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转移性透明细胞肾细胞癌患者的长期生存。344 例患者真实研究结果。

Long survival of patients with metastatic clear cell renal cell carcinoma. Results of real life study of 344 patients.

机构信息

Clinique Victor Hugo, Le Mans, France.

Centre Eugène Marquis, Rennes, France.

出版信息

Int J Cancer. 2020 Mar 15;146(6):1643-1651. doi: 10.1002/ijc.32578. Epub 2019 Aug 1.

Abstract

The treatment landscape in metastatic renal cell carcinoma has changed fundamentally over the last decade by the development of antiangiogenic agents, mammalian target of rapamycin inhibitors and immunotherapy. Outside of the context of a clinical trial, the treatments are used sequentially. We describe results under real-life conditions of a sequential treatment strategy, before the era of immunotherapy. All patients were treated according to their prognostic score (either Memorial Sloan Kettering Cancer Center or International Metastatic Renal Cell Carcinoma Database Consortium) for advanced renal cell carcinoma. A treatment strategy involving 1 to 4 lines was determined including a rechallenge criterion for the repeat use of a treatment class. Three hundred forty-four patients were included over 3 years. Overall survival was 57 months in patients with good or intermediate prognosis and 19 months in patients with poor prognosis. In the former group, the proportions of patients treated with 2 to 4 treatment lines were 70%, 38% and 16%, respectively. The best objective response rates for lines 1 to 4 were 46%, 36%, 16% and 17%, respectively. Grade III/IV toxicity did not appear to be cumulative. The recommended strategy was followed in 68% of patients. A large proportion of patients with good or intermediate prognosis who progress after two lines of treatment still have a performance status good enough to receive a systemic treatment, which justifies such a strategy. Overall survival of patients with good and intermediate prognosis was long, suggesting a benefit from the applied approach. These results might be used as selection criterion for the treatment of patients in the era of immune checkpoint inhibitors.

摘要

过去十年,抗血管生成药物、哺乳动物雷帕霉素靶蛋白抑制剂和免疫疗法的发展从根本上改变了转移性肾细胞癌的治疗格局。在临床试验之外,这些治疗方法是按顺序使用的。我们描述了免疫治疗时代之前,真实环境下序贯治疗策略的结果。所有患者均根据其晚期肾细胞癌的预后评分(MSKCC 或 IMDC)接受治疗。根据治疗方案,确定了包括重复使用治疗类别的重挑战标准的 1 到 4 线治疗策略。在 3 年期间共纳入 344 例患者。预后良好或中等的患者总生存期为 57 个月,预后不良的患者总生存期为 19 个月。在前一组中,接受 2 到 4 线治疗的患者比例分别为 70%、38%和 16%。1 到 4 线的最佳客观缓解率分别为 46%、36%、16%和 17%。3/4 级毒性似乎没有累积。68%的患者遵循了推荐的治疗策略。在接受两线治疗后进展的预后良好或中等的患者中,很大一部分仍有足够的体能状态接受系统治疗,这证明了这种策略是合理的。预后良好和中等的患者的总生存期较长,表明所采用的方法有益。这些结果可作为免疫检查点抑制剂治疗患者的选择标准。

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