原发性胰腺神经内分泌肿瘤切除伴不可切除肝转移的生存获益:一项荟萃分析。

IF 1.7 4区 医学 Q3 GASTROENTEROLOGY & HEPATOLOGY
Jie Gong, Ben-Jian Gao, Ze-Hua Lei
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引用次数: 0

摘要

背景:胰腺神经内分泌肿瘤(PNETs)是一种罕见的恶性肿瘤,常伴有肝转移(LM)。原发性肿瘤切除(PTR)对不可切除LM患者的益处仍存在争议。本研究通过整合来自系统评价、荟萃分析和监测、流行病学和最终结果(SEER)数据库分析的证据,评估PTR对总生存期(OS)和肿瘤分级的影响。目的:评价PTR治疗PNETs合并LM患者的生存获益。方法:本研究按照PRISMA指南进行。使用PubMed、Web of Science、EMBASE、Cochrane Library和CNKI 5个数据库进行系统的文献检索和meta分析,记录时间截止到2025年2月。共纳入16项研究(n = 8761,包括1项前瞻性研究和15项回顾性研究)。随机效应模型应用于OS的风险比和肿瘤分级的优势比,并通过i2统计量评估异质性。使用ROBINS-I工具评估偏倚风险。此外,基于SEER数据库(n = 791),采用Kaplan-Meier生存曲线和log-rank检验进行独立分析。结果:meta分析结果显示,PTR显著改善PNETs和LM患者的OS(风险比= -1.10,95%可信区间:-1.43 ~ -0.71,P < 0.0001)。亚组分析显示,研究设计(前瞻性与回顾性)和样本量(< 400 vs≥400)均未显著影响生存获益。在肿瘤分级方面,手术组与非手术组比较,差异无统计学意义(优势比为1.60,95%可信区间为0.70 ~ 3.63,P = 0.26)。SEER数据库的独立分析(n = 791)进一步证实了PTR在不同肿瘤分化水平上的生存优势,手术组和非手术组的OS差异有统计学意义(P < 0.05)。结论:PTR可显著改善PNET合并LM患者的OS。然而,它对肿瘤分级的影响尚不清楚,需要进一步的前瞻性研究来完善这一人群的手术策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Survival benefit of primary tumor resection in pancreatic neuroendocrine tumors with unresectable liver metastases: A meta-analysis.

Survival benefit of primary tumor resection in pancreatic neuroendocrine tumors with unresectable liver metastases: A meta-analysis.

Survival benefit of primary tumor resection in pancreatic neuroendocrine tumors with unresectable liver metastases: A meta-analysis.

Survival benefit of primary tumor resection in pancreatic neuroendocrine tumors with unresectable liver metastases: A meta-analysis.

Background: Pancreatic neuroendocrine tumors (PNETs) are rare malignancies frequently associated with liver metastases (LM). The benefit of primary tumor resection (PTR) in patients with unresectable LM remains controversial. This study evaluates the impact of PTR on overall survival (OS) and tumor grading by integrating evidence from a systematic review, meta-analysis, and Surveillance, Epidemiology, and End Results (SEER) database analysis.

Aim: To evaluate the survival benefits of PTR in patients with PNETs and LM.

Methods: This study was conducted in accordance with the PRISMA guidelines. A systematic literature search and meta-analysis were performed using five databases: PubMed, Web of Science, EMBASE, Cochrane Library, and CNKI, with records included up to February 2025. A total of 16 studies (n = 8761; including 1 prospective and 15 retrospective studies) were included. A random-effects model was applied to pool hazard ratios for OS and odds ratios for tumor grading, with heterogeneity assessed by the I 2 statistic. Risk of bias was evaluated using the ROBINS-I tool. In addition, an independent analysis based on the SEER database (n = 791) was conducted using Kaplan-Meier survival curves and log-rank tests.

Results: Meta-analysis results revealed that PTR significantly improved OS in patients with PNETs and LM (hazard ratio = -1.10, 95% confidence interval: -1.43 to -0.71, P < 0.0001). Subgroup analyses showed that neither study design (prospective vs. retrospective) nor sample size (< 400 vs ≥ 400) significantly influenced the survival benefit. In terms of tumor grading, no statistically significant difference was observed between the surgical and non-surgical groups (odds ratio = 1.60, 95% confidence interval: 0.70-3.63, P = 0.26). Independent analysis of the SEER database (n = 791) further confirmed the survival advantage of PTR across different tumor differentiation levels, with significant differences in OS between surgical and non-surgical groups (P < 0.05).

Conclusion: PTR significantly improves OS in PNET patients with LM. However, its effect on tumor grading remains unclear, warranting further prospective studies to refine surgical strategies for this population.

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