间皮素作为癌症免疫治疗的生物标志物和治疗靶点
Mesothelin as Biomarker and Therapeutic Target for Immunotherapy in Cancer.
癌症仍是一个关键的全球健康问题,原因在于发现晚、耐药和高死亡率。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Application of immune checkpoint inhibitors and microsatellite instability in gastric cancer.
Application of immune checkpoint inhibitors and microsatellite instability in gastric cancer.
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在这篇社论中,我们对Li发表在近期《World Journal of Gastroenterology》上的文章进行评论。
我们特别关注免疫检查点抑制剂(ICIs)和微卫星不稳定性(MSI)在胃癌(GC)中的应用。长期以来,GC管理被认为有四大支柱,包括手术、化疗、放疗和靶向治疗。
然而,免疫治疗最近作为“第五支柱”出现,其应用正在迅速扩大。肿瘤免疫治疗有四种主要策略:ICIs、肿瘤疫苗、过继性免疫治疗和非特异性免疫调节剂。其中,ICIs是GC最先进和最广泛应用的癌症免疫治疗类型。ICIs最近的突破性成果为癌症免疫治疗的新时代铺平了道路。特别是,使用ICIs抑制PD-1/PD-L1轴,包括nivolumab和pembrolizumab,已成为晚期GC的一种新型治疗策略。不幸的是,这些治疗有时与常常微妙但可能致命的免疫相关不良事件(irAEs)相关,包括皮炎、腹泻、结肠炎、内分泌病、肝毒性、神经病和肺炎。
我们必须意识到这些irAEs,并改进对这些过程的检测,以防止不适当的出院、急诊科再访和下游并发症。最近的研究表明,MSI-high或错配修复缺陷肿瘤,无论其原发部位如何,对ICIs都有良好的反应。因此,在应用ICIs治疗GC之前检测MSI很重要。
In this editorial we comment on the article by Li published in the recent issue of the World Journal of Gastroenterology .
We focus specifically on the application of immune checkpoint inhibitors (ICIs) and microsatellite instability (MSI) in gastric cancer (GC). The four pillars of GC management have long been considered, including surgery, chemotherapy, radiotherapy and targeted therapy.
However, immunotherapy has recently emerged as a "fifth pillar", and its use is rapidly expanding. There are four principal strategies for tumor immunotherapy: ICIs, tumor vaccines, adoptive immunotherapy and nonspecific immunomodulators. Of them, ICIs are the most advanced and widespread type of cancer immunotherapy for GC. Recent breakthrough results for ICIs have paved the way to a new era of cancer immunotherapy.
In particular, inhibition of the PD-1/PD-L1 axis with ICIs, including nivolumab and pembrolizumab, has emerged as a novel treatment strategy for advanced GC. Unfortunately, these therapies are sometimes associated with often subtle, potentially fatal immune-related adverse events (irAEs), including dermatitis, diarrhea, colitis, endocrinopathy, hepatotoxicity, neuropathy and pneumonitis.
We must be aware of these irAEs and improve the detection of these processes to prevent inappropriate discharges, emergency department revisits, and downstream complications. Recent studies have revealed that MSI-high or mismatch- repair-deficient tumors, regardless of their primary site, have a promising response to ICIs. So, it is important to detect MSI before applying ICIs for treatment of GC.
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