Literature DB >> 9504634

Vitamin D treatment in myelodysplastic syndromes.

L Mellibovsky1, A Díez, E Pérez-Vila, S Serrano, M Nacher, J Aubía, A Supervía, R R Recker.   

Abstract

Myelodysplastic syndromes (MDS) are a group of clonal disturbances with defective cellular differentiation. Vitamin D3 (VD) analogues can act on the differentiation and maturity of different cell lines. We studied the effects of VD on a series of patients with MDS in an open-design trial. Nineteen patients, 12 men and seven women, with MDS were included. Patients were 74.8 +/- 5.6 years (mean +/- SD), seven had refractory anaemia with ringed sideroblasts, five had refractory anaemia, one had refractory anaemia with excess of blasts and six had chronic myelomonocytic leukaemia. All the patients were in a low to intermediate risk group. Mean follow-up period was 26.21 months, range 9-75. Responders were defined as follows: granulocyte or platelet count increase by 50%, or haemoglobin increase of 1.5 g/dl or transfusion needs decrease by 50%. The first five patients received 266 microg of calcifediol three times a week and the other 14 received calcitriol (0.25-0.75 microg/d). Response was observed in 11 patients. In the calcifediol-treated group, one case responded, three were nonresponders, and one showed progression. In the calcitriol group, 10 were responders (two with major response), and four were non-responders. No correlation was observed between baseline levels of vitamin D metabolites and the presence of response. No hypercalcaemia was observed. Treatment with vitamin D3 metabolites could induce a long-standing response of the haematological disturbance in some low-intermediate risk MDS patients without inducing hypercalcaemia.

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Year:  1998        PMID: 9504634     DOI: 10.1046/j.1365-2141.1998.00598.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


  11 in total

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2.  A phase I study to determine the maximum tolerated dose and safety of oral LR-103 (1α,24(S)Dihydroxyvitamin D2) in patients with advanced cancer.

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Review 3.  Vitamin D in hematological disorders and malignancies.

Authors:  Paige M Kulling; Kristine C Olson; Thomas L Olson; David J Feith; Thomas P Loughran
Journal:  Eur J Haematol       Date:  2016-11-21       Impact factor: 2.997

4.  19-nor-1alpha,25-dihydroxyvitamin D(2) (paricalcitol): effects on clonal proliferation, differentiation, and apoptosis in human leukemic cell lines.

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Journal:  J Cancer Res Clin Oncol       Date:  2003-02-12       Impact factor: 4.553

Review 5.  Effect of Vitamin D on Graft-versus-Host Disease.

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Journal:  Biomedicines       Date:  2022-04-24

6.  Phase II study of doxercalciferol for the treatment of myelodysplastic syndrome.

Authors:  Adam Petrich; Brad Kahl; Howard Bailey; Kyungmann Kim; Nancy Turman; Mark Juckett
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Review 7.  Vitamin D3-driven signals for myeloid cell differentiation--implications for differentiation therapy.

Authors:  Philip J Hughes; Ewa Marcinkowska; Elzbieta Gocek; George P Studzinski; Geoffrey Brown
Journal:  Leuk Res       Date:  2009-10-06       Impact factor: 3.156

8.  Clinical experience using vitamin d and analogs in the treatment of myelodysplasia and acute myeloid leukemia: a review of the literature.

Authors:  Jonathan S Harrison; Alexander Bershadskiy
Journal:  Leuk Res Treatment       Date:  2012-07-30

9.  Bryostatin-1, Fenretinide and 1α,25 (OH)(2)D(3) Induce Growth Inhibition, Apoptosis and Differentiation in T and B Cell-Derived Acute Lymphoblastic Leukemia Cell Lines (CCRF-CEM and Nalm-6).

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Review 10.  The role of vitamin D in hematologic disease and stem cell transplantation.

Authors:  Aric C Hall; Mark B Juckett
Journal:  Nutrients       Date:  2013-06-18       Impact factor: 5.717

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