg/kg + 6 mg/kg q3w | Breast cancer | 1195 | 29.4 (5.8 - 59.5) | 178 (117 - 291) | 1373 (736 - 2245) |
| MGC | 274 | 23.1 (6.1 - 50.3) | 132 (84.2 - 225) | 1109 (588 - 1938) | |
| 4 mg/kg + 2 mg/kg qw | Breast cancer | 1195 | 37.7 (12.3 - 70.9) | 88.3 (58 - 144) | 1066 (586 - 1754) |
| Schedule | Primary tumor type | N | Cmin,ss
*
(µg/mL) | Cmax,ss
†
(µg/mL) | AUCss, 0-21 days
(µg.day/mL) | Time to steady-state (week) | Total CL range at steady-state (L/day) |
|---|---|---|---|---|---|---|---|
| 8 mg/kg + 6 mg/kg q3w | Breast cancer | 1195 | 47.4 (5 - 115) | 179 (107 - 309) | 1794 (673 - 3618) | 12 | 0.173 - 0.283 |
| MGC | 274 | 32.9 (6.1 - 88.9) | 131 (72.5 - 251) | 1338 (557 - 2875) | 9 | 0.189 - 0.337 | |
| 4 mg/kg + 2 mg/kg qw | Breast cancer | 1195 | 66.1 (14.9 - 142) | 109 (51.0 - 209) | 1765 (647 - 3578) | 12 | 0.201 - 0.244 |
Specific Populations
Based on a population pharmacokinetic analysis, no clinically significant differences were observed in the pharmacokinetics of trastuzumab based on age (< 65 (n = 1294); ≥ 65 (n = 288)), race (Asian (n = 264); non-Asian (n = 1324)) and renal impairment (mild (creatinine clearance [CLcr] 60 to 90 mL/min) (n = 636) or moderate (CLcr 30 to 60 mL/min) (n = 133)). The pharmacokinetics of trastuzumab in patients with severe renal impairment, end-stage renal disease with or without hemodialysis, or hepatic impairment is unknown.
Drug Interaction Studies
There have been no formal drug interaction studies performed with Herceptin in humans. Clinically significant interactions between Herceptin and concomitant medications used in clinical trials have not been observed.
Paclitaxel and doxorubicin: Concentrations of paclitaxel and doxorubicin and their major metabolites (i.e., 6-α hydroxyl-paclitaxel [POH], and doxorubicinol [DOL], respectively) were not altered in the presence of trastuzumab when used as combination therapy in clinical trials. Trastuzumab concentrations were not altered as part of this combination therapy.
Docetaxel and carboplatin: When Herceptin was administered in combination with docetaxel or carboplatin, neither the plasma concentrations of docetaxel or carboplatin nor the plasma concentrations of trastuzumab were altered.
Cisplatin and capecitabine: In a drug interaction substudy conducted in patients in ToGA, the pharmacokinetics of cisplatin, capecitabine and their metabolites were not altered when administered in combination with Herceptin.
The observed incidence of anti-drug antibodies is highly dependent on the sensitivity and specificity of the assay. Differences in assay methods preclude meaningful comparisons of the incidence of anti-drug antibodies in the studies described below with the incidence of anti-drug antibodies in other studies, including those of HERCEPTIN or of other trastuzumab products.
Among 903 women with metastatic breast cancer, human anti human antibody (HAHA) to Herceptin was detected in one patient using an enzyme linked immunosorbent assay (ELISA). This patient did not experience an allergic reaction. Samples for assessment of HAHA were not collected in studies of adjuvant breast cancer.
The clinical relevance of the development of anti-trastuzumab antibodies after treatment with HERCEPTIN is not known.
Herceptin has not been tested for carcinogenic potential.
No evidence of mutagenic activity was observed when trastuzumab was tested in the standard Ames bacterial and human peripheral blood lymphocyte mutagenicity assays at concentrations of up to 5000 mcg/mL. In an in vivo micronucleus assay, no evidence of chromosomal damage to mouse bone marrow cells was observed following bolus intravenous doses of up to 118 mg/kg of trastuzumab.
A fertility study was conducted in female Cynomolgus monkeys at doses up to 25 times the weekly recommended human dose of 2 mg/kg of trastuzumab and has revealed no evidence of impaired fertility, as measured by menstrual cycle duration and female sex hormone levels.
The safety and efficacy of Herceptin in women receiving adjuvant chemotherapy for HER2 overexpressing breast cancer were evaluated in an integrated analysis of two randomized, open-label, clinical trials (NSABP B31 and NCCTG N9831) with a total of 4063 women at the protocol-specified final overall survival analysis, a third randomized, open-label, clinical trial (HERA) with a total of 3386 women at definitive Disease-Free Survival analysis for one-year Herceptin treatment versus observation, and a fourth randomized, open-label clinical trial with a total of 3222 patients (BCIRG006).
NSABP B31 and NCCTG N9831
In NSABP B31 and NCCTG N9831, breast tumor specimens were required to show HER2 overexpression (3+ by IHC) or gene amplification (by FISH). HER2 testing was verified by a central laboratory prior to randomization (NCCTG N9831) or was required to be performed at a reference laboratory (NSABP B31). Patients with a history of active cardiac disease based on symptoms, abnormal electrocardiographic, radiologic, or left ventricular ejection fraction findings or uncontrolled hypertension (diastolic > 100 mm Hg or systolic > 200 mm Hg) were not eligible.
Patients were randomized (1:1) to receive doxorubicin and cyclophosphamide followed by paclitaxel (AC→paclitaxel) alone or paclitaxel plus Herceptin (AC→paclitaxel + Herceptin). In both trials, patients received four 21-day cycles of doxorubicin 60 mg/m2 and cyclophosphamide 600 mg/m2. Paclitaxel was administered either weekly (80 mg/m2) or every 3 weeks (175 mg/m2) for a total of 12 weeks in NSABP B31; paclitaxel was administered only by the weekly schedule in NCCTG N9831. Herceptin was administered at 4 mg/kg on the day of initiation of paclitaxel and then at a dose of 2 mg/kg weekly for a total of 52 weeks. Herceptin treatment was permanently discontinued in patients who developed congestive heart failure, or persistent/recurrent LVEF decline [see Dosage and Administration (2.5)]. Radiation therapy, if administered, was initiated after the completion of chemotherapy. Patients with ER+ and/or PR+ tumors received hormonal therapy. The major efficacy outcome measure of the combined efficacy analysis was Disease-Free Survival (DFS), defined as the time from randomization to recurrence, occurrence of contralateral breast cancer, other second primary cancer, or death. An additional efficacy outcome measure was overall survival (OS).
A total of 3752 patients were included in the joint efficacy analysis of DFS following a median follow-up of 2.0 years in the AC→paclitaxel + Herceptin arm. The pre-planned final OS analysis from the joint analysis included 4063 patients and was performed when 707 deaths had occurred after a median follow-up of 8.3 years in the AC→paclitaxel + Herceptin arm. The data from both arms in NSABP B31 and two of the three study arms in NCCTG N9831 were pooled for efficacy analyses.
The patients included in the DFS analysis had a median age of 49 years (range, 22–80 years; 6% > 65 years), 84% were White, 7% Black, 4% Hispanic, and 4% Asian/Pacific Islander. Disease characteristics included 90% infiltrating ductal histology, 38% T1, 91% nodal involvement, 27% intermediate and 66% high grade pathology, and 53% ER+ and/or PR+ tumors.
HERA
In HERA, breast tumor specimens were required to show HER2 overexpression (3+ by IHC) or gene amplification (by FISH) as determined at a central laboratory. Patients with node-negative disease were required to have ≥ T1c primary tumor. Patients with a history of congestive heart failure or LVEF < 55%, uncontrolled arrhythmias, angina requiring medication, clinically significant valvular heart disease, evidence of transmural infarction on ECG, poorly controlled hypertension (systolic > 180 mm Hg or diastolic > 100 mm Hg) were not eligible.
Patients were randomized (1:1:1) upon completion of definitive surgery, and at least four cycles of chemotherapy to receive no additional treatment, or one year of Herceptin treatment or two years of Herceptin treatment. Patients undergoing a lumpectomy had also completed standard radiotherapy. Patients with ER+ and/or PgR+ disease received systemic adjuvant hormonal therapy at investigator discretion. Herceptin was administered with an initial dose of 8 mg/kg followed by subsequent doses of 6 mg/kg once every three weeks. The major efficacy outcome measure was Disease-Free Survival (DFS), defined as in NSABP B31 and NCCTG N9831.
HERA was designed to compare one and two years of once every three week Herceptin treatment versus observation in patients with HER2 positive EBC following surgery, established chemotherapy and radiotherapy (if applicable). A protocol specified interim efficacy analysis comparing one-year Herceptin treatment to observation was performed at a median follow-up duration of 12.6 months in the Herceptin arm.
Among the 3386 patients randomized to the observation (n = 1693) and Herceptin one-year (n = 1693) treatment arms, the median age was 49 years (range 21–80), 83% were White, and 13% were Asian. Disease characteristics: 94% infiltrating ductal carcinoma, 50% ER+ and/or PgR+, 57% node positive, 32% node negative, and in 11% of patients, nodal status was not assessable due to prior neo-adjuvant chemotherapy. Ninety-six percent (1055/1098) of patients with node-negative disease had high-risk features: among the 1098 patients with node-negative disease, 49% (543) were ER– and PgR–, and 47% (512) were ER and/or PgR+ and had at least one of the following high-risk features: pathological tumor size greater than 2 cm, Grade 2–3, or age < 35 years. Prior to randomization, 94% of patients had received anthracycline-based chemotherapy regimens.
After the DFS results comparing observation to one-year Herceptin treatment were disclosed, a prospectively planned analysis that included comparison of one year versus two years of Herceptin treatment at a median follow-up duration of 8 years was performed. Based on this analysis, extending Herceptin treatment for a duration of two years did not show additional benefit over treatment for one year [Hazard Ratios of two-years Herceptin versus one-year Herceptin treatment in the intent to treat (ITT) population for Disease-Free Survival (DFS) = 0.99 (95% CI: 0.87, 1.13), p-value = 0.90 and Overall Survival (OS) = 0.98 (0.83, 1.15); p-value = 0.78].
BCIRG006
In BCIRG006, breast tumor specimens were required to show HER2 gene amplification (FISH+ only) as determined at a central laboratory. Patients were required to have either node-positive disease, or node-negative disease with at least one of the following high-risk features: ER/PR-negative, tumor size > 2 cm, age < 35 years, or histologic and/or nuclear Grade 2 or 3. Patients with a history of CHF, myocardial infarction, Grade 3 or 4 cardiac arrhythmia, angina requiring medication, clinically significant valvular heart disease, poorly controlled hypertension (diastolic > 100 mm Hg), any T4 or N2, or known N3 or M1 breast cancer were not eligible.
Patients were randomized (1:1:1) to receive doxorubicin and cyclophosphamide followed by docetaxel (AC-T), doxorubicin and cyclophosphamide followed by docetaxel plus Herceptin (AC-TH), or docetaxel and carboplatin plus Herceptin (TCH). In both the AC-T and AC-TH arms, doxorubicin 60 mg/m2 and cyclophosphamide 600 mg/m2 were administered every 3 weeks for four cycles; docetaxel 100 mg/m2 was administered every 3 weeks for four cycles. In the TCH arm, docetaxel 75 mg/m2 and carboplatin (at a target AUC of 6 mg/mL/min as a 30- to 60-minute infusion) were administered every 3 weeks for six cycles. Herceptin was administered weekly (initial dose of 4 mg/kg followed by weekly dose of 2 mg/kg) concurrently with either T or TC, and then every 3 weeks (6 mg/kg) as monotherapy for a total of 52 weeks. Radiation therapy, if administered, was initiated after completion of chemotherapy. Patients with ER+ and/or PR+ tumors received hormonal therapy. Disease-Free Survival (DFS) was the major efficacy outcome measure.
Among 3222 patients, the median age was 49 (range 22 to 74 years; 6% ≥ 65 years). Disease characteristics included 54% ER+ and/or PR+ and 71% node positive. Prior to randomization, all patients underwent primary surgery for breast cancer.
The results for DFS for the integrated analysis of NSABP B31 and NCCTG N9831, HERA, and BCIRG006 and OS results for the integrated analysis of NSABP B31 and NCCTG N9831, and HERA are presented in Table 9. For NSABP B31 and NCCTG N9831, the duration of DFS following a median follow-up of 2.0 years in the AC→TH arm is presented in Figure 4, and the duration of OS after a median follow-up of 8.3 years in the AC→TH arm is presented in Figure 5. The duration of DFS for BCIRG006 is presented in Figure 6. For NSABP B31 and NCCTG N9831, the OS hazard ratio was 0.64 (95% CI: 0.55, 0.74). At 8.3 years of median follow-up [AC→TH], the survival rate was estimated to be 86.9% in the AC→TH arm and 79.4% in the AC→T arm. The final OS analysis results from NSABP B31 and NCCTG N9831 indicate that OS benefit by age, hormone receptor status, number of positive lymph nodes, tumor size and grade, and surgery/radiation therapy was consistent with the treatment effect in the overall population. In patients ≤ 50 years of age (n = 2197), the OS hazard ratio was 0.65 (95% CI: 0.52, 0.81) and in patients > 50 years of age (n = 1866), the OS hazard ratio was 0.63 (95% CI: 0.51, 0.78). In the subgroup of patients with hormone receptor-positive disease (ER-positive and/or PR-positive) (n = 2223), the hazard ratio for OS was 0.63 (95% CI: 0.51, 0.78). In the subgroup of patients with hormone receptor-negative disease (ER-negative and PR-negative) (n = 1830), the hazard ratio for OS was 0.64 (95% CI: 0.52, 0.80). In the subgroup of patients with tumor size ≤ 2 cm (n = 1604), the hazard ratio for OS was 0.52 (95% CI: 0.39, 0.71). In the subgroup of patients with tumor size > 2 cm (n = 2448), the hazard ratio for OS was 0.67 (95% CI: 0.56, 0.80).
| DFS events | DFS Hazard ratio (95% CI) p-value | Deaths (OS events) | OS Hazard ratio p-value | |
|---|---|---|---|---|
| CI = confidence interval. | ||||
| NSABP B31 and NCCTG N9831* | ||||
| AC→TH (n = 1872)† (n = 2031)‡ | 133† | 0.48†
,
§
(0.39, 0.59) p< 0.0001¶ | 289‡ | 0.64‡
,
§
(0.55, 0.74) p< 0.0001¶ |
| AC→T (n = 1880)† (n = 2032)‡ | 261† | 418‡ | ||
| HERA# | ||||
| Chemo→ Herceptin (n = 1693) | 127 | 0.54 (0.44, 0.67) p< 0.0001♠ | 31 | 0.75 p = NS♥ |
| Chemo→ Observation (n = 1693) | 219 | 40 | ||
| BCIRG006♦ | ||||
| TCH (n = 1075) | 134 | 0.67 (0.54 – 0.84) p=0.0006¶ , ♣ | 56 | |
| AC→TH (n = 1074) | 121 | 0.60 (0.48 – 0.76) p< 0.0001¶ , ♦ | 49 | |
| AC→T (n = 1073) | 180 | 80 | ||
* NSABP B31 and NCCTG N9831 regimens: doxorubicin and cyclophosphamide followed by paclitaxel (AC→T) or paclitaxel plus Herceptin (AC→TH).
† Efficacy evaluable population, for the primary DFS analysis, following a median follow-up of 2.0 years in the AC→TH arm.
‡ Efficacy evaluable population, for the final OS analysis, following 707 deaths (8.3 years of median follow-up in the AC→TH arm).
§ Hazard ratio estimated by Cox regression stratified by clinical trial, intended paclitaxel schedule, number of positive nodes, and hormone receptor status.
¶ stratified log-rank test.
# At definitive DFS analysis with median duration of follow-up of 12.6 months in the one-year Herceptin treatment arm.
♠ log-rank test.
♥ NS = non-significant.
♦ BCIRG006 regimens: doxorubicin and cyclophosphamide followed by docetaxel (AC→T) or docetaxel plus Herceptin (AC→TH); docetaxel and carboplatin plus Herceptin (TCH).
♣ A two-sided alpha level of 0.025 for each comparison.
|
|
|
Exploratory analyses of DFS as a function of HER2 overexpression or gene amplification were conducted for patients in Studies 2 and 3, where central laboratory testing data were available. The results are shown in Table 10. The number of events in NCCTG N9831 was small with the exception of the IHC 3+/FISH+ subgroup, which constituted 81% of those with data. Definitive conclusions cannot be drawn regarding efficacy within other subgroups due to the small number of events. The number of events in HERA was adequate to demonstrate significant effects on DFS in the IHC 3+/FISH unknown and the FISH+/IHC unknown subgroups.
| NCCTG N9831 | HERA* | |||
|---|---|---|---|---|
| HER2 Assay Result† | Number of Patients | Hazard Ratio DFS (95% CI) | Number of Patients | Hazard Ratio DFS (95% CI) |
| IHC 3+ | ||||
| FISH (+) | 1170 | 0.42 (0.27, 0.64) | 91 | 0.56 (0.13, 2.50) |
| FISH (-) | 51 | 0.71 (0.04, 11.79) | 8 | — |
| FISH Unknown | 51 | 0.69 (0.09, 5.14) | 2258 | 0.53 (0.41, 0.69) |
| IHC < 3+ / FISH (+) | 174 | 1.01 (0.18, 5.65) | 299‡ | 0.53 (0.20, 1.42) |
| IHC unknown / FISH (+) | — | — | 724 | 0.59 (0.38, 0.93) |
The safety and efficacy of Herceptin in treatment of women with metastatic breast cancer were studied in a randomized, controlled clinical trial in combination with chemotherapy (H0648g, n = 469 patients) and an open-label, single agent clinical trial (H0649g, n = 222 patients). Both trials studied patients with metastatic breast cancer whose tumors overexpress the HER2 protein. Patients were eligible if they had 2 or 3 levels of overexpression (based on a 0 to 3 scale) by immunohistochemical assessment of tumor tissue performed by a central testing lab.
Previously Untreated Metastatic Breast Cancer (H0648g)
H0648g was a multicenter, randomized, open-label clinical trial conducted in 469 women with metastatic breast cancer who had not been previously treated with chemotherapy for metastatic disease. Tumor specimens were tested by IHC (Clinical Trial Assay, CTA) and scored as 0, 1+, 2+, or 3+, with 3+ indicating the strongest positivity. Only patients with 2+ or 3+ positive tumors were eligible (about 33% of those screened). Patients were randomized to receive chemotherapy alone or in combination with Herceptin given intravenously as a 4 mg/kg loading dose followed by weekly doses of Herceptin at 2 mg/kg. For those who had received prior anthracycline therapy in the adjuvant setting, chemotherapy consisted of paclitaxel (175 mg/m2 over 3 hours every 21 days for at least six cycles); for all other patients, chemotherapy consisted of anthracycline plus cyclophosphamide (AC: doxorubicin 60 mg/m2 or epirubicin 75 mg/m2 plus 600 mg/m2 cyclophosphamide every 21 days for six cycles). Sixty-five percent of patients randomized to receive chemotherapy alone in this study received Herceptin at the time of disease progression as part of a separate extension study.
Based upon the determination by an independent response evaluation committee, the patients randomized to Herceptin and chemotherapy experienced a significantly longer median time to disease progression (TTP), a higher overall response rate (ORR), and a longer median duration of response (DoR) as compared with patients randomized to chemotherapy alone. Patients randomized to Herceptin and chemotherapy also had a longer median overall survival (OS) (see Table 11). These treatment effects were observed both in patients who received Herceptin plus paclitaxel and in those who received Herceptin plus AC; however, the magnitude of the effects was greater in the paclitaxel subgroup.
| Combined Results | Paclitaxel Subgroup | AC* Subgroup | ||||
|---|---|---|---|---|---|---|
| Herceptin + All Chemotherapy (n = 235) | All Chemotherapy (n = 234) | Herceptin + Paclitaxel (n = 92) | Paclitaxel (n = 96) | Herceptin + AC*
(n = 143) | AC*
(n = 138) | |
| Time to Disease Progression (TTP) | ||||||
| Median (months)† , ‡ | 7.2 | 4.5 | 6.7 | 2.5 | 7.6 | 5.7 |
| 95% CI | 7, 8 | 4, 5 | 5, 10 | 2, 4 | 7, 9 | 5, 7 |
| p-value§ | < 0.0001 | < 0.0001 | 0.002 | |||
| Overall Response Rate (ORR)† | ||||||
| Events (n) | 45 | 29 | 38 | 15 | 50 | 38 |
| 95% CI | 39, 51 | 23, 35 | 28, 48 | 8, 22 | 42, 58 | 30, 46 |
| p-value¶ | < 0.001 | < 0.001 | 0.10 | |||
| Duration of Response (DoR) | ||||||
| Median (months) † , ‡ | 8.3 | 5.8 | 8.3 | 4.3 | 8.4 | 6.4 |
| 25%, 75% Quartile | 6, 15 | 4, 8 | 5, 11 | 4, 7 | 6, 15 | 4, 8 |
| Overall Survival (OS) | ||||||
| Median (months)‡ | 25.1 | 20.3 | 22.1 | 18.4 | 26.8 | 21.4 |
| 95% CI | 22, 30 | 17, 24 | 17, 29 | 13, 24 | 23, 33 | 18, 27 |
| p-value§ | 0.05 | 0.17 | 0.16 | |||
* AC = Anthracycline (doxorubicin or epirubicin) and cyclophosphamide
† Assessed by an independent Response Evaluation Committee
‡ Kaplan-Meier Estimate
§ log-rank test
¶ χ2-test.
Data from H0648g suggest that the beneficial treatment effects were largely limited to patients with the highest level of HER2 protein overexpression (3+) (see Table 12).
| HER2 Assay Result | Number of Patients (N) | Relative Risk* for Time to Disease Progression (95% CI) | Relative Risk* for Mortality (95% CI) |
|---|---|---|---|
| CTA 2+ or 3+ | 469 | 0.49 (0.40, 0.61) | 0.80 (0.64, 1.00) |
| FISH (+)† | 325 | 0.44 (0.34, 0.57) | 0.70 (0.53, 0.91) |
| FISH (–)† | 126 | 0.62 (0.42, 0.94) | 1.06 (0.70, 1.63) |
| CTA 2+ | 120 | 0.76 (0.50, 1.15) | 1.26 (0.82, 1.94) |
| FISH (+) | 32 | 0.54 (0.21, 1.35) | 1.31 (0.53, 3.27) |
| FISH (–) | 83 | 0.77 (0.48, 1.25) | 1.11 (0.68, 1.82) |
| CTA 3+ | 349 | 0.42 (0.33, 0.54) | 0.70 (0.51, 0.90) |
| FISH (+) | 293 | 0.42 (0.32, 0.55) | 0.67 (0.51, 0.89) |
| FISH (–) | 43 | 0.43 (0.20, 0.94) | 0.88 (0.39, 1.98) |
Previously Treated Metastatic Breast Cancer (H0649g)
Herceptin was studied as a single agent in a multicenter, open-label, single-arm clinical trial (H0649g) in patients with HER2 overexpressing metastatic breast cancer who had relapsed following one or two prior chemotherapy regimens for metastatic disease. Of 222 patients enrolled, 66% had received prior adjuvant chemotherapy, 68% had received two prior chemotherapy regimens for metastatic disease, and 25% had received prior myeloablative treatment with hematopoietic rescue. Patients were treated with a loading dose of 4 mg/kg IV followed by weekly doses of Herceptin at 2 mg/kg IV.
The ORR (complete response + partial response), as determined by an independent Response Evaluation Committee, was 14%, with a 2% complete response rate and a 12% partial response rate. Complete responses were observed only in patients with disease limited to skin and lymph nodes. The overall response rate in patients whose tumors tested as CTA 3+ was 18% while in those that tested as CTA 2+, it was 6%.
The safety and efficacy of Herceptin in combination with cisplatin and a fluoropyrimidine (capecitabine or 5-fluorouracil) were studied in patients previously untreated for metastatic gastric or gastroesophageal junction adenocarcinoma (ToGA). In this open-label, multi-center trial, 594 patients were randomized 1:1 to Herceptin in combination with cisplatin and a fluoropyrimidine (FC+H) or chemotherapy alone (FC). Randomization was stratified by extent of disease (metastatic vs. locally advanced), primary site (gastric vs. gastroesophageal junction), tumor measurability (yes vs. no), ECOG performance status (0,1 vs. 2), and fluoropyrimidine (capecitabine vs. 5-fluorouracil). All patients were either HER2 gene amplified (FISH+) or HER2 overexpressing (IHC 3+). Patients were also required to have adequate cardiac function (e.g., LVEF > 50%).
On the Herceptin-containing arm, Herceptin was administered as an IV infusion at an initial dose of 8 mg/kg followed by 6 mg/kg every 3 weeks until disease progression. On both study arms cisplatin was administered at a dose of 80 mg/m2 Day 1 every 3 weeks for 6 cycles as a 2 hour IV infusion. On both study arms, capecitabine was administered at 1000 mg/m2 dose orally twice daily (total daily dose 2000 mg/m2) for 14 days of each 21 day cycle for 6 cycles. Alternatively, continuous intravenous infusion (CIV) 5-fluorouracil was administered at a dose of 800 mg/m2/day from Day 1 through Day 5 every three weeks for 6 cycles.
The median age of the study population was 60 years (range: 21–83); 76% were male; 53% were Asian, 38% Caucasian, 5% Hispanic, 5% other racial/ethnic groups; 91% had ECOG PS of 0 or 1; 82% had primary gastric cancer and 18% had primary gastroesophageal adenocarcinoma. Of these patients, 23% had undergone prior gastrectomy, 7% had received prior neoadjuvant and/or adjuvant therapy, and 2% had received prior radiotherapy.
The main outcome measure of ToGA was overall survival (OS), analyzed by the unstratified log-rank test. The final OS analysis based on 351 deaths was statistically significant (nominal significance level of 0.0193). An updated OS analysis was conducted at one year after the final analysis. The efficacy results of both the final and the updated analyses are summarized in Table 13 and Figure 7.
| FC* + Herceptin Arm N = 298 | FC* Arm N = 296 | |
|---|---|---|
| Overall Survival (interim analysis) | ||
| N (%) | 167 (56.0%) | 184 (62.2%) |
| Median (months) | 13.5 | 11.0 |
| 95% CI | (11.7, 15.7) | (9.4, 12.5) |
| Hazard Ratio | 0.73 | |
| 95% CI | (0.60, 0.91) | |
| p-value† | 0.0038 | |
| Overall Survival (updated) | ||
| N (%) | 221 (74.2%) | 227 (76.7%) |
| Median (months) | 13.1 | 11.7 |
| 95% CI | (11.9, 15.1) | (10.3, 13.0) |
| Hazard Ratio | 0.80 | |
| 95% CI | (0.67, 0.97) | |
* FC = capecitabine vs. 5-fluorouracil
† Two sided p-value comparing with the nominal significance level of 0.0193.
|
An exploratory analysis of OS in patients based on HER2 gene amplification (FISH) and protein overexpression (IHC) testing is summarized in Table 14.
| FC (N = 296)* | FC+H (N = 298)† | |
|---|---|---|
| FISH+ / IHC 0, 1+ subgroup (N=133) | ||
| No. Deaths / n (%) | 57/71 (80%) | 56/62 (90%) |
| Median OS Duration (mos.) | 8.8 | 8.3 |
| 95% CI (mos.) | (6.4, 11.7) | (6.2, 10.7) |
| Hazard ratio (95% CI) | 1.33 (0.92, 1.92) | |
| FISH+ / IHC2+ subgroup (N=160) | ||
| No. Deaths / n (%) | 65/80 (81%) | 64/80 (80%) |
| Median OS Duration (mos.) | 10.8 | 12.3 |
| 95% CI (mos.) | (6.8, 12.8) | (9.5, 15.7) |
| Hazard ratio (95% CI) | 0.78 (0.55, 1.10) | |
| FISH+ or FISH- / IHC3+‡ subgroup (N=294) | ||
| No. Deaths / n (%) | 104/143 (73%) | 96/151 (64%) |
| Median OS Duration (mos.) | 13.2 | 18.0 |
| 95% CI (mos.) | (11.5, 15.2) | (15.5, 21.2) |
| Hazard ratio (95% CI) | 0.66 (0.50, 0.87) | |
* Two patients on the FC arm who were FISH+ but IHC status unknown were excluded from the exploratory subgroup analyses.
† Five patients on the Herceptin-containing arm who were FISH+, but IHC status unknown were excluded from the exploratory subgroup analyses.
‡ Includes 6 patients on chemotherapy arm, 10 patients on Herceptin arm with FISH–, IHC3+ and 8 patients on chemotherapy arm, 8 patients on Herceptin arm with FISH status unknown, IHC 3+.
150 mg Single-dose vial
Herceptin (trastuzumab) for injection 150 mg/vial is supplied in a single-dose vial as a preservative-free, white to pale yellow lyophilized sterile powder, under vacuum. Available in a carton containing one single-dose vial (NDC 50242-132-01) and a carton containing 10 single-dose vials (NDC 50242-132-10).
Store Herceptin vials in the refrigerator at 2°C to 8°C (36°F to 46°F) until time of reconstitution.
Cardiomyopathy
Embryo-Fetal Toxicity
HERCEPTIN® [trastuzumab]
Manufactured by:
Genentech, Inc.
A Member of the Roche Group
1 DNA Way
South San Francisco, CA 94080-4990
US License No.1048
Herceptin® is a registered trademark of Genentech, Inc.
©2026 Genentech, Inc.
NDC 50242-132-01
Herceptin®
trastuzumab
For Injection
150 mg per vial
For Intravenous Infusion
After Reconstitution.
Single-Dose Vial.
Discard Unused Portion.
No preservative.
KEEP REFRIGERATED
Genentech
Rx only
10187107
| Class | Version | Type | Effective |
|---|---|---|---|
| TRASTUZUMAB Pharmacologic Class Indexing | 3 | Indexing - Pharmacologic Class | 20180813 |
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| bd11614e-4776-4a92-aaca-2bcbb5f710ed | Product name | 1 | 20210115 |
| b914e981-d6dc-4748-bd51-accd6b85b817 | Product name | 1 | 20190618 |
| 9397f6d4-17a1-42b4-beda-fa2c0ea40c8c | Product name | 1 | 20190610 |
| 0ca1d589-929b-4b33-bc5b-1d84abdafa6a | Product name | 1 | 20150324 |
| fc363c46-397b-4476-ac0f-70e43e8e4592 | Product name | 1 | 20150324 |
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 50242-132-01 | EA - Each | 50242-132 | 57463a6f-9e34-44d8-8fc7-5785545ee60a | 1 | 2017-06-15 |
| 50242-132-10 | EA - Each | 50242-132 | 7208e0ba-85f6-4923-91ba-0c850b304599 | 1 | 2019-06-19 |
| Product | Base substance | Indexed substance code | Indexed substance | Application | Indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|---|---|
| OGIVRI | TRASTUZUMAB | P188ANX8CK-DKST-01 | trastuzumab-dkst | BLA761074 | 23350e95-44fb-4806-a16d-566522d2298e | 1 | 2017-12-01 |
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| TRASTUZUMAB | ACTIVE INGREDIENT | P188ANX8CK | 7 | |
| TRASTUZUMAB | ACTIVE MOIETY | P188ANX8CK | 7 | |
| BENZYL ALCOHOL | INACTIVE INGREDIENT | LKG8494WBH | 7 | |
| HISTIDINE | INACTIVE INGREDIENT | 4QD397987E | 7 | |
| HISTIDINE MONOHYDROCHLORIDE | INACTIVE INGREDIENT | 1D5Q932XM6 | 7 | |
| POLYSORBATE 20 | INACTIVE INGREDIENT | 7T1F30V5YH | 7 | |
| TREHALOSE DIHYDRATE | INACTIVE INGREDIENT | 7YIN7J07X4 | 7 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 50242-132 | 50242-132-01 |
| BLA | Proprietary name | Proper name | License type | Status | Latest source |
|---|---|---|---|---|---|
| 103792 | Herceptin | trastuzumab | 351(a) | Disc* | 2026-09-01 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| TRASTUZUMAB | P188ANX8CK | ACTIB |
| HISTIDINE HYDROCHLORIDE MONOHYDRATE | X573657P6P | IACT |
| HISTIDINE | 4QD397987E | IACT |
| TREHALOSE DIHYDRATE | 7YIN7J07X4 | IACT |
| POLYSORBATE 20 | 7T1F30V5YH | IACT |
| Version | Effective date | Source | Hydrated |
|---|---|---|---|
| 26 | 2024-11-18 | full-release | 2026-05-31 21:17:39 |
Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| POLYSORBATE 20 | POLYSORBATE 20 | 7T1F30V5YH | INJECTION, POWDER, FOR SOLUTION / INTRAVENOUS | NA | ||
| HISTIDINE | HISTIDINE | 4QD397987E | INJECTION / INTRAVENOUS | 465 mg | ||
| BENZYL ALCOHOL | BENZYL ALCOHOL | LKG8494WBH | INJECTION, SOLUTION / INTRAVENOUS | 400 mg | ||
| BENZYL ALCOHOL | BENZYL ALCOHOL | LKG8494WBH | LIQUID / INTRAVENOUS | 1.04 %w/v | ||
| BENZYL ALCOHOL | BENZYL ALCOHOL | LKG8494WBH | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRACAVITARY | 8.4 mg | ||
| HISTIDINE | HISTIDINE | 4QD397987E | INJECTION, SUSPENSION, LIPOSOMAL / INTRAVENOUS | 0.16 %w/v | ||
| HISTIDINE | HISTIDINE | 4QD397987E | INJECTION / INTRAVENOUS | 465 mg | ||
| BENZYL ALCOHOL | BENZYL ALCOHOL | LKG8494WBH | INJECTION / INTRAVENOUS | 1620 mg | ||
| POLYSORBATE 20 | POLYSORBATE 20 | 7T1F30V5YH | INJECTION, POWDER, FOR SOLUTION / INTRAVENOUS | NA | ||
| HISTIDINE | HISTIDINE | 4QD397987E | INJECTION, SUSPENSION, LIPOSOMAL / INTRAVENOUS | 0.16 %w/v | ||
| TREHALOSE DIHYDRATE | TREHALOSE DIHYDRATE | 7YIN7J07X4 | INJECTION, POWDER, FOR SOLUTION / INTRADERMAL | 4 mg | ||
| TREHALOSE DIHYDRATE | TREHALOSE DIHYDRATE | 7YIN7J07X4 | INJECTION, SOLUTION / SUBCUTANEOUS | 22 mg | ||
| HISTIDINE | HISTIDINE | 4QD397987E | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / SUBCUTANEOUS | 3.88 mg | ||
| BENZYL ALCOHOL | BENZYL ALCOHOL | LKG8494WBH | LIQUID / INTRAVENOUS | 1.04 %w/v | ||
| TREHALOSE DIHYDRATE | TREHALOSE DIHYDRATE | 7YIN7J07X4 | INJECTION, POWDER, FOR SOLUTION / INTRADERMAL | 4 mg | ||
| BENZYL ALCOHOL | BENZYL ALCOHOL | LKG8494WBH | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRACAVERNOUS | 18 mg | ||
| BENZYL ALCOHOL | BENZYL ALCOHOL | LKG8494WBH | INJECTION, EMULSION / INTRAVENOUS | 45 mg | ||
| BENZYL ALCOHOL | BENZYL ALCOHOL | LKG8494WBH | SOLUTION / INTRAVENOUS | 242 mg | ||
| HISTIDINE | HISTIDINE | 4QD397987E | INJECTABLE, LIPOSOMAL / INTRAVENOUS | 63 mg | ||
| POLYSORBATE 20 | POLYSORBATE 20 | 7T1F30V5YH | INJECTION / INTRAVENOUS | 30 mg | ||
| BENZYL ALCOHOL | BENZYL ALCOHOL | LKG8494WBH | INJECTION, EMULSION / INTRAVENOUS | 45 mg | ||
| HISTIDINE | HISTIDINE | 4QD397987E | INJECTABLE, LIPOSOMAL / INTRAVENOUS | 63 mg | ||
| HISTIDINE | HISTIDINE | 4QD397987E | INJECTION, SUSPENSION, LIPOSOMAL / INTRAVENOUS | 0.16 %w/v | ||
| BENZYL ALCOHOL | BENZYL ALCOHOL | LKG8494WBH | SOLUTION / INTRAVENOUS | 242 mg | ||
| BENZYL ALCOHOL | BENZYL ALCOHOL | LKG8494WBH | INJECTION / INTRAVENOUS | 1620 mg | ||
| BENZYL ALCOHOL | BENZYL ALCOHOL | LKG8494WBH | INJECTION, SOLUTION / INTRAVENOUS | 400 mg | ||
| BENZYL ALCOHOL | BENZYL ALCOHOL | LKG8494WBH | INJECTION, POWDER, FOR SOLUTION / INTRAVENOUS | 144 mg | ||
| BENZYL ALCOHOL | BENZYL ALCOHOL | LKG8494WBH | INJECTION, EMULSION / INTRAVENOUS | 45 mg | ||
| BENZYL ALCOHOL | BENZYL ALCOHOL | LKG8494WBH | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRACAVERNOUS | 18 mg | ||
| POLYSORBATE 20 | POLYSORBATE 20 | 7T1F30V5YH | INJECTION, SOLUTION / INTRAVENOUS | 30 mg | ||
| HISTIDINE | HISTIDINE | 4QD397987E | INJECTABLE, LIPOSOMAL / INTRAVENOUS | 63 mg | ||
| HISTIDINE | HISTIDINE | 4QD397987E | INJECTION, SOLUTION / INTRAVENOUS | 0.09 %w/v | ||
| TREHALOSE DIHYDRATE | TREHALOSE DIHYDRATE | 7YIN7J07X4 | INJECTION, POWDER, FOR SOLUTION / SUBCUTANEOUS | 4 mg | ||
| POLYSORBATE 20 | POLYSORBATE 20 | 7T1F30V5YH | INJECTION / INTRAVENOUS | 30 mg | ||
| POLYSORBATE 20 | POLYSORBATE 20 | 7T1F30V5YH | INJECTION / INTRAVENOUS | 30 mg | ||
| BENZYL ALCOHOL | BENZYL ALCOHOL | LKG8494WBH | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRACAVITARY | 8.4 mg | ||
| BENZYL ALCOHOL | BENZYL ALCOHOL | LKG8494WBH | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRACAVITARY | 8.4 mg | ||
| HISTIDINE | HISTIDINE | 4QD397987E | INJECTION, SOLUTION / INTRAVENOUS | 0.09 %w/v | ||
| POLYSORBATE 20 | POLYSORBATE 20 | 7T1F30V5YH | INJECTION, SOLUTION / INTRAVENOUS | 30 mg | ||
| HISTIDINE | HISTIDINE | 4QD397987E | INJECTION, SOLUTION / INTRAVENOUS | 0.09 %w/v | ||
| HISTIDINE | HISTIDINE | 4QD397987E | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / SUBCUTANEOUS | 3.88 mg | ||
| BENZYL ALCOHOL | BENZYL ALCOHOL | LKG8494WBH | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRACAVERNOUS | 18 mg | ||
| TREHALOSE DIHYDRATE | TREHALOSE DIHYDRATE | 7YIN7J07X4 | INJECTION, SOLUTION / SUBCUTANEOUS | 22 mg | ||
| BENZYL ALCOHOL | BENZYL ALCOHOL | LKG8494WBH | INJECTION, SOLUTION / INTRAVENOUS | 400 mg | ||
| HISTIDINE | HISTIDINE | 4QD397987E | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / SUBCUTANEOUS | 3.88 mg | ||
| POLYSORBATE 20 | POLYSORBATE 20 | 7T1F30V5YH | INJECTION, SOLUTION / INTRAVENOUS | 30 mg | ||
| TREHALOSE DIHYDRATE | TREHALOSE DIHYDRATE | 7YIN7J07X4 | INJECTION, POWDER, FOR SOLUTION / SUBCUTANEOUS | 4 mg | ||
| TREHALOSE DIHYDRATE | TREHALOSE DIHYDRATE | 7YIN7J07X4 | INJECTION, SOLUTION / SUBCUTANEOUS | 22 mg | ||
| TREHALOSE DIHYDRATE | TREHALOSE DIHYDRATE | 7YIN7J07X4 | INJECTION, POWDER, FOR SOLUTION / INTRADERMAL | 4 mg | ||
| BENZYL ALCOHOL | BENZYL ALCOHOL | LKG8494WBH | INJECTION / INTRAVENOUS | 1620 mg | ||
| BENZYL ALCOHOL | BENZYL ALCOHOL | LKG8494WBH | SOLUTION / INTRAVENOUS | 242 mg | ||
| BENZYL ALCOHOL | BENZYL ALCOHOL | LKG8494WBH | LIQUID / INTRAVENOUS | 1.04 %w/v | ||
| BENZYL ALCOHOL | BENZYL ALCOHOL | LKG8494WBH | INJECTION, POWDER, FOR SOLUTION / INTRAVENOUS | 144 mg | ||
| HISTIDINE | HISTIDINE | 4QD397987E | INJECTION / INTRAVENOUS | 465 mg | ||
| POLYSORBATE 20 | POLYSORBATE 20 | 7T1F30V5YH | INJECTION, POWDER, FOR SOLUTION / INTRAVENOUS | NA | ||
| TREHALOSE DIHYDRATE | TREHALOSE DIHYDRATE | 7YIN7J07X4 | INJECTION, POWDER, FOR SOLUTION / SUBCUTANEOUS | 4 mg | ||
| BENZYL ALCOHOL | BENZYL ALCOHOL | LKG8494WBH | INJECTION, POWDER, FOR SOLUTION / INTRAVENOUS | 144 mg |
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Herceptin | TRASTUZUMAB | Genentech, Inc. | 492dbdb2-077e-4064-bff3-372d6af0a7a2 | 2026-05-29 | Boxed warning, Warnings, Adverse reactions | 50242-132-01 50242-132 50242013201 7517f775-6a10-4ddd-8dfb-6704ece413d0 492dbdb2-077e-4064-bff3-372d6af0a7a2 |
Adverse event summaries are temporarily unavailable. Other product information remains available.
