Combination of PARP Inhibitor and Antiangiogenic Therapy Following Disease Progression in Patients With Epithelial Ovarian Cancer Undergoing PARP Inhibitor Maintenance Therapy: A Real‐World Study

医学 内科学 PARP抑制剂 肿瘤科 无进展生存期 联合疗法 维持疗法 胃肠病学 癌症 人口 外科 化疗 聚ADP核糖聚合酶 生物化学 聚合酶 基因 化学 环境卫生
作者
Nan Zhang,Hong Zheng,Yunong Gao,Tong Shu,Hongguo Wang,Yan Cai
出处
标识
DOI:10.1111/1471-0528.18179
摘要

ABSTRACT Objective To investigate whether the combination of antiangiogenic therapy and poly‐ADP‐ribose polymerase inhibitors (PARPi) can enhance the effectiveness of maintenance therapy in patients with progressive ovarian cancer who are progressing after PARPi maintenance therapy. Design Retrospective cohort study. Setting Single‐centre tertiary hospital in Beijing, China. Population Patients treated with combination therapy. Methods We retrospectively reviewed the clinicopathological data of patients with epithelial ovarian cancer. Telephone follow‐ups were performed for eligible participants to verify disease progression and survival status. Main Outcome Measures Clinical endpoints included objective response rate (ORR), disease control rate (DCR), time‐to‐symptomatic progression (TTSP), and progression‐free survival. Results Overall, 25 patients were analysed. Overall confirmed ORR was 44%, and the DCR was 68%. The median TTSP was 12.0 months (95% CI: 2.05–24.73). In the progression‐free interval (PFI) > 12 months group ( n = 15), the ORR was 60% (9/15), and the DCR was 73.3%. In the PFI ≤ 12 months group ( n = 10), the ORR was 20% (2/10), and the DCR was 60%. The median TTSP was not reached in the PFI > 12 months group and was 4.0 months (95% CI: 2.988–5.012) for the PFI ≤ 12 months group. The 6‐month progression‐free survival rates were 58% and 40%, respectively. Among the 10 patients who received subsequent chemotherapy, seven achieved partial response (PR), and one had stable disease. The respective ORR and DCR values were 70% and 80%. Conclusions Combining antiangiogenic therapy with the original PARPi may benefit patients with ascites‐free ovarian cancer and a low tumour burden who experience disease progression following PARPi maintenance therapy.
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