All

What are you looking for?

All
Projects
Results
Organizations

Quick search

  • Projects supported by TA ČR
  • Excellent projects
  • Projects with the highest public support
  • Current projects

Smart search

  • That is how I find a specific +word
  • That is how I leave the -word out of the results
  • “That is how I can find the whole phrase”

A comparative study of deferasirox and deferiprone in the treatment of iron overload in patients with myelodysplastic syndromes

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14110%2F13%3A00071203" target="_blank" >RIV/00216224:14110/13:00071203 - isvavai.cz</a>

  • Alternative codes found

    RIV/65269705:_____/13:#0002114 RIV/00179906:_____/13:10191710 RIV/00023736:_____/13:00010730 RIV/00064165:_____/13:10191710

  • Result on the web

    <a href="http://dx.doi.org/10.1016/j.leukres.2013.07.021" target="_blank" >http://dx.doi.org/10.1016/j.leukres.2013.07.021</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.leukres.2013.07.021" target="_blank" >10.1016/j.leukres.2013.07.021</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    A comparative study of deferasirox and deferiprone in the treatment of iron overload in patients with myelodysplastic syndromes

  • Original language description

    One hundred thirteen patients with myelodysplastic syndromes (MDS) with &lt;10% of bone marrow blasts received either deferiprone in a daily dose of 40-90 mg/kg (48 patients) or deferasirox in a daily dose of 10-40 mg/kg (65 patients). Median duration oftreatment was 10,9 months for deferiprone and 13,7 months for deferasirox. A substantial reduction of iron stores evaluated as a decrease in serum ferritin of more than 50% of pretreatment level was achieved in 18 patients in deferasirox group (27.7%) but not in any patient treated with deferiprone, The incidence of adverse effects (mostly gastrointestinal symptoms) was similar after administration of both the drugs. The symptoms of deferasirox toxicity were mild and mostly transient and no drug related myelosuppresive effect was observed in contrast to deferiprone where agranulocytosis occurred in 4% of patients and the treatment had to be discontinued due to side effects in 20% of patients.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    FD - Oncology and haematology

  • OECD FORD branch

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2013

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Leukemia Research

  • ISSN

    0145-2126

  • e-ISSN

  • Volume of the periodical

    37

  • Issue of the periodical within the volume

    12

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    4

  • Pages from-to

    1612-1615

  • UT code for WoS article

    000327539700004

  • EID of the result in the Scopus database