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首页> 外文期刊>Journal of Cancer Research and Clinical Oncology >A phase II trial of dose-intensive interleukin-2 in metastatic renal cell carcinoma.
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A phase II trial of dose-intensive interleukin-2 in metastatic renal cell carcinoma.

机译:剂量密集型白介素2在转移性肾细胞癌的II期试验。

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PURPOSE: High-dose bolus interleukin-2 (IL-2) is currently the sole agent approved by the Food and Drug Administration for the treatment of advanced renal cell carcinoma. This phase II study was designed to evaluate the clinical activity and toxicity spectrum of a regime consisting of dose-intensive IL-2 in both previously treated and untreated patients with advanced renal cell carcinoma. PATIENTS AND METHODS: Twenty eligible, sequential patients received IL-2 at a dose of 24 mlU m(-2) dose(-1) (1.33 mg m(-2) dose(-1)) every 8 h on days 1-5 and 15 19, for a maximum of 28 boluses. Patients achieving stable disease or a response were treated every 10 weeks for a maximum of five cycles/year. RESULTS: Out of 20 study participants 8 patients (40%; 95% confidence interval, 18.5%-61.4%) demonstrated a response. Three of these responses were complete (CR; 15%) while 5 were partial (PR; 25%) and about 75% of the responses occurred in patients with extensive tumor burdens. All 3 CR continue to respond after 28+ to 30+ months. With a median follow-up time of 26 months, the median overall survival duration for all patients is 18.0 months (95% confidence interval 12-24 months). Response was observed to correlate significantly with the IL-2 dose intensity. A dose intensity below 1440 mlU m(-2) year(-1) and at least 1440 mlU m(-2) year(-1) correlated highly with failure to achieve CR and the successful achieving of CR respectively (P < 0.01). An analysis of the present study database in the context of five previous similar trials demonstrated a significant correlation between IL-2 dose intensity and response rate by regression analysis (r=0.89; P < 0.019). Finally, all toxicities were reversible once the dosing had concluded. CONCLUSIONS: IL-2 dose intensity appears to represent a significant determinant of successful clinical outcomes. This dose-intensive approach led to a high proportion of durable responses. Further evaluation of this regimen is warranted.
机译:目的:大剂量推注白介素2(IL-2)是目前由美国食品药品监督管理局批准用于治疗晚期肾细胞癌的唯一药物。这项II期研究旨在评估在先前治疗和未治疗的晚期肾细胞癌患者中,由剂量密集型IL-2组成的治疗方案的临床活性和毒性谱。患者与方法:20名符合条件的连续患者在第1天每8小时接受24 mlU m(-2)剂量(-1)(1.33 mg m(-2)剂量(-1))的IL-2 5和15 19,最多28个推注。每10周对达到稳定疾病或反应的患者进行治疗,每年最多五个周期。结果:在20名研究参与者中,有8名患者(40%; 95%置信区间,18.5%-61.4%)表现出缓解。这些反应中有3例是完全反应(CR; 15%),而5例是部分反应(PR; 25%),其中约75%的反应是在肿瘤负担较重的患者中发生的。所有3个CR在28+到30+个月后继续响应。中位随访时间为26个月,所有患者的平均总生存时间为18.0个月(95%置信区间12-24个月)。观察到反应与IL-2剂量强度显着相关。低于1440 mlU m(-2)年(-1)和至少1440 mlU m(-2)年(-1)的剂量强度分别与未能实现CR和成功实现CR高度相关(P <0.01) 。在五个先前相似试验的背景下对本研究数据库进行的分析表明,通过回归分析,IL-2剂量强度与缓解率之间存在显着相关性(r = 0.89; P <0.019)。最后,一旦给药结束,所有毒性都是可逆的。结论:IL-2剂量强度似乎代表成功临床结果的重要决定因素。这种剂量密集的方法导致很大比例的持久反应。有必要对该方案进行进一步评估。

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