Dacarbazine, Cisplatin, and Interferon-Alfa-2b With or Without Interleukin-2 in Metastatic Melanoma: A Randomized Phase III Trial (18951) of the European Organisation for Research and Treatment of Cancer Melanoma Group

Author:

Keilholz Ulrich1,Punt Cornelis J.A.1,Gore Martin1,Kruit Wim1,Patel Poulam1,Lienard Danielle1,Thomas Jose1,Proebstle Thomas M.1,Schmittel Alexander1,Schadendorf Dirk1,Velu Thierry1,Negrier Sylvie1,Kleeberg Ulrich1,Lehman Frederic1,Suciu Stefan1,Eggermont Alexander M.M.1

Affiliation:

1. From the Department of Medicine III, Charité, Campus Benjamin Franklin, Berlin; Department of Dermatology, University of Ulm, Ulm; Department of Dermatology, University of Heidelberg, Heidelberg; Haematologisch-Onkologische Praxis Altona, Hamburg, Germany; Department of Medical Oncology, University Medical Center, Nijmegen; Daniel den Hoed Cancer Center, University of Rotterdam, Rotterdam, Netherlands; Royal Marsden Hospital, London; Cancer Research UK Clinical Center, St James’s University Hospital,...

Abstract

Background Based on phase II trial results, chemoimmunotherapy combinations have become the preferred treatment for patients with metastatic melanoma in many institutions. This study was performed to determine whether interleukin-2 (IL-2) as a component of chemoimmunotherapy influences survival of patients with metastatic melanoma. Patients and Methods Patients with advanced metastatic melanoma were randomly assigned to receive dacarbazine 250 mg/m2 and cisplatin 30 mg/m2 on days 1 to 3 combined with interferon-alfa-2b 10 × 106 U/m2 subcutaneously on days 1 through 5 without (arm A) or with (arm B) a high-dose intravenous decrescendo regimen of IL-2 on days 5 through 10 (18 × 106 U/m2/6 hours, 18 × 106 U/m2/12 hours, 18 × 106 U/m2/24 hours, and 4.5 × 106 U/m2 for 3 × 24 hours). Treatment cycles were repeated in the absence of disease progression every 28 days to a maximum of four cycles. Results Three hundred sixty-three patients with advanced metastatic melanoma were accrued. The median survival was 9 months in both arms, with a 2-year survival rate of 12.9% and 17.6% in arms A and B, respectively (P = .32; hazard ratio, 0.90; 95% CI, 0.72 to 1.11). There was also no statistically significant difference regarding progression-free survival (median, 3.0 v 3.9 months) and response rate (22.8% v 20.8%). Conclusion Despite its activity in melanoma as a single agent or in combination with interferon-alfa-2b, the chosen schedule of IL-2 added to the chemoimmunotherapy combination had no clinically relevant activity.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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