Moriceau Guillaume, Rivoirard Romain, Méry Benoîte, Vallard Alexis, Pacaut Cécile, Trone Jane-Chloé, Espenel Sophie, Bosacki Claire, Jacquin Jean-Philippe, Magné Nicolas
Chemotherapy. 2016;61(3):122-6. doi: 10.1159/000441378. Epub 2016 Jan 12.
Trabectedin plus pegylated liposomal doxorubicin (PLD) proved efficacious as second-line treatment for patients with recurrent ovarian cancer (ROC).
We report a single-center retrospective analysis of the efficacy and tolerance of trabectedin 1.1 mg/m2 every 3 weeks in a cohort of real-life ROC patients.
From February 2012 to January 2014, 17 patients were treated with trabectedin alone or combined with PLD. Median age was 61 years (range: 48-78). Performance status was 0-1 in 16 patients (94%). Disease response rate was 53% and disease control rate was 76%. At the end of the follow-up, 8 patients (47%) were alive. Median overall survival was 17.6 months (95% CI 13.6 to not reached). Median progression-free survival was 6.7 months (95% CI 5.4-10.0). The most frequent grade 3-4 toxicities were neutropenia (n = 4, 24%) and nausea/vomiting (n = 4, 24%).
Trabectedin combined with PLD seems efficient in and well tolerated by real-life ROC patients.
曲贝替定联合聚乙二醇化脂质体阿霉素(PLD)被证明对复发性卵巢癌(ROC)患者是有效的二线治疗方案。
我们报告了一项单中心回顾性分析,研究了在一组真实世界的ROC患者中,每3周使用1.1mg/m²曲贝替定的疗效和耐受性。
从2012年2月至2014年1月,17例患者接受了单独使用曲贝替定或联合PLD的治疗。中位年龄为61岁(范围:48 - 78岁)。16例患者(94%)的体能状态为0 - 1。疾病缓解率为53%,疾病控制率为76%。随访结束时,8例患者(47%)存活。中位总生存期为17.6个月(95%置信区间13.6至未达到)。中位无进展生存期为6.7个月(95%置信区间5.4 - 10.0)。最常见的3 - 4级毒性反应是中性粒细胞减少(n = 4,24%)和恶心/呕吐(n = 4,24%)。
曲贝替定联合PLD在真实世界的ROC患者中似乎有效且耐受性良好。