Darzi Ali, Shokouhfar Mahla, Farajee Narges, Ghafari Arezoo, Deldar Fatemeh, Eini Pooya, Vanan Ahmad Ghorbani, Bahrami Nastaran
School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
School of medicine, Islamic Azad university of Tehran medical sciences, Tehran, Iran.
Biomed Pharmacother. 2025 Dec;193:118875. doi: 10.1016/j.biopha.2025.118875. Epub 2025 Dec 4.
Renal cell carcinoma (RCC) represents a major therapeutic challenge due to its highly immunosuppressive tumor microenvironment. Over the past decade, immune checkpoint inhibitors (ICIs) have revolutionized the management of advanced RCC, shifting treatment paradigms from cytokine- and VEGF-based therapies toward immunotherapy-driven strategies. This review highlights the mechanisms of immune evasion in RCC, focusing on the roles of tumor-associated macrophages, regulatory T cells, and cancer-associated fibroblasts, as well as the key checkpoints PD-1/PD-L1 and CTLA-4. We summarize pivotal clinical trials that established ICIs as the standard of care, including monotherapy and combination regimens with tyrosine kinase inhibitors (TKIs) and mTOR inhibitors, which have demonstrated superior objective response rates, progression-free survival, and overall survival compared to conventional therapies. Despite these advances, primary and acquired resistance remain significant barriers, driven by adaptive signaling pathways and immune exhaustion. Emerging strategies such as dual checkpoint blockade, metabolic and angiogenic co-targeting, and biomarker-guided personalization are under investigation to overcome resistance. Furthermore, the integration of multi-omics profiling, artificial intelligence, and microbiome modulation may refine patient selection and optimize therapeutic outcomes. Collectively, ICIs have transformed RCC treatment, yet future progress will depend on deeper biological insight, rational combination design, and individualized immunotherapy approaches.
肾细胞癌(RCC)因其高度免疫抑制的肿瘤微环境而成为一个重大的治疗挑战。在过去十年中,免疫检查点抑制剂(ICI)彻底改变了晚期RCC的治疗方式,将治疗模式从基于细胞因子和VEGF的疗法转向免疫治疗驱动的策略。本综述重点介绍了RCC中的免疫逃逸机制,着重探讨肿瘤相关巨噬细胞、调节性T细胞和癌症相关成纤维细胞的作用,以及关键检查点PD-1/PD-L1和CTLA-4。我们总结了将ICI确立为标准治疗方法的关键临床试验,包括单药治疗以及与酪氨酸激酶抑制剂(TKI)和mTOR抑制剂的联合方案,这些方案与传统疗法相比,已显示出更高的客观缓解率、无进展生存期和总生存期。尽管取得了这些进展,但由适应性信号通路和免疫耗竭驱动的原发性和获得性耐药仍然是重大障碍。正在研究诸如双重检查点阻断、代谢和血管生成共同靶向以及生物标志物指导的个性化等新兴策略以克服耐药性。此外,多组学分析、人工智能和微生物群调节的整合可能会优化患者选择并改善治疗效果。总体而言,ICI已经改变了RCC的治疗方式,但未来的进展将取决于更深入的生物学见解、合理的联合设计和个性化免疫治疗方法。