Randomized trial comparing epirubicin, cisplatin, and fluorouracil versus fluorouracil, doxorubicin, and methotrexate in advanced esophagogastric cancer

被引:745
作者
Webb, A
Cunningham, D
Scarffe, JH
Harper, P
Norman, A
Joffe, JK
Hughes, M
Mansi, J
Findlay, M
Hill, A
Oates, J
Nicolson, M
Hickish, T
OBrien, M
Iveson, T
Watson, M
Underhill, C
Wardley, A
Meehan, M
机构
[1] ROYAL MARSDEN HOSP,MED SECT,CRC,SUTTON SM2 5PT,SURREY,ENGLAND
[2] ROYAL MARSDEN HOSP,GASTROINTESTINAL UNIT,SUTTON SM2 5PT,SURREY,ENGLAND
[3] INST CANC RES,SUTTON,SURREY,ENGLAND
[4] CHRISTIE HOSP,CRC,DEPT MED ONCOL,MANCHESTER,LANCS,ENGLAND
[5] GUYS HOSP,DEPT MED ONCOL,LONDON,ENGLAND
[6] ST GEORGE HOSP,DEPT MED ONCOL,LONDON,ENGLAND
[7] CRC,DEPT MED ONCOL,GLASGOW,LANARK,SCOTLAND
[8] ST JAMES HOSP,IMPERIAL CANC RES FUND,CANC RES UNIT,LEEDS LS9 7TF,W YORKSHIRE,ENGLAND
关键词
D O I
10.1200/JCO.1997.15.1.261
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: We report the results of a prospectively randomized study that compared the combination of epirubicin, cisplatin, and protracted venous infusion fluorouracil (5-FU) (ECF regimen) with the standard combination of 5-FU, doxorubicin, and methotrexate (FAMTX) in previously untreated patients with advanced esophagogastric cancer. Patients and Methods: Two hundred seventy-four patients with adenocarcinoma or undifferentiated carcinoma were randomized and analyzed for survival, tumor response, toxicity, and quality of life (QL). Results: The overall response rate was 45% (95% confidence interval [CI], 36% to 54%) with ECF and 21% (95% CI, 13% to 29%) with FAMTX (P = .0002). Toxicity was tolerable and there were only three toxic deaths. The FAMTX regimen caused more hematologic toxicity and serious infections, but ECF caused more emesis and alopecia. The median survival duration was 8.9 months with ECF and 5.7 months with FAMTX (P = .0009); at 1 year, 36% (95% CI, 27% to 45%) of ECF and 21% (95% CI, 14% to 29%) of FAMTX patients were alive. The median failure-free survival duration was 7.4 months with ECF and 3.4 months with FAMTX (P = .00006). The global QL scores were better for ECF at 24 weeks, but the remaining QL data showed no differences between either arm of the study. Hospital-based cost analysis on a subset of patients was similar for each arm and translated into an increment cost of $975 per life-year gained. Conclusion: The ECF regimen results in a survival and response advantage, tolerable toxicity, better QL and cost-effectiveness compared with FAMTX chemotherapy. This regimen should now be considered the standard treatment for advanced esophagogastric cancer. (C) 1997 by American Society of Clinical Oncology.
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页码:261 / 267
页数:7
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