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韩国前瞻性临床测序中晚期泛癌症患者的基因组特征及临床应用:K-MASTER 计划。

Genomic Landscape and Clinical Utility in Korean Advanced Pan-Cancer Patients from Prospective Clinical Sequencing: K-MASTER Program.

机构信息

Division of Medical Oncology/Hematology, Department of Internal Medicine, Korea University Anam Hospital, Korea University College of Medicine, Seoul, Republic of Korea.

K-MASTER Cancer Precision Medicine Diagnosis and Treatment Enterprise, Korea University Anam Hospital, Korea University College of Medicine, Seoul, Republic of Korea.

出版信息

Cancer Discov. 2022 Apr 1;12(4):938-948. doi: 10.1158/2159-8290.CD-21-1064.

Abstract

UNLABELLED

The fundamental principle of precision oncology is centralized on the identification of therapeutically exploitable targets that provides individual patients with cancer an opportunity to make informed decisions on a personalized level. To facilitate and adopt such concepts within clinical practice, we have initiated a nationwide, multi-institutional precision oncology screening program to examine and enroll patients into the most appropriate clinical trial based on their tumor's unique molecular properties. To determine the prevalence of essential major driver mutations and to explore their dynamic associations at both molecular and pathway levels, we present a comprehensive overview on the genomic properties of East Asian patients with cancer. We further delineate the extent of genomic diversity as well as clinical actionability in patients from Western and Eastern cultures at the pan-cancer and single-tumor entity levels. To support fellow oncology communities in future investigations involving large-scale analysis, all data have been made accessible to the public (https://kmportal.or.kr).

SIGNIFICANCE

We present a comprehensive overview of molecular properties of East Asian pan-cancer patients and demonstrate significant diversity in terms of genomic characteristics as well as clinical utility compared with patients with European ancestry. The results of this study will lay the groundwork for designing personalized treatments in the clinical setting. See related commentary by Moyers and Subbiah, p. 886. This article is highlighted in the In This Issue feature, p. 873.

摘要

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精准肿瘤学的基本原则集中在鉴定有治疗潜力的靶点上,为癌症患者提供了在个性化层面上做出知情决策的机会。为了在临床实践中促进和采用这些概念,我们启动了一项全国性的多机构精准肿瘤学筛选计划,根据肿瘤的独特分子特性,为患者检查并选择最合适的临床试验。为了确定主要驱动突变的基本流行率,并探索它们在分子和途径水平上的动态关联,我们全面概述了东亚癌症患者的基因组特征。我们进一步描述了在泛癌和单一肿瘤实体水平上,来自西方和东方文化的患者的基因组多样性以及临床可操作性的程度。为了支持肿瘤学领域的同行在未来涉及大规模分析的研究中,我们将所有数据提供给公众(https://kmportal.or.kr)。

意义

我们全面概述了东亚泛癌患者的分子特征,并展示了与欧洲血统患者相比,在基因组特征和临床应用方面存在显著的多样性。这项研究的结果将为在临床环境中设计个性化治疗奠定基础。请参阅 Moyers 和 Subbiah 的相关评论,第 886 页。本文在本期特色文章中重点介绍,第 873 页。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d7c/9387587/1a1fc884fffa/938fig1.jpg

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