Roshandel Elham, Kaviani Saeid, Hajifathali Abbas, Soleimani Masoud
Department of Hematology, Tarbiat Modares University, Tehran, Iran.
Hematopoietic Stem Cell Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran; Taleghani Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Transfus Apher Sci. 2020 Aug;59(4):102810. doi: 10.1016/j.transci.2020.102810. Epub 2020 May 13.
Thrombocytopenia is a common consequence of leukemia that affects the outcome of hematopoietic stem cell transplantation (HSCT). The stromal damage of bone marrow following pre-HSCT conditioning regimens can delay the hematopoietic engraftment and increased blood product transfusions. We tried to define threshold based on pre-transplant platelet count as a biomarker to predict engraftment time and blood product requirements in allogeneic HSCT patients.
This retrospective study was performed on 194 patients who received allogeneic HSCT. The median for platelet (PLT) count of patients at the admission day was considered as a cut off value. The association of platelet count with white blood cell (WBC) and PLT engraftment time and also the requirement of packed red blood cell or PLT transfusions as outcomes of interest were investigated.
164 patients (84.5 %) had successful WBC engraftment, and PLT engraftment was seen in 155 patients (79.9 %) in 30 and 50 days after HSCT, respectively. The patients with PLT count higher than 154,000/μL had better PLT engraftment (P = 0.060), and WBC engraftment (P = 0.014) than those with PLT count lower than this cut off. The pre-transplant PLT count had negative relations with SD platelet requests after HSCT (P = 0.008).
The thrombocytopenia before HSCT might delay the platelet and WBC engraftment time, which should be taken into account before transplantation. Since the blood product transfusion is one of the factors associated with engraftment, the pre-transplant platelet count can be used as a predictive biomarker to manage the blood product requirement during the HSCT until engraftment occurs.
血小板减少是白血病的常见后果,会影响造血干细胞移植(HSCT)的结果。HSCT预处理方案后骨髓的基质损伤会延迟造血植入并增加血液制品的输注。我们试图基于移植前血小板计数定义一个阈值作为生物标志物,以预测异基因HSCT患者的植入时间和血液制品需求。
对194例接受异基因HSCT的患者进行了这项回顾性研究。将患者入院当天血小板(PLT)计数的中位数作为临界值。研究血小板计数与白细胞(WBC)及PLT植入时间的关联,以及作为感兴趣结局的浓缩红细胞或PLT输血需求。
164例患者(84.5%)白细胞成功植入,155例患者(79.9%)分别在HSCT后30天和50天出现PLT植入。PLT计数高于154,000/μL的患者比低于该临界值的患者有更好的PLT植入(P = 0.060)和白细胞植入(P = 0.014)。移植前PLT计数与HSCT后血小板需求标准差呈负相关(P = 0.008)。
HSCT前的血小板减少可能会延迟血小板和白细胞的植入时间,这在移植前应予以考虑。由于血液制品输注是与植入相关的因素之一,移植前血小板计数可作为预测生物标志物,用于管理HSCT期间直至植入发生时的血液制品需求。