Interferon alfa-2a and interleukin-2 with or without cisplatin in metastatic melanoma: A randomized trial of the European organization for research and treatment of cancer melanoma cooperative group

Ulrich Keilholz, Swan Hoo Goey, Cornelis J.A. Punt, Thomas M. Proebstle, Ralph Salzmann, Carmen Scheibenbogen, Dirk Schadendorf, Danielle Liénard, Alexander Enk, Reinhard Dummer, Birgit Hantich, Anne Marie Geueke, Alexander M.M. Eggermont

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198 Citaten (Scopus)

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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.

Originele taal-2Engels
Pagina's (van-tot)2579-2588
Aantal pagina's10
TijdschriftJournal of Clinical Oncology
Volume15
Nummer van het tijdschrift7
DOI's
StatusGepubliceerd - jul. 1997
Extern gepubliceerdJa

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