两例Lynch综合征患者的错配修复熟练结肠腺癌。

IF 2.9 3区 医学 Q2 GENETICS & HEREDITY
Binny Khandakar, Jill Lacy, Joanna A Gibson
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引用次数: 0

摘要

筛查Lynch综合征(LS)在结直肠癌(CRC)诊断中是必不可少的。LS结直肠癌的标志是错配修复(MMR)缺陷,这是一种重要的生物标志物,通过肿瘤中MMR蛋白的微卫星不稳定性(MSI)分析和/或免疫组织化学(IHC)染色来评估,也可以预测对免疫检查点抑制剂的反应。我们报告了两例LS患者发展为MMR熟练的crc。患者A具有致病性MSH6种系变异,表现为两种MMR不一致的crc:直肠MMRd/MSI腺癌和乙状结肠MMR精通(MMRp)和微卫星稳定(MSS)腺癌,导致转移。虽然MMRd/MSI癌在派姆单抗治疗后早期被发现并表现出完全的病理反应,但MMRp/MSS腺癌未被充分认识,对治疗反应较差。另一名携带致病性PMS2变异的患者也发展为MMRp型结直肠癌。这些病例强调了结直肠癌发展的复杂生物学途径以及分子分类对治疗的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mismatch Repair Proficient Colorectal Adenocarcinoma in Two Patients With Lynch Syndrome.

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.

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来源期刊
Clinical Genetics
Clinical Genetics 医学-遗传学
CiteScore
6.50
自引率
0.00%
发文量
175
审稿时长
3-8 weeks
期刊介绍: Clinical Genetics links research to the clinic, translating advances in our understanding of the molecular basis of genetic disease for the practising clinical geneticist. The journal publishes high quality research papers, short reports, reviews and mini-reviews that connect medical genetics research with clinical practice. Topics of particular interest are: • Linking genetic variations to disease • Genome rearrangements and disease • Epigenetics and disease • The translation of genotype to phenotype • Genetics of complex disease • Management/intervention of genetic diseases • Novel therapies for genetic diseases • Developmental biology, as it relates to clinical genetics • Social science research on the psychological and behavioural aspects of living with or being at risk of genetic disease
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