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Real-world safety and effectiveness of maintenance niraparib for platinum-sensitive recurrent ovarian cancer: A GEICO retrospective observational study within the Spanish expanded-access programme

医学 不利影响 加药 卵巢癌 内科学 回顾性队列研究 人口 观察研究 置信区间 无进展生存期 肿瘤科 癌症 外科 化疗 环境卫生
作者
Juan Cueva,Isabel Palacio,Cristina Churruca,Ana Herrero,Beatriz Pardo,Manuel Constenla,Ana Santaballa,Luís Manso,Purificación Estévez,Constanza Maximiano,Marta Legerén,Gloria Marquina,Ana De Juan,María Quindós,Luisa Sánchez,Arántzazu Barquín,Isaura Fernández,Cristina Martín,Asunción Juárez,Teresa Gómez
出处
期刊:European Journal of Cancer [Elsevier BV]
卷期号:182: 3-14 被引量:10
标识
DOI:10.1016/j.ejca.2022.12.023
摘要

To describe patient characteristics, effectiveness and safety in a real-world population treated with niraparib in the Spanish expanded-access programme.This retrospective observational study included women with platinum-sensitive recurrent high-grade serous ovarian cancer who received maintenance niraparib within the Spanish niraparib expanded-access programme. Eligible patients had received ≥2 previous lines of platinum-containing therapy, remained platinum-sensitive after the penultimate line of platinum and had responded to the most recent platinum-containing therapy. Niraparib dosing was at the treating physician's discretion (300 mg/day fixed starting dose or individualised starting dose [ISD] according to baseline body weight and platelet count). Safety, impact of dose adjustments, patient characteristics and effectiveness were analysed using data extracted from medical records.Among 316 eligible patients, 80% had BRCA wild-type tumours and 66% received an ISD. Median niraparib duration was 7.8 months. The most common adverse events typically occurred within 3 months of starting niraparib. Median progression-free survival was 8.6 (95% confidence interval [CI] 7.6-10.0) months. One- and 2-year overall survival rates were 86% (95% CI 81-89%) and 65% (95% CI 59-70%), respectively. Dose interruptions, dose reductions, haematological toxicities and asthenia/fatigue were less common with ISD than fixed starting dose niraparib, but progression-free survival was similar irrespective of dosing strategy. Subsequent therapy included platinum in 71% of patients who received further treatment.Outcomes in this large real-world dataset of niraparib-treated patients are consistent with phase III trials, providing reassuring evidence of the tolerability and activity of niraparib maintenance therapy for platinum-sensitive recurrent ovarian cancer.NCT04546373.
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