使用循环肿瘤DNA在不同测试条件下预测结直肠癌复发的14个基因小组。

IF 4.3 2区 医学 Q1 Medicine
Cancer Science Pub Date : 2025-06-30 DOI:10.1111/cas.70114
Yuichi Hisamatsu, Koji Ando, Kensuke Kudo, Ryota Nakanishi, Tetsuro Kawazoe, Yoko Zaitsu, Tetsuya Kusumoto, Taishi Hata, Yoshinori Kagawa, Tomoharu Yoshizumi, Naoko Ashida, Hayato Niiro, Takashi Hirose, Eiji Oki
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引用次数: 0

摘要

术后检测最小残留病变是评估结直肠癌复发风险的关键。传统的方法,包括组织学和癌胚抗原检测,灵敏度有限。由于循环肿瘤DNA已成为一种有希望的最小残留疾病生物标志物,我们使用敏感的靶向14基因面板Sysmex Plasma-Safe-SeqS结直肠癌检测来评估可切除结直肠癌病例中的循环肿瘤DNA检测。我们招募了46名术前诊断为II期结直肠癌的日本患者,他们在三家机构接受了手术。术前、术后均采集血浆标本。进行肿瘤知情、血浆知情和肿瘤初始血浆安全- seqs结直肠癌检测。通过临床评估和计算机断层扫描对患者进行中位随访1169天(范围148-1476)。46例中有45例(98%)在肿瘤组织中检测到变异。术前循环肿瘤DNA检测32例(70%),术后循环肿瘤DNA检测16例(35%)。术后循环肿瘤DNA预测复发的阳性率分别为肿瘤告知、血浆告知和肿瘤初始检测的33%、38%和25%。术后循环肿瘤dna阳性的病例,肿瘤初始检测比其他方法检测到的更多。由于肿瘤初始方法不需要术前基因分析,因此在成本和易于在常规临床实践中实施方面具有显着优势。需要进一步的大规模研究来优化检测策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A 14-Gene Panel for Predicting Colorectal Cancer Recurrence Using Circulating Tumor DNA in Different Testing Conditions.

Detecting minimal residual disease after surgery is critical for assessing colorectal cancer recurrence risk. Traditional methods, including histology and carcinoembryonic antigen testing, have limited sensitivity. As circulating tumor DNA has emerged as a promising minimal residual disease biomarker, we evaluated circulating tumor DNA detection using a sensitive, targeted 14-gene panel, the Sysmex Plasma-Safe-SeqS colorectal cancer assay, in resectable colorectal cancer cases. We enrolled 46 Japanese patients with preoperatively diagnosed stage II colorectal cancer who underwent surgery at three institutions. Plasma samples were collected pre- and postoperatively. Tumor-informed, plasma-informed, and tumor-naive Plasma-Safe-SeqS colorectal cancer assays were performed. Patients were followed for a median of 1169 (range 148-1476) days using clinical assessments and computed tomography scans. Variants in tumor tissue were detected in 45 of 46 cases (98%). Preoperative circulating tumor DNA was detected in 32 (70%) and postoperative circulating tumor DNA in 16 (35%) patients. Postoperative circulating tumor DNA predicted recurrence with 33%, 38%, and 25% of positive percent agreement for tumor-informed, plasma-informed, and tumor-naive assays, respectively. The tumor-naive assay detected more postoperative circulating tumor DNA-positive cases than the others. As the tumor-naive approach does not require preoperative genetic profiling, it offers significant advantages in cost and ease of implementation in routine clinical practice. Further large-scale studies are warranted to optimize detection strategies.

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来源期刊
Cancer Science
Cancer Science ONCOLOGY-
CiteScore
9.90
自引率
3.50%
发文量
406
审稿时长
17 weeks
期刊介绍: Cancer Science (formerly Japanese Journal of Cancer Research) is a monthly publication of the Japanese Cancer Association. First published in 1907, the Journal continues to publish original articles, editorials, and letters to the editor, describing original research in the fields of basic, translational and clinical cancer research. The Journal also accepts reports and case reports. Cancer Science aims to present highly significant and timely findings that have a significant clinical impact on oncologists or that may alter the disease concept of a tumor. The Journal will not publish case reports that describe a rare tumor or condition without new findings to be added to previous reports; combination of different tumors without new suggestive findings for oncological research; remarkable effect of already known treatments without suggestive data to explain the exceptional result. Review articles may also be published.
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