Mismatch Repair Proficient Colorectal Adenocarcinoma in Two Patients With Lynch Syndrome

被引:0
作者
Khandakar, Binny [1 ]
Lacy, Jill [2 ]
Gibson, Joanna A. [3 ]
机构
[1] Donald & Barbara Zucker Sch Med Hofstra Northwell, Dept Pathol & Lab Med, New York, NY USA
[2] Yale Univ, Sch Med, Dept Internal Med, Med Oncol, New Haven, CT USA
[3] Yale Univ, Sch Med, Dept Pathol, New Haven, CT 06520 USA
关键词
colorectal carcinoma; immunotherapy; Lynch syndrome; mismatch repair; MMR deficient; MMR proficient; MSH6; next generation sequencing; predictive biomarker; RISK;
D O I
10.1111/cge.14670
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Screening for Lynch syndrome (LS) is essential in colorectal carcinoma (CRC) diagnosis. The hallmark of CRC in LS is mismatch repair (MMR) deficiency, a vital biomarkers assessed by microsatellite instability (MSI) analysis and/or immunohistochemistry (IHC) staining of the MMR proteins in the tumor, that also predict response to immune checkpoint inhibitors. We report two LS patients who developed MMR proficient CRCs. Patient A, with a pathogenic MSH6 germline variant, presented with two MMR discordant CRCs: a rectal MMRd/MSI adenocarcinoma, and a sigmoid MMR proficient (MMRp) and microsatellite stable (MSS) adenocarcinoma, leading to metastasis. While the MMRd/MSI carcinoma was recognized early and showed complete pathologic response after pembrolizumab treatment, the MMRp/MSS adenocarcinoma was underrecognized and poorly responsive to treatment. A second patient, with a pathogenic PMS2 variant, also developed a MMRp CRC. These cases highlight the complex biological pathways in CRC development and the impact of molecular classification on treatment.
引用
收藏
页码:469 / 474
页数:6
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