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一种高度敏感的泛癌微卫星不稳定性检测方法。

A Highly Sensitive Pan-Cancer Test for Microsatellite Instability.

机构信息

R&D Clinical Diagnostics, Promega Corporation, Madison, Wisconsin; Department of Medicine, University of Wisconsin, Madison, Wisconsin.

R&D Clinical Diagnostics, Promega Corporation, Madison, Wisconsin.

出版信息

J Mol Diagn. 2023 Nov;25(11):806-826. doi: 10.1016/j.jmoldx.2023.07.003. Epub 2023 Aug 5.

DOI:10.1016/j.jmoldx.2023.07.003
PMID:37544360
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10629437/
Abstract

Microsatellite instability (MSI) is an evolving biomarker for cancer detection and treatment. MSI was first used to identify patients with Lynch syndrome, a hereditary form of colorectal cancer (CRC), but has recently become indispensable in predicting patient response to immunotherapy. To address the need for pan-cancer MSI detection, a new multiplex assay was developed that uses novel long mononucleotide repeat (LMR) markers to improve sensitivity. A total of 469 tumor samples from 20 different cancer types, including 319 from patients with Lynch syndrome, were tested for MSI using the new LMR MSI Analysis System. Results were validated by using deficient mismatch repair (dMMR) status according to immunohistochemistry as the reference standard and compared versus the Promega pentaplex MSI panel. The sensitivity of the LMR panel for detection of dMMR status by immunohistochemistry was 99% for CRC and 96% for non-CRC. The overall percent agreement between the LMR and Promega pentaplex panels was 99% for CRC and 89% for non-CRC tumors. An increased number of unstable markers and the larger size shifts observed in dMMR tumors using the LMR panel increased confidence in MSI determinations. The LMR MSI Analysis System expands the spectrum of cancer types in which MSI can be accurately detected.

摘要

微卫星不稳定性 (MSI) 是一种用于癌症检测和治疗的新兴生物标志物。MSI 最初用于识别林奇综合征(一种遗传性结直肠癌 (CRC) 形式)患者,但最近已成为预测患者对免疫疗法反应的不可或缺的指标。为了解决泛癌种 MSI 检测的需求,开发了一种新的多重分析方法,该方法使用新的长单核苷酸重复 (LMR) 标记物来提高灵敏度。总共对来自 20 种不同癌症类型的 469 个肿瘤样本(包括 319 个来自林奇综合征患者的样本)进行了 MSI 检测,使用新的 LMR MSI 分析系统。结果通过根据免疫组织化学的缺陷错配修复 (dMMR) 状态作为参考标准进行验证,并与 Promega 五重 MSI 面板进行比较。LMR 面板检测免疫组织化学 dMMR 状态的灵敏度对于 CRC 为 99%,对于非 CRC 为 96%。对于 CRC,LMR 和 Promega 五重面板之间的总体一致性百分比为 99%,对于非 CRC 肿瘤为 89%。LMR 面板观察到的不稳定标记物数量增加和更大的大小移位增加了 MSI 测定的可信度。LMR MSI 分析系统扩展了可以准确检测 MSI 的癌症类型范围。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd09/10629437/c73cfcbb413c/figs10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd09/10629437/13de78615982/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd09/10629437/02a5ae67eb34/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd09/10629437/fc8b939c2d8c/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd09/10629437/3b6696c47798/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd09/10629437/363b6cca492e/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd09/10629437/d95550a539b3/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd09/10629437/a832beeac073/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd09/10629437/72f8e3bf91c2/figs1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd09/10629437/8f626c7a04e8/figs2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd09/10629437/b4d78a7b0163/figs3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd09/10629437/3cb93a72c8eb/figs4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd09/10629437/c0acee00d954/figs5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd09/10629437/9fe97db7858e/figs6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd09/10629437/70f8fa676596/figs7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd09/10629437/377c7b2282bf/figs8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd09/10629437/234af89e28a2/figs9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd09/10629437/c73cfcbb413c/figs10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd09/10629437/13de78615982/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd09/10629437/02a5ae67eb34/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd09/10629437/fc8b939c2d8c/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd09/10629437/3b6696c47798/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd09/10629437/363b6cca492e/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd09/10629437/d95550a539b3/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd09/10629437/a832beeac073/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd09/10629437/72f8e3bf91c2/figs1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd09/10629437/8f626c7a04e8/figs2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd09/10629437/b4d78a7b0163/figs3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd09/10629437/3cb93a72c8eb/figs4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd09/10629437/c0acee00d954/figs5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd09/10629437/9fe97db7858e/figs6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd09/10629437/70f8fa676596/figs7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd09/10629437/377c7b2282bf/figs8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd09/10629437/234af89e28a2/figs9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd09/10629437/c73cfcbb413c/figs10.jpg

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