Intravenous Vitamin C Supplementation in Allogeneic Hematopoietic Cell Transplant Recipients: Salutary Impact on Clinical Outcomes.
Amir ToorGary SimmonsRoy SaboMay AzizErika J MartinRobyn BernardManjari SripaCody McIntireElizabeth KreigerDonald BrophyRamesh NatarajanAlpha FowlerCatherine RobertsPublished in: Research square (2023)
Intravenous (IV) vitamin C improves organ function and reduces inflammation in sepsis, an inflammatory state like the post-hematopoietic stem cell transplant (HCT) milieu. The safety and efficacy of parenteral vitamin C after allogeneic HCT were evaluated in a phase I/II trial. Clinical outcomes were compared with a propensity score - matched historical control. Methods: Patients with advanced hematologic malignancies received IV vitamin C, 50mg/kg/d, divided into 3 doses given on days 1-14 after HCT, followed by 500 mg bid oral from day 15 until 6 months post-SCT. Results 55 patients received IV vitamin C. All patients were deficient in vitamin C at day 0. Vitamin C recipients had lower non-relapse mortality (NRM) (p = 0.07) and improved survival compared to historical controls (p=0.06), with no attributable grade 3 and 4 toxicities. Vitamin C recipients had similar relapse rate and acute graft versus host disease (GVHD) (p=0.35), but lower severe chronic GVHD (p=0.35). Patients with myeloid malignancies had improved survival (p=0.02) and NRM (p=0.009), as well as chronic GVHD, with similar relapse rates compared to controls. Conclusions: In patients undergoing allogeneic HCT the administration of IV vitamin C is safe and reduces non-relapse mortality and chronic GVHD improving overall survival.
Keyphrases
- hematopoietic stem cell
- free survival
- end stage renal disease
- stem cell transplantation
- bone marrow
- patients undergoing
- chronic kidney disease
- ejection fraction
- newly diagnosed
- oxidative stress
- allogeneic hematopoietic stem cell transplantation
- high dose
- peritoneal dialysis
- prognostic factors
- clinical trial
- stem cells
- acute myeloid leukemia
- risk factors
- type diabetes
- low dose
- cardiovascular disease
- patient reported outcomes
- study protocol
- dendritic cells
- coronary artery disease
- respiratory failure