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尼拉帕利维持治疗铂敏感复发性卵巢癌患者:西班牙医院的真实世界经验

Niraparib Maintenance Therapy in Patients with Platinum-Sensitive Recurrent Ovarian Cancer: Real-World Experience at Hospitals in Spain.

作者信息

Rodríguez Sagrado Miguel Angel, Alvarez Criado Javier, Arenaza Peña Ainhoa Elisa, Escudero-Vilaplana Vicente, Folguera Olias Carlos, Herrero Fernandez Marta, Martinez Nieto Concepción, Rubio Salvador Ana Rosa, Sanmartin Fenollera Patricia, Vazquez Castillo Maria José

机构信息

Pharmacy Service, Hospital Universitario Ramón y Cajal, Madrid, Spain.

Pharmacy Service, H. La Paz, Madrid, Spain.

出版信息

Target Oncol. 2025 Mar;20(2):319-327. doi: 10.1007/s11523-024-01121-5. Epub 2025 Jan 24.

Abstract

BACKGROUND

The reported benefit of poly (ADP-ribose) polymerase inhibitor (PARPi) maintenance in patients with newly diagnosed and platinum (Pt)-sensitive recurrent ovarian cancer (OC) included in randomized clinical trials needs to be corroborated in a less selected population.

OBJECTIVE

The aim is to increase the evidence on niraparib in a real-world setting.

METHODS

This is a retrospective observational study including women with platinum-sensitive relapsed high-grade serous OC who started niraparib maintenance between August 2019 (marketing data, Spain) and May 2022. Patients received ≥ 2 previous lines of therapy with complete or partial response to prior chemotherapy. Patient characteristics, niraparib dose, adequacy of dose individualization, effectiveness (progression-free survival [PFS] and overall survival), safety, and economic savings with an individualized starting dose (ISD) strategy were assessed.

RESULTS

The study included 217 patients with a median of 8.9 months of niraparib duration: breast cancer gene (BRCA) wild-type OC, 70%; two prior treatment lines, 49%; Research on Adverse Drug Events and Reports (RADAR) criteria, 82% (receiving mainly 200 mg of niraparib, 79%). Median PFS was 10.8 months (95% confidence interval [CI], 8.4-14.8) without statistically significant differences based on starting dose strategy, contrary to what was observed on the basis of prior lines, response to prior chemotherapy, BRCA mutational status, and International Federation of Gynecology and Obstetrics (FIGO) stage at diagnosis. The last three variables also showed a statistically significant predictive prognostic value for effectiveness. Dose interruptions due to toxicity were required in 7% of patients, and dose adjustments in 56% were mainly due to hematologic toxicities. The actual dose of niraparib reveals economic savings versus the theoretical cost.

CONCLUSION

This large real-world analysis corroborates the tolerability and activity of niraparib maintenance for platinum-sensitive recurrent OC and economic savings.

摘要

背景

随机临床试验纳入的新诊断且铂敏感复发卵巢癌(OC)患者中,聚(ADP - 核糖)聚合酶抑制剂(PARPi)维持治疗的已报道益处需在选择范围较小的人群中得到证实。

目的

旨在增加尼拉帕利在真实世界中的证据。

方法

这是一项回顾性观察性研究,纳入2019年8月(西班牙上市数据)至2022年5月开始尼拉帕利维持治疗的铂敏感复发高级别浆液性OC女性患者。患者接受过≥2线先前治疗且对先前化疗有完全或部分缓解。评估患者特征、尼拉帕利剂量、剂量个体化的适宜性、有效性(无进展生存期[PFS]和总生存期)、安全性以及个体化起始剂量(ISD)策略的经济节省情况。

结果

该研究纳入217例患者,尼拉帕利治疗持续时间中位数为8.9个月:乳腺癌基因(BRCA)野生型OC患者占70%;接受过2线先前治疗的患者占49%;药物不良事件和报告研究(RADAR)标准符合率为82%(主要接受200mg尼拉帕利的患者占79%)。中位PFS为10.8个月(95%置信区间[CI],8.4 - 14.8),基于起始剂量策略无统计学显著差异,这与基于先前治疗线数、对先前化疗的反应、BRCA突变状态以及诊断时国际妇产科联合会(FIGO)分期所观察到的情况相反。后三个变量对有效性也显示出统计学显著的预测预后价值。7%的患者因毒性需要中断剂量,56%的患者进行剂量调整主要是由于血液学毒性。与理论成本相比,尼拉帕利的实际剂量显示出经济节省。

结论

这项大型真实世界分析证实了尼拉帕利维持治疗对铂敏感复发OC的耐受性、活性及经济节省情况。

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