INTERFERON ALFA-2A AND INTERLEUKIN-2 WITH OR WITHOUT CISPLATIN IN METASTATIC MELANOMA - A RANDOMIZED TRIAL OF THE -ORGANIZATION-FOR-RESEARCH-AND-TREATMENT-OF-CANCER MELANOMA COOPERATIVE GROUP
U. Keilholz et al., INTERFERON ALFA-2A AND INTERLEUKIN-2 WITH OR WITHOUT CISPLATIN IN METASTATIC MELANOMA - A RANDOMIZED TRIAL OF THE -ORGANIZATION-FOR-RESEARCH-AND-TREATMENT-OF-CANCER MELANOMA COOPERATIVE GROUP, Journal of clinical oncology, 15(7), 1997, pp. 2579-2588
Purpose: The combination of interferon alfa-2a (IFN alpha) and high-do
se interleukin-2 (IL-2) is active in metastatic melanoma. The addition
of cisplatin (CDDP) has resulted in response rates greater than 50%,
This study was performed to determine whether the addition of CDDP to
a cytokine treatment regimen with IFN alpha and high-dose IL-2 influen
ces survival of patients with metastatic melanoma. Patients and Method
s: Patients with advanced metastatic melanoma were randomly assigned t
o receive treatment with IFN alpha 10 x 10(6) U/m(2) subcutaneously on
days 1 through 5 and a high-dose intravenous decrescendo regimen of I
L-2 on days 3 through 8 (18 mIU/m(2)/6 hours, 18 mIU/m(2)/12 hours, 18
mIU/m(2)/24 hours, and 4.5 mIU/m(2)/24 hours x 3) without (arm A) or
with (arm B) CDDP 100 mg/m(2) on day 1. Treatment cycles were repeated
every 28 days to a maximum of four cycles. Results: One hundred thirt
y-eight patients with advanced metastatic melanoma, of whom 87% had vi
sceral metastases, were accrued for the trial, Both regimens were feas
ible in a multicenter setting, The objective response rate was 18% wit
hout and 33% with CDDP (P = .04). The progression-free survival was 53
days without and 92 days with CDDP (P = .02, Wilcoxon; P = .09, log-r
ank). There was no statistically significant difference in survival be
tween treatment arms, with a median overall survival duration for all
patients of 9 months. Conclusion: The addition of CDDP to cytokine tre
atment with IFN alpha and IL-2 does not influence survival of patients
with advanced metastatic melanoma, despite a significant increase in
response rate and progression-free survival. (C) 1997 by American Soci
ety of Clinical Oncology.