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错配修复蛋白缺陷并不影响 I 型子宫内膜癌的无病生存。

Mismatch Repair Protein Deficiency Does Not Affect Disease Free Survival in Type I Endometrial Carcinoma.

机构信息

Department of Obstetric & Gynaecology, Oncology Division, Airlangga University, Surabaya, Indonesia.

Department of Pathology Anatomy, Airlangga University, Surabaya, Indonesia.

出版信息

Asian Pac J Cancer Prev. 2023 Sep 1;24(9):3229-3234. doi: 10.31557/APJCP.2023.24.9.3229.

DOI:10.31557/APJCP.2023.24.9.3229
PMID:37774076
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10762745/
Abstract

BACKGROUND

This study aimed to analyze the correlation between the 3-year disease-free survival (DFS) and mismatch repair (MMR) protein levels in patients with type 1 endometrial carcinoma. Many studies have reported different results regarding the role of MMR in the prognosis of endometrial carcinoma; therefore, we aimed to identify this association in our hospital.

METHODS

This observational study employed a historical cohort design and included patients with type 1 endometrial carcinoma who underwent surgery at Dr. Soetomo Hospital between January 2017 and December 2019. Medical records and paraffin blocks meeting these criteria were obtained. MMR proteins (MLH1 and MSH2) were assessed using immunohistochemistry.

RESULTS

A total of 46 patients with type 1 endometrial carcinoma were analyzed. We observed MMR deficiency (dMMR) in 12 patients (26.1%) and MMR proficiency (pMMR) in 34 patients (73.9%). Of the 12 patients with dMMR, nine cases (75%) were diagnosed as stage I and 7 (58.33%) as low grade. The 3-year DFS in patients with dMMR and pMMR was 83.3% and 67.6%, respectively (Hazard Ratio 2.31, 95% CI 0.5135-10.475, p=0.27). Higher stages had a 5.42 times increased risk of recurrence (95% CI 1.3378-21.9358, p=0.018). Higher histopathological grades were also associated with 8.65 times increased risk of recurrence (95% CI 2.5020-29.8738, p=0.001).

CONCLUSION

Patients with dMMR had a better DFS compared to those with pMMR; however, the difference was not statistically significant. The tumor stage and histopathological grade were independent risk factors for recurrence.

摘要

背景

本研究旨在分析 1 型子宫内膜癌患者 3 年无病生存率(DFS)与错配修复(MMR)蛋白水平的相关性。许多研究报告了 MMR 在子宫内膜癌预后中的作用的不同结果;因此,我们旨在在我院确定这种相关性。

方法

本观察性研究采用历史队列设计,纳入 2017 年 1 月至 2019 年 12 月在苏托莫医院接受手术的 1 型子宫内膜癌患者。获取符合这些标准的病历和石蜡块。使用免疫组织化学法评估 MMR 蛋白(MLH1 和 MSH2)。

结果

共分析了 46 例 1 型子宫内膜癌患者。我们观察到 12 例(26.1%)存在 MMR 缺陷(dMMR),34 例(73.9%)存在 MMR 功能正常(pMMR)。在 12 例 dMMR 患者中,9 例(75%)诊断为 I 期,7 例(58.33%)为低级别。dMMR 和 pMMR 患者的 3 年 DFS 分别为 83.3%和 67.6%(风险比 2.31,95%CI 0.5135-10.475,p=0.27)。较高的分期复发风险增加 5.42 倍(95%CI 1.3378-21.9358,p=0.018)。较高的组织病理学分级也与 8.65 倍的复发风险相关(95%CI 2.5020-29.8738,p=0.001)。

结论

dMMR 患者的 DFS 优于 pMMR 患者,但差异无统计学意义。肿瘤分期和组织病理学分级是复发的独立危险因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50d5/10762745/d4749dd3a0ad/APJCP-24-3229-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50d5/10762745/d1700b80dccd/APJCP-24-3229-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50d5/10762745/77f57dae1ae9/APJCP-24-3229-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50d5/10762745/d4749dd3a0ad/APJCP-24-3229-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50d5/10762745/d1700b80dccd/APJCP-24-3229-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50d5/10762745/77f57dae1ae9/APJCP-24-3229-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50d5/10762745/d4749dd3a0ad/APJCP-24-3229-g003.jpg

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本文引用的文献

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TCGA Molecular Prognostic Groups of Endometrial Carcinoma: Current Knowledge and Future Perspectives.TCGA 子宫内膜癌分子预后分组:当前认识与未来展望。
Int J Mol Sci. 2022 Oct 2;23(19):11684. doi: 10.3390/ijms231911684.
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Current and Emerging Prognostic Biomarkers in Endometrial Cancer.子宫内膜癌中当前及新出现的预后生物标志物
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Time to first recurrence, pattern of recurrence, and survival after recurrence in endometrial cancer according to the molecular classification.
根据分子分类的子宫内膜癌首次复发时间、复发模式及复发后的生存情况
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Endometrial Cancer.子宫内膜癌
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Int J Gynecol Cancer. 2020 Jun;30(6):783-788. doi: 10.1136/ijgc-2019-000910. Epub 2020 Apr 30.
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Mismatch Repair Deficiency in Endometrial Cancer: Immunohistochemistry Staining and Clinical Implications.子宫内膜癌中的错配修复缺陷:免疫组织化学染色及临床意义
Appl Immunohistochem Mol Morphol. 2019 Oct;27(9):678-682. doi: 10.1097/PAI.0000000000000641.
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