Phase II Trial of Cetuximab With or Without Paclitaxel in Patients With Advanced Urothelial Tract Carcinoma

被引:112
作者
Wong, Yu-Ning [1 ]
Litwin, Samuel [1 ]
Vaughn, David [2 ]
Cohen, Seth [5 ]
Plimack, Elizabeth R. [1 ]
Lee, James [6 ]
Song, Wei [3 ]
Dabrow, Michael [4 ]
Brody, Marion [1 ]
Tuttle, Holly [1 ]
Hudes, Gary [1 ]
机构
[1] Fox Chase Canc Ctr, Philadelphia, PA 19111 USA
[2] Univ Penn, Philadelphia, PA 19104 USA
[3] Pottstown Mem Med Ctr, Pottstown, PA USA
[4] Paoli Canc Ctr, Paoli, PA USA
[5] St Lukes Roosevelt Hosp, New York, NY 10025 USA
[6] Virtua Canc Ctr, Mt Holly, NJ USA
关键词
TRANSITIONAL-CELL CARCINOMA; GROWTH-FACTOR-RECEPTOR; METASTATIC COLORECTAL-CANCER; BLADDER-CANCER; 2ND-LINE TREATMENT; PROGNOSTIC-FACTORS; PLUS IRINOTECAN; CHEMOTHERAPY; GEMCITABINE; EXPRESSION;
D O I
10.1200/JCO.2012.41.9572
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose The benefit of salvage chemotherapy is modest in metastatic urothelial cancer. We conducted a randomized, noncomparative phase II study to measure the efficacy of cetuximab with or without paclitaxel in patients with previously treated urothelial cancer. Patients and Methods Patients with metastatic urothelial cancer who received one line of chemotherapy in the perioperative or metastatic setting were randomly assigned to 4-week cycles of cetuximab 250 mg/m(2) with or without paclitaxel 80 mg/m2 per week. We used early progression as an indicator of futility. Either arm would close if seven of the initial 15 patients in that arm progressed at the first disease evaluation at 8 weeks. Results We enrolled 39 evaluable patients. The single-agent cetuximab arm closed after nine of the first 11 patients progressed by 8 weeks. The combination arm completed the full accrual of 28 patients, of whom 22 patients (78.5%) had visceral disease. Twelve of 28 patients had progression-free survival greater than 16 weeks. The overall response rate was 25% (95% CI, 11% to 45%; three complete responses and four partial responses). The median progression-free survival was 16.4 weeks (95% CI, 12 to 25.1 weeks), and the median overall survival was 42 weeks (95% CI, 30.4 to 78 weeks). Treatment-related grade 3 and 4 adverse events that occurred in at least two patients were rash (six cases), fatigue (five cases), and low magnesium (three cases). Conclusion Although it had limited activity as a single agent, cetuximab appears to augment the antitumor activity of paclitaxel in previously treated urothelial cancers. The cetuximab and paclitaxel combination merits additional study to establish its role in the treatment of urothelial cancers. J Clin Oncol 30:3545-3551. (C) 2012 by American Society of Clinical Oncology
引用
收藏
页码:3545 / 3551
页数:7
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