^
Association details:
Biomarker:BRCA1 mutation
Cancer:Prostate Cancer
Drug:Talzenna (talazoparib) (PARP inhibitor)
Direction:Sensitive
Evidence:
Evidence Level:
Sensitive: C1 - Off-label
  (Approved for HER2 Negative Breast Cancer)
New
Title:

Regulator OKs Pfizer's BRCA mutation breast cancer treatment

Excerpt:
Pfizer Korea said that the Ministry of Food and Drug Safety has approved Talzenna, its BRCA (Breast Cancer Susceptibility Gene) mutation breast cancer targeted therapy....treatment as monotherapy for germline BRCA (gBRCA) mutations and HER2 (human epithelial cell growth factor receptor 2) negative locally advanced or metastatic breast cancer patients have previously had chemotherapy.
Evidence Level:
Sensitive: C2 – Inclusion Criteria
New
Title:

Measuring the Effects of Talazoparib in Patients With Advanced Cancer and DNA Repair Variations

Excerpt:
...- Deleterious BRCA1 or BRCA2 mutations...
Trial ID:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
New
Title:

Talazoparib, an Oral PARP Inhibitor, in Patients With Advanced Solid Tumors and Aberrations in Genes Involved in DNA Damage Response

Excerpt:
...- Deleterious BRCA1 or BRCA2 mutations...
Trial ID:
Less C2 evidence
Evidence Level:
Sensitive: C3 – Early Trials
Source:
Title:

TALAPRO-1: Phase II study of talazoparib (TALA) in patients (pts) with DNA damage repair alterations (DDRm) and metastatic castration-resistant prostate cancer (mCRPC) – updated interim analysis (IA).

Published date:
05/13/2020
Excerpt:
TALA monotherapy has encouraging antitumor activity in docetaxel-pretreated mCRPC pts with BRCA1/2 alterations and was generally well tolerated. also Refer table,
DOI:
10.1200/JCO.2020.38.15_suppl.5566
Trial ID:
Evidence Level:
Sensitive: C3 – Early Trials
Title:

TALAPRO-1: A phase II study of talazoparib (TALA) in men with DNA damage repair mutations (DDRmut) and metastatic castration-resistant prostate cancer (mCRPC)—First interim analysis (IA).

Published date:
02/13/2020
Excerpt:
Overall ORR (95% CI) was 25.6% (13.5–41.2), ORRBRCA1/2 50.0% (27.2–72.8), ORRATM 7.1% (0.2–33.9). Overall median (95% CI) rPFS was 5.6 months (mo) (3.5–8.2), rPFSBRCA1/2 8.2 mo (5.6–NE), rPFSATM 3.5 mo (1.7–8.1).
Trial ID: