首页> 外文期刊>Journal of interferon and cytokine research: The official journal of the International Society for Interferon and Cytokine Research >Randomized multicenter phase II trial of subcutaneous recombinant human interleukin-12 versus interferon-alpha 2a for patients with advanced renal cell carcinoma.
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Randomized multicenter phase II trial of subcutaneous recombinant human interleukin-12 versus interferon-alpha 2a for patients with advanced renal cell carcinoma.

机译:皮下重组人白细胞介素12与干扰素-α2a皮下注射治疗晚期肾细胞癌的随机多中心II期试验。

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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 II study of rHuIL-12 compared with interferon-alpha (IFN-alpha) evaluated clinical response for patients with previously untreated, advanced RCC. Patients were randomly assigned 2:1 to receive either rHuIL-12 or IFN-alpha2a. 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 microg/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 microg/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.
机译:重组人白细胞介素12(rHuIL-12)是一种多效细胞因子,在临床前模型和I期试验中具有抗肾细胞癌(RCC)的抗癌活性。与干扰素-α(IFN-α)相比,rHuIL-12的II期随机研究评估了先前未经治疗的晚期RCC患者的临床反应。患者被随机分配为2:1接受rHuIL-12或IFN-alpha2a。在每个28天周期的第1、8和15天通过皮下(s.c.)注射来施用rHuIL-12。在周期1期间将IL-12的剂量增加至1.25μg/ kg的维持剂量。 s.c. IFN以900万单位给药。每周注射三次。在第1周期第15天(剂量3)给予第一个全剂量1.25 microg / kg的剂量后,在接受rHuIL-12治疗的10例患者中获得血清IL-12,IFN-γ,IL-10和新蝶呤的浓度,并再次进行在周期2的第15天(剂量6)多次给药后,用rHuIL-12治疗30例患者,并用IFN-α治疗16例患者。在使用rHuIL-12治疗的30例患者中,有2例(7%)达到了部分缓解,该试验因缓解率低而无法招募。皮下注射后IL-12迅速吸收。给药,两个周期约12小时出现峰值血清浓度。多次给药后血清IL-12浓度保持稳定。 γ-干扰素,IL-10和新蝶呤的水平随rHuIL-12的升高而升高,并维持在第2周期。rHuIL-12是一种新型的细胞因子,具有独特的药理和药效学特征,正在研究中,用于治疗恶性肿瘤和其他医学疾病。鉴于临床前数据,与rHuIL-12单药治疗转移性RCC相关的低应答比例令人失望。 rHuIL-12在其他医学疾病中的进一步研究正在进行中。对于RCC,研究新细胞因子是最优先的。

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