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索引结直肠病变中该基因第7外显子的体细胞突变与异时性腺瘤的早期发生相关。

Somatic Mutations in Exon 7 of the Gene in Index Colorectal Lesions Are Associated with the Early Occurrence of Metachronous Adenoma.

作者信息

Hálková Tereza, Ptáčková Renata, Semyakina Anastasiya, Suchánek Štěpán, Traboulsi Eva, Ngo Ondřej, Hejcmanová Kateřina, Májek Ondřej, Bureš Jan, Zavoral Miroslav, Minárik Marek, Benešová Lucie

机构信息

Centre for Applied Genomics of Solid Tumors (CEGES), Genomac Research Institute, Drnovská 1112/60, 161 00 Prague, Czech Republic.

Department of Medicine, 1st Faculty of Medicine, Charles University and Military University Hospital Prague, U Vojenské Nemocnice 1200, 169 02 Prague, Czech Republic.

出版信息

Cancers (Basel). 2022 Jun 7;14(12):2823. doi: 10.3390/cancers14122823.

Abstract

(1) Background: this prospective study was focused on detailed analysis of the mutation heterogeneity in colorectal lesions removed during baseline (index) colonoscopy to identify patients at high risk of early occurrence of metachronous adenomas. (2) Methods: a total of 120 patients after endoscopic therapy of advanced colorectal neoplasia size ≥10 mm (index lesion) with subsequent surveillance colonoscopy after 10-18 months were included. In total, 143 index lesions and 84 synchronous lesions in paraffin blocks were divided into up to 30 samples. In each of them, the detection of somatic mutations in 11 hot spot gene loci was performed. Statistical analysis to correlate the mutation profiles and the degree of heterogeneity of the lesions with the risk of metachronous adenoma occurrence was undertaken. (3) Results: mutation in exon 7 of the gene found in the index lesion significantly correlated with the early occurrence of metachronous adenoma (log-rank test = 0.003, hazard ratio 2.73, 95% confidence interval 1.14-6.56). We did not find an association between the risk of metachronous adenomas and other markers monitored. (4) Conclusions: the findings of this study could lead to an adjustment of existing recommendations for surveillance colonoscopies in a specific group of patients with mutations in exon 7 of the gene in an index lesion, where a shortening of surveillance interval may be warranted.

摘要

(1) 背景:本前瞻性研究聚焦于对基线(索引)结肠镜检查时切除的结直肠病变中的突变异质性进行详细分析,以识别异时性腺瘤早期发生风险较高的患者。(2) 方法:纳入120例接受内镜治疗的直径≥10 mm的晚期结直肠肿瘤(索引病变)患者,在10 - 18个月后进行后续的监测结肠镜检查。石蜡块中的143个索引病变和84个同步病变总共被分成多达30个样本。对每个样本进行11个热点基因位点的体细胞突变检测。进行统计分析以关联突变谱和病变的异质性程度与异时性腺瘤发生风险。(3) 结果:在索引病变中发现的 基因外显子7突变与异时性腺瘤的早期发生显著相关(对数秩检验 = 0.003,风险比2.73,95%置信区间1.14 - 6.56)。我们未发现异时性腺瘤风险与所监测的其他标志物之间存在关联。(4) 结论:本研究结果可能导致对特定组患者(索引病变中 基因外显子7发生突变)的现有监测结肠镜检查建议进行调整,在这些患者中可能有必要缩短监测间隔。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3e3/9221022/6947d802c5e2/cancers-14-02823-g001.jpg

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