TY - JOUR
T1 - Interferon alfa-2a and interleukin-2 with or without cisplatin in metastatic melanoma
T2 - A randomized trial of the European organization for research and treatment of cancer melanoma cooperative group
AU - Keilholz, Ulrich
AU - Goey, Swan Hoo
AU - Punt, Cornelis J.A.
AU - Proebstle, Thomas M.
AU - Salzmann, Ralph
AU - Scheibenbogen, Carmen
AU - Schadendorf, Dirk
AU - Liénard, Danielle
AU - Enk, Alexander
AU - Dummer, Reinhard
AU - Hantich, Birgit
AU - Geueke, Anne Marie
AU - Eggermont, Alexander M.M.
PY - 1997/7
Y1 - 1997/7
N2 - Purpose: The combination of interferon alfa-2a (IFNα) and high-dose 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 IFNα and high-dose IL-2 influences survival of patients with metastatic melanoma. Patients and Methods: Patients with advanced metastatic melanoma were randomly assigned to receive treatment with IFNα 10 x 106 U/m2 subcutaneously on days 1 through 5 and a high- dose intravenous decrescendo regimen of IL-2 on days 3 through 8 (18 mIU/m2/6 hours, 18 mIU/m2/12 hours, 18 mIU/m2/24 hours, and 4.5 mIU/m2/24 hours x 3) without (arm A) or with (arm B) CDDP 100 mg/m2 on day 1. Treatment cycles were repeated every 28 days to a maximum of four cycles. Results: One hundred thirty-eight patients with advanced metastatic melanoma, of whom 87% had visceral metastases, were accrued for the trial. Both regimens were feasible in a multicenter setting. The objective response rate was 18% without 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-rank). There was no statistically significant difference in survival between treatment arms, with a median overall survival duration for all patients of 9 months. Conclusion: The addition of CDDP to cytokine treatment with and IL-2 does not influence survival of patients with advanced metastatic melanoma, despite a significant increase in response rate and progression-free survival.
AB - Purpose: The combination of interferon alfa-2a (IFNα) and high-dose 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 IFNα and high-dose IL-2 influences survival of patients with metastatic melanoma. Patients and Methods: Patients with advanced metastatic melanoma were randomly assigned to receive treatment with IFNα 10 x 106 U/m2 subcutaneously on days 1 through 5 and a high- dose intravenous decrescendo regimen of IL-2 on days 3 through 8 (18 mIU/m2/6 hours, 18 mIU/m2/12 hours, 18 mIU/m2/24 hours, and 4.5 mIU/m2/24 hours x 3) without (arm A) or with (arm B) CDDP 100 mg/m2 on day 1. Treatment cycles were repeated every 28 days to a maximum of four cycles. Results: One hundred thirty-eight patients with advanced metastatic melanoma, of whom 87% had visceral metastases, were accrued for the trial. Both regimens were feasible in a multicenter setting. The objective response rate was 18% without 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-rank). There was no statistically significant difference in survival between treatment arms, with a median overall survival duration for all patients of 9 months. Conclusion: The addition of CDDP to cytokine treatment with and IL-2 does not influence survival of patients with advanced metastatic melanoma, despite a significant increase in response rate and progression-free survival.
UR - http://www.scopus.com/inward/record.url?scp=0342894822&partnerID=8YFLogxK
U2 - 10.1200/JCO.1997.15.7.2579
DO - 10.1200/JCO.1997.15.7.2579
M3 - Article
AN - SCOPUS:0342894822
SN - 0732-183X
VL - 15
SP - 2579
EP - 2588
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 7
ER -