The therascreen pik3ca rgq pcr kit is a real-time qualitative pcr test for the detection of 11 mutations in the phosphatidylinositol 3-kinase catalytic subunit alpha (pik3ca) gene (exon 7: c420r; exon 9: e542k, e545a, e545d [1635g>t only], e545g, e545k, q546e, q546r; and exon 20: h1047l, h1047r, h1047y) using genomic dna (gdna) extracted from formalin-fixed, paraffin-embedded (ffpe) breast tumor tissue or circulating tumor dna (ctdna) from plasma derived from k2edta anticoagulated peripheral whole blood taken from patients with breast cancer. The test is intended to aid clinicians in identifying breast cancer patients who may be eligible for treatment with piqray® (alpelisib) based on a pik3ca mutation detected result. Patients whose ffpe tissue or plasma specimen produces a positive therascreen pik3ca rgq pcr kit test result for the presence of one or more pik3ca mutations are eligible for treatment with piqray (alpelisib). Patients whose plasma specimen produces a negative result using this test should be reflexed to testing with ffpe tumor tissue for the presence of pik3ca mutations. Ffpe tumor specimens are processed using the qiaamp dsp dna ffpe tissue kit for manual sample preparation. K2edta anticoagulated whole peripheral venous blood plasma specimens are processed using the qiaamp dsp circulating nucleic acid kit for manual sample preparation. For both specimen types, the rotor-gene q (rgq) mdx (us) instrument is used for automated amplification and detection. The kit is to be used by trained personnel in a professional laboratory environment.
| Device | therascreen PIK3CA RGQ PCR Kit |
| Classification Name | Somatic Gene Mutation Detection System |
| Generic Name | Somatic Gene Mutation Detection System |
| Applicant | QIAGEN GMBH |
| Date Received | 2019-01-17 |
| Decision Date | 2019-05-24 |
| PMA | P190001 |
| Supplement | S |
| Product Code | OWD |
| Advisory Committee | Molecular Genetics |
| Expedited Review | No |
| Combination Product | No |
| Applicant Address | QIAGEN GMBH qiagen Strasse 1 hilden 40724 |
| Post-Approval Study: | Show Report Schedule and Study Progress |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P190001 | Original Filing | |
| S001 | 2020-03-04 | 30-day Notice |