Page last updated: 2024-10-25

deferoxamine and Leukemia, Myeloid, Acute

deferoxamine has been researched along with Leukemia, Myeloid, Acute in 12 studies

Deferoxamine: Natural product isolated from Streptomyces pilosus. It forms iron complexes and is used as a chelating agent, particularly in the mesylate form.
desferrioxamine B : An acyclic desferrioxamine that is butanedioic acid in which one of the carboxy groups undergoes formal condensation with the primary amino group of N-(5-aminopentyl)-N-hydroxyacetamide and the second carboxy group undergoes formal condensation with the hydroxyamino group of N(1)-(5-aminopentyl)-N(1)-hydroxy-N(4)-[5-(hydroxyamino)pentyl]butanediamide. It is a siderophore native to Streptomyces pilosus biosynthesised by the DesABCD enzyme cluster as a high affinity Fe(III) chelator.

Leukemia, Myeloid, Acute: Clonal expansion of myeloid blasts in bone marrow, blood, and other tissue. Myeloid leukemias develop from changes in cells that normally produce NEUTROPHILS; BASOPHILS; EOSINOPHILS; and MONOCYTES.

Research Excerpts

ExcerptRelevanceReference
"Deferoxamine (DFO) is an iron chelator that is known to inhibit acute non-lymphocytic leukemia cells in vitro."5.28Failure to alter the course of acute myelogenous leukemia in the rat with subcutaneous deferoxamine. ( Arena, VC; Blatt, J; Boegel, F; Hedlund, BE; Shadduck, RK, 1991)
"Deferoxamine (DFO) is an iron chelator that is known to inhibit acute non-lymphocytic leukemia cells in vitro."1.28Failure to alter the course of acute myelogenous leukemia in the rat with subcutaneous deferoxamine. ( Arena, VC; Blatt, J; Boegel, F; Hedlund, BE; Shadduck, RK, 1991)

Research

Studies (12)

TimeframeStudies, this research(%)All Research%
pre-19904 (33.33)18.7374
1990's3 (25.00)18.2507
2000's1 (8.33)29.6817
2010's3 (25.00)24.3611
2020's1 (8.33)2.80

Authors

AuthorsStudies
Batsivari, A1
Grey, W1
Bonnet, D1
Merkel, DG1
Nagler, A1
Rose, C1
Brechignac, S1
Vassilief, D1
Pascal, L1
Stamatoullas, A1
Guerci, A1
Larbaa, D1
Dreyfus, F1
Beyne-Rauzy, O1
Chaury, MP1
Roy, L1
Cheze, S1
Morel, P1
Fenaux, P1
Armand, P1
Sainvil, MM1
Kim, HT1
Rhodes, J1
Cutler, C1
Ho, VT1
Koreth, J1
Alyea, EP1
Neufeld, EJ1
Kwong, RY1
Soiffer, RJ1
Antin, JH1
Schmidt, D1
Finke, J1
Bridges, KR1
Cudkowicz, A1
Mattia, E1
Rao, K1
Shapiro, DS1
Sussman, HH1
Klausner, RD1
Weiss, G1
Goossen, B1
Doppler, W1
Fuchs, D1
Pantopoulos, K1
Werner-Felmayer, G1
Grünewald, K1
Wachter, H1
Hentze, MW1
Ammon, A1
Rumpf, KW1
Hommerich, CP1
Behrens-Baumann, W1
Rüchel, R1
Blatt, J1
Boegel, F1
Hedlund, BE1
Arena, VC1
Shadduck, RK1
Kaplinsky, C1
Estrov, Z1
Freedman, MH1
Gelfand, EW1
Cohen, A2
Barankiewicz, J1

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
A Pilot Study of Deferoxamine Before and During Myeloablative Allogeneic Stem Cell Transplantation for Patients With Myelodysplastic Syndromes or Acute Leukemia and Iron Overload[NCT00658411]5 participants (Actual)Interventional2008-08-31Terminated (stopped due to Closed due to slow patient accrual)
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

1-year Post-Transplant Survival

Survival information for the 5 patients who were treated with deferoxamine was collected. This information was used to determine transplant-related mortality, relapse, disease-free and overall survival. (NCT00658411)
Timeframe: 1 year

Interventionparticipants (Number)
Transplant-Related Mortality (Deferoxamine)0
Relapse (Deferoxamine)0
Disease-Free Survival (Deferoxamine)5
Overall Survival (Deferoxamine)0

Safety of Deferoxamine Therapy Determined by the Number of Participants With Grade 3 or Higher Toxicities.

"All patients meeting the criteria for Severe iron overload as defined by BOTH:~ferritin ≥ 1000 ng/ml and liver iron content(LIC) ≥ 5 mg/gdw were enrolled and received chelation therapy with Deferoxamine. All patients who received chelation therapy were monitored for grade 3 or above toxicity Attributable to Deferoxamine(grades defined by the CTCAE Version 3). The number of participants with grade 3 or higher toxicities were measured and used to determine the safety of chelation therapy." (NCT00658411)
Timeframe: Baseline , 6 month, 1 year

InterventionParticipants (Number)
Baseline6 month1 year
Deferoxamine500

Reviews

2 reviews available for deferoxamine and Leukemia, Myeloid, Acute

ArticleYear
Understanding of the crosstalk between normal residual hematopoietic stem cells and the leukemic niche in acute myeloid leukemia.
    Experimental hematology, 2021, Volume: 95

    Topics: Animals; Antineoplastic Agents; Cell Communication; Cell Hypoxia; Deferoxamine; Disease Progression;

2021
Toward resolving the unsettled role of iron chelation therapy in myelodysplastic syndromes.
    Expert review of anticancer therapy, 2014, Volume: 14, Issue:7

    Topics: Administration, Oral; Benzoates; Blood Transfusion; Chelation Therapy; Deferasirox; Deferiprone; Def

2014

Trials

1 trial available for deferoxamine and Leukemia, Myeloid, Acute

ArticleYear
Pre-transplantation iron chelation in patients with MDS or acute leukemia and iron overload undergoing myeloablative allo-SCT.
    Bone marrow transplantation, 2013, Volume: 48, Issue:1

    Topics: Adult; Chelation Therapy; Deferoxamine; Drug Monitoring; Early Termination of Clinical Trials; Feasi

2013

Other Studies

9 other studies available for deferoxamine and Leukemia, Myeloid, Acute

ArticleYear
Does iron chelation therapy improve survival in regularly transfused lower risk MDS patients? A multicenter study by the GFM (Groupe Francophone des Myélodysplasies).
    Leukemia research, 2010, Volume: 34, Issue:7

    Topics: Aged; Aged, 80 and over; Chelation Therapy; Comorbidity; Deferoxamine; Disease Progression; Female;

2010
[Bull's-Eye Maculopathy with Deferoxamine Treatment].
    Klinische Monatsblatter fur Augenheilkunde, 2004, Volume: 221, Issue:3

    Topics: Aged; Anemia; Deferoxamine; Electroretinography; Erythrocyte Transfusion; Ferritins; Fluorescein Ang

2004
Effect of iron chelators on the transferrin receptor in K562 cells.
    The Journal of biological chemistry, 1984, Nov-10, Volume: 259, Issue:21

    Topics: Apoproteins; Cell Line; Cell Membrane; Deferoxamine; Humans; Iron; Iron Chelating Agents; Kinetics;

1984
Biosynthetic regulation of the human transferrin receptor by desferrioxamine in K562 cells.
    The Journal of biological chemistry, 1984, Mar-10, Volume: 259, Issue:5

    Topics: Animals; Cell Line; Deferoxamine; Humans; Kinetics; Leukemia, Myeloid, Acute; Poly A; Protein Biosyn

1984
Stimulation of IRE-BP activity of IRF by tetrahydrobiopterin and cytokine dependent induction of nitric oxide synthase.
    Advances in experimental medicine and biology, 1994, Volume: 356

    Topics: Amino Acid Oxidoreductases; Animals; Arginine; Biopterins; Cell Line; Chloramphenicol O-Acetyltransf

1994
[Rhinocerebral mucormycosis during deferoxamine therapy].
    Deutsche medizinische Wochenschrift (1946), 1992, Sep-18, Volume: 117, Issue:38

    Topics: Adult; Blindness; Brain Diseases; Cellulitis; Combined Modality Therapy; Deferoxamine; Female; Human

1992
Failure to alter the course of acute myelogenous leukemia in the rat with subcutaneous deferoxamine.
    Leukemia research, 1991, Volume: 15, Issue:5

    Topics: Animals; Deferoxamine; Dose-Response Relationship, Drug; Drug Administration Schedule; Female; Injec

1991
Effect of deferoxamine on DNA synthesis, DNA repair, cell proliferation, and differentiation of HL-60 cells.
    Leukemia, 1987, Volume: 1, Issue:5

    Topics: Antigens, Surface; Benzamides; Cell Cycle; Cell Differentiation; Deferoxamine; DNA Repair; DNA, Neop

1987
Impairment of nucleotide metabolism by iron-chelating deferoxamine.
    Biochemical pharmacology, 1987, Jul-15, Volume: 36, Issue:14

    Topics: Cell Division; Cell Line; Deferoxamine; Depression, Chemical; Humans; Iron; Leukemia, Myeloid, Acute

1987