Clinical Experience Using Vitamin D and Analogs in the Treatment of Myelodysplasia and Acute Myeloid Leukemia: A Review of the Literature. (30th July 2012)

• Record Type: Journal Article
• Authors: Harrison, Jonathan S.; Bershadskiy, Alexander
• Other Names: Studzinski George P. Academic Editor.
• Is Part Of: Leukemia research and treatment. Volume 2012(2012)
• Publication Date: 2012-07-30
• Subjects: Leukemia -- Periodicals; Leukemia -- Treatment -- Periodicals; Leukemia; Leukemia -- therapy; Leukemia; Leukemia -- Treatment; Leukemia -- Periodicals; Leukemia -- Treatment -- Periodicals; Leukemia -- therapy -- Periodicals; Electronic journals; Periodicals; Periodicals; 616.99419
• DOI: 10.1155/2012/125814
• Languages: English
• ISSNs: 2090-3219

Abstract

Abstract : Despite progress in understanding the biology of acute myeloid leukemia (AML), and despite advances in treatment, the majority of patients with AML die from the disease. The observation that Vitamin D can induce AML blast cells in vitro to differentiate along the monocytic lineage was made 30 years ago; however, it remains to translate this into a clinically meaningful strategy. This is a review of published clinical experience regarding the use of Vitamin D and its analogs, either alone or in combination with other agents, to treat AML. In many of these reports, investigators included patients with myelodysplasia (MDS) as well as AML patients in their treatment cohorts; therefore reports of Vitamin D and its analogs in treating MDS are included. This review documents heterogeneity in selection criteria for patients treated in these studies, the spectrum of Vitamin D analogs used in various studies, and the differing dosing strategies employed by investigators. Despite examples of occasional clinical efficacy, barriers remain to the successful application of Vitamin D in the treatment of MDS and AML. These include the lack of definition of a particularly sensitive target population, and the as yet unknown optimal choice of Vitamin D analog and dosing schedule.