Apsel Winger Beth, Long Susie E, Brooks Jordan, Gupta Ashish O, Dvorak Christopher C, Long-Boyle Janel Renee
Division of Allergy, Immunology, and Bone Marrow Transplantation, Department of Pediatrics, University of California, San Francisco, San Francisco, CA, United States.
Division of Hematology and Oncology, Department of Pediatrics, University of California, San Francisco, San Francisco, CA, United States.
Front Pediatr. 2021 Jul 19;9:713091. doi: 10.3389/fped.2021.713091. eCollection 2021.
Pediatric diseases treated by allogeneic hematopoietic stem cell transplantation (alloHCT) are complex and associated with significant comorbidities and medication requirements that can complicate the transplant process. It is critical to reconcile pre-transplant concomitant medications (pcon-meds) in the weeks prior to alloHCT and to consider the potential for pcon-meds to cause harmful drug-drug interactions (DDIs) or overlapping toxicities with conditioning agents. In this perspective, we describe a systematic process to review pcon-meds and determine the drug modifications needed to avoid DDIs with conditioning regimens. We provide an extensive appendix with timelines for discontinuation or modification of common pcon-meds that patients are taking when presenting to the HCT medical team. The timelines are based on the pharmacokinetic (PK) properties of both the pcon-meds and the planned conditioning medications, as well as anticipated DDIs. They also account for the ages seen at pediatric transplant centers (0-30 years old). Common scenarios, such as when pcon-med discontinuation is not an option, are discussed. Since alloHCT patients are often dependent upon psychiatric medications with problematic DDIs, a table of alternative, non-interacting psychiatric medications is also presented. The appendix provides details regarding how to adjust pcon-meds prior to the start of chemotherapy for children and young adults undergoing alloHCT, however patient-specific circumstances always need to be taken into account. Careful attentiveness to pcon-meds at the time the decision is made to pursue transplant will result in more consistent HCT outcomes, with lower toxicity and increased efficacy of conditioning agents.
通过异基因造血干细胞移植(alloHCT)治疗的儿科疾病复杂,伴有显著的合并症和用药需求,这可能使移植过程复杂化。在alloHCT前数周协调移植前的合并用药(pcon-meds)并考虑pcon-meds与预处理药物发生有害药物相互作用(DDIs)或重叠毒性的可能性至关重要。从这个角度出发,我们描述了一个系统的流程来审查pcon-meds,并确定避免与预处理方案发生DDIs所需的药物调整。我们提供了一个详细的附录,其中包含患者向HCT医疗团队就诊时正在服用的常见pcon-meds的停药或调整时间表。这些时间表基于pcon-meds和计划的预处理药物的药代动力学(PK)特性以及预期的DDIs。它们还考虑了儿科移植中心所见的年龄(0至30岁)。讨论了常见情况,例如当pcon-meds停药不可行时的情况。由于alloHCT患者通常依赖于具有问题DDIs的精神科药物,因此还列出了替代的、无相互作用的精神科药物表。附录提供了有关如何在接受alloHCT的儿童和年轻人开始化疗前调整pcon-meds的详细信息,然而始终需要考虑患者的具体情况。在决定进行移植时仔细关注pcon-meds将导致更一致的HCT结果,降低毒性并提高预处理药物的疗效。