The impact of waiting time and delayed treatment on the outcomes of patients with hepatocellular carcinoma: A systematic review and meta-analysis.

IF 1.1 Q4 GASTROENTEROLOGY & HEPATOLOGY Annals of hepato-biliary-pancreatic surgery Pub Date : 2024-02-29 Epub Date: 2023-12-14 DOI:10.14701/ahbps.23-090
Feng Yi Cheo, Celeste Hong Fei Lim, Kai Siang Chan, Vishal Girishchandra Shelat
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Abstract

Hepatocellular carcinoma (HCC) is the sixth most diagnosed cancer worldwide. Healthcare resource constraints may predispose treatment delays. We aim to review existing literature on whether delayed treatment results in worse outcomes in HCC. PubMed, Embase, The Cochrane Library, and Scopus were systematically searched from inception till December 2022. Primary outcomes were overall survival (OS) and disease-free survival (DFS). Secondary outcomes included post-treatment mortality, readmission rates, and complications. Fourteen studies with a total of 135,389 patients (delayed n = 25,516, no delay n = 109,873) were included. Age, incidence of male patients, Child-Pugh B cirrhosis, and Barcelona Clinic Liver Cancer Stage 0/A HCC were comparable between delayed and no delay groups. Tumor size was significantly smaller in delayed versus no delay group (mean difference, -0.70 cm; 95% confidence interval [CI]: -1.14, 0.26; p = 0.002). More patients received radiofrequency ablation in delayed versus no delay group (OR, 1.22; 95% CI: 1.16, 1.27; p < 0.0001). OS was comparable between delayed and no delay in HCC treatment (hazard ratio [HR], 1.13; 95% CI: 0.99, 1.29; p = 0.07). Comparable DFS between delayed and no delay groups (HR, 0.99; 95% CI: 0.75, 1.30; p = 0.95) was observed. Subgroup analysis of studies that defined treatment delay as > 90 days showed comparable OS in the delayed group (HR, 1.04; 95% CI: 0.93, 1.16; p = 0.51). OS and DFS for delayed treatment were non-inferior compared to no delay, but might be due to better tumor biology/smaller tumor size in the delayed group.

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等待时间和延迟治疗对肝细胞癌患者预后的影响:系统回顾和荟萃分析。
肝细胞癌(HCC)是全球第六大确诊癌症。医疗资源的限制可能会导致治疗延迟。我们旨在回顾现有文献,了解延迟治疗是否会导致 HCC 的预后更差。我们对 PubMed、Embase、The Cochrane Library 和 Scopus 进行了系统检索,检索时间从开始到 2022 年 12 月。主要结果为总生存期(OS)和无病生存期(DFS)。次要结果包括治疗后死亡率、再入院率和并发症。14项研究共纳入135,389名患者(延迟n=25,516,无延迟n=109,873)。延迟组和非延迟组的年龄、男性患者发病率、Child-Pugh B肝硬化和巴塞罗那临床肝癌0/A期HCC的发病率相当。延迟组与无延迟组相比,肿瘤体积明显较小(平均差异为-0.70厘米;95%置信区间[CI]:-1.14,0.26;P = 0.002)。与无延迟组相比,延迟组接受射频消融的患者更多(OR,1.22;95% 置信区间[CI]:1.16,1.27;P < 0.0001)。延迟和不延迟治疗 HCC 的 OS 相当(危险比 [HR],1.13;95% CI:0.99, 1.29;P = 0.07)。延迟和不延迟组的 DFS 具有可比性(HR,0.99;95% CI:0.75,1.30;P = 0.95)。对将延迟治疗定义为大于90天的研究进行的亚组分析显示,延迟治疗组的OS相当(HR,1.04;95% CI:0.93,1.16;P = 0.51)。与不延迟治疗相比,延迟治疗的OS和DFS并不劣于不延迟治疗,但这可能是由于延迟治疗组的肿瘤生物学特性更好/肿瘤体积更小。
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