Retrospective Analysis of Clinical Outcomes With Neoadjuvant Cisplatin-Based Regimens for Muscle-Invasive Bladder Cancer

被引:30
作者
Pal, Sumanta K. [1 ]
Ruel, Nora H. [2 ]
Wilson, Timothy G. [3 ]
Yuh, Bertram E. [3 ]
机构
[1] City Hope Comprehens Canc Ctr, Dept Med Oncol & Expt Therapeut, Duarte, CA 91010 USA
[2] City Hope Comprehens Canc Ctr, Div Biostat, Dept Informat Sci, Duarte, CA 91010 USA
[3] City Hope Comprehens Canc Ctr, Div Urol, Dept Surg, Duarte, CA 91010 USA
关键词
Adriamycin; Cisplatin; Doxorubicin; Gemcitabine; Methotrexate; Muscle-invasive bladder cancer; Neoadjuvant; Response; Survival; Vinblastine; GEMCITABINE PLUS CISPLATIN; UROTHELIAL CARCINOMA; CHEMOTHERAPY; METHOTREXATE; VINBLASTINE; TRIAL;
D O I
10.1016/j.clgc.2012.08.004
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In a retrospective series, we showed that neoadjuvant chemotherapy with cisplatin-gemcitabine (CG) for muscle-invasive bladder cancer (MIBC) may yield efficacy similar to that of methotrexate, vinblastine, doxorubicin (Adriamycin), and cisplatin (MVAC). Although warranting prospective validation, our data suggest that CG is a possible alternative neoadjuvant approach to traditional regimens such as MVAC for patients with MIBC. Background: The benefit of neoadjuvant methotrexate, vinblastine, doxorubicin (Adriamycin), and cisplatin (MVAC) for muscle-invasive bladder cancer (MIBC) has been prospectively demonstrated in a phase III study. Extrapolating from comparative data in the metastatic setting, platinum doublets such as cisplatin-gemcitabine (CG) have been adopted. We sought to compare clinical outcomes in patients treated for MIBC with neoadjuvant CG and MVAC at our institution. Patients and Methods: Patients with MIBC were identified from a prospectively maintained registry. Clinicopathologic information and clinical outcome data were obtained directly from the registry. When available, pharmacy records were reviewed to ascertain the use of growth factors and chemotherapy dose intensity (DI). Survival was compared in subgroups divided by the regimen of chemotherapy rendered (ie, CG vs. MVAC) using the Kaplan-Meier method. Results: Median overall survival (OS) in the overall cohort (N = 61) was 23 months. OS was improved in patients receiving either MVAC or CG chemotherapy compared with patients receiving "other" chemotherapy (35.3 vs. 16.3 months; P = .055). Although the median OS associated with neoadjuvant CG numerically exceeded the survival associated with neoadjuvant MVAC (104.3 and 21.8 months, respectively), this was not statistically significant (P = .73). Pathologic downstaging predicted improved OS with both neoadjuvant CG and MVAC, and the rates of downstaging were similar with both regimens. Conclusions: Although warranting prospective validation, our data suggest that CG is a possible alternative neoadjuvant approach to traditional regimens such as MVAC for patients with MIBC.
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页码:246 / 250
页数:5
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