First-Line Treatment with Olaparib for Early Stage BRCA-Positive Ovarian Cancer: May It Be Possible? Hypothesis Potentially Generating a Line of Research
- PMID: 32765062
- PMCID: PMC7369298
- DOI: 10.2147/CMAR.S194874
First-Line Treatment with Olaparib for Early Stage BRCA-Positive Ovarian Cancer: May It Be Possible? Hypothesis Potentially Generating a Line of Research
Abstract
Olaparib is currently approved in maintenance treatment of advanced ovarian cancer after response to first-line chemotherapy for breast related cancer antigens (BRCA) mutated patients. The use of this agent is based on data from SOLO1 study that observed a decreased risk of disease progression or death and a median progression-free survival about 36 months longer in case of therapy with olaparib. However, this trial recruited only patients with advanced stage ovarian cancer. The aim of this review is to retrace the available data in order to clarify the potential efficacy and feasibility of olaparib administration in newly diagnosed epithelial ovarian cancer also in early stages.
Keywords: BRCA mutation; PARPinhibitors; early stage ovarian cancer; newly diagnosed ovarian cancer; olaparib.
© 2020 Tomao et al.
Conflict of interest statement
Drs Nicoletta Colombo reports personal fees from Roche, Pharmamar, Astra Zeneca, Clovis, Tesaro, GSK, Pfizer, Amgen, Immunogen, and Biocad, outside the submitted work. The authors report no other conflicts of interest in this work.
References
-
- Heintz AP, Odicino F, Maisonneuve P, et al. Carcinoma of the ovary. J Epidemiol Biostat. 2001;6(1):107–138. - PubMed
-
- Percent of cases & 5-year relative survival by stage at diagnosis: ovarian cancer. Available from: https://seer.cancer.gov/statfacts/html/ovary.html. Accessed January30, 2020.
-
- Morice P, Leblanc E, Rey A, et al. Conservative treatment in epithelial ovarian cancer: results of a multicentre study of the GCCLCC (Groupe des Chirurgiens de Centre de Lutte Contre le Cancer) and SFOG (Société Francaise d’Oncologie Gynécologique). Hum Reprod. 2005;20(5):1379–1385. doi: 10.1093/humrep/deh777 - DOI - PubMed
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