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首页> 外文期刊>International journal of clinical oncology >A low-dose combination therapy of interleukin-2 and interferon-alpha is effective for lung metastasis of renal cell carcinoma: a multicenter open study.
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A low-dose combination therapy of interleukin-2 and interferon-alpha is effective for lung metastasis of renal cell carcinoma: a multicenter open study.

机译:低剂量白细胞介素2和干扰素-α的联合治疗对肾细胞癌的肺转移有效:一项多中心开放研究。

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BACKGROUND: To confirm the usefulness of a combination therapy of interleukin-2 (IL-2) and interferon-alpha (IFN-alpha) against metastatic renal cell carcinoma, the recommended dose of IFN-alpha to use in combination with low-dose IL-2 was determined (phase 1). Efficacy and safety at this dose was evaluated (phase 2). METHODS: In phase 1, the dose of IL-2 was fixed at 0.7 x 10(6) Japan reference unit (JRU)/person for 5 days a week. The dose of IFN-alpha was increased from 3 x 10(6) IU for 3 days a week (level I) to 6 x 10(6) IU for 3 days a week (level II) and to 6 x 10(6) IU for 5 days a week (level III). RESULTS: In phase 1, 10 patients were registered, with 9 (3 at each level) able to be evaluated. Because grade 3 and grade 4 neutropenia were observed at level III in 1 patient each, level II was found to be the recommended regimen. The response rate in phase 1 was 44.4% (4/9). In phase 2, 46 patients were registered, with a response rate in 37 patients, classified as per protocol set (PPS), of 21.6%(8/37). Toxicities observed were primarily flu-like symptoms due to cytokines, and gastrointestinal symptoms. Leukocyte abnormalities were observed, but they were milder and tolerable. CONCLUSION: In the 46 patients evaluated in phase 1 and phase 2, the response rate was 26.1% (12/46), being highest in 38.7% (12/31) of those who were nephrectomized, and with only lung metastases.
机译:背景:为了证实白介素2(IL-2)和干扰素-α(IFN-α)联合治疗对转移性肾细胞癌的有效性,推荐剂量的IFN-α与小剂量IL联合使用确定为-2(阶段1)。评估了该剂量下的疗效和安全性(第2期)。方法:在第1阶段,每周5天将IL-2的剂量固定为0.7 x 10(6)日本参考单位(JRU)/人。 IFN-α的剂量从每周3天的3 x 10(6)IU(I级)增加到每周3天的6 x 10(6)IU(II级)和6 x 10(6)IU IU一周5天(III级)。结果:在第一阶段,登记了10例患者,其中9例(每个级别3例)能够进行评估。由于每位1名患者在III级观察到3级和4级中性粒细胞减少,因此推荐使用II级。第一阶段的响应率为44.4%(4/9)。在第2阶段,登记了46例患者,按方案集(PPS)分类的37例患者的缓解率为21.6%(8/37)。观察到的毒性主要是由于细胞因子引起的流感样症状和胃肠道症状。观察到白细胞异常,但它们较轻且可耐受。结论:在阶段1和阶段2评估的46例患者中,有肾切除并仅有肺转移的患者的有效率为26.1%(12/46),在38.7%(12/31)的患者中最高。

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