Randomized multicenter phase II trial of subcutaneous recombinant human interleukin-12 versus interferon-α2a for patients with advanced renal cell carcinoma

被引:82
|
作者
Motzer, RJ
Rakhit, A
Thompson, JA
Nemunaitis, J
Murphy, BA
Ellerhorst, J
Schwartz, LH
Berg, WJ
Bukowski, RM
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Med, Div Solid Tumor Oncol, Genitourinary Oncol Serv, New York, NY 10021 USA
[2] Mem Sloan Kettering Canc Ctr, Dept Med Imaging, New York, NY 10021 USA
[3] Hoffmann La Roche Inc, Nutley, NJ 07110 USA
[4] Univ Washington, Seattle, WA 98195 USA
[5] US Oncol, Dallas, TX USA
[6] Vanderbilt Univ, Nashville, TN USA
[7] Univ Texas, MD Anderson Canc Ctr, Houston, TX 77030 USA
[8] Cleveland Clin Fdn, Cleveland, OH 44195 USA
来源
JOURNAL OF INTERFERON AND CYTOKINE RESEARCH | 2001年 / 21卷 / 04期
关键词
D O I
10.1089/107999001750169934
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Recombinant human interleukin-12 (rHuIL-12) is a pleiotropic cytokine with anticancer activity against renal cell carcinoma (RCC) in preclinical models and in a phase I trial. A randomized phase LT study of rHuIL-12 compared with interferon-a (IFN-a) evaluated clinical response for patients with previously untreated, advanced RCC, Patients were randomly assigned 2:1 to receive either rHuIL-12 or IFN-alpha 2a, rHuIL-12 was administered by subcutaneous (s.c.) injection on days 1, 8, and 15 of each 28-day cycle. The dose of IL-12 was escalated during cycle 1 to a maintenance dose of 1.25 mug/kg. IFN was administered at 9 million units by s.c. injection three times per week. Serum concentrations of IL-12, IFN-gamma, IL-10, and neopterin were obtained in 10 patients treated with rHuIL-12 after the first full dose of 1.25 mug/kg given on day 15 (dose 3) of cycle 1 and again after multiple doses on day 15 (dose 6) of cycle 2, Thirty patients were treated with rHuIL-12, and 16 patients were treated with IFN-alpha. Two (7%) of 30 patients treated with rHuIL-12 achieved a partial response, and the trial was closed to accrual based on the low response proportion. IL-12 was absorbed rapidly after s.c. drug administration, with the peak serum concentration appearing at approximately 12 h in both cycles. Serum IL-12 concentrations remained stable on multiple dosing. Levels of IFN-gamma, IL-10, and neopterin increased with rHuIL-12 and were maintained in cycle 2, rHuIL-12 is a novel cytokine with unique pharmacologic and pharmacodynamic features under study for the treatment of malignancy and other medical conditions. The low response proportion associated with rHuIL-12 single-agent therapy against metastatic RCC was disappointing, given the preclinical data. Further study of rHuIL-12 for other medical conditions is underway. For RCC, the study of new cytokines is of the highest priority.
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收藏
页码:257 / 263
页数:7
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