实体肿瘤患者接受全身治疗后静脉血栓栓塞的预后因素:系统综述。

TH Open: Companion Journal to Thrombosis and Haemostasis Pub Date : 2021-09-30 eCollection Date: 2021-07-01 DOI:10.1055/a-1642-4572
Sandra Lee, Anika Shenoy, Daniel Shi, Mootaz Husien, Pablo E Serrano, Sameer Parpia
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引用次数: 0

摘要

背景:接受全身癌症治疗的患者易发生静脉血栓栓塞(VTE)。静脉血栓栓塞最相关的预后因素尚不清楚。本系统综述旨在总结该人群中与静脉血栓栓塞相关的预后因素。方法检索MEDLINE、Embase和CENTRAL数据库,寻找使用肿瘤类型和/或转移性疾病调整的多变量分析来模拟静脉血栓栓塞风险的观察性或随机研究。对所有纳入的研究收集每个预后因素的调整后的效应估计。使用预后因素研究质量(QUIPS)工具评估偏倚风险。结果从5988个搜索结果中,确定了15个符合条件的研究和42个预后因素。共纳入8554例患者,其中456例(5.33%)发生静脉血栓栓塞。14项研究有高偏倚风险,1项研究有中等偏倚风险。最常报道的预后因素包括年龄、性别、肿瘤部位、转移、表现状态和全身治疗类型。在大多数研究中,表现不佳和使用含铂化疗化合物与静脉血栓栓塞风险增加有关。证据表明,确定的其他预后因素与静脉血栓栓塞的发展有关,尚无定论。一些单独的研究发现了静脉血栓栓塞的新生物标志物。统计方法和预后因素定义的异质性妨碍了meta分析。结论总体而言,确定了许多预后因素;然而,大多数因素与静脉血栓栓塞相关的证据尚无定论。纳入研究的高异质性和偏倚风险限制了研究结果。
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Prognostic Factors for Venous Thromboembolism in Patients with Solid Tumours on Systemic Therapy: A Systematic Review.

Background  Patients undergoing systemic cancer therapy are susceptible to developing venous thromboembolism (VTE). The most pertinent prognostic factors for VTE remain unclear. This systematic review aims to summarize prognostic factors associated with VTE in this population. Methods  MEDLINE, Embase, and CENTRAL databases were searched for observational or randomized studies that used multivariable analysis adjusted for tumor type and/or metastatic disease to model the risk of VTE. Adjusted effect estimates for each prognostic factor were collected for all of the included studies. Risk of bias was assessed using the Quality in Prognostic Factor Studies (QUIPS) tool. Results  From 5,988 search results, 15 eligible studies and 42 prognostic factors were identified. A total of 8,554 patients of whom 456 (5.33%) developed VTE were included. Fourteen studies had a high risk of bias and one study had a moderate risk. The most commonly reported prognostic factors include age, gender, tumor site, metastasis, performance status, and systemic therapy type. Poor performance status and the use of platinum-based chemotherapy compounds were associated with an increased risk of VTE across the majority of studies. The evidence to suggest that the other prognostic factors identified were associated with VTE development was inconclusive. Several individual studies identified novel biomarkers for VTE. Heterogeneity in statistical methods and prognostic factor definitions across studies precluded meta-analysis. Conclusion  Overall, many prognostic factors were identified; however, the evidence for association with development of VTE for most of the factors is inconclusive. Findings were limited by high heterogeneity and risk of bias in the included studies.

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