Evidence map›Paper›PMID 23086508›Full record

ArticleAnnals of hematology2013

Efficacy and safety of deferasirox at low and high iron burdens: results from the EPIC magnetic resonance imaging substudy.

J B Porter, M S Elalfy, A T Taher, Y Aydinok, L L Chan, S-H Lee, P Sutcharitchan, D Habr, N Martin, A El-Beshlawy

Open access · hybridAbstract readComparative Study
In one paragraph

Article in Annals of hematology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.0field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Secondary Iron Overload and the Liver: A Comprehensive Review.Journal of clinical and translational hepatology · 2023
    Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Deferasirox: Over a Decade of Experience in Thalassemia.Mediterranean journal of hematology and infectious diseases · 2018
    Review
  10. Iron overload in thalassemia: different organs at different rates.Hematology. American Society of Hematology. Education Program · 2017
    Review
  11. How we manage iron overload in sickle cell patients.British journal of haematology · 2017
    Review
  12. Review
  13. Article
  14. Biopsy-based calibration of T2* magnetic resonance for estimation of liver iron concentration and comparison with R2 Ferriscan.Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance · 2014
    Article
  15. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 10 institutions in 9 countries.

J B PorterUCL Cancer Institute, Department of Haematology, University College London, 72 Huntley Street, London, UK. j.porter@ucl.ac.uk
M S Elalfy
A T Taher
Y Aydinok
L L Chan
S-H Lee
P Sutcharitchan
D Habr
N Martin
A El-Beshlawy
Ain Shams University · EGAmerican University of Beirut · LBCairo University · EGEge University · TRKing Chulalongkorn Memorial Hospital · THNovartis (Switzerland) · CHNovartis (United States) · USSouth Australia Pathology · AUUniversity College London · GBUniversity Malaya Medical Centre · MY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The effect of deferasirox dosing tailored for iron burden and iron loading based on liver iron concentration (LIC) was assessed over 1 year in less versus more heavily iron-overloaded patients in a substudy of the Evaluation of Patients' Iron Chelation with Exjade®. Deferasirox starting dose was 10-30 mg/kg/day, depending on blood transfusion frequency, with recommended dose adjustments every 3 months. Therapeutic goals were LIC maintenance or reduction in patients with baseline LIC <7 or ≥7 mg Fe/g dry weight (dw), respectively. Changes in LIC (R2-magnetic resonance imaging) and serum ferritin after 1 year were assessed. Adverse events (AEs) and laboratory parameters were monitored throughout. Of 374 patients, 71 and 303 had baseline LIC <7 and ≥7 mg Fe/g dw, respectively; mean deferasirox doses were 20.7 and 27.1 mg/kg/day (overall average time to dose increase, 24 weeks). At 1 year, mean LIC and median serum ferritin levels were maintained in the low-iron cohort (-0.02 ± 2.4 mg Fe/g dw, -57 ng/mL; P = not significant) and significantly decreased in the high-iron cohort (-6.1 ± 9.1 mg Fe/g dw, -830 ng/mL; P < 0.0001). Drug-related gastrointestinal AEs, mostly mild to moderate, were more frequently reported in the <7 versus ≥7 mg Fe/g dw cohort (39.4 versus 20.8 %; P = 0.001) and were not confounded by diagnosis, dosing, ethnicity, or hepatitis B and/or C history. Reported serum creatinine increases did not increase in low- versus high-iron cohort patients. Deferasirox doses of 20 mg/kg/day maintained LIC <7 mg Fe/g dw and doses of 30 mg/kg/day were required for net iron reduction in the high-iron cohort, with clinically manageable safety profiles. The higher incidence of gastrointestinal AEs at lower iron burdens requires further investigation.

Indexed as

Chelation TherapyMagnetic Resonance ImagingAdolescentAdultBenzoatesChildChild, PreschoolCholelithiasisClinical Trials, Phase III as TopicCreatinineDeferasiroxEdemaEthnicityFemaleFerritinsGastrointestinal DiseasesBenzoatesCreatinineDeferasiroxFerritinsIronIron Chelating AgentsTriazoles

Identifiers

PMID23086508
PMCPMC3542426
OpenAlexW2103826687

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.