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Review
. 2022 Jul 28;15(1):88.
doi: 10.1186/s13048-022-01020-1.

Maintenance therapy for newly diagnosed epithelial ovarian cancer- a review

Affiliations
Review

Maintenance therapy for newly diagnosed epithelial ovarian cancer- a review

Shona Nag et al. J Ovarian Res. .

Abstract

Epithelial ovarian cancer (EOC) is the most lethal gynaecological cancer among women worldwide, with the 5-year survival rate ranging between 30 and 40%. Due to the asymptomatic nature of the condition, it is more likely to be diagnosed at an advanced stage, requiring an aggressive therapeutic approach. Cytoreductive surgery (CRS) along with systemic chemotherapy with paclitaxel and carboplatin has been the mainstay of the treatment in the frontline management of EOC. In recent years, neo-adjuvant chemotherapy, followed by interval CRS has become an important strategy for the management of advanced EOC. Due to the high rate of recurrence, the oncology community has begun to shift its focus to molecular-targeted agents and maintenance therapy in the frontline settings. The rationale for maintenance therapy is to delay the progression or relapse of the disease, as long as possible after first-line treatment, irrespective of the amount of residual disease. Tumours with homologous recombination deficiency (HRD) including BReast CAncer gene (BRCA) mutations are found to be sensitive to polyadenosine diphosphate-ribose polymerase (PARP) inhibitors and understanding of HRD status has become important in the frontline setting. PARP inhibitors are reported to provide a significant improvement in progression-free survival and have an acceptable safety profile. PARP inhibitors have also been found to act regardless of BRCA status. Recently, PARP inhibitors as maintenance therapy in the frontline settings showed encouraging results in EOC; however, the results from further trials and survival data from ongoing trials are awaited for understanding the role of this pathway in treatment of EOC. This review discusses an overview of maintenance strategies in newly diagnosed EOC along with considerations for maintenance therapy in EOC with a focus on PARP inhibitors.

Keywords: Anti-angiogenic agents; Epithelial ovarian cancer; Maintenance therapy; Molecular-targeted therapy; PARP inhibitors.

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Conflict of interest statement

Authors don’t have any competing interests to disclose.

Figures

Fig. 1
Fig. 1
Evolution of Maintenance Strategy for Epithelial Ovarian Cancer *Future prospects

References

    1. Cancer today. n.d. https://gco.iarc.fr/today/online-analysis-table?v=2020&mode=cancer&mode_.... Accessed 25 May 2021.
    1. Cancer tomorrow. n.d. https://gco.iarc.fr/tomorrow/en/dataviz/tables?cancers=25&populations=35.... Accessed 25 May 2021.
    1. Sankaranarayanan R, Ferlay J. Worldwide burden of gynaecological cancer: the size of the problem. Best Pract Res Clin Obstet Gynaecol. 2006;20:207–225. doi: 10.1016/j.bpobgyn.2005.10.007. - DOI - PubMed
    1. Pavlidis N, Rassy E, Vermorken JB, Assi T, Kattan J, Boussios S, et al. The outcome of patients with serous papillary peritoneal cancer, fallopian tube cancer, and epithelial ovarian cancer by treatment eras: 27 years data from the SEER registry. Cancer Epidemiol. 2021;75:102045. doi: 10.1016/j.canep.2021.102045. - DOI - PubMed
    1. Allemani C, Weir HK, Carreira H, Harewood R, Spika D, Wang X-S, et al. Global surveillance of cancer survival 1995-2009: analysis of individual data for 25,676,887 patients from 279 population-based registries in 67 countries (CONCORD-2) Lancet. 2015;385:977–1010. doi: 10.1016/S0140-6736(14)62038-9. - DOI - PMC - PubMed

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