Sunnybrook Odette Cancer Centre, Toronto, ON, Canada.
Lancet Oncol. 2013 Jul;14(8):769-76. doi: 10.1016/S1470-2045(13)70162-1. Epub 2013 May 22.
No standard treatment exists for patients with platinum-refractory urothelial cancer. Taxanes and vinflunine are commonly used, but response is less than 20% with no survival benefit. In this phase 2 study, we assessed efficacy and tolerability of nanoparticle albumin-bound (nab) paclitaxel in platinum-refractory urothelial cancer.
We did an open-label, single-group, two-stage study at five centres in Canada. We enrolled patients aged at least 18 years with histologically confirmed, locally advanced, or metastatic measurable urothelial cancer, with documented progression on or within 12 months of treatment with one previous platinum-containing regimen. Patients received nab-paclitaxel at 260 mg/m(2) intravenously every 3 weeks. Treatment continued until disease progression or occurrence of unacceptable toxic effects. The primary endpoint was objective tumour response, defined by a complete response (CR) or partial response (PR) according to Response Evaluation Criteria In Solid Tumors (version 1.0) criteria. Tumour response and safety were assessed in all patients who received at least one cycle of nab-paclitaxel. This study is registered with ClinicalTrials.gov, number NCT00683059.
We enrolled 48 patients between Oct 16, 2008, and June 23, 2010. Patients received a median of six cycles (range one to 15). 47 patients were evaluable; one (2·1%) had a CR and 12 (25·5%) had PRs, resulting in an overall response of 27·7% (95% CI 17·3-44·4). The most frequently recorded adverse events of any grade were fatigue (38 of 48; 79%), pain (37 of 48; 77%), alopecia (34 of 48; 71%), and neuropathy (30 of 48; 77%). The most frequently recorded adverse events of grade 3 or higher were pain (11 of 48; 23%), fatigue (five of 48; 23%), hypertension (three of 48; 6%), neuropathy (three of 48, 6%), and joint stiffness or pain (two of 48; 4%).
Nab-paclitaxel was well tolerated in this population of patients with pretreated advanced urothelial cancer with an encouraging tumour response. These results warrant further study of nab-paclitaxel in second-line treatment of urothelial cancer.
Abraxis Bioscience, Celgene.
铂类耐药性尿路上皮癌患者尚无标准治疗方法。紫杉醇和 vinflunine 通常被使用,但反应率低于 20%,且无生存获益。在这项 2 期研究中,我们评估了纳米白蛋白结合紫杉醇(nab-紫杉醇)在铂类耐药性尿路上皮癌中的疗效和耐受性。
我们在加拿大的五家中心进行了一项开放标签、单组、两阶段研究。我们招募了年龄至少 18 岁的组织学证实的局部晚期或转移性可测量的尿路上皮癌患者,这些患者在先前的含铂方案治疗期间或治疗后 12 个月内有疾病进展。患者接受nab-紫杉醇 260mg/m2 静脉注射,每 3 周一次。治疗持续到疾病进展或出现不可接受的毒性作用。主要终点是根据实体瘤反应评价标准(版本 1.0)标准评估的客观肿瘤反应,定义为完全缓解(CR)或部分缓解(PR)。所有接受至少一个周期 nab-紫杉醇治疗的患者均评估了肿瘤反应和安全性。这项研究在 ClinicalTrials.gov 注册,编号为 NCT00683059。
我们于 2008 年 10 月 16 日至 2010 年 6 月 23 日期间纳入了 48 名患者。患者接受了中位数为 6 个周期(范围为 1 至 15 个)的治疗。47 名患者可评估;1 名(2.1%)患者有 CR,12 名(25.5%)患者有 PR,总缓解率为 27.7%(95%CI 17.3-44.4)。任何级别最常记录的不良事件是疲劳(48 例中的 38 例;79%)、疼痛(48 例中的 37 例;77%)、脱发(48 例中的 34 例;71%)和周围神经病变(48 例中的 30 例;77%)。3 级或以上最常记录的不良事件是疼痛(48 例中的 11 例;23%)、疲劳(48 例中的 5 例;23%)、高血压(48 例中的 3 例;6%)、周围神经病变(48 例中的 3 例;6%)和关节僵硬或疼痛(48 例中的 2 例;4%)。
nab-紫杉醇在先前接受过治疗的晚期尿路上皮癌患者中耐受性良好,肿瘤反应令人鼓舞。这些结果证明了 nab-紫杉醇在尿路上皮癌二线治疗中的进一步研究是合理的。
Abraxis Bioscience,Celgene。