Vitamin D and Hemopoietic Stem Cell Transplantation: Clinical Guidance for GVHD Management and Post-Transplant Outcomes.
- 2026-03-17
- Cancers 18(6)
- Manlio Fazio
- Maria Elisa Nasso
- Sebastiano Gangemi
- Adele Bottaro
- Luca Gammeri
- Fabio Stagno
- Alessandro Allegra
- PubMed: 41899574
- DOI: 10.3390/cancers18060972
Study Design
- Type
- Review
Vitamin D is a pleiotropic secosteroid with endocrine and intracrine actions that influence key phases of allogeneic hematopoietic stem cell transplantation. Epithelial barriers, antigen-presenting cells and effector lymphocytes express the vitamin D receptor and enzymes required for local activation, allowing circulating 25-hydroxyvitamin D to be converted into its active form and modulate immune interactions. During the peri-transplant period, sunlight deprivation, reduced intake, mucosal injury, cholestasis and corticosteroid exposure markedly reduce vitamin D levels at a time when antigen presentation and immune reconstitution occur. This review integrates mechanistic immunology with clinical observations and interventional data to outline strategies that prevent severe deficiency. It summarizes epidemiology before and after transplantation, associations with acute and chronic graft-versus-host disease, relapse, engraftment, infections, bone health and survival, and evaluates dosing approaches including pre-conditioning loading and reassessment at day thirty with escalation if needed. Absorption-savvy formulations such as oral thin-film and intramuscular cholecalciferol are considered when gastrointestinal function is compromised. Given the high prevalence of deficiency, biological plausibility, safety and low cost, a structured approach that includes screening, repletion and monitoring to achieve concentrations of at least thirty nanograms per milliliter by day thirty represents a pragmatic and low-risk component of supportive care pending definitive evidence.
Research Insights
associations with ... bone health and survival
- Effect
- Neutral
- Effect size
- Small
- Dose
- pre-conditioning loading and reassessment at day thirty with escalation if needed; target ≥30 ng/mL by day 30
associations with ... engraftment, infections, bone health and survival
- Effect
- Neutral
- Effect size
- Small
- Dose
- pre-conditioning loading and reassessment at day thirty with escalation if needed; target ≥30 ng/mL by day 30
associations with ... survival
- Effect
- Neutral
- Effect size
- Small
- Dose
- pre-conditioning loading and reassessment at day thirty with escalation if needed; target ≥30 ng/mL by day 30
associations with acute and chronic graft-versus-host disease
- Effect
- Neutral
- Effect size
- Small
- Dose
- pre-conditioning loading and reassessment at day thirty with escalation if needed; target ≥30 ng/mL by day 30
associations with acute and chronic graft-versus-host disease
- Effect
- Neutral
- Effect size
- Small
- Dose
- pre-conditioning loading and reassessment at day thirty with escalation if needed; target ≥30 ng/mL by day 30
associations with ... infections, bone health and survival
- Effect
- Neutral
- Effect size
- Small
- Dose
- pre-conditioning loading and reassessment at day thirty with escalation if needed; target ≥30 ng/mL by day 30
associations with ... relapse, engraftment, infections, bone health and survival
- Effect
- Neutral
- Effect size
- Small
- Dose
- pre-conditioning loading and reassessment at day thirty with escalation if needed; target ≥30 ng/mL by day 30
Adverse Events Reported
sunlight deprivation, reduced intake, mucosal injury, cholestasis and corticosteroid exposure markedly reduce vitamin D levels
- Finding
- Reported
- Grade
- severe