Oki Ryosuke, Takemura Kosuke, Urasaki Tetsuya, Fujiwara Ryo, Numao Noboru, Yonese Junji, Miura Yuji, Yuasa Takeshi
Department of Medical Oncology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.
Department of Genitourinary Oncology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.
Expert Rev Anticancer Ther. 2025 Jun;25(6):643-655. doi: 10.1080/14737140.2025.2491647. Epub 2025 Apr 14.
The management of metastatic renal cell carcinoma (mRCC) has advanced with recent therapies, yet optimizing treatment remains challenging due to disease heterogeneity and the growing number of options. Integrating systemic and local treatments requires a multidisciplinary approach to improve outcomes.
This review summarizes recent developments in treatment for mRCC. Upfront immuno-oncology (IO)-based combinations have improved survival, though concerns about overtreatment and toxicity persist. While the role of cytoreductive nephrectomy (CN) has declined to some extent, it may still benefit well-selected patients. Metastasis-directed therapies, including metastasectomy and stereotactic radiotherapy, provide prognostic value, particularly for oligometastatic lesions or brain metastases. Comprehensive genomic profiling (CGP) holds promise for personalized treatment but is currently limited by the lack of actionable mutations and predictive biomarkers.
A personalized, multimodal approach is essential for optimizing mRCC management. Careful patient selection is key to balancing the benefits of treatment with the risks of toxicity. While CN and metastasis-directed therapies remain useful in select cases, advancing individualized care requires the development of validated biomarkers and broader application of CGP.
转移性肾细胞癌(mRCC)的治疗随着近期疗法的出现而取得进展,但由于疾病的异质性和治疗选择的不断增加,优化治疗仍然具有挑战性。整合全身治疗和局部治疗需要多学科方法来改善治疗结果。
本综述总结了mRCC治疗的最新进展。基于免疫肿瘤学(IO)的初始联合治疗提高了生存率,尽管对过度治疗和毒性的担忧仍然存在。虽然减瘤性肾切除术(CN)的作用在一定程度上有所下降,但它可能仍使精心挑选的患者受益。针对转移灶的治疗,包括转移灶切除术和立体定向放射治疗,具有预后价值,特别是对于寡转移病灶或脑转移。全面基因组分析(CGP)有望实现个性化治疗,但目前受到可操作突变和预测性生物标志物缺乏的限制。
个性化的多模式方法对于优化mRCC管理至关重要。仔细选择患者是平衡治疗益处与毒性风险的关键。虽然CN和针对转移灶的治疗在特定病例中仍然有用,但推进个体化治疗需要开发经过验证的生物标志物并更广泛地应用CGP。