Abstract
Background/Aim: Olaparib was approved in 2014 by the European Medicines Agency (EMA) as maintenance treatment for patients with breast cancer gene (BRCA)-mutated platinum-sensitive relapsed high-grade epithelial ovarian cancer (EOC) following the results of the Study 19. We present the results of a national real-world study on the effectiveness of olaparib in relapsed BRCA-mutated EOC patients. Patients and Methods: Patients with EOC, peritoneal, and/or fallopian-tube cancer treated with olaparib in a French Center between May 2014 and March 2017 were included. The primary endpoint of the study was progression-free survival. Results: Of the 128 patients analyzed, 89 were treated according to the EMA label. The median progression-free survival was 17.0 months. The most common treatment-related toxicity was fatigue. Treatment-related myelodysplastic syndrome (n=5) and a second cancer (n=1) were diagnosed. Conclusion: In this real-life setting, olaparib confirmed its efficacy and safety profile, as previously shown in clinical trials.
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Bourien, H., Lefevre, L. B., Mouret-Reynier, M. A., Asselain, B., Lucas, B., Gavoille, C., … de la Motte Rouge, T. (2023). Real-World Data on Olaparib in Relapsed BRCA-mutated Ovarian Cancer: A Multicenter GINECO RETROLA Cohort Study. Anticancer Research, 43(2), 653–662. https://doi.org/10.21873/anticanres.16202
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