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Intravenous Vitamin C Supplementation in Allogeneic Hematopoietic Cell Transplant Recipients: Salutary Impact on Clinical Outcomes

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 wer...

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Autores principales: Toor, Amir, Simmons, Gary, Sabo, Roy, Aziz, May, Martin, Erika, Bernard, Robyn, Sriparna, Manjari, McIntire, Cody, Kreiger, Elizabeth, Brophy, Donald, Natarajan, Ramesh, Fowler, Alpha, Roberts, Catherine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Journal Experts 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10659544/
https://www.ncbi.nlm.nih.gov/pubmed/37986783
http://dx.doi.org/10.21203/rs.3.rs-3538792/v1
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author Toor, Amir
Simmons, Gary
Sabo, Roy
Aziz, May
Martin, Erika
Bernard, Robyn
Sriparna, Manjari
McIntire, Cody
Kreiger, Elizabeth
Brophy, Donald
Natarajan, Ramesh
Fowler, Alpha
Roberts, Catherine
author_facet Toor, Amir
Simmons, Gary
Sabo, Roy
Aziz, May
Martin, Erika
Bernard, Robyn
Sriparna, Manjari
McIntire, Cody
Kreiger, Elizabeth
Brophy, Donald
Natarajan, Ramesh
Fowler, Alpha
Roberts, Catherine
author_sort Toor, Amir
collection PubMed
description 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.
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spelling pubmed-106595442023-11-20 Intravenous Vitamin C Supplementation in Allogeneic Hematopoietic Cell Transplant Recipients: Salutary Impact on Clinical Outcomes Toor, Amir Simmons, Gary Sabo, Roy Aziz, May Martin, Erika Bernard, Robyn Sriparna, Manjari McIntire, Cody Kreiger, Elizabeth Brophy, Donald Natarajan, Ramesh Fowler, Alpha Roberts, Catherine Res Sq Article 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. American Journal Experts 2023-11-10 /pmc/articles/PMC10659544/ /pubmed/37986783 http://dx.doi.org/10.21203/rs.3.rs-3538792/v1 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
Toor, Amir
Simmons, Gary
Sabo, Roy
Aziz, May
Martin, Erika
Bernard, Robyn
Sriparna, Manjari
McIntire, Cody
Kreiger, Elizabeth
Brophy, Donald
Natarajan, Ramesh
Fowler, Alpha
Roberts, Catherine
Intravenous Vitamin C Supplementation in Allogeneic Hematopoietic Cell Transplant Recipients: Salutary Impact on Clinical Outcomes
title Intravenous Vitamin C Supplementation in Allogeneic Hematopoietic Cell Transplant Recipients: Salutary Impact on Clinical Outcomes
title_full Intravenous Vitamin C Supplementation in Allogeneic Hematopoietic Cell Transplant Recipients: Salutary Impact on Clinical Outcomes
title_fullStr Intravenous Vitamin C Supplementation in Allogeneic Hematopoietic Cell Transplant Recipients: Salutary Impact on Clinical Outcomes
title_full_unstemmed Intravenous Vitamin C Supplementation in Allogeneic Hematopoietic Cell Transplant Recipients: Salutary Impact on Clinical Outcomes
title_short Intravenous Vitamin C Supplementation in Allogeneic Hematopoietic Cell Transplant Recipients: Salutary Impact on Clinical Outcomes
title_sort intravenous vitamin c supplementation in allogeneic hematopoietic cell transplant recipients: salutary impact on clinical outcomes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10659544/
https://www.ncbi.nlm.nih.gov/pubmed/37986783
http://dx.doi.org/10.21203/rs.3.rs-3538792/v1
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