Department of Pathology and Laboratory Medicine, Cardiovascular Research Institute, Hemostasis and Thrombosis Research Division, Loyola University Chicago, Health Sciences Division, Maywood, IL, USA.
Head of Intensive care unit, Lymphoma Centre, Clinic for Hematology, Clinical Center Serbia, University of Belgrade, Belgrade, Serbia.
Clin Appl Thromb Hemost. 2020 Jan-Dec;26:1076029620983466. doi: 10.1177/1076029620983466.
The prevalence of thrombosis in lymphoma patients is reportedly high and ranges from 3-10%. Vascular malfunction and inflammatory processes further contribute to the thrombotic activation process in these patients. Andexanet alfa (AA) is an antidote for factor Xa inhibitors and its usage has been reported with thrombotic complications. This study was designed to compare the effect of AA on the thrombin generation (TG) potential. Blood samples from 78 patients with confirmed diagnosis of non-Hodgkin lymphoma (NHL), Hodgkin lymphoma (HL) and Chronic lymphocytic leukemia (CLL) were collected from the University of Belgrade Clinic, Serbia. Normal human plasma (NHP) was used for referencing purposes. Individual samples were supplemented with AA at 100 ug/ml. TG studies were carried out using a commercially available fluorogenic substrate method. TG parameters such as peak thrombin (PT), lag time (LT) and area under the curve (AUC) were compiled. Cumulatively, lymphoma patients showed an increase in LT compared to NHP which decreases with AA. The PT and AUC levels were decreased compared to NHP and increases with AA. Upon sub-grouping of lymphoma patients, PT levels for all sub-groups were increased with AA. The AUC values increased for HL and NHL and decreased for CLL with AA. Variations in lag time were noted in all 3 sub-groups. Lymphoma represents a heterogenous group of patients where both the hypercoagulable state and inflammatory responses simultaneously occur. Increased thrombin generation in post AA supplemented samples suggest that the use of this agent may potentially be associated with thrombotic complications.
据报道,淋巴瘤患者的血栓形成患病率较高,范围为 3-10%。血管功能障碍和炎症过程进一步促进了这些患者的血栓形成激活过程。Andexanet alfa (AA) 是一种针对 Xa 因子抑制剂的解毒剂,已报道其用于治疗血栓并发症。本研究旨在比较 AA 对凝血酶生成 (TG) 潜力的影响。从塞尔维亚贝尔格莱德大学诊所收集了 78 例确诊为非霍奇金淋巴瘤 (NHL)、霍奇金淋巴瘤 (HL) 和慢性淋巴细胞白血病 (CLL) 的患者的血液样本。正常人类血浆 (NHP) 用于参考。将个体样本用 100ug/ml 的 AA 补充。使用商业上可用的荧光底物法进行 TG 研究。编译了 TG 参数,如最大凝血酶 (PT)、滞后时间 (LT) 和曲线下面积 (AUC)。累积起来,与 NHP 相比,淋巴瘤患者的 LT 增加,而 LT 随着 AA 的增加而减少。与 NHP 相比,PT 和 AUC 水平降低,而随着 AA 的增加而增加。对淋巴瘤患者进行亚组分析后,所有亚组的 PT 水平均随 AA 升高。HL 和 NHL 的 AUC 值增加,而 CLL 的 AUC 值随 AA 降低。在所有 3 个亚组中均观察到滞后时间的变化。淋巴瘤是一组异质性患者,同时存在高凝状态和炎症反应。AA 补充后样本中凝血酶生成增加表明,该药物的使用可能与血栓形成并发症有关。