Treatment stratification and prognosis assessment using circulating tumor DNA in locally advanced rectal cancer: A systematic review and meta-analysis

被引:3
作者
Mi, Junjie [1 ,3 ]
Wang, Rong [1 ]
Han, Xiaofang [2 ]
Ma, Ruijun [1 ]
Zhao, Danyu [1 ]
机构
[1] Shanxi Med Univ, Shanxi Prov Peoples Hosp, Hosp 5, Dept Gastroenterol, Taiyuan, Peoples R China
[2] Shanxi Med Univ, Shanxi Prov Peoples Hosp, Hosp 5, Core Lab, Taiyuan, Peoples R China
[3] Shanxi Med Univ, Shanxi Prov Peoples Hosp, Hosp 5, Dept Gastroenterol, 29, Shuang ta si St, Taiyuan, Peoples R China
来源
CANCER MEDICINE | 2023年 / 12卷 / 17期
关键词
circulating tumor DNA; locally advanced rectal cancer; pathological complete response; prognosis; recurrence; TOTAL MESORECTAL EXCISION; CLINICAL COMPLETE RESPONDERS; SHORT-COURSE RADIOTHERAPY; NEOADJUVANT CHEMORADIOTHERAPY; COLORECTAL-CANCER; COLON-CANCER; FOLLOW-UP; CHEMORADIATION; MULTICENTER; SURVIVAL;
D O I
10.1002/cam4.6434
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Circulating tumor DNA (ctDNA) is an emerging biomarker for locally advanced rectal cancer (LARC), giving hope for stratified treatment. As the completed studies have small sample sizes and different experimental methods, systematic review and meta-analysis were performed to explore their role in predicting pathological complete response (pCR), tumor recurrence, and prognosis.Methods: PubMed, Embase, and the Web of Science were searched for potentially eligible studies published up to September 6, 2022. Pooled relative risk (RR) was calculated to predict pCR and tumor recurrence, and pooled hazard ratio (HR) was calculated to evaluate the prognosis of overall survival (OS), recurrence-free survival (RFS), and metastasis-free survival (MRS).Results: Twelve studies published between 2018 and 2022 included 931 patients, and 2544 serum samples were eventually included in the meta-analysis. The pooled revealed that ctDNA-negative patients were more likely to have a pCR (RR = 1.64, 95% confidence interval [CI]: 1.26-2.12). The pooled revealed that ctDNA-positive patients were at high risk of recurrence (RR = 3.37, 95% CI: 2.34-4.85) and had a poorer prognosis for OS (HR = 3.03, 95% CI: 1.86-4.95), RFS (HR = 7.08, 95% CI: 4.12-12.14), and MRS (HR = 2.77, 95% CI: 2.01-3.83).Conclusion: ctDNA may be useful for stratifying treatment and assessing prognosis in patients with LARC, but its clinical application still needs to be confirmed in a prospective multicenter study with large samples.
引用
收藏
页码:17934 / 17944
页数:11
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