Prognostic factors for survival and factors associated with long-term remission in patients with advanced melanoma receiving cytokine-based treatments:: second analysis of a randomised EORTC Melanoma Group trial comparing interferon-α2a (IFNα) and interleukin 2 (IL-2) with or without cisplatin

被引:39
作者
Keilholz, U
Martus, P
Punt, CJA
Kruit, W
Mooser, G
Schadendorf, D
Liénard, D
Dummer, R
Koller, J
Voit, C
Eggermont, AMM
机构
[1] Free Univ Berlin, Med Klin 3, UKBF, D-12200 Berlin, Germany
[2] Free Univ Berlin, Dept Biostat, UKBF, Berlin, Germany
[3] Univ Nijmegen Hosp, Dept Med Oncol, NL-6500 HB Nijmegen, Netherlands
[4] Dr Daniel Den Hoed Canc Ctr, Dept Med Oncol, NL-3008 AE Rotterdam, Netherlands
[5] Univ Ulm, Dept Dermatol, Ulm, Germany
[6] Univ Hosp Rudolf Virchow, Dept Dermatol, Berlin, Germany
[7] CHU Vaudois, Ctr Pluridisciplinaire Oncol, CH-1011 Lausanne, Switzerland
[8] Univ Zurich, Dept Dermatol, CH-8006 Zurich, Switzerland
[9] Salzburg Univ, Dept Dermatol, A-5020 Salzburg, Austria
[10] Humboldt Univ, Charite, Dept Dermatol, Berlin, Germany
[11] Dr Daniel Den Hoed Canc Ctr, Dept Surg Oncol, NL-3008 AE Rotterdam, Netherlands
关键词
melanoma; IL-2; cytokines; prognostic factors;
D O I
10.1016/S0959-8049(02)00123-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The aim of this study,vas to define prognostic factors for survival, and especially for long-term survival in a mature data-set of patients with stage IV melanoma treated within a randomised trial of cytokine-based protocols. Long-term follow-up data on patients enrolled into a European Organization for Research and Treatment of Cancer (EORTC) trial comparing interferon-alpha (IFNalpha) plus interleukin-2 (IL-2) with or without cisplatin were collected. Univariate and multivariate Cox regression analyses wereperformed to define prognostic factors for survival. The characteristics of patients alive at 2 and 5 years after randomisation were compared with the entire cohort using the chi(2) test. The Minimum potential follow-up of the 131 evaluable patients was 5 years. 18 patients (14%) were alive 2 years after randomisation, and 11 (8%) 5 years after randomisation. Pretreatment performance status (PS), serum lactate dehydrogenase (LDH) and tumour mass were significant predictors for survival, whereas site of metastases and number of sites were non-significant. PS and LDH were the only independent prognostic factors. All except I patient alive at 2 and 5 years had a pretreatment PS of 100%. and only three long-term survivors had elevated pretreatment LDH. There was no association between the site of metastases and long-term survival. Response to treatment was a major predictor for long-term survival, whereas addition of cisplatin did not impact upon overall survival probability or on long-term survival. The probability of long-term survival in stage IV melanoma patients after IL-2-based treatments is governed by pretreatment PS, serum LDH and response to treatment. Site of metastases, the basis for the M-subcategories of the new AJCC staging system, was not informative in this study. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1501 / 1511
页数:11
相关论文
共 46 条
[1]  
Agarwala SS, 1999, CANCER, V85, P1979, DOI 10.1002/(SICI)1097-0142(19990501)85:9<1979::AID-CNCR15>3.0.CO
[2]  
2-G
[3]  
AHMANN DL, 1989, CANCER, V63, P224, DOI 10.1002/1097-0142(19890115)63:2<224::AID-CNCR2820630203>3.0.CO
[4]  
2-I
[5]   ANALYSIS OF SURVIVAL BY TUMOR RESPONSE [J].
ANDERSON, JR ;
CAIN, KC ;
GELBER, RD .
JOURNAL OF CLINICAL ONCOLOGY, 1983, 1 (11) :710-719
[6]   High-dose recombinant interleukin 2 therapy for patients with metastatic melanoma: Analysis of 270 patients treated between 1985 and 1993 [J].
Atkins, MB ;
Lotze, MT ;
Dutcher, JP ;
Fisher, RI ;
Weiss, G ;
Margolin, K ;
Abrams, J ;
Sznol, M ;
Parkinson, D ;
Hawkins, M ;
Paradise, C ;
Kunkel, L ;
Rosenberg, SA .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (07) :2105-2116
[7]   MULTICENTER RANDOMIZED TRIAL OF DACARBAZINE ALONE OR IN COMBINATION WITH 2 DIFFERENT DOSES AND SCHEDULES OF INTERFERON ALFA-2A IN THE TREATMENT OF ADVANCED MELANOMA [J].
BAJETTA, E ;
DILEO, A ;
ZAMPINO, MG ;
SERTOLI, MR ;
COMELLA, G ;
BARDUAGNI, M ;
GIANNOTTI, B ;
QUEIROLO, P ;
TRIBBIA, G ;
BERNENGO, MG ;
MENICHETTI, ET ;
PALMERI, S ;
RUSSO, A ;
CRISTOFOLINI, M ;
ERBAZZI, A ;
FOWST, C ;
CRISCUOLO, D ;
BUFALINO, R ;
ZILEMBO, N ;
CASCINELLI, N .
JOURNAL OF CLINICAL ONCOLOGY, 1994, 12 (04) :806-811
[8]   A MULTIFACTORIAL ANALYSIS OF MELANOMA .4. PROGNOSTIC FACTORS IN 200 MELANOMA PATIENTS WITH DISTANT METASTASES (STAGE III) [J].
BALCH, CM ;
SOONG, SJ ;
MURAD, TM ;
SMITH, JW ;
MADDOX, WA ;
DURANT, JR .
JOURNAL OF CLINICAL ONCOLOGY, 1983, 1 (02) :126-134
[9]   Final version of the American Joint Committee on Cancer staging system for cutaneous melanoma [J].
Balch, CM ;
Buzaid, AC ;
Soong, SJ ;
Atkins, MB ;
Cascinelli, N ;
Coit, DG ;
Fleming, ID ;
Gershenwald, JE ;
Houghton, A ;
Kirkwood, JM ;
McMasters, KM ;
Mihm, MF ;
Morton, DL ;
Reintgen, DS ;
Ross, MI ;
Sober, A ;
Thompson, JA ;
Thompson, JF .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (16) :3635-3648
[10]  
Barth A, 1995, J Am Coll Surg, V181, P193