Arsenic trioxide at conventional dosage does not aggravate hemorrhage in the first-line treatment of adult acute promyelocytic leukemia
Arsenic trioxide at conventional dosage does not aggravate hemorrhage in the first-line treatment of adult acute promyelocytic leukemia
复制标题
常规剂量的三氧化二砷在成人急性早幼粒细胞白血病一线治疗中不会加重出血。
DOI:
10.1111/ejh.13018
复制
发表时间:
2018-04-01
影响因子:
3.1
通讯作者:
Mi, Jian-Qing
中科院分区:
文献类型:
--
作者:
Cui, Wen;Wang, Jin;Mi, Jian-Qing
ObjectivesThe arsenic trioxide (ATO) plus all-trans retinoic acid (ATRA) therapy has demonstrated a tremendous success in the first-line treatment of acute promyelocytic leukemia (APL). Actually, early death (ED) is currently thought as a major challenge in APL. ATO has been reported to inhibit platelet function in vitro, and whether it increases the ED rate by exacerbating the hemorrhagic symptoms remains to be investigated.MethodsEffects of ATO on platelet aggregation and adhesion were evaluated in vitro and in thirty-two complete remission (CR) and four newly diagnosed APL patients. Furthermore, concentrations of plasma total arsenic were monitored in APL patients via ICP-MS.ResultsThe inhibition of platelet function, either aggregation or adhesion, did occur in vitro when the concentration of ATO reached 2mol/L. However, in CR APL patients receiving ATO with normal platelet count, the platelets responded normally when being activated and so did those in the newly diagnosed patients with thrombocytopenia. Our data further showed that the conventional dosage of ATO reached a plasma concentration substantially below the required concentration to inhibit platelets.ConclusionsIn the first-line treatment of APL, the use of ATO is safe and effective and does not compromise the hemostatic potential that may eventually increase ED rate.