Leon-Rodriguez Eucario, Rivera-Franco Monica M
Stem Cell Transplantation Program, Hematology and Oncology Department, Instituto Nacional de Ciencias Medicas Y Nutricion Salvador Zubiran, Vasco de Quiroga 15, Belisario Dominguez Seccion XVI, Tlalpan, 14080, Mexico City, Mexico.
Int J Hematol. 2016 Dec;104(6):644-646. doi: 10.1007/s12185-016-2098-8. Epub 2016 Oct 8.
Busulfan (Bu), an alkylating agent, has been used in pre-transplant conditioning regimens since the 1950s, due to its potent myeloablative effect. Questions have been raised regarding oral or intravenous formulations, although both are known to be associated with serious side effects, including hepatic veno-occlusive disease, and neurotoxicity. The administration of anticonvulsant prophylaxis has become more common during high-dose Bu-based conditioning regimen; however, anticonvulsants can interfere with Bu pharmacokinetics and may have their own side effects, which can affect the outcome of the transplant. Our objective was to analyze the incidence of neurotoxicity in patients who underwent stem cell transplantation with high-dose Bu-based conditioning regimens without anticonvulsant prophylaxis. Ninety-seven patients were included, either having received a dose of 12 mg/kg (n = 73) for allogeneic transplantation or 16 mg/kg (n = 24) for autologous transplantation. The incidence of seizures was 0.01 %. We conclude that anticonvulsant prophylactic regimens may be unnecessary, and reduction of their use may help to avoid potential drug interactions and undesired side effects.
白消安(Bu)是一种烷化剂,自20世纪50年代以来一直用于移植前预处理方案,因其具有强大的清髓作用。尽管口服和静脉制剂都已知会伴有严重副作用,包括肝静脉闭塞病和神经毒性,但关于这两种制剂仍存在一些问题。在基于大剂量白消安的预处理方案中,预防性使用抗惊厥药物已变得更为常见;然而,抗惊厥药物会干扰白消安的药代动力学,且可能有其自身的副作用,这会影响移植结果。我们的目的是分析在接受基于大剂量白消安的预处理方案且未进行抗惊厥药物预防的干细胞移植患者中神经毒性的发生率。纳入了97例患者,其中73例接受12 mg/kg剂量进行异基因移植,24例接受16 mg/kg剂量进行自体移植。癫痫发作的发生率为0.01%。我们得出结论,抗惊厥药物预防方案可能没有必要,减少其使用可能有助于避免潜在的药物相互作用和不良副作用。