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甲羟孕酮、干扰素α-2a、白细胞介素2或两者联合用于中度预后转移性肾癌患者:一项随机对照试验的结果

Medroxyprogesterone, interferon alfa-2a, interleukin 2, or combination of both cytokines in patients with metastatic renal carcinoma of intermediate prognosis: results of a randomized controlled trial.

作者信息

Negrier Sylvie, Perol David, Ravaud Alain, Chevreau Christine, Bay Jacques-Olivier, Delva Remy, Sevin Emmanuel, Caty Armelle, Escudier Bernard

机构信息

Université de Lyon, Department of Medical Oncology and Cytokines & Cancer Research Unit, Leon Berard Center, INSERM U590, Lyon, France.

出版信息

Cancer. 2007 Dec 1;110(11):2468-77. doi: 10.1002/cncr.23056.

Abstract

BACKGROUND

Few randomized trials have compared the survival benefit of interferon-alfa over controls in metastatic renal cell carcinoma, and none has been performed using interleukin-2. The Programme Etude Rein Cytokines (PERCY) Quattro trial was designed to evaluate both cytokines for their survival benefit to intermediate prognosis patients, who represent the majority of candidates for these treatments.

METHODS

Patients were randomized in a 2-by-2 factorial design to medroxyprogesterone acetate 200 mg daily, interferon-alfa 9 million IU 3 times a week, subcutaneous interleukin-2 9 million IU daily, or a combination of both cytokines. Tumor response was evaluated at Week 12 and Month 6; progression-free patients received further identical treatment for a maximum of 3 additional months. Primary endpoint was overall survival; secondary endpoints were disease-free survival, response rate, toxicity, and quality of life. Survival was analyzed on an intent-to-treat basis.

RESULTS

From January 2000 to July 2004, 492 patients were enrolled. Analysis was performed after a 29.2-month median follow-up (range, 0 months to 54.6 months). There were no significant survival differences between the 244 interferon-alfa-treated patients and 248 noninterferon-alfa patients (hazard ratio, 1.00; 95% CI, 0.81-1.24) or between the 247 interleukin-2 and 245 noninterleukin-2-treated patients (hazard ratio, 1.07; 95% CI, 0.87-1.33; log rank, 0.99 and 0.52, respectively). Grade 3-4 toxicities were significantly more frequent in cytokine-treated patients than in medroxyprogesterone-treated patients.

CONCLUSIONS

Subcutaneous interleukin-2 and/or interferon-alfa provide no survival benefit in metastatic renal cancers of intermediate prognosis, and they induce a significant risk of toxicity. Newly available angiogenesis inhibitors should be preferred for these patients.

摘要

背景

很少有随机试验比较过干扰素-α与对照组相比在转移性肾细胞癌中的生存获益情况,且尚无使用白细胞介素-2进行的此类试验。细胞因子治疗肾癌研究项目(PERCY)四号试验旨在评估这两种细胞因子对中期预后患者的生存获益,这类患者是这些治疗的主要候选对象。

方法

患者按2×2析因设计随机分组,分别接受每日200毫克醋酸甲羟孕酮、每周3次皮下注射900万国际单位干扰素-α、每日皮下注射900万国际单位白细胞介素-2或两种细胞因子联合治疗。在第12周和第6个月评估肿瘤反应;病情无进展的患者最多再接受3个月相同治疗。主要终点为总生存期;次要终点为无病生存期、缓解率、毒性和生活质量。生存期分析采用意向性治疗原则。

结果

2000年1月至2004年7月,共纳入492例患者。在中位随访29.2个月(范围0个月至54.6个月)后进行分析。244例接受干扰素-α治疗的患者与248例未接受干扰素-α治疗的患者之间无显著生存差异(风险比为1.00;95%置信区间为0.81 - 1.24),247例接受白细胞介素-2治疗的患者与245例未接受白细胞介素-2治疗的患者之间也无显著生存差异(风险比为1.07;95%置信区间为0.87 - 1.33;对数秩检验分别为0.99和0.52)。细胞因子治疗组患者3 - 4级毒性反应明显比醋酸甲羟孕酮治疗组更常见。

结论

皮下注射白细胞介素-2和/或干扰素-α对中期预后的转移性肾癌患者无生存获益,且会带来显著的毒性风险。对于这些患者,应优先选用新出现的血管生成抑制剂。

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