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PARP inhibitors (PARPi) prolongation after local therapy for oligo-metastatic progression in relapsed ovarian cancer patients

医学 卵巢癌 内科学 肿瘤科 癌症 癌症研究 生物化学 化学 聚合酶 聚ADP核糖聚合酶 基因
作者
Thibault Gauduchon,Maria Kfoury,Domenica Lorusso,Anne Floquet,Jole Ventriglia,Hélène Salaün,Malak Moubarak,Romain Rivoirard,Laura Polastro,Laure Favier,Benoît You,Dominique Berton,Thibault De La Motte Rouge,Laura Mansi,Cyril Abdeddaim,Karine Prulhière,Laurence Lecomte,Magali Provansal,Cécile Dalban,I. L. Ray-Coquard
出处
期刊:Gynecologic Oncology [Elsevier BV]
卷期号:173: 98-105 被引量:30
标识
DOI:10.1016/j.ygyno.2023.04.002
摘要

PARP inhibitors (PARPi) have revolutionized the management of high-grade epithelial ovarian cancer (HGOC) treatment. However, a significant number of patients relapse or progress under PARPi, leading to the introduction of a new line of systemic therapy such as chemotherapy. In patients with a limited number of metastatic sites at progression, -referred to as an oligometastatic progression- a potential indication for local therapy followed by re-introduction or continuation of PARPi treatment rather than initiating a new line of chemotherapy could be proposed. However, the impact of such strategies on progression free survival (PFS) in these patients remains unknown.This international multicenter retrospective study evaluated the efficacy of PARPi continuation or re-introduction in patients with HGOC after local treatment for oligometastatic progression. The main objective was to assess PFS under PARPi after local therapy (PFS post-LT). Secondary objectives included safety and overall survival (OS).74 patients were identified in 20 centers between April 2020 and November 2021. 65% of patients were BRCA mutated and 92% had received ≥2 lines of prior systemic chemotherapy before the initial introduction of PARPi. Main progression sites were lymph nodes (42%), peritoneum (27%), liver (16%), other visceral (16%) and abdominal wall (4%). Local therapies included radiotherapy (45%), surgery (43%), both (7%), percutaneous thermal ablation (4%) or chemoembolization (1%). Median PFS post-LT was 11.5 months [95% CI 7.4; 17.2]. After a median follow up of 14.8 months, 6 patients (8.1%) discontinued PARPi due to toxicity. The 1-year overall survival rate was 90.7% [95% CI 79.1; 96.0].With close to one year without progression or introduction of a new line of systemic therapy, this study reports the feasibility and potential benefit of this original strategy in patients with oligometastatic progression under PARPi.
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