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舒尼替尼治疗低危和中危转移性肾细胞癌患者的疗效——立陶宛国家癌症研究所的经验。

Efficacy of Sunitinib in Patients With Favorable and Intermediate Risk Metastatic Renal Cell Carcinoma - Lithuanian National Cancer Institute Experience.

机构信息

Institute of Biosciences, Life Sciences Center, Vilnius University, Vilnius, Lithuania;

National Cancer Institute, Vilnius, Lithuania.

出版信息

Anticancer Res. 2024 Jan;44(1):213-219. doi: 10.21873/anticanres.16804.

Abstract

BACKGROUND/AIM: According to the European Society for Medical Oncology (ESMO) and National Comprehensive Cancer Network (NCCN) recommendations, sunitinib is one of the recommended regimens for favorable and intermediate-risk metastatic renal cell carcinoma (mRCC) patients. The objective of this study was to evaluate sunitinib efficacy as a first-line treatment for mRCC patients with favorable/intermediate prognostic risk in a real-world setting.

PATIENTS AND METHODS

Patients diagnosed with mRCC and confirmed as appropriate candidates for the first-line systemic treatment were included in this retrospective study. The prognostic risk was evaluated according to the model of the International Metastatic RCC Database Consortium (IMDC).

RESULTS

Patients received sunitinib as a first-line treatment. A total of 94 patients were enrolled from 2019 to the 2020and 67 of them were included in the detailed analysis. Median progression-free survival (PFS) was 23.4 (95%CI=17.3-29.5), and median overall survival (OS) was 66 months (95%CI=44.9-87.1). The age over 60 years was a significant negative predictor for PFS and OS. Regarding the IMDC model for disease risk prediction, the number of two risk factors in the intermediate risk group was a significant predictor for a shorter response to the first-line therapy.

CONCLUSION

Sunitinib is an effective tyrosine kinase inhibitor, which can be used as a first-line treatment in favorable/intermediate-risk groups of patients with mRCC, especially in countries where novel systemic treatment modalities are not yet available.

摘要

背景/目的:根据欧洲肿瘤内科学会(ESMO)和美国国家综合癌症网络(NCCN)的建议,舒尼替尼是转移性肾细胞癌(mRCC)患者中有利和中危的推荐方案之一。本研究的目的是评估舒尼替尼作为一线治疗药物在真实环境中治疗有利/中危预后的 mRCC 患者的疗效。

患者和方法

本回顾性研究纳入了诊断为 mRCC 且被确认为一线系统治疗合适候选者的患者。预后风险根据国际转移性肾细胞癌数据库联盟(IMDC)模型进行评估。

结果

患者接受舒尼替尼作为一线治疗。共纳入了 94 名患者,其中 67 名患者被纳入详细分析。中位无进展生存期(PFS)为 23.4 个月(95%CI=17.3-29.5),中位总生存期(OS)为 66 个月(95%CI=44.9-87.1)。60 岁以上的年龄是 PFS 和 OS 的显著负预测因素。关于疾病风险预测的 IMDC 模型,中危组的两个风险因素数量是一线治疗反应较短的显著预测因素。

结论

舒尼替尼是一种有效的酪氨酸激酶抑制剂,可作为 mRCC 有利/中危患者的一线治疗药物,特别是在尚无新型系统治疗方法的国家。

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