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晚期肾细胞癌治疗的下一波目标。

Next Wave of Targets in the Treatment of Advanced Renal Cell Carcinoma.

机构信息

Department of Oncology, Juravinski Cancer Centre, McMaster University, Hamilton, ON L8V 5C2, Canada.

London Regional Cancer Program, London Health Sciences Centre, Western University, London, ON N6A 5W9, Canada.

出版信息

Curr Oncol. 2022 Jul 30;29(8):5426-5441. doi: 10.3390/curroncol29080429.

DOI:10.3390/curroncol29080429
PMID:36005167
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9406353/
Abstract

While surgical resection has remained the mainstay of treatment in early-stage renal cell carcinoma (RCC), therapeutic options in the advanced setting have remarkably expanded over the last 20 years. Tyrosine kinase inhibitors targeting the vascular endothelial growth factor receptor (VEGF-TKIs) and anti-programmed cell death 1 (PD-1)/anti-programmed death-ligand 1 (PD-L1)-based immune checkpoint inhibitors (ICIs) have become globally accepted options in the upfront metastatic setting, with different ICI-based combination strategies improving overall survival compared to single-agent Sunitinib. Although some patients benefit from long-term responses, most eventually develop disease progression. Ongoing efforts to better understand the biology of RCC and the different mechanisms of acquired resistance have led to the identification of promising therapeutic targets. Belzutifan, a novel agent targeting the angiogenic pathway involving hypoxia-inducible factors (HIFs), has already been approved for the treatment of early-stage tumors associated with VHL disease and represents a very promising therapy in advanced RCC. Other putative targets include epigenetic regulation enzymes, as well as several metabolites such as adenosine, glutaminase and tryptophan, which are critical players in cancer cell metabolism and in the tumor microenvironment. Different methods of immune regulation are also being investigated, including CAR-T cell therapy and modulation of the gut microbiome, in addition to novel agents targeting the interleukin-2 (IL-2) pathway. This review aims to highlight the emergent novel therapies for RCC and their respective completed and ongoing clinical trials.

摘要

虽然手术切除仍然是治疗早期肾细胞癌 (RCC) 的主要方法,但在过去的 20 年中,晚期治疗的选择已经显著扩大。针对血管内皮生长因子受体 (VEGF-TKIs) 的酪氨酸激酶抑制剂和抗程序性细胞死亡 1 (PD-1)/抗程序性死亡配体 1 (PD-L1) 的免疫检查点抑制剂 (ICIs) 已成为全球公认的一线转移性疾病治疗选择,与单药舒尼替尼相比,不同的 ICI 联合策略改善了总生存期。尽管一些患者从长期反应中受益,但大多数最终还是出现了疾病进展。为了更好地了解 RCC 的生物学和获得性耐药的不同机制,人们正在努力寻找有前途的治疗靶点。贝伐珠单抗是一种针对缺氧诱导因子 (HIF) 参与的血管生成途径的新型药物,已被批准用于治疗与 VHL 疾病相关的早期肿瘤,是晚期 RCC 非常有前途的治疗药物。其他潜在的靶点包括表观遗传调节酶,以及几种代谢物,如腺苷、谷氨酰胺酶和色氨酸,它们是癌细胞代谢和肿瘤微环境中的关键因素。目前还在研究不同的免疫调节方法,包括 CAR-T 细胞疗法和肠道微生物组的调节,以及针对白细胞介素-2 (IL-2) 途径的新型药物。本文旨在强调 RCC 的新兴新型疗法及其各自已完成和正在进行的临床试验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de97/9406353/1e2bf23595e4/curroncol-29-00429-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de97/9406353/1e2bf23595e4/curroncol-29-00429-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de97/9406353/1e2bf23595e4/curroncol-29-00429-g001.jpg

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Gut microbiota influence immunotherapy responses: mechanisms and therapeutic strategies.肠道微生物群影响免疫治疗反应:机制和治疗策略。
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