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结肠腺癌患者微卫星不稳定性与临床病理数据的比较

英文原题:Comparison of Microsatellite Instability With Clinicopathologic Data in Patients With Colon Adenocarcinoma.

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Comparison of Microsatellite Instability With Clinicopathologic Data in Patients With Colon Adenocarcinoma.

PubMed 2024/04/08(内容时间) Cureus

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中文摘要

背景 微卫星不稳定性(MSI)是一种由DNA修复基因错误引起的遗传状态,可导致结直肠癌(CRC)。文献中关于散发性CRC中MSI的发生频率及其对预后的影响存在矛盾。

本研究探讨了临床病理特征的分布以及MSI与生存结局之间的关系。方法 这是一项对101例连续CRC病例的回顾性研究及免疫组化研究。所有病例均经回顾性复查,并从病理切片重新评估组织学分级、淋巴血管侵犯、神经周围侵犯、肿瘤边界、脏坏死、TIL(肿瘤浸润淋巴细胞)(TILs)、克罗恩样淋巴反应、黏液及髓样分化以及肿瘤出芽。在合适的蜡块上进行免疫组化研究,使用MLH-1、MSH-2、MSH-6和PMS-2。

我们从患者的临床资料中收集临床分期、病理肿瘤分期、淋巴结转移、年龄、性别、肿瘤直径、远处转移、定位及生存信息。结果 两组患者在年龄、性别、肿瘤直径、组织学分级、肿瘤边界、脏坏死、TILs、N和M分期、神经周围及淋巴血管侵犯、黏液分化、髓样分化及肿瘤出芽特征方面差异无统计学意义。MSI-H组更常位于右半结肠和横结肠(p < 0.001),且其T分期高于MSI-L组(p = 0.014)。多因素回归分析显示,MSI状态对生存时间无显著影响。年龄及N和M分期是结肠癌预后的独立预后因素。结论 我们的研究呈现了101例区域性CRC患者的临床病理特征分布及其与MSI的关系。MSI状态通过免疫组化检测。识别CRC中的MSI可能有助于个性化治疗规划。由于这些特征的分布可能因人群而异,关于此主题需要进一步研究。

展开英文摘要原文

Background Microsatellite instability (MSI) is a genetic condition caused by errors in DNA repair genes that cause colorectal cancer (CRC). The literature contradicts the frequency of MSI in sporadic CRCs and its effect on prognosis.

This study investigated the distribution of clinicopathologic features and the relationship between MSI and survival outcomes. Methodology This is a retrospective study of 101 consecutive cases of CRC and immunohistochemical studies.

All cases were retrospectively reviewed and reevaluated by histological grade, lymphovascular invasion, perineural invasion, tumor borders, dirty necrosis, tumor-infiltrating lymphocytes (TILs), Crohn's-like lymphoid reaction, mucinous and medullary differentiation, and tumoral budding from pathological slides. An immunohistochemical study was performed in appropriate blocks for using MLH-1, MSH-2, MSH-6, and PMS-2.

We collected the clinical stage, pathological tumor stage, lymph node metastasis, age, sex, tumor diameter, distant metastasis, localization, and survival information from patients' clinical data. Results There was no statistically significant difference between the two groups regarding age, gender, tumor diameter, histological grade, tumor border, dirty necrosis, TILs, N and M stage, perineural and lymphovascular invasion, mucinous differentiation, medullary differentiation, and tumor budding characteristics of the patients. The MSI-H group was more frequently located in the right colon and transverse colon (p < 0.

001), and the T stage was higher among them than in the MSI-L group (p = 0. 014). Upon multivariate regression analysis, MSI status had no significant effect on survival time. Age and stage N and M were independent prognostic factors for colon cancer prognosis.

Conclusions Our study presented the distribution of clinicopathological features and their relationship with MSI for 101 regional CRC patients. MSI status was detected by immunohistochemistry. Identifying MSI in CRCs may help personalize therapy planning. As the distribution of the features may vary from population to population, further investigations are needed on this topic.

论文信息

作者
Cesmecioglu Karavin E、Sağnak Yılmaz Z、Yazici H、Ersoz S、Mungan S
第一作者单位
Pathology, Marmara University Pendik Training and Research Hospital, Istanbul, TUR.Turkey
通讯作者单位
Pathology, Karadeniz Technical University Faculty of Medicine, Trabzon, TUR.Turkey
期刊
Cureus2024 Apr
原文标识
PubMed 38590982 · DOI 10.7759/cureus.57814