Prognostic utility of preoperative and postoperative KRAS-mutated circulating tumor DNA (ctDNA) in resected pancreatic ductal adenocarcinoma: A systematic review and meta-analysis

被引:2
|
作者
Alqahtani, Ali [1 ,2 ]
Alloghbi, Abdurahman [3 ,4 ]
Coffin, Philip [5 ]
Yin, Chao [1 ]
Mukherji, Reetu [1 ]
Weinberg, Benjamin A. [1 ,6 ]
机构
[1] Georgetown Univ, Lombardi Comprehens Canc Ctr, Ruesch Ctr Cure Gastrointestinal Canc, Med Ctr, Washington, DC 20057 USA
[2] King Faisal Specialist Hosp & Res Ctr, Med Oncol Dept, Riyadh, Saudi Arabia
[3] King Khalid Univ, Canc Res Unit, Abha, Saudi Arabia
[4] King Khalid Univ, Dept Oncol, Abha, Saudi Arabia
[5] Georgetown Univ, Med Ctr, Dept Internal Med, Washington, DC 20007 USA
[6] 3800 Reservoir Rd NW, Washington, DC 20007 USA
来源
SURGICAL ONCOLOGY-OXFORD | 2023年 / 51卷
关键词
Biomarkers; Circulating tumor DNA; Liquid biopsy; Pancreatic adenocarcinoma; Minimal residual disease; ADJUVANT CHEMOTHERAPY; LIQUID BIOPSY; CANCER; ONCOLOGY; MARKER;
D O I
10.1016/j.suronc.2023.102007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Pancreatic ductal adenocarcinoma (PDAC) is a challenging disease, with surgery being the only possible cure. However, despite surgery, the majority of patients experience recurrence. Recent evidence suggests that perioperative KRAS-mutated circulating tumor DNA (ctDNA) may have prognostic value. Therefore, we conducted a systematic review and meta-analysis to explore the prognostic significance of preoperative and postoperative KRAS-mutated ctDNA testing in resected PDAC. Methods: We searched PubMed/MEDLINE, Embase, and Cochrane Central Register of Controlled Trials databases for studies that reported the effect of preoperative and postoperative KRAS-mutated ctDNA on overall survival (OS) and/or relapse-free survival (RFS) in resected PDAC. We used a random-effects model to determine the pooled OS and RFS hazard ratios (HR) and their corresponding 95 % confidence intervals (CI). Results: We identified 15 studies (868 patients) eligible for analysis. In the preoperative setting, positive ctDNA correlated with worse RFS in 8 studies (HR, 2.067; 95 % CI, 1.346-3.174, P < 0.001) and worse OS in 10 studies (HR, 2.170; 95 % CI, 1.451-3.245, P < 0.001) compared to negative ctDNA. In the postoperative setting, positive ctDNA correlated with worse RFS across 9 studies (HR, 3.32; 95 % CI, 2.19-5.03, P < 0.001) and worse OS in 6 studies (HR, 6.62; 95 % CI, 2.18-20.16, P < 0.001) compared to negative ctDNA. Conclusion: Our meta-analysis supports the utility of preoperative and postoperative KRAS-mutated ctDNA testing as a prognostic marker for resected PDAC. Further controlled studies are warranted to confirm these results and to investigate the potential therapeutic implications of positive KRAS-mutated ctDNA.
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页数:9
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