Hensley Martee L, Enserro Danielle, Hatcher Helen, Ottevanger Petronella B, Krarup-Hansen Anders, Blay Jean-Yves, Fisher Cyril, Moxley Katherine M, Lele Shashikant B, Lea Jayanthi S, Tewari Krishnansu S, Thaker Premal H, Zivanovic Oliver, O'Malley David M, Robison Katina, Miller David S
Martee L. Hensley, Memorial Sloan Kettering Cancer Center; Martee L. Hensley and Oliver Zivanovic, Weill Cornell Medical College, New York City; Danielle Enserro and Shashikant B. Lele, Roswell Park Comprehensive Cancer Center, Buffalo, NY; Helen Hatcher, Cambridge University Hospitals National Health Service Foundation Trust, Cambridge; Cyril Fisher, University of Birmingham, Birmingham, United Kingdom; Petronella B. Ottevanger, Radboud University Medical Center, Nijmegen, the Netherlands; Anders Krarup-Hansen, University Hospital Copenhagen, Copenhagen, Denmark; Jean-Yves Blay, Centre Leon Berard, Lyon, France; Katherine M. Moxley, University of Oklahoma Health Sciences Center, Oklahoma City, OK; Jayanthi S. Lea, and David S. Miller, The University of Texas Southwestern Medical Center, Dallas, TX; Krishnansu S. Tewari, University of California at Irvine, Orange, CA; Premal H. Thaker, Washington University School of Medicine, and Siteman Cancer Center, St Louis, MO; David M. O'Malley, The Ohio State University College of Medicine, Columbus, OH; Katina Robison, Women and Infants Hospital in Rhode Island, Providence, RI.
J Clin Oncol. 2018 Oct 5;36(33):JCO1800454. doi: 10.1200/JCO.18.00454.
We conducted a randomized phase III trial to determine whether adjuvant chemotherapy improves survival in women with uterine leiomyosarcoma.
Women with uterus-confined, high-grade leiomyosarcoma who were confirmed disease free by imaging were randomly assigned to four cycles of gemcitabine plus docetaxel, followed by four cycles of doxorubicin, or to observation. All were followed for evidence of recurrence. The primary end point was overall survival (OS).
With international collaboration, 38 of the targeted accrual of 216 patients were enrolled, after which the study was closed by the National Cancer Institute for accrual futility. Twenty patients were assigned to chemotherapy, 18 to observation. Among the 17 patients treated with at least one cycle of chemotherapy, grade 3 or 4 toxicities were observed in 47%; among the 18 patients assigned to observation, one had grade 3 hypertension. There were six deaths (chemotherapy, n = 5; observation, n = 1), all due to disease. The restricted mean survival time for OS was estimated as 34.3 months (95% CI, 25.3 to 43.3 months) in the chemotherapy arm and as 46.4 months (95% CI, 43.6 to 49.1 months) in the observation arm. There were eight recurrences in each arm. The restricted mean survival time for recurrence-free survival was estimated as 18.1 (95% CI, 14.2 to 22.0) months in the chemotherapy arm and as 14.6 months (95% CI, 10.3 to 19.0 months) in the observation arm. Neither survival outcome comparison was considered statistically robust, due to the small sample size.
Despite international collaboration to test the role of adjuvant chemotherapy in uterine-confined leiomyosarcoma, this study was closed for accrual futility. Although the sample size precludes robust statistical comparison, observed OS and recurrence-free survival data do not show superior outcomes with adjuvant chemotherapy.
我们开展了一项随机III期试验,以确定辅助化疗能否提高子宫平滑肌肉瘤女性患者的生存率。
经影像学检查确认无疾病的子宫局限性高级别平滑肌肉瘤女性患者被随机分配接受四个周期的吉西他滨加多西他赛治疗,随后接受四个周期的阿霉素治疗,或接受观察。所有患者均接受随访以观察复发情况。主要终点为总生存期(OS)。
通过国际合作,在目标入组的216例患者中,有38例入组,之后该研究因入组无效被美国国立癌症研究所关闭。20例患者被分配接受化疗,18例接受观察。在接受至少一个周期化疗的17例患者中,47%出现3级或4级毒性反应;在分配接受观察的18例患者中,1例出现3级高血压。共有6例死亡(化疗组5例,观察组1例),均因疾病死亡。化疗组的OS受限平均生存时间估计为34.3个月(95%CI,25.3至43.3个月),观察组为46.4个月(95%CI,43.6至49.1个月)。每组均有8例复发。化疗组无复发生存期的受限平均生存时间估计为18.1(95%CI,14.2至22.0)个月,观察组为14.6个月(95%CI,10.3至19.0个月)。由于样本量小,两种生存结果比较均未被认为具有统计学稳健性。
尽管开展了国际合作以测试辅助化疗在子宫局限性平滑肌肉瘤中的作用,但该研究因入组无效而关闭。虽然样本量不足以进行稳健的统计学比较,但观察到的OS和无复发生存数据并未显示辅助化疗有更好的结果。