Feasibility of intravenous vitamin C supplementation in allogeneic hematopoietic cell transplant recipients

Author:

Simmons Gary L.1,Sabo Roy2,Qayyum Rehan3,Aziz May4,Martin Erika4,Bernard Robyn J.5,Sriparna Manjari5,McIntire Cody5,Krieger Elizabeth6,Brophy Donald F.4,Natarajan Ramesh1,III Alpha Fowler1,Roberts Catherine H.1ORCID,Toor Amir17ORCID

Affiliation:

1. Department of Internal Medicine Virginia Commonwealth University Richmond Virginia USA

2. Department of Biostatistics Virginia Commonwealth University Richmond Virginia USA

3. Department of Internal Medicine Eastern Virginia Medical School Norfolk Virginia USA

4. School of Pharmacy Virginia Commonwealth University Richmond Virginia USA

5. Department of Medicine Virginia Commonwealth University Richmond Virginia USA

6. Department of Pediatrics Virginia Commonwealth University Richmond Virginia USA

7. Topper Cancer Institute Lehigh Valley Health Network Allentown Pennsylvania USA

Abstract

AbstractIntroductionIntravenous vitamin C was administered following hematopoietic stem cell transplant to mitigate nonrelapse mortality (NRM) in a Phase II clinical trial.MethodsPatients with advanced hematologic malignancies received IV vitamin C, 50 mg/kg/day, in three divided doses on days 1–14 after HSCT, followed by 500 mg bid oral until 6 months.ResultsAll patients enrolled (55) were deficient in vitamin C at day 0 and had restoration to normal levels. Vitamin C recipients had a trend for lower nonrelapse mortality (NRM, 11% vs. 25%, p‐value = 0.07) compared with propensity score‐matched historical controls. A similar trend toward improved survival was observed (82% vs. 62% p = 0.06), with no attributable grade 3 and 4 toxicities to vitamin C.ConclusionIn patients undergoing allogeneic HSCT, repletion of vitamin C is feasible and may reduce NRM and improve overall survival. Randomized trials in large uniform cohorts of patients are needed to confirm the utility of this easily available and inexpensive therapy.

Publisher

Wiley

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