Heterogeneous effects of cytotoxic chemotherapies for platinum-resistant ovarian cancer

Author:

Nara Katsuhiko1,Taguchi Ayumi1ORCID,Yamamoto Takehito1,Hara Konan2,Tojima Yuri1,Honjoh Harunori1,Nishijima Akira1,Eguchi Satoko1,Miyamoto Yuichiro1,Sone Kenbun1,Mori Mayuyo1,Takada Tappei1,Osuga Yutaka1

Affiliation:

1. The University of Tokyo: Tokyo Daigaku

2. UA: The University of Arizona

Abstract

Abstract Background: Single-agent chemotherapy with or without bevacizumab (Bev) is a standard therapy for platinum-resistant ovarian cancer (PR-OC). However, there is a lack of literature on chemotherapy agent selection in heterogenous PR-OC. Therefore, we aimed to clarify the heterogeneous treatment effects of each chemotherapy agent. Methods: Patients who underwent single-drug chemotherapy agents or Bev combination therapy for PR-OC between January 2009 and June 2022 were included in this study. We assessed the impact of each chemotherapy agent on the time to treatment failure (TTF) according to histological type, platinum-free interval (PFI), and Bev usage. Results: A total of 158 patients received 343 different chemotherapy regimens. In patients with clear cell carcinoma/mucinous carcinoma (CC/MC), gemcitabine (GEM) had the strongest effect with a median TTF of 5.3 months, whilst nedaplatin (NDP) had the lowest effect with a median TTF of 1.4 months. In contrast, in the non-CC/MC group, irinotecan (CPT-11) and NDP had a better TTF than GEM and pegylated liposomal doxorubicin (PLD). There were notable differences in the treatment efficacy of NDP according to PFI. Specifically, NDP prolonged the TTF in patients with a PFI ≥3 months. Compared with GEM alone, GEM+Bev tended to prolong the TTF more effectively; however, an additive effect was not observed with PLD+Bev. Conclusions: This study demonstrated that the effect of chemotherapy agents differed according to the tumor and background characteristics of the patient. Our findings will improve selection of effective therapies for patients with PR-OC by considering their background characteristics.

Publisher

Research Square Platform LLC

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