RANDOMIZED, SURGICAL ADJUVANT CLINICAL-TRIAL OF RECOMBINANT INTERFERON ALFA-2A IN SELECTED PATIENTS WITH MALIGNANT-MELANOMA

被引:187
作者
CREAGAN, ET
DALTON, RJ
AHMANN, DL
JUNG, SH
MORTON, RF
LANGDON, RM
KUGLER, J
RODRIGUE, LJ
机构
[1] MAYO CLIN & MAYO FDN, DIV MED ONCOL, ROCHESTER, MN 55905 USA
[2] MAYO CLIN & MAYO FDN, CANC STAT UNIT, ROCHESTER, MN 55905 USA
[3] DULUTH COMMUNITY CLIN ONCOL PROGRAM, DULUTH, MN USA
[4] IOWA ONCOL RES ASSOC, COMMUNITY CLIN ONCOL PROGRAM, DES MOINES, IA USA
[5] CREIGHTON UNIV, NEBRASKA ONCOL GRP, OMAHA, NE USA
[6] UNIV NEBRASKA, MED CTR & ASSOCIATES, LINCOLN, NE 68583 USA
[7] UNIV NEBRASKA, MED CTR, OMAHA, NE USA
[8] ILLINOIS ONCOL RES ASSOC, COMMUNITY CLIN ONCOL PROGRAM, PEORIA, IL USA
[9] SASKATCHEWAN CANC FDN, ALLAN BLAIR MEM CLIN, REGINA, SK, CANADA
关键词
D O I
10.1200/JCO.1995.13.11.2776
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: We conducted a randomized prospective trial in selected patients with fully resected high-risk stage I and II malignant melanoma. Patients and methods: Interferon alfa-2a (IFN-alpha 2a) 20 x 10(6) U/m(2) was administered three times each week for 12 weeks by the intramuscular route, Both the treatment group (n = 131) and the control group (n = 131) were evenly balanced with regard to relevant prognostic discriminants. Results: The median disease-free survival (DFS) time was 2.4 years for the IFN-alpha 2a group and 2.0 years for the observation group (log-rank P = 0.19), The median survival times were 6.6 years for IFN-alpha 2a and 5.0 years for observation (log-rank P = .40). For stage I patients (n = 102), there was no apparent therapeutic advantage from IFN-alpha 2a therapy. The DFS for stage II patients was a median of 10.8 months in the control group versus 17 months in the treatment group. The overall survival time was 4.1 years for the treatment group versus 2.7 years for the control group, The differences in DFS for stage II patient were significant in a Cox model. These results must be interpreted cautiously because of subset analysis. A severe fly-like toxicity occurred in 44% of patients, 13% lost at least 10% of their baseline weight, and 45% experienced a worsening of Eastern Cooperative Oncology Group (ECOG) performance score. Conclusion: Our findings indicate trends that suggest a possible benefit for selected patients with high-risk malignant melanoma, The results will require further study in a larger patient population for confirmation. (C) 1995 by American Society of Clinical Oncology.
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页码:2776 / 2783
页数:8
相关论文
共 41 条
[1]   A MULTIFACTORIAL ANALYSIS OF MELANOMA .3. PROGNOSTIC FACTORS IN MELANOMA PATIENTS WITH LYMPH-NODE METASTASES (STAGE-II) [J].
BALCH, CM ;
SOONG, SJ ;
MURAD, TM ;
INGALLS, AL ;
MADDOX, WA .
ANNALS OF SURGERY, 1981, 193 (03) :377-388
[2]  
BALCH CM, 1979, SURGERY, V86, P343
[3]  
BANZET P, 1978, CANCER, V41, P1240, DOI 10.1002/1097-0142(197804)41:4<1240::AID-CNCR2820410404>3.0.CO
[4]  
2-J
[5]   TUMOR THICKNESS, LEVEL OF INVASION AND NODE DISSECTION IN STAGE-1 CUTANEOUS MELANOMA [J].
BRESLOW, A .
ANNALS OF SURGERY, 1975, 182 (05) :572-575
[6]   FACTORS PROGNOSTIC FOR SURVIVAL IN PATIENTS WITH MALIGNANT-MELANOMA SPREAD TO THE REGIONAL LYMPH-NODES [J].
CALLERY, C ;
COCHRAN, AJ ;
ROE, DJ ;
REES, W ;
NATHANSON, SD ;
BENEDETTI, JK ;
ELASHOFF, RM ;
MORTON, DL .
ANNALS OF SURGERY, 1982, 196 (01) :69-75
[7]   RESULTS OF ADJUVANT INTERFERON STUDY IN WHO MELANOMA PROGRAM [J].
CASCINELLI, N ;
BUFALINO, R ;
MORABITO, A ;
MACKIE, R .
LANCET, 1994, 343 (8902) :913-914
[8]  
CLARK WH, 1969, CANCER RES, V29, P705
[9]  
COX DR, 1972, J R STAT SOC B, V34, P187
[10]  
CREAGAN ET, 1978, CANCER, V42, P2206, DOI 10.1002/1097-0142(197811)42:5<2206::AID-CNCR2820420518>3.0.CO