Randomized phase III trial of 2nd line gemcitabine and paclitaxel chemotherapy in patients with advanced bladder cancer: short-term versus prolonged treatment [German Association of Urological Oncology (AUO) trial AB 20/99]

被引:111
作者
Albers, P. [1 ]
Park, S. -I. [2 ]
Niegisch, G. [1 ]
Fechner, G. [2 ]
Steiner, U. [3 ]
Lehmann, J. [4 ]
Heimbach, D. [5 ]
Heidenreich, A. [6 ]
Fimmers, R. [7 ]
Siener, R. [2 ]
机构
[1] Univ Dusseldorf, Dept Urol, D-40225 Dusseldorf, Germany
[2] Univ Bonn, Dept Urol, D-5300 Bonn, Germany
[3] Charite, Dept Urol, Berlin, Germany
[4] Univ Homburg, Dept Urol, D-6650 Homburg, Germany
[5] St Vincenz Hosp, Dept Urol, Datteln, Germany
[6] Univ Aachen, Dept Urol, D-5100 Aachen, Germany
[7] Univ Bonn, Inst Med Biometry Informat & Epidemiol, D-5300 Bonn, Germany
关键词
bladder cancer; chemotherapy; clinical trial; phase III; second-line; transitional cell carcinoma; TRANSITIONAL-CELL CARCINOMA; ADVANCED UROTHELIAL CARCINOMA; PLATINUM-CONTAINING REGIMEN; 2ND-LINE CHEMOTHERAPY; SOLID TUMORS; CISPLATIN; PLUS; VINFLUNINE; TRACT;
D O I
10.1093/annonc/mdq398
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The second-line chemotherapeutic treatment for metastatic urothelial cancer (UC) after failure of cisplatin-based first-line therapy needs to be improved. Based on encouraging phase II data of gemcitabine and paclitaxel (Taxol) (GP), this trial was designed to compare a short-term (arm A) versus a prolonged (arm B) second-line combination chemotherapy of GP. Patients and methods: Of 102 randomized patients, 96 were eligible for analysis. Primary end point was overall survival (OS). Secondary end points were progression-free survival (PFS), objective response rates (ORR) and toxicity. Results: Neither OS [arm A: 7.8 (95% CI: 4.2-11.4), arm B: 8.0 (95% CI: 4.9-11.1) months] and PFS [ arm A: 4.0 (95% CI: 0-8.0), arm B: 3.1 (95% CI: 1.9-4.2) months] nor ORR (arm A: 37.5%, arm B: 41.5%) were significantly different. On prolonged treatment, more patients experienced severe anemia (arm A: 6.7% versus arm B: 26.7% grade III/IV anemia; P = 0.011). In six patients, treatment was stopped during the first cycle due to disease progression or toxicity. Two patients died due to treatment-related toxic effects. Conclusion: Due to rapid tumor progression and toxicity at this dosage and schedule in a multicenter setting, it was not feasible to deliver a prolonged regimen. However, a high response rate of similar to 40% makes GP a promising second-line treatment option for patients with metastatic UC.
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页码:288 / 294
页数:7
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