Falanga Anna, Schieppati Francesca, Russo Laura
Department of Transfusion Medicine and Hematology, Hospital Papa Giovanni XXIII, Bergamo, Italy.
University of Milan Bicocca, School of Medicine and Surgery, Monza, Italy.
Cancer Treat Res. 2019;179:11-36. doi: 10.1007/978-3-030-20315-3_2.
Thrombosis is a major cause of morbidity and mortality in cancer patients. The pathogenesis of blood coagulation activation in oncological patients is complex and involves both clinical and biological factors. Abnormalities in one or more coagulation test are common in cancer patients, even without thrombotic manifestations, indicating an ongoing hypercoagulable condition. Moreover, venous thromboembolism (VTE) can be the first symptom of an occult malignancy in an otherwise healthy individual. The levels of laboratory markers of activation of blood coagulation parallel the development of malignancy, being the coagulant mechanisms important for both thrombogenesis and tumor progression. Besides general clinical risk factors for VTE, also disease-specific clinical factors, i.e., type and stage of the tumor, and anticancer therapies increase the thrombotic risk in these patients. Furthermore, biological factors, including the cancer cell-specific prothrombotic properties together with the host cell inflammatory response to the tumor, are relevant as well as unique players in the pathogenesis of the cancer-associated hypercoagulability. Cancer cells produce and release procoagulant and fibrinolytic proteins, inflammatory cytokines, and procoagulant microparticles. They also express adhesion molecules binding to the receptors of host vascular cells (i.e., endothelial cells, platelets, and leukocytes), thereby stimulating the prothrombotic properties of these normal cells, including the shed of cell-specific microparticles and neutrophil extracellular traps. Of interest, several genes responsible for the cellular neoplastic transformation drive the programs of hemostatic properties expressed by cancer tissues. A better understanding of such mechanisms will help the development of novel strategies to prevent and treat the Trousseau's syndrome (i.e., cancer-associated thrombosis).
血栓形成是癌症患者发病和死亡的主要原因。肿瘤患者凝血激活的发病机制复杂,涉及临床和生物学因素。即使没有血栓形成表现,癌症患者一项或多项凝血检测异常也很常见,这表明存在持续的高凝状态。此外,静脉血栓栓塞(VTE)可能是原本健康个体隐匿性恶性肿瘤的首发症状。凝血激活的实验室标志物水平与恶性肿瘤的发展平行,凝血机制对血栓形成和肿瘤进展都很重要。除了VTE的一般临床危险因素外,疾病特异性临床因素,即肿瘤的类型和分期以及抗癌治疗也会增加这些患者的血栓形成风险。此外,生物学因素,包括癌细胞特异性的促血栓形成特性以及宿主细胞对肿瘤的炎症反应,也是癌症相关高凝状态发病机制中的相关因素和独特因素。癌细胞产生并释放促凝和纤溶蛋白、炎性细胞因子和促凝微粒。它们还表达与宿主血管细胞(即内皮细胞、血小板和白细胞)受体结合的粘附分子,从而刺激这些正常细胞的促血栓形成特性,包括细胞特异性微粒和中性粒细胞胞外陷阱的脱落。有趣的是,一些负责细胞肿瘤转化的基因驱动着癌症组织表达的止血特性程序。更好地理解这些机制将有助于开发预防和治疗Trousseau综合征(即癌症相关血栓形成)的新策略。