Division of Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
University of Cincinnati College of Medicine, Cincinnati, OH.
Blood Adv. 2023 Aug 22;7(16):4555-4562. doi: 10.1182/bloodadvances.2023009855.
Vitamin D deficiency is common in childhood, pervasive before and after bone marrow transplant, and is associated with increased incidence of graft-versus-host disease (GVHD) and decreased survival in patients undergoing hematopoietic stem cell transplant (HSCT). Numerous barriers impede replacement, including malabsorption secondary to gut GVHD, mucositis, inability to take capsules, kidney disease, liver disease, and infection; many patients remain refractory despite vitamin D therapy. We hypothesized that a different formulation of cholecalciferol, administered on the tongue as a readily dissolving oral thin film (OTF), would ease administration and facilitate therapeutic vitamin D levels (>35 ng/mL) in patients who are refractory. In this prospective pilot study, we evaluated 20 patients after HSCT (range, day +21 - day +428 at enrollment) with serum vitamin D levels ≤35 ng/mL. Cholecalciferol OTF strips were administered for 12 weeks. Dosing was based on patient body weight and titrated per individual pharmacokinetics. Wilcoxon matched-pairs signed-rank test demonstrated marked improvement in all 20 patients who were formerly refractory, increasing from a median baseline vitamin D level of 29.2 ng/mL to 58 ng/mL at end of study (P < .0001). All patients demonstrated improvement in serum vitamin D level by week 4 on study, some of whom had been refractory for years prior. Median dose was 1 OTF strip (40 000 IU) per week. No toxicity was observed. This formulation proved to be safe, effective, efficient, and well received. We are eager to explore other patient populations, which might benefit from this promising development, and other therapeutics that might be optimized using this mode of delivery. This trial was registered at www.clinicaltrials.gov as #NCT04818957.
维生素 D 缺乏在儿童中很常见,在骨髓移植前后普遍存在,并且与移植物抗宿主病 (GVHD) 的发生率增加和接受造血干细胞移植 (HSCT) 的患者生存率降低有关。许多障碍阻碍了替代治疗,包括肠道 GVHD 引起的吸收不良、黏膜炎、无法服用胶囊、肾脏疾病、肝脏疾病和感染;尽管进行了维生素 D 治疗,但许多患者仍然没有反应。我们假设,一种不同形式的胆钙化醇,作为一种易于溶解的口腔薄膜 (OTF) 施用于舌头上,将减轻管理并促进治疗性维生素 D 水平 (>35ng/mL) 在那些有反应的患者中。在这项前瞻性试点研究中,我们评估了 20 名 HSCT 后的患者(范围为+21 天至+428 天入组时),血清维生素 D 水平≤35ng/mL。胆钙化醇 OTF 条在 12 周内给药。剂量根据患者体重和个体药代动力学进行滴定。Wilcoxon 配对符号秩检验显示,所有 20 名以前有反应的患者均有显著改善,从中位数基线维生素 D 水平 29.2ng/mL 增加到研究结束时的 58ng/mL(P<.0001)。所有患者在研究的第 4 周时血清维生素 D 水平均有改善,其中一些患者在之前的几年中一直有反应。中位数剂量为每周 1 个 OTF 条(40000IU)。未观察到毒性。这种制剂被证明是安全、有效、高效且深受欢迎的。我们渴望探索其他可能受益于这一有前途的发展的患者群体,以及可能通过这种给药方式优化的其他治疗方法。该试验在 www.clinicaltrials.gov 上注册为 #NCT04818957。