Circulating Tumor DNA Predicts Conversion Therapy Response and Prognosis in Initially Unresectable Colorectal Liver-Limited Metastases: A Retrospective Study.

IF 1 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL
British journal of hospital medicine Pub Date : 2025-03-26 Epub Date: 2025-03-18 DOI:10.12968/hmed.2024.0695
Bohan Han, Cailu Shen, Huabin Hu, Jianwei Zhang, Xiaoyu Xie, Qinli Mo, Yanhong Deng
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引用次数: 0

Abstract

Aims/Background Effective molecular biomarkers for predicting prognosis and guiding treatment in patients with initially unresectable colorectal liver metastases (CRLMs) undergoing conversion therapy are currently lacking. This study investigated the predictive value of circulating tumor DNA (ctDNA) conversion therapy outcomes in initially unresectable CRLMs. Methods A retrospective analysis was conducted on 81 patients with CRLMs treated at the Sixth Affiliated Hospital, Sun Yat-sen University from January 2017 to April 2021. The relationships between baseline and treatment ctDNA levels and clinical responses were evaluated using group comparisons based on data type. The impact of ctDNA on survival outcomes was analyzed through Cox regression survival analysis. Results Analysis of 81 patients with ctDNA-positive at baseline showed that patients in the ctDNA low-level group had a significantly longer median progression-free survival (mPFS) (p = 0.039). Among 45 patients who underwent ctDNA testing during systemic therapy, the proportion of patients in the ctDNA-negative group receiving local ablative treatment (LAT) was significantly higher (70.0% vs 26.7%, p = 0.006). Furthermore, 50% of patients in the ctDNA-negative group achieved no evidence of disease (NED) status, compared to 6.7% in the ctDNA-positive group (p = 0.004). Both mPFS and median overall survival (mOS) were significantly longer in ctDNA-negative patients compared to ctDNA-positive patients (p < 0.05). Of the 61 patients who underwent LAT, 37 received ctDNA testing at the same time as imaging assessment for NED. The proportion of patients with ctDNA clearance who achieved NED status was markedly higher than that of patients with ctDNA non-clearance (78.6% vs 33.3%, p = 0.036). Patients with ctDNA clearance demonstrated significantly improved mOS compared to those with ctDNA non-clearance (not reached vs 30.1 months, p = 0.036). Conclusion Dynamic changes in ctDNA levels can predict both long-term survival and the effectiveness of conversion therapy in patients with initially unresectable CRLMs.

循环肿瘤DNA预测最初不可切除的结直肠癌肝局限性转移的转化治疗反应和预后:一项回顾性研究。
目的/背景对于最初不可切除的结肠肝转移(crlm)患者进行转化治疗,目前缺乏预测预后和指导治疗的有效分子生物标志物。本研究探讨了循环肿瘤DNA (ctDNA)转换治疗结果对最初不可切除的crlm的预测价值。方法回顾性分析中山大学附属第六医院2017年1月至2021年4月收治的81例crlm患者。使用基于数据类型的组比较来评估基线和治疗ctDNA水平与临床反应之间的关系。通过Cox回归生存分析分析ctDNA对生存结局的影响。结果对81例基线时ctDNA阳性患者的分析显示,ctDNA低水平组患者的中位无进展生存期(mPFS)显著延长(p = 0.039)。在45例全身治疗期间进行ctDNA检测的患者中,ctDNA阴性组接受局部消融治疗(LAT)的患者比例显著高于对照组(70.0% vs 26.7%, p = 0.006)。此外,ctdna阴性组中50%的患者无疾病(NED)状态,而ctdna阳性组为6.7% (p = 0.004)。ctdna阴性患者的mPFS和中位总生存期(mOS)均明显长于ctdna阳性患者(p < 0.05)。在61例接受LAT的患者中,37例在进行NED影像学评估的同时接受了ctDNA检测。ctDNA清除的患者达到NED状态的比例明显高于ctDNA未清除的患者(78.6% vs 33.3%, p = 0.036)。ctDNA清除的患者与ctDNA未清除的患者(未达到vs 30.1个月,p = 0.036)相比,mOS显着改善。结论ctDNA水平的动态变化可以预测最初不可切除的crlm患者的长期生存和转换治疗的有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
British journal of hospital medicine
British journal of hospital medicine 医学-医学:内科
CiteScore
1.50
自引率
0.00%
发文量
176
审稿时长
4-8 weeks
期刊介绍: British Journal of Hospital Medicine was established in 1966, and is still true to its origins: a monthly, peer-reviewed, multidisciplinary review journal for hospital doctors and doctors in training. The journal publishes an authoritative mix of clinical reviews, education and training updates, quality improvement projects and case reports, and book reviews from recognized leaders in the profession. The Core Training for Doctors section provides clinical information in an easily accessible format for doctors in training. British Journal of Hospital Medicine is an invaluable resource for hospital doctors at all stages of their career. The journal is indexed on Medline, CINAHL, the Sociedad Iberoamericana de Información Científica and Scopus.
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