University of Southern California, Norris Comprehensive Cancer Center, Los Angeles, CA.
University of Kansas, Lawrence, KS.
J Clin Oncol. 2019 Oct 10;37(29):2682-2688. doi: 10.1200/JCO.19.00861. Epub 2019 Aug 7.
Patients with metastatic urothelial carcinoma are often ineligible for cisplatin-based treatments. A National Cancer Institute Cancer Therapy Evaluation Program-sponsored trial assessed the tolerability and efficacy of a gemcitabine-eribulin combination in this population.
Patients with treatment-naïve advanced or recurrent metastatic urothelial carcinoma of the bladder, ureter, or urethra not amenable to curative surgery and not candidates for cisplatin-based therapy were eligible. Cisplatin ineligibility was defined as creatinine clearance less than 60 mL/min (but ≥ 30 mL/min), grade 2 neuropathy, or grade 2 hearing loss. Treatment was gemcitabine 1,000 mg/m intravenously followed by eribulin 1.4 mg/m, both on days 1 and 8, repeated in 21-day cycles until progression or unacceptable toxicity. A Simon two-stage phase II trial design was used to distinguish between Response Evaluation Criteria in Solid Tumors, version 1.1 objective response rates of 20% versus 50%.
Between June 2015 and March 2017, 24 eligible patients with a median age of 73 years (range, 62 to 88 years) underwent therapy. Performance status of 0, 1, or 2 was seen in 11, 11, and two patients, respectively. Sites of disease included: lymph nodes, 16; lungs, nine; liver, seven; bladder, five; bones, two. Median number of cycles received was four (range, one to 16). Of 24 patients, 12 were confirmed responders; the observed objective response rate was 50% (95% CI, 29% to 71%). Median overall survival was 11.9 months (95% CI, 5.6 to 20.4 months), and median progression-free survival was 5.3 months (95% CI, 4.5 to 6.7 months). The most common treatment-related any-grade toxicities were fatigue (83% of patients), neutropenia (79%), anemia (63%), alopecia (50%), elevated AST (50%), and constipation, nausea, and thrombocytopenia (42% each).
Gemcitabine-eribulin treatment response and survival for cisplatin-ineligible patients compare favorably to other regimens. Additional research is needed.
患有转移性尿路上皮癌的患者通常不符合顺铂类治疗的条件。一项由美国国家癌症研究所癌症治疗评估计划赞助的试验评估了吉西他滨联合艾立布林在这一人群中的耐受性和疗效。
患有不可治愈的晚期或复发性转移性膀胱、输尿管或尿道尿路上皮癌且不适合手术治疗且不符合顺铂类治疗条件的患者有资格参加。顺铂类药物不适用的定义为肌酐清除率低于 60 mL/min(但≥ 30 mL/min)、2 级神经病变或 2 级听力损失。治疗方法为吉西他滨 1000 mg/m2 静脉注射,随后艾立布林 1.4 mg/m2,均在第 1 天和第 8 天给药,每 21 天重复一次,直至疾病进展或出现不可接受的毒性。采用 Simon 两阶段二期临床试验设计,以区分实体瘤反应评价标准 1.1 的客观缓解率为 20%与 50%。
2015 年 6 月至 2017 年 3 月期间,24 名中位年龄为 73 岁(范围,62 岁至 88 岁)的合格患者接受了治疗。分别有 11、11 和 2 名患者的表现状态为 0、1 或 2。疾病部位包括:淋巴结 16 处,肺部 9 处,肝脏 7 处,膀胱 5 处,骨骼 2 处。接受的中位周期数为 4 个(范围,1 至 16 个)。24 名患者中,12 名患者得到确认的缓解;观察到的客观缓解率为 50%(95%CI,29%至 71%)。中位总生存期为 11.9 个月(95%CI,5.6 至 20.4 个月),中位无进展生存期为 5.3 个月(95%CI,4.5 至 6.7 个月)。最常见的治疗相关任何级别毒性是疲劳(83%的患者)、中性粒细胞减少症(79%)、贫血(63%)、脱发(50%)、AST 升高(50%)以及便秘、恶心和血小板减少症(各 42%)。
吉西他滨联合艾立布林治疗对不符合顺铂类药物条件的患者的治疗反应和生存率优于其他方案。需要进一步的研究。