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Association details:
Biomarker:BRCA2 mutation
Cancer:Breast Cancer
Drug:veliparib (ABT-888) (PARP inhibitor)
Direction:Sensitive
Evidence:
Evidence Level:
Sensitive: B - Late Trials
Source:
Title:

Veliparib monotherapy following carboplatin/paclitaxel plus veliparib combination therapy in patients with germline BRCA-associated advanced breast cancer: results of exploratory analyses from the phase III BROCADE3 trial

Published date:
11/30/2021
Excerpt:
Veliparib monotherapy following carboplatin/paclitaxel plus veliparib combination therapy in patients with germline BRCA-associated advanced breast cancer...In this blinded monotherapy subgroup, investigator-assessed median PFS from randomization was 25.7 months with veliparib versus 14.6 months with placebo….Veliparib maintenance monotherapy had a tolerable safety profile and may extend PFS following combination chemotherapy.
DOI:
https://doi.org/10.1016/j.annonc.2021.11.018
Trial ID:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
New
Title:

Cisplatin With or Without Veliparib in Treating Patients With Recurrent or Metastatic Triple-Negative and/or BRCA Mutation-Associated Breast Cancer With or Without Brain Metastases

Excerpt:
...previously confirmed deleterious breast cancer 1, early onset (BRCA1) or breast cancer 2, early onset (BRCA2) germline mutation or suspected deleterious BRCA1 or BRCA2 germline mutation if the classification being used is the 5-tier classification; documentation of germline test results are required...
Trial ID:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
New
Title:

Response to PARP Inhibitor Predicted by the RAD51 Assay

Excerpt:
...Subjects must have triple negative breast cancer (maximum 10% ER expression), platinum sensitive (≥ 6 months since last platinum containing therapy) high grade serous ovarian cancer or BRCA1/2 mutated (non-)breast and (non-)ovarian cancer....
Trial ID:
More C2 evidence
Evidence Level:
Sensitive: C2 – Inclusion Criteria
New
Title:

A Phase I Study of ABT-888 in Combination With Temozolomide in Cancer Patients

Excerpt:
...- BRCA deficient tumor status*: advanced breast cancer (with soft tissue disease), or advanced ovarian cancer, or advanced primary peritoneal cancer, or advanced fallopian tube cancer* *Patients must have histologically or cytologically confirmed solid tumors with a positive genetic test result documenting BRCA 1 or BRCA 2 mutation status, to be considered eligible....
Trial ID:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
New
Title:

Phase II ABT-888 With Cyclophosphamide

Excerpt:
...- BRCA-positive ovarian cancer (documented deleterious BRCA1/2 mutation or a BRCAPRO score of greater than or equal to 30%)...
Trial ID:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
New
Title:

Veliparib, Cisplatin, and Vinorelbine Ditartrate in Treating Patients With Recurrent and/or Metastatic Breast Cancer

Excerpt:
...- Confirmed BRCA1 or BRCA2 mutation associated breast cancer...
Trial ID:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
New
Title:

Veliparib, Oxaliplatin, and Capecitabine in Treating Patients With Advanced Solid Tumors

Excerpt:
...- BRCA1/2 mutation and a BRCA-related malignancy...
Trial ID:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
New
Title:

ABT-888 and Temozolomide for Metastatic Breast Cancer and BRCA1/2 Breast Cancer

Excerpt:
...To determine Safety and Efficacy in an Expansion Cohort of BRCA1/2 Mutation Carriers....
Trial ID:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
New
Go to data
Title:

Study Evaluating Efficacy And Tolerability Of Veliparib in Combination With Temozolomide (TMZ) or In Combination With Carboplatin and Paclitaxel Versus Placebo in Participants With Breast Cancer Gene (BRCA)1 and BRCA2 Mutation and Metastatic Breast Cancer

Excerpt:
...- Must have a documented deleterious Breast Cancer Gene BRCA1 or BRCA2 germline mutation....
Trial ID:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
New
Title:

Expanded Access With ABT-888 (Veliparib) to Treat Metastatic Breast Cancer

Excerpt:
...- Confirmed HER2-, BRCA1 or BRCA2 mutation-associated breast cancer or sporadic triple negative breast cancer....
Trial ID:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
New
Title:

Veliparib in Treating Patients With Malignant Solid Tumors That Do Not Respond to Previous Therapy

Excerpt:
...- Have a documented BRCA1/2 mutation and a BRCA related malignancy (primarily breast or ovarian cancers, but also may include prostate or pancreatic cancers);...
Trial ID:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
New
Title:

Veliparib and Carboplatin in Treating Patients With HER2-Negative Metastatic Breast Cancer

Excerpt:
...- HER negative with a known germline BRCA1/2 mutation...
Trial ID:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
New
Title:

A Study to Evaluate the Safety, Pharmacokinetics and Oral Bio Availability of Veliparib in Subjects With Solid Tumors

Excerpt:
...Subjects must also 1) have a documented BRCA1 or BRCA2 mutation that is considered to be deleterious by the investigator, OR 2) have high grade serous ovarian, fallopian tube, or peritoneal cancer....
Trial ID:
Less C2 evidence
Evidence Level:
Sensitive: C3 – Early Trials
Title:

Exposure-response analysis to inform the optimal dose of veliparib in combination with carboplatin and paclitaxel in BRCA-mutated advanced breast cancer patients

Published date:
08/29/2019
Excerpt:
The exposure-response analysis suggested that intermittent 7-day veliparib 120 mg BID dosing in a 21-day cycle provided additional efficacy without meaningfully impacting the safety and tolerability when co-administered with carboplatin and paclitaxel in patients with BRCA-deficient breast cancer.
DOI:
10.1007/s00280-019-03930-2
Evidence Level:
Sensitive: C3 – Early Trials
New
Title:

Abstract S2-05: Efficacy and tolerability of veliparib (V; ABT-888) in combination with carboplatin (C) and paclitaxel (P) vs placebo (Plc)+C/P in patients (pts) with BRCA1 or BRCA2 mutations and metastatic breast cancer: A randomized, phase 2 study

Excerpt:
A total of 196 pts (193 BRCA+ per central lab) were randomized to receive double blinded V+C/P (n=97) or Plc+C/P (n=99)….The V+C/P arm demonstrated numeric improvements for both PFS and OS compared to the Plc+C/P arm; improvement in ORR was statistically significant...This is the first randomized phase 2 trial of a PARP inhibitor in combination with platinum-based therapy for treatment of BRCA1/2-mutated advanced breast cancer. V+C/P demonstrated significantly higher ORR and symptom improvement compared to Plc+C/P, with nonsignificant trends for improved OS and PFS.
Secondary therapy:
carboplatin + paclitaxel
DOI:
10.1158/1538-7445.SABCS16-S2-05
Trial ID: