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Association details:
Biomarker:BAP1 mutation
Cancer:Mesothelioma
Drug:Lynparza (olaparib) (PARP inhibitor)
Direction:Resistant
Evidence:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
New
Title:

Olaparib in Patients With HRD Malignant Mesothelioma

Excerpt:
...- Participant must show evidence of specific DNA changes/genetic mutations defined as follows: A) BAP1 loss (the loss of a protein called ubiquitin carboxyl-terminal hydrolase) verified by physicians at the University of Chicago using sampling tests AND/OR B) A mutation (abnormal change) in the participant's germ cells (reproductive cells) or somatic cells (non-reproductive cells) that disrupts protein function in at least one of the patient's genes....
Trial ID:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
New
Go to data
Title:

Olaparib in People With Malignant Mesothelioma

Excerpt:
...Percentage of Participants With Breast Cancer Type 1 Associated Protein-1 (BAP1) Somatic Mutations Who Experienced Partial or Complete Response.`...
Trial ID:
Less C2 evidence
Evidence Level:
Resistant: C3 – Early Trials
Title:

Phase 2 Study of Olaparib in Malignant Mesothelioma and Correlation of Efficacy With Germline or Somatic Mutations in BAP1 Gene

Published date:
09/17/2021
Excerpt:
Olaparib has limited activity in previously treated mesothelioma including patients with BAP1 mutations. Germline BAP1 mutations were associated with decreased PFS and OS.
DOI:
10.1016/j.jtocrr.2021.100231
Evidence Level:
Resistant: C3 – Early Trials
Source:
Title:

Phase II study of olaparib in malignant mesothelioma (MM) to correlate efficacy with germline and somatic mutations in DNA repair genes.

Published date:
05/13/2020
Excerpt:
Phase II single-center study (NCT03531840) enrolled patients with advanced pleural or peritoneal mesothelioma...Olaparib has limited anti-tumor activity in previously treated MM patients including those with germline or somatic BAP1 mutations. Presence of germline BAP1 mutations was associated with decreased PFS and OS.
DOI:
10.1200/JCO.2020.38.15_suppl.9054
Trial ID: