Resistance to PARP Inhibitors After First-Line Platinum-Based Chemotherapy in a Patient with Advanced Ovarian Cancer with a Pathogenic Somatic BRCA1 Mutation.

Pharmgenomics Pers Med

Department of Obstetrics and Gynecology, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, 610041, People's Republic of China.

Published: March 2023

AI Article Synopsis

  • PARP inhibitors are used as maintenance therapy after first-line platinum-based chemotherapy for advanced ovarian cancer patients with specific BRCA1/2 mutations, but some patients can develop resistance to these treatments.* -
  • A patient with a specific BRCA1 mutation displayed resistance to olaparib, prompting a plasma ctDNA analysis since a tissue biopsy was not feasible.* -
  • The ctDNA analysis revealed an absence of the original BRCA1 mutation, suggesting that chemotherapy eliminated the tumor cells with this mutation, allowing non-mutant cells to grow and cause recurrence.*

Article Abstract

PARP inhibitors (PARPi) are the maintenance therapy after first line platinum-based chemotherapy for patients with advanced epithelial ovarian cancer (EOC) with germline and pathogenic somatic BRCA1/2 mutations. However, as with chemotherapy, patients can develop resistance to PARPi. The selective pressure generated by heterogeneous somatic BRCA mutations may give rise to chemotherapy or PARPi resistant tumors. Here, we present the case of a patient harboring a pathogenic p.Glu143* (c.427G>T) somatic BRCA1 mutation conferring resistance to olaparib following cytoreductive surgery and platinum-based chemotherapy. We ordered a plasma ctDNA analysis (tissue biopsy of recurrent lesions was contraindicated due to their anatomical location) to figure out the possible resistance mechanism. Analysis of ctDNA did not detect the pathogenic somatic BRCA1 p.Glu143* (c.427G>T) mutation seen before. The tumor cells harboring the pathogenic BRCA1 mutation were probably eliminated by the platinum-based chemotherapy, leaving only those without BRCA mutations to proliferate.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10024533PMC
http://dx.doi.org/10.2147/PGPM.S397827DOI Listing

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