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首页> 外文期刊>Journal of Clinical Oncology >Interferon-alfa as a comparative treatment for clinical trials of new therapies against advanced renal cell carcinoma.
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Interferon-alfa as a comparative treatment for clinical trials of new therapies against advanced renal cell carcinoma.

机译:干扰素-α作为针对晚期肾细胞癌的新疗法的临床试验的比较治疗。

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PURPOSE: To define outcome data and prognostic criteria for patients with metastatic renal cell carcinoma (RCC) treated with interferon-alfa as initial systemic therapy. The data can be applied to design and interpretation of clinical trials of new agents and treatment programs against this refractory malignancy. PATIENTS AND METHODS: Four hundred sixty-three patients with advanced RCC administered interferon-alpha as first-line systemic therapy on six prospective clinical trials were the subjects of this retrospective analysis. Three risk categories for predicting survival were identified on the basis of five pretreatment clinical features by a stratified Cox proportional hazards model. RESULTS: The median overall survival time was 13 months. The median time to progression was 4.7 months. Five variables were used as risk factors for short survival: low Karnofsky performance status, high lactate dehydrogenase, low serum hemoglobin, high corrected serum calcium, and time from initial RCC diagnosis to start of interferon-alpha therapy of less than one year. Each patient was assigned to one of three risk groups: those with zero risk factors (favorable risk), those with one or two (intermediate risk), and those with three or more (poor risk). The median time to death of patients deemed favorable risk was 30 months. Median survival time in the intermediate-risk group was 14 months. In contrast, the poor-risk group had a median survival time of 5 months. CONCLUSION: Progression-free and overall survival with interferon-alpha treatment can be compared with new therapies in phase II and III clinical investigations. The prognostic model is suitable for risk stratification of phase III trials using interferon-alpha as the comparative treatment arm.
机译:目的:为转移性肾细胞癌(RCC)接受干扰素-α治疗作为初始全身性治疗的患者,定义结局数据和预后标准。该数据可用于设计和解释针对这种难治性恶性肿瘤的新药和治疗方案的临床试验。患者与方法:回顾性分析的对象为463例晚期RCC患者,在6项前瞻性临床试验中将干扰素-α作为一线系统治疗。根据分层的Cox比例风险模型,基于五个预处理的临床特征,确定了三个预测生存的风险类别。结果:中位总生存时间为13个月。平均进展时间为4.7个月。五个变量被用作短期生存的危险因素:低的卡氏性能状态,高的乳酸脱氢酶,低的血红蛋白,高的校正的血清钙以及从最初的RCC诊断到开始干扰素-α治疗的时间少于一年。每个患者被分配到三个风险组之一:风险因子为零(有利风险)的患者,风险因子为一或两个(中度风险)的患者和风险因子为三个或三个以上的人群(低风险)。被认为是有利风险的患者中位死亡时间为30个月。中危组的中位生存时间为14个月。相比之下,低风险组的中位生存时间为5个月。结论:干扰素-α治疗的无进展生存期和总生存期可与II期和III期临床研究中的新疗法进行比较。该预后模型适用于以干扰素-α作为比较治疗组的III期临床试验的风险分层。

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