Interleukin-2, Interferon-α and Interleukin-2 plus Interferon-α in Renal Cell Carcinoma. A Randomized Phase Ii Trial

Author:

Boccardo Francesco1,Rubagotti Alessandra2,Canobbio Luciano1,Galligioni Enzo3,Sorio Roberto4,Lucenti Antonio4,Cognetti Francesco5,Ruggeri Enrico5,Landonio Giuseppe6,Baiocchi Claudia6,Besana Carlo7,Citterio Giovanni7,De Rosa Marisa8,Calabresi Federico5

Affiliation:

1. Department of Medical Oncology II, National Institute for Cancer Research, Genoa

2. Biostatistics Unit, Chair of Medical Oncology, University, Genoa

3. Department of Medical Oncology, S. Chiara Hospital, Trent

4. Department of Medical Oncology, Centro di Riferimento Oncologico, Aviano

5. Department of Medical Oncology I, Istituto Regina Elena, Rome

6. Department of Medical Oncology “Falck”, Niguarda Hospital, Milan

7. Chair of Internal Medicine, University, Milan

8. CINECA, Bologna, Italy

Abstract

Background The purpose of the present study was to investigate the therapeutic effectiveness of interleukin-2 (IL-2) and interferon (IFN), either alone or in combination, in comparable groups of patients affected by advanced renal cell carcinoma (RCC). Patients and methods In order to limit selection biases, treatment was allocated on a random basis. Patients randomized to IL-2 alone were scheduled to receive eight rIL-2 24-hour i.v. infusion cycles, days 1 to 4, at a daily dose of 18 x 106 IU/m2 for a total of 25 weeks. Patients randomized to IFN alone were scheduled to receive rIFN-α at a daily dose of 6 x 106 IU/m2, days 1, 3 and 5, every week for a total of 52 weeks. Patients randomized to the combination of IFN and IL-2 were given the same drugs at the same daily doses for a total of 24 weeks. Drug dose was modified according to toxicity. Results Twenty-three percent (95% CI: ± 17.5) of patients treated with IL-2 alone showed an objective response to treatment (9% CR). The corresponding figures in patients treated with IFN alone or IFN plus IL-2 were 9% (95% CI: ± 11.9) and 9% (95% CI: ± 11.9), respectively. Complete responses were observed only in patients treated with IL-2. The median duration of response in the IL-2 arm was 18 months (range, 9.5-24). The duration of the two responses achieved by IFN alone was seven and nine, months, respectively. The corresponding figures in the two patients responding to the combination of IFN with IL-2 were 19 and 27 months, respectively. Total IL-2 dose appeared to be a major predictor of response. Only a minority of patients experienced grade 3-4 toxicity, the incidence being higher in those treated with IL-2 or IL-2 plus IFN. Conclusions Neither IFN nor IL-2 or the combination of the two appear to be very active in patients with advanced RCC, even when trial entry was restricted to patients with relatively indolent disease. This stresses the need for the development of new approaches.

Publisher

SAGE Publications

Subject

Cancer Research,Oncology,General Medicine

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