Phase II Study of Gemcitabine, Carboplatin, and Bevacizumab in Patients With Advanced Unresectable or Metastatic Urothelial Cancer

被引:91
作者
Balar, Arjun V. [1 ,2 ]
Apolo, Andrea B. [1 ,2 ]
Ostrovnaya, Irina [1 ]
Mironov, Svetlana [1 ]
Iasonos, Alexia [1 ]
Trout, Alisa [1 ]
Regazzi, Ashley M. [1 ]
Garcia-Grossman, Ilana R. [1 ]
Gallagher, David J. [1 ,2 ]
Milowsky, Matthew I. [1 ,2 ]
Bajorin, Dean F. [1 ,2 ]
机构
[1] Mem Sloan Kettering Canc Ctr, New York, NY 10021 USA
[2] Cornell Univ, Weill Med Coll, New York, NY 10021 USA
关键词
TRANSITIONAL-CELL CARCINOMA; ENDOTHELIAL GROWTH-FACTOR; CISPLATIN-BASED CHEMOTHERAPY; LONG-TERM-SURVIVAL; PACLITAXEL PLUS BEVACIZUMAB; BLADDER-CANCER; THROMBOEMBOLIC EVENTS; RANDOMIZED-TRIAL; ANGIOGENESIS; UNFIT;
D O I
10.1200/JCO.2012.42.5215
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Purpose Although gemcitabine and carboplatin (GCa) is a standard option for patients with advanced urothelial cancer (UC) who are ineligible for cisplatin, outcomes remain poor. This trial evaluated the efficacy and safety of bevacizumab with GCa in advanced UC. Patients and Methods Patients with Karnofsky performance status of 60% to 70%, creatinine clearance less than 60 mL/min, visceral metastasis, or solitary kidney were eligible and received a lead-in dose of bevacizumab 10 mg/kg followed 2 weeks later by gemcitabine 1,000 mg/m(2) on days 1 and 8 and carboplatin at area under the [concentration-time] curve (AUC) 5.0 or 4.5 and bevacizumab 15 mg/kg on day 1 every 21 days for six cycles. Patients achieving at least stable disease (SD) continued bevacizumab 15 mg/kg every 21 days for 18 additional cycles. The study was powered to detect a 50% improvement in median progression-free survival (PFS) over a historical control. Results Fifty-one patients, median age 67 years (range, 42 to 83 years), were enrolled onto the study and were evaluable for toxicity. Twenty (39%) experienced grade 3 to 4 toxicity, and 10 (20%) had thromboembolic events (deep venous thrombosis or pulmonary embolism). Four received one or fewer cycles leaving 47 evaluable for outcomes. Twenty-three (49%) achieved response (three complete; 20 partial), and 11 had SD. Median PFS was 6.5 months (95% CI, 4.7 to 7.8 months); PFS was greater in the carboplatin AUC 5.0 group (P = .04). Median overall survival (OS) was 13.9 months. Conclusion The 95% one-sided lower confidence bound of 4.77 months for median PFS did not meet the predesignated PFS of more than 4.8 months considered sufficient for further study. Median OS was greater than expected. An ongoing phase III trial in patients who are eligible for therapy with cisplatin will define the role of bevacizumab in UC. J Clin Oncol 31:724-730. (C) 2013 by American Society of Clinical Oncology
引用
收藏
页码:724 / 730
页数:7
相关论文
共 46 条
[1]
Apolo AB, 2009, J CLIN ONCOL S, V27, p252s
[2]
Long-term survival in metastatic transitional-cell carcinoma and prognostic factors predicting outcome of therapy [J].
Bajorin, DF ;
Dodd, PM ;
Mazumdar, M ;
Fazzari, M ;
McCaffrey, JA ;
Scher, HI ;
Herr, H ;
Higgins, G ;
Boyle, MG .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (10) :3173-3181
[3]
Bajorin DF, 2007, J CLIN ONCOL, V25, p248s
[4]
A feasibility study of carboplatin with fixed dose of gemcitabine in 'unfit' patients with advanced bladder cancer [J].
Bellmunt, J ;
de Wit, R ;
Albanell, J ;
Baselga, J .
EUROPEAN JOURNAL OF CANCER, 2001, 37 (17) :2212-2215
[5]
ANGIOGENESIS IN BLADDER-CANCER - RELATIONSHIP BETWEEN MICROVESSEL DENSITY AND TUMOR PROGNOSIS [J].
BOCHNER, BH ;
COTE, RJ ;
WEIDNER, N ;
GROSHEN, S ;
CHEN, SC ;
SKINNER, DG ;
NICHOLS, PW .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1995, 87 (21) :1603-1612
[6]
BROWN LF, 1993, AM J PATHOL, V143, P1255
[7]
Phase III trial of bevacizumab (BEV) in the primary treatment of advanced epithelial ovarian cancer (EOC), primary peritoneal cancer (PPC), or fallopian tube cancer (FTC): A Gynecologic Oncology Group study [J].
Burger, R. A. ;
Brady, M. F. ;
Bookman, M. A. ;
Walker, J. L. ;
Homesley, H. D. ;
Fowler, J. ;
Monk, B. J. ;
Greer, B. E. ;
Boente, M. ;
Liang, S. X. .
JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (18)
[8]
Carboplatin-gemcitabine treatment of patients with transitional cell carcinoma of the bladder and impaired renal function [J].
Carles, J ;
Nogué, M ;
Domènech, M ;
Pérez, C ;
Saigí, E ;
Villadiego, K ;
Guasch, I ;
Ibeas, R .
ONCOLOGY, 2000, 59 (01) :24-27
[9]
URINE FROM PATIENTS WITH TRANSITIONAL-CELL CARCINOMA STIMULATES MIGRATION OF CAPILLARY ENDOTHELIAL-CELLS [J].
CHODAK, GW ;
SCHEINER, CJ ;
ZETTER, BR .
NEW ENGLAND JOURNAL OF MEDICINE, 1981, 305 (15) :869-874
[10]
INCREASED IMMUNODETECTION OF ACIDIC FIBROBLAST GROWTH-FACTOR IN BLADDER-CANCER, DETECTABLE IN URINE [J].
CHOPIN, DK ;
CARUELLE, JP ;
COLOMBEL, M ;
PALCY, S ;
RAVERY, V ;
CARUELLE, D ;
ABBOU, CC ;
BARRITAULT, D .
JOURNAL OF UROLOGY, 1993, 150 (04) :1126-1130