Interleukin-2, interferon-α and interleukin-2 plus interferon-α in renal cell carcinoma.: A randomized phase II trial

被引:22
作者
Boccardo, F
Rubagotti, A
Canobbio, L
Galligioni, E
Sorio, R
Lucenti, A
Cognetti, F
Ruggeri, E
Landonio, G
Baiocchi, C
Besana, C
Citterio, G
De Rosa, M
Calabresi, F
机构
[1] Ist Nazl Ric Canc, Serv Oncol Med 2, Dept Med Oncol 2, I-16132 Genoa, Italy
[2] Univ Genoa, Chair Med Oncol, Biostat Unit, Genoa, Italy
[3] S Chiara Hosp, Dept Med Oncol, Trent, Italy
[4] Ctr Riferimento Oncol, Dept Med Oncol, I-33081 Aviano, Italy
[5] Ist Regina Elena, Dept Med Oncol 1, I-00161 Rome, Italy
[6] Niguarda Hosp, Dept Med Oncol Falck, Milan, Italy
[7] Univ Milan, Chair Internal Med, Milan, Italy
[8] CINECA, Bologna, Italy
关键词
interferon-alpha; interleukin-2; interferon-alpha plus interleukin-2; renal cell carcinoma;
D O I
10.1177/030089169808400505
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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 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 10(6) IU/m(2) for a total of 25 weeks. Patients randomized to IFN alone were scheduled to receive rIFN-alpha at a daily dose of 6 x 10(6) IU/m(2), 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.
引用
收藏
页码:534 / 539
页数:6
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