PO.CL09.02 · 临床研究
既往心脏病对胰腺癌生存和术后结局的影响:一项TriNetX分析
Impact of preexisting heart disease on survival and postoperative outcomes in pancreatic cancer: A TriNetX analysis
作者与单位 Authors & Affiliations
摘要 Abstract
中文摘要
背景:心血管合并症在胰腺导管腺癌(PDAC)患者中常见,可能影响长期生存和围手术期风险,但其在当代实践中的影响尚未充分明确。我们利用TriNetX(一个多国去标识化数据集)开展了一项回顾性数据库研究,以识别PDAC患者并检查心脏病、生存与胰十二指肠切除术(PD)并发症之间的关联。
方法:利用TriNetX数据库,我们识别出PDAC患者,并按有无心脏病(缺血性、结构性、心力衰竭)对队列进行分层。对接受PD的患者进行亚组分析。主要结局为总生存期,次要结局为PD后并发症发生率。针对年龄、性别、分期和合并症进行倾向评分匹配。采用Kaplan-Meier曲线和log-rank检验确定组间生存,采用多变量logistic回归评估心脏病与术后并发症之间的关联。在接受PD的患者中,次要结局包括术后胰漏、心肌梗死(MI)、急性肾损伤(AKI)、手术部位感染(SSI)和静脉血栓栓塞(VTE),采用多变量logistic回归评估其发生率。
结果:我们识别出226,966例PDAC患者,其中45,936例(20%)有既往心脏病,181,030例(80%)无;12,840例接受了PD。倾向匹配后,无心脏病患者的中位总5年生存期为703天,而有心脏病者为611天(HR = 0.90,p < 0.0001)。在匹配的手术队列中,既往心脏病与术后心肌梗死风险增加(RR = 3.34,p < 0.0001)和急性肾损伤(RR = 1.34,p < 0.0001)相关,但与术后胰漏(RR = 1.11,p = 0.18)、脓肿(RR = 1.15,p = 0.16)或手术部位感染(RR = 1.13,p = 0.16)无关。在接受和未接受PD的PDAC合并心脏病患者的倾向匹配队列中,接受PD者1年总生存期显著改善(82%对63%,p < 0.0001)。
结论:在这一大型真实世界PDAC患者队列中,既往心脏病是总生存和围手术期发病率的重要决定因素,中位生存和术后并发症谱存在具有临床意义的差异。PD的获益似乎并未因心脏危险因素而丧失,接受PD的组中观察到总生存显著改善。这些发现可为这一高风险人群的风险分层、治疗选择和围手术期优化策略提供参考。
查看英文原文 English abstract
Background: Cardiovascular comorbidity is common among patients with pancreatic ductal adenocarcinoma (PDAC) and may influence both long-term survival and perioperative risk, yet its impact in contemporary practice is not well defined. We performed a retrospective database study using TriNetx, a multinational deidentified dataset, to identify patients with PDAC and to examine associations between heart disease, survival, and complications of pancreaticoduodenectomy (PD).
Methods: Using the TriNetx database, we identified patients with PDAC and stratified the cohort by presence or absence of heart disease (ischemic, structural, heart failure). Subgroup analysis was performed of patients who underwent PD. The primary outcome is overall survival, and secondary outcome is rate of post-PD complications. Propensity score matching was performed for age, sex, stage, and comorbidities. Kaplan-Meier curves and log-rank testing were used to determine survival between the groups and multivariable logistic regression was used to evaluate associations between heart disease and postoperative complications. Among patients undergoing PD, secondary outcomes include postoperative pancreatic leak, myocardial infarction (MI), acute kidney injury (AKI), surgical site infection (SSI), and venous thromboembolism (VTE), rates were evaluated using multivariable logistic regression.
Results: We identified 226,966 patients with PDAC, of whom 45,936 (20%) had preexisting heart disease and 181,030 (80%) did not; 12,840 underwent PD. Propensity matched median overall 5-year survival was 703 days for patients without heart disease versus 611 days for those without (HR = 0.90, p < 0.0001). In the matched surgical cohort, preexisting heart disease was associated with increased risk of post-operative myocardial infarction (RR = 3.34, p < 0.0001) and acute kidney injury (RR = 1.34, p < 0.0001) but not associated with post-operative pancreatic leak (RR = 1.11, p = 0.18), abscess (RR = 1.15, p = 0.16), or surgical site infection (RR = 1.13, p = 0.16). Among propensity matched cohorts of patients with PDAC and heart disease who did and did not undergo PD, those who underwent PD had significant improvement in 1-year overall survival (82% vs 63%, p < 0.0001).
Conclusions: In this large, real-world cohort of patients with PDAC, preexisting heart disease was an important determinant of overall survival and perioperative morbidity, with clinically meaningful differences in median survival and postoperative complication profiles. The benefit of PD does not seem to be lost to patients with cardiac risk factors, with significant improvement in overall survival seen in the group who underwent PD. These findings may inform risk stratification, treatment selection, and perioperative optimization strategies for this high-risk population.
利益披露 Disclosure
C. Burch, None..
J. Lambdin, None..
W. Royster, None..
L. Fernandez, None..
R. Louie, None..
R. Bello, None..
J. G. Trevino, None.