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从组织非特异性治疗到个体化治疗:精准医疗范式的(R)演进。

From Tissue-Agnostic to N-of-One Therapies: (R)Evolution of the Precision Paradigm.

机构信息

Department of Internal Medicine, University of South Florida, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.

Department of Investigational Cancer Therapeutics (A Phase 1 Program), The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

出版信息

Trends Cancer. 2021 Jan;7(1):15-28. doi: 10.1016/j.trecan.2020.08.009. Epub 2020 Sep 29.

Abstract

Precision medicine has exploited next-generation sequencing (NGS) and gene/immune-targeted drug deployment to transform the outlook for several lethal cancers. For instance, there are now several FDA-approved medications that target the sequelae of aberrant genes in a tissue-agnostic approach: pembrolizumab [microsatellite instability and tumor mutational burden (TMB) ≥10 mutations/megabase (mut/Mb)] and larotrectinib/entrectinib (NTRK fusions). Molecular interrogation further reveals the disruptive reality that metastatic cancers are tremendously complex and individually distinct. Therefore, optimized treatment often requires drug combinations (rather than monotherapy) and N-of-one customization. Early studies of this approach suggest feasibility, safety, and efficacy. Real-world data/master registry trials may also provide massive, clinically relevant datasets that further fuel the (r)evolution in oncology.

摘要

精准医学利用下一代测序(NGS)和基因/免疫靶向药物的应用,改变了几种致命癌症的预后。例如,现在有几种美国食品和药物管理局(FDA)批准的药物,采用组织非特异性方法针对异常基因的后果:pembrolizumab[微卫星不稳定性和肿瘤突变负荷(TMB)≥10 个突变/兆碱基(mut/Mb)]和 larotrectinib/entrectinib(NTRK 融合)。分子检测进一步揭示了转移性癌症极其复杂和个体独特的破坏性现实。因此,优化治疗通常需要药物联合治疗(而不是单一疗法)和个性化定制。这种方法的早期研究表明其具有可行性、安全性和疗效。真实世界的数据/主登记试验也可能提供大量具有临床意义的数据集,进一步推动肿瘤学的(r)evolution。

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