HIGH-DOSE RECOMBINANT INTERLEUKIN-2 ALONE - A REGIMEN WITH LIMITED ACTIVITY IN THE TREATMENT OF ADVANCED RENAL-CELL CARCINOMA

被引:58
作者
ABRAMS, JS
RAYNER, AA
WIERNIK, PH
PARKINSON, DR
EISENBERGER, M
ARONSON, FR
GUCALP, R
ATKINS, MB
HAWKINS, MJ
机构
[1] ALBERT EINSTEIN CANC CTR,NEW YORK,NY
[2] NCI,CANC THERAPY EVALUAT PROGRAM,BETHESDA,MD 20205
[3] UNIV CALIF SAN FRANCISCO,SAN FRANCISCO,CA 94143
[4] TUFTS UNIV,NEW ENGLAND MED CTR,BOSTON,MA 02111
关键词
D O I
10.1093/jnci/82.14.1202
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Sixteen patients with metastatic renal cell carcinoma were treated with high-dose bolus recombinant interleukin-2 (rIL-2) alone at a dose and schedule identical to those that produced a 35% response rate among 72 patients in a trial reported by the Surgery Branch, National Cancer Institute (NCI), Bethesda, Md, in which rIL-2 plus lymphokine-activated killer (LAK) cells was used for the treatment of renal cell carcinoma. Patients received two 5-day cycles of 100,000 Cetus U/kg (600,000 IU/kg) of rIL-2 infused intravenously over 15 minutes every 8 hours; each treatment cycle was separated by 1 week. No objective responses were seen. The toxicity of rIL-2 given alone at these high doses was similar to that noted with high-dose rIL-2-LAK cell therapy. The lack of responses seen in this trial also differed from the 21% response rate observed by the NCI Surgery Branch, using rIL-2 alone at an identical schedule and dose in 56 patients with renal cell carcinoma. Only minor differences in such recognized prognostic variables as performance status, tumor burden, and rIL-2 dose intensity were noted between this study and other trials reported by the NCI Surgery Branch and by the IL-2-LAK Working Group. Our analysis indicates that, because of the smaller number of patients in our trial, not enough subjects were included with the ideal characteristics to attain the 21% response rate seen in the NCI study. However, the precise nature of these characteristics remains unclear. [J Natl Cancer Inst 82:1202-1206, 1990]. © 1990 Oxford University Press.
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页码:1202 / 1206
页数:5
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