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癌症相关血栓形成的生物标志物

Biomarkers of Cancer-Associated Thromboembolism.

作者信息

Mahajan Anjlee, Wun Ted

机构信息

Division of Hematology and Oncology, UC Davis School of Medicine, UC Davis Cancer Center, 4501 X Street, Sacramento, CA, 95817, USA.

UC Davis School of Medicine, Clinical and Translational Sciences Center (CTSC), Sacramento, USA.

出版信息

Cancer Treat Res. 2019;179:69-85. doi: 10.1007/978-3-030-20315-3_5.

Abstract

Venous thromboembolism is known to be associated with an increase in morbidity and mortality in patients with malignancy. Predictive laboratory biomarkers of venous thromboembolism (VTE) have long been sought after to improve outcomes and help guide clinical decision making. Previously studied biomarkers include C reactive protein (CRP), tissue factor expressing microparticles (TF MP), D-dimer, soluble P-selectin (sP-selectin), plasminogen activator inhibitor 1 (PAI-1), factor VIII, platelet count, and leukocyte counts. This chapter will focus on these possible biomarkers for cancer-associated thrombosis (CAT) with particular emphasis on the pathophysiology behind thrombosis formation as well as data from clinical studies in patients with malignancy. The incorporation of the above biomarkers into risk assessment tools to predict CAT will also be reviewed, as will risk factors for recurrent VTE in patients with malignancy. Further studies are ongoing to develop readily available biomarkers that can be incorporated into future risk assessment models with the goal of reducing morbidity and mortality due to cancer-associated thrombosis.

摘要

已知静脉血栓栓塞与恶性肿瘤患者的发病率和死亡率增加有关。长期以来一直在寻找静脉血栓栓塞(VTE)的预测性实验室生物标志物,以改善治疗结果并帮助指导临床决策。先前研究的生物标志物包括C反应蛋白(CRP)、表达组织因子的微粒(TF MP)、D-二聚体、可溶性P-选择素(sP-选择素)、纤溶酶原激活物抑制剂1(PAI-1)、因子VIII、血小板计数和白细胞计数。本章将重点讨论这些可能的癌症相关血栓形成(CAT)生物标志物,特别强调血栓形成背后的病理生理学以及恶性肿瘤患者临床研究的数据。还将回顾将上述生物标志物纳入风险评估工具以预测CAT的情况,以及恶性肿瘤患者复发性VTE的危险因素。正在进行进一步研究,以开发易于获得的生物标志物,这些生物标志物可纳入未来的风险评估模型,目标是降低癌症相关血栓形成导致的发病率和死亡率。

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