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子宫浆液性癌的发病机制与临床管理

Pathogenesis and Clinical Management of Uterine Serous Carcinoma.

作者信息

Zhang Li, Kwan Suet Ying, Wong Kwong Kwok, Solaman Pamela T, Lu Karen H, Mok Samuel C

机构信息

Department of Gynecologic Oncology and Reproductive Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.

The University of Texas Graduate School of Biomedical Sciences at Houston, Houston, TX 77030, USA.

出版信息

Cancers (Basel). 2020 Mar 14;12(3):686. doi: 10.3390/cancers12030686.

Abstract

Uterine serous carcinoma (USC) is an aggressive variant of endometrial cancer that has not been well characterized. It accounts for less than 10% of all endometrial cancers and 80% of endometrial cancer-related deaths. Currently, staging surgery together with chemotherapy or radiotherapy, especially vaginal cuff brachytherapy, is the main treatment strategy for USC. Whole-exome sequencing combined with preclinical and clinical studies are verifying a series of effective and clinically accessible inhibitors targeting frequently altered genes, such as and , in varying USC patient populations. Some progress has also been made in the immunotherapy field. The PD-1/PD-L1 pathway has been found to be activated in many USC patients, and clinical trials of PD-1 inhibitors in USC are underway. This review updates the progress of research regarding the molecular pathogenesis and putative clinical management of USC.

摘要

子宫浆液性癌(USC)是一种侵袭性子宫内膜癌变体,其特征尚未完全明确。它占所有子宫内膜癌的比例不到10%,但却导致了80%的子宫内膜癌相关死亡。目前,分期手术联合化疗或放疗,尤其是阴道残端近距离放疗,是USC的主要治疗策略。全外显子测序结合临床前和临床研究正在验证一系列针对不同USC患者群体中频繁改变基因(如 和 )的有效且临床可用的抑制剂。免疫治疗领域也取得了一些进展。已发现许多USC患者的PD-1/PD-L1通路被激活,并且针对USC的PD-1抑制剂临床试验正在进行中。本综述更新了关于USC分子发病机制和假定临床管理的研究进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b271/7140057/2e41d98361b4/cancers-12-00686-g001.jpg

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