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卵巢癌中的下一代测序与分子生物标志物——靶向治疗的机遇

Next Generation Sequencing and Molecular Biomarkers in Ovarian Cancer-An Opportunity for Targeted Therapy.

作者信息

Harbin Laura M, Gallion Holly H, Allison Derek B, Kolesar Jill M

机构信息

Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, University of Kentucky Markey Cancer Center, 800 Rose Street, Lexington, KY 40536-0596, USA.

Department of Pathology & Laboratory Medicine, University of Kentucky College of Medicine, Lexington, KY 40536-0596, USA.

出版信息

Diagnostics (Basel). 2022 Mar 29;12(4):842. doi: 10.3390/diagnostics12040842.

Abstract

Ovarian cancer is the deadliest of all gynecologic malignancies claiming the lives of nearly 14,000 women in the United States annually. Despite therapeutic advances, the ovarian cancer mortality rate has remained stagnant since the 1980's. The molecular heterogeneity of ovarian cancers suggest they may be more effectively treated via precision medicine. Current guidelines recommend germline and somatic testing for all new epithelial ovarian cancer diagnoses to assist providers in identifying candidates for targeted therapies. Next generation sequencing (NGS) identifies targetable, driver, and novel mutations used to guide treatment decisions. Performing NGS is standard of care in many other malignancies, but for ovarian cancer the use of NGS in daily practice is still emerging. This review discusses the targetable genetic mutations and role of NGS and molecular biomarker testing in the treatment of ovarian cancer.

摘要

卵巢癌是所有妇科恶性肿瘤中致死率最高的,在美国每年有近14000名女性死于该病。尽管治疗取得了进展,但自20世纪80年代以来,卵巢癌的死亡率一直停滞不前。卵巢癌的分子异质性表明,通过精准医学可能会更有效地治疗它们。目前的指南建议对所有新诊断的上皮性卵巢癌进行种系和体细胞检测,以帮助医疗人员确定靶向治疗的候选者。下一代测序(NGS)可识别用于指导治疗决策的可靶向、驱动和新的突变。在许多其他恶性肿瘤中,进行NGS是护理标准,但在卵巢癌中,NGS在日常实践中的应用仍在兴起。本文综述讨论了可靶向的基因突变以及NGS和分子生物标志物检测在卵巢癌治疗中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/671d/9030726/fddf53bbebb2/diagnostics-12-00842-g001.jpg

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