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Published on: July 25, 2020
Case report: olaparib use in metastatic lung adenocarcinoma with BRCA2 pathogenic variant
Jonathan Soon Jian Hao1, Chan Sock Hoai1, Daniel Tan Shao Weng2,3
1Cancer Genetics Service, National Cancer Centre Singapore, Singapore 169610, Singapore.
Abstract:
Poly (ADP-ribose) polymerase (PARP) inhibitors have been approved in malignancies associated with germline BRCA1 or BRCA2 pathogenic variants, such as breast, ovarian, prostate, and pancreatic cancer. In malignancies not associated with germline BRCA1 or BRCA2 pathogenic variants, the therapeutic relevance of PARP inhibitors is less clear. Non-small-cell lung cancer (NSCLC) is known to demonstrate somatic alterations in BRCA1 or BRCA2 gene. The current report is on a gentleman with metastatic lung adenocarcinoma with a somatic BRCA2 pathogenic variant, who was effectively treated with olaparib. Furthermore, we discuss the existing data for use of PARP inhibitors in NSCLC. This study highlights the utility of next-generation sequencing in identifying gene mutations and demonstrates how such information can be used to select targeted therapies in patients with actionable molecular alterations.
Insights
Poly (ADP-ribose) polymerase (PARP) inhibitors show promise in treating lung adenocarcinoma with somatic BRCA2 mutations. Next-generation sequencing can identify these mutations for targeted therapy selection.
Area of Science:
- Oncology
- Genetics
- Pharmacology
Background:
- Poly (ADP-ribose) polymerase (PARP) inhibitors are approved for cancers with germline BRCA1/BRCA2 mutations.
- Their efficacy in cancers without germline BRCA1/BRCA2 alterations is less understood.
- Non-small-cell lung cancer (NSCLC) can exhibit somatic BRCA1/BRCA2 alterations.
Observation:
- A patient with metastatic lung adenocarcinoma presented with a somatic BRCA2 pathogenic variant.
- The patient received olaparib, a PARP inhibitor, as treatment.
- The treatment with olaparib was effective for the patient.
Findings:
- This case report details the successful treatment of lung adenocarcinoma with a somatic BRCA2 mutation using olaparib.
- The study discusses current data on PARP inhibitor use in NSCLC.
- Next-generation sequencing (NGS) is highlighted as crucial for identifying actionable molecular alterations.
Implications:
- Somatic BRCA2 mutations in NSCLC may represent a target for PARP inhibitor therapy.
- NGS is a valuable tool for guiding personalized treatment strategies in lung cancer.
- This approach can lead to improved outcomes for patients with specific molecular profiles.
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