Pre-Treatment SEPTIN9 Gene Methylation Ratio Predicts Tumor Response to Total Neoadjuvant Therapy in Patients with Locally Advanced Rectal Cancer.

IF 4.4 2区 医学 Q1 ONCOLOGY Cancers Pub Date : 2025-03-13 DOI:10.3390/cancers17060965
Víctor Domínguez-Prieto, Miguel León-Arellano, Rocío Olivera-Salazar, Luz Vega-Clemente, Cristina Caramés, Eva Ruiz-Hispán, Raquel Fuentes-Mateos, Diana Rosero-Rodríguez, Héctor Guadalajara, Mariano García-Arranz, Damián García-Olmo
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Abstract

Background and objective: Multiple markers have been proposed, but there are no reliable pre-treatment markers that predict tumor response to total neoadjuvant therapy in patients with locally advanced rectal cancer. The objective of this study is to evaluate the usefulness of pre-treatment SEPTIN9 gene methylation ratio as a predictor of tumor response to total neoadjuvant therapy and its correlation with tumor size and tumor stage in patients with locally advanced rectal cancer. Methods: Patients with locally advanced rectal cancer (T3/4 and/or N+ histologically confirmed rectal cancer) undergoing total neoadjuvant therapy were included. Tumor size and tumor stage were determined by magnetic resonance. SEPTIN9 gene methylation in plasmatic cfDNA was analyzed by droplet digital PCR at the time of diagnosis. After completing total neoadjuvant therapy, tumor response was assessed by magnetic resonance and proctoscopy. The correlation between pre-treatment SEPTIN9 gene methylation ratio, tumor size, tumor stage and tumor response was analyzed. Results: 39 patients with locally advanced rectal cancer were included. Pre-treatment SEPTIN9 gene methylation ratio (p = 0.033) and tumor size (p = 0.026), but not tumor stage, significantly correlated with tumor response to total neoadjuvant therapy. Pre-treatment SEPTIN9 gene methylation ratio also correlated with N stage (p = 0.040) and tumor size (p = 0.001), but not with T stage (p = 0.846). Conclusions: Pre-treatment SEPTIN9 gene methylation ratio correlates with tumor size and N stage and can predict tumor response to total neoadjuvant therapy in patients with locally advanced rectal cancer.

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治疗前SEPTIN9基因甲基化率预测局部晚期直肠癌患者对总新辅助治疗的肿瘤反应。
背景与目的:已经提出了多种标志物,但没有可靠的治疗前标志物来预测局部晚期直肠癌患者对新辅助治疗的肿瘤反应。本研究的目的是评估治疗前SEPTIN9基因甲基化率作为局部晚期直肠癌患者肿瘤对总新辅助治疗反应的预测指标及其与肿瘤大小和肿瘤分期的相关性。方法:局部晚期直肠癌患者(组织学证实为T3/4和/或N+)接受全新辅助治疗。磁共振法测定肿瘤大小及分期。诊断时采用液滴数字PCR分析血浆cfDNA中SEPTIN9基因甲基化。完成全部新辅助治疗后,通过磁共振和直肠镜检查评估肿瘤反应。分析治疗前SEPTIN9基因甲基化率与肿瘤大小、肿瘤分期及肿瘤反应的相关性。结果:39例局部晚期直肠癌患者入选。治疗前SEPTIN9基因甲基化率(p = 0.033)和肿瘤大小(p = 0.026)与肿瘤对总新辅助治疗的反应显著相关,但与肿瘤分期无关。治疗前SEPTIN9基因甲基化率与N分期(p = 0.040)和肿瘤大小(p = 0.001)相关,但与T分期无关(p = 0.846)。结论:局部晚期直肠癌患者治疗前SEPTIN9基因甲基化率与肿瘤大小和N分期相关,可预测肿瘤对新辅助治疗的反应。
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来源期刊
Cancers
Cancers Medicine-Oncology
CiteScore
8.00
自引率
9.60%
发文量
5371
审稿时长
18.07 days
期刊介绍: Cancers (ISSN 2072-6694) is an international, peer-reviewed open access journal on oncology. It publishes reviews, regular research papers and short communications. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
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