Department of Haematology, University Hospital Basel, Basel, Switzerland.
Eur J Haematol. 2019 Nov;103(5):472-477. doi: 10.1111/ejh.13310. Epub 2019 Aug 27.
In this study, we analyzed the changes of thrombin generation as marker of coagulation activation and von Willebrand factor (vWF) levels as a marker of endothelial activation in patients undergoing chemotherapy, autologous, or allogeneic HSCT. We studied possible associations to triggering factors, including acute GVHD, thrombosis, time to engraftment, and bleeding complications.
Seventy-six patients treated for hematologic malignancies at the University Hospital Basel between 2005 and 2008 took part in this study. Blood samples were collected before the start of chemotherapy or conditioning regime (median day -2), in an early phase (median day + 12), and at a later point in time (median day + 24).
Thrombin generation decreased in all three groups to about 50% of the initial value. Patients undergoing autologous or allogeneic HSCT showed significantly (P = .026 and P = .01) higher vWF levels than patients undergoing chemotherapy. Eighteen patients (42%) receiving allogeneic HSCT developed GVHD, vWF levels in patients with GVHD were significantly (P = .008) higher than in patients without GVHD.
Patients receiving autologous or allogeneic HSCT had significantly higher vWF levels in the acute phase after the transplant than patients receiving chemotherapy alone, implicating a persistent stimulation of the endothelium, possibly within the context of GVHD.
在这项研究中,我们分析了接受化疗、自体或同种异体 HSCT 的患者凝血激活标志物凝血酶生成和血管性血友病因子 (vWF) 水平作为内皮细胞激活标志物的变化。我们研究了与触发因素的可能关联,包括急性移植物抗宿主病 (GVHD)、血栓形成、植入时间和出血并发症。
2005 年至 2008 年期间,巴塞尔大学医院收治的 76 例血液系统恶性肿瘤患者参与了这项研究。在化疗或预处理方案开始前(中位数为-2 天)、早期(中位数为+12 天)和后期(中位数为+24 天)采集血液样本。
三组患者的凝血酶生成均下降至初始值的 50%左右。接受自体或同种异体 HSCT 的患者的 vWF 水平明显高于接受化疗的患者(P=0.026 和 P=0.01)。18 名(42%)接受同种异体 HSCT 的患者发生了 GVHD,患有 GVHD 的患者的 vWF 水平明显高于没有 GVHD 的患者(P=0.008)。
接受自体或同种异体 HSCT 的患者在移植后的急性期 vWF 水平明显高于仅接受化疗的患者,这表明内皮细胞持续受到刺激,可能与 GVHD 有关。