Phase III trial of fluorouracil, interferon alfa-2b, and cisplatin versus methotrexate, vinblastine, doxorubicin, and cisplatin in metastatic or unresectable urothelial cancer

被引:59
作者
Siefker-Radtke, AO
Millikan, RE
Tu, SM
Moore, DF
Smith, TL
Williams, D
Logothetis, CJ
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Genitourinary Med Oncol, Houston, TX 77030 USA
[2] Univ Texas, MD Anderson Canc Ctr, Dept Biostat, Houston, TX 77030 USA
[3] Ctr Canc Kansas, Wichita Community Clin Oncol Program, Wichita, KS USA
关键词
D O I
10.1200/JCO.20.5.1361
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose : Previously, we developed a novel biochemotherapy regimen combining interferon alfa-2b with fluorouracil and cisplatin (FAP). We now report the results of a prospective randomized trial comparing FAP with methotrexate, vinblastine, doxorubicin, and cisplatin (M-VAC), the standard chemotherapy regimen for locally advanced and metastatic urothelial cancer. The purpose of this study was to compare the response rates and overall survival of patients with metastatic or unresectable urothelial cancer treated with these two chemotherapy regimens. Patients and Methods: Between October 1992 and September 1999, 172 previously untreated patients were registered and randomly assigned to treatment with either FAP or M-VAC. Patients were followed until their death. Results: The pretreatment clinical characteristics of the groups were similar except for sex (P < .01). Sex did not affect prognosis or survival. The objective response rate for patients assigned to FAP was 42% (35 of 83 patients), with complete response observed in eight (10%) of 83 patients. Among the patients assigned to M-VAC, 51 (59%) of 86 had an objective response, with complete response observed in 21 (24%) of 86. The Kaplan-Meier estimate of median survival was 12.5 months for both groups. Both regimens were quite toxic, with more mucocutaneous toxicity in the FAP arm and more myelosuppression in the M-VAC arm. Conclusion. Although overall survival was not significantly different, patients assigned to M-VAC had a much better chance of responding to front-line therapy. Thus, FAP is very likely to be inferior to M-VAC and is certainly no less toxic. FAP cannot be recommended as part of the standard armamentarium for urothelial cancer. (C) 2002 by American Society of Clinical Oncology.
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收藏
页码:1361 / 1367
页数:7
相关论文
共 27 条
  • [11] ESCALATED DOSAGES OF METHOTREXATE, VINBLASTINE, DOXORUBICIN, AND CISPLATIN PLUS RECOMBINANT HUMAN GRANULOCYTE-COLONY-STIMULATING FACTOR IN ADVANCED UROTHELIAL CARCINOMA - AN EASTERN-COOPERATIVE-ONCOLOGY-GROUP TRIAL
    LOEHRER, PJ
    ELSON, P
    DREICER, R
    HAHN, R
    NICHOLS, CR
    WILLIAMS, R
    EINHORN, LH
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1994, 12 (03) : 483 - 488
  • [12] A RANDOMIZED COMPARISON OF CISPLATIN ALONE OR IN COMBINATION WITH METHOTREXATE, VINBLASTINE, AND DOXORUBICIN IN PATIENTS WITH METASTATIC UROTHELIAL CARCINOMA - A COOPERATIVE GROUP-STUDY
    LOEHRER, PJ
    EINHORN, LH
    ELSON, PJ
    CRAWFORD, ED
    KUEBLER, P
    TANNOCK, I
    RAGHAVAN, D
    STUARTHARRIS, R
    SAROSDY, MF
    LOWE, BA
    BLUMENSTEIN, B
    TRUMP, D
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1992, 10 (07) : 1066 - 1073
  • [13] LOGOTHETIS C, 1992, Proceedings of the American Association for Cancer Research Annual Meeting, V33, P221
  • [14] ESCALATED MVAC WITH OR WITHOUT RECOMBINANT HUMAN GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR FOR THE INITIAL TREATMENT OF ADVANCED MALIGNANT UROTHELIAL TUMORS - RESULTS OF A RANDOMIZED TRIAL
    LOGOTHETIS, CJ
    FINN, LD
    SMITH, T
    KILBOURN, RG
    ELLERHORST, JA
    ZUKIWSKI, AA
    SELLA, A
    TU, SM
    AMATO, RJ
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1995, 13 (09) : 2272 - 2277
  • [15] A PROSPECTIVE RANDOMIZED TRIAL COMPARING MVAC AND CISCA CHEMOTHERAPY FOR PATIENTS WITH METASTATIC UROTHELIAL TUMORS
    LOGOTHETIS, CJ
    DEXEUS, FH
    FINN, L
    SELLA, A
    AMATO, RJ
    AYALA, AG
    KILBOURN, RG
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1990, 8 (06) : 1050 - 1055
  • [16] LOGOTHETIS CJ, 1994, ANTICANCER RES, V14, P1265
  • [17] Petrioli R, 1996, CANCER, V77, P344, DOI 10.1002/(SICI)1097-0142(19960115)77:2<344::AID-CNCR18>3.0.CO
  • [18] 2-1
  • [19] Slaton JW, 1999, CLIN CANCER RES, V5, P2726
  • [20] Chemotherapy and management of bladder tumours
    Sternberg, CN
    Calabrò, F
    [J]. BJU INTERNATIONAL, 2000, 85 (05) : 599 - 610