推进精准肿瘤学:子宫内膜癌全基因组测序液基细胞学。

Reika Takamatsu, Kohei Nakamura, Tatsuyuki Chiyoda, Kosuke Tsuji, Ryutaro Kawano, Naoki Yoshimi, Wataru Yamagami, Hiroshi Nishihara
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摘要

背景子宫内膜癌的诊断策略一直在不断发展,细胞学分析因其微创性和对各种评估的适应性而被视为综合肿瘤诊断的关键方法。液基细胞学(LBC)已成为一种很有前景的完整保存DNA的方法;它在下一代测序等高级测序应用中表现出更高的效率。然而,尽管 LBC 可用于面板检测,但其在全外显子组测序(WES)中用于全面基因组剖析的应用仍未得到充分探索:研究是否可以利用 LBC 标本的 DNA 在 WES 基础上进行分子分类:我们将 WES 与靶向基因面板分析相结合,比较了从 7 例子宫内膜癌中获得的 LBC 和传统组织样本的基因组结果。我们研究了致病突变、肿瘤突变负荷和微卫星不稳定性,并实现了高准确度的分子分类:我们发现 LBC 与传统组织样本在致病突变检测方面具有很高的一致性,LBC 样本的匹配率为 95%,组织样本的匹配率为 94%。值得注意的是,我们的研究结果强调了将 WES 与基于面板的分析相结合,对确定面板分析中遗漏的病例的超突变状态的重要性:我们的研究结果强调了 LBC 样本在对子宫内膜癌病例进行精确、无创基因组分析方面的潜力,并为精准肿瘤学诊断和治疗策略的开发提供了一条新途径。
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Advancing Precision Oncology: Whole-Exome Sequencing in Endometrial Cancer Liquid-Based Cytology.

Context.—: Diagnostic strategies for endometrial cancer have been evolving, with cytologic analysis being considered a key method in integrated oncologic diagnostics because of its less invasive nature and adaptability to various assessments. Liquid-based cytology (LBC) has emerged as a promising method for intact DNA preservation; it exhibits improved efficiency in advanced sequencing applications such as next-generation sequencing. However, despite the use of LBC in panel assays, its application in whole-exome sequencing (WES) for comprehensive genomic profiling remains underexplored.

Objective.—: To investigate whether molecular classification is possible based on WES using DNA derived from LBC specimens.

Design.—: We combined WES with targeted gene panel analysis to compare genomic findings of LBC and traditional tissue samples obtained from 7 cases of endometrial cancer. We investigated pathogenic mutations, tumor mutational burden, and microsatellite instability, and achieved molecular classification with high accuracy.

Results.—: We found a substantial concordance between LBC and traditional tissue samples in terms of pathogenic mutation detection, with a 95% match in the LBC samples and 94% in the tissue samples. Notably, our results highlight the importance of combining WES with panel-based analysis in identifying the ultramutated status of a case that had been missed during panel analysis.

Conclusions.—: Our findings emphasize the potential of LBC samples in the precise and noninvasive genomic analysis of cases of endometrial cancer and offer a new avenue for developing diagnostic and therapeutic strategies in precision oncology.

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