Evidence map›Paper›PMID 42108919›Full record

ArticleAmerican journal of hematology2026

Management of Iron Overload in Infants and Toddlers With Diamond-Blackfan Anemia Syndrome: A French-Italian Study.

Francesca Torchio, Baptiste Lecalvez, Emanuela Garelli, Coralie Mallebranche, Adriana Carando, Marie-Pierre Castex, Nathalie Garnier, Marco Zecca, Nathalie Aladjidi, Elisa Bertoni and 10 more

Abstract readMulticenter Study
In one paragraph

Article in American journal of hematology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
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

20 authors.

Francesca TorchioDepartment of Public Health and Pediatric Sciences, University of Turin, Turin, Italy.ORCID https://orcid.org/0009-0007-5861-9307
Baptiste LecalvezDepartment of Pediatric Hematology and Immunology, Robert Debré Academic Hospital, GHU AP-HP Nord Université Paris Cité, Paris, France.
Emanuela GarelliDepartment of Public Health and Pediatric Sciences, University of Turin, Turin, Italy.
Coralie MallebrancheUniversité Angers, Université de Nantes, CHU Angers, Inserm, CNRS, CRCI2NA, SFR ICAT, Angers, France.
Adriana CarandoDepartment of Public Health and Pediatric Sciences, University of Turin, Turin, Italy.
Marie-Pierre CastexPediatric Oncology and Hematology Department, Hôpital Des Enfants, University Hospital Center of Toulouse, Toulouse, France.
Nathalie GarnierInstitut D'Hematologie et D'Oncologie Pediatrique, Hospices Civils de Lyon, Lyon, France.
Marco ZeccaPediatric Hematology/Oncology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.ORCID https://orcid.org/0000-0002-8818-1744
Nathalie AladjidiPaediatric Clinical Immunology, Pellegrin Hospital, CIC1401, INSERM CICP, Bordeaux University Hospital, Bordeaux, France.
Elisa BertoniPediatric Oncohematology and Bone Marrow Transplant (BMT) Unit, Children's Hospital, Spedali Civili, Brescia, Italy.
Arthur SterinDepartment of Pediatric Hematology, Immunology and Oncology, La Timone Children's Hospital, Marseille, France.
Maria LicciardelloPediatric Hematology and Oncology Unit, Department of Clinical and Experimental Medicine, University of Catania, Catania, Italy.
Anne SirventPediatric Haematology and Oncology Department, CHU Montpellier, Montpellier, France.
Antonella SauDepartment of Hematology and Oncology, Santo Spirito Hospital, Pescara, Italy.
Isabelle MarieFrench National Reference Center for Aplastic Anemia and PNH, CeRAMIC, Saint-Louis Hospital, Paris, France.
Benedicte BrunoDepartment of Pediatric Hematology-Oncology, Jeanne de Flandre Hospital, Lille, France.ORCID https://orcid.org/0000-0002-6453-6395
Lydie M Da CostaFrench National Reference Center for Aplastic Anemia and PNH, CeRAMIC, Saint-Louis Hospital, Paris, France.
Franca FagioliDepartment of Public Health and Pediatric Sciences, University of Turin, Turin, Italy.
Paola QuarelloDepartment of Public Health and Pediatric Sciences, University of Turin, Turin, Italy.
Thierry LeblancDepartment of Pediatric Hematology and Immunology, Robert Debré Academic Hospital, GHU AP-HP Nord Université Paris Cité, Paris, France.ORCID https://orcid.org/0000-0003-2463-9346

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diamond-Blackfan Anemia Syndrome (DBAS) is a rare congenital anemia often requiring chronic red blood cell transfusions from infancy. Without appropriate chelation, iron overload develops early and may be severe; however, no data are available on chelation in patients under 3 years of age. To address this, we conducted a retrospective, multicenter study collecting data from the French and Italian DBAS national registries. A total of 167 transfused DBAS patients were screened. Of these, 64 (38%) initiated chelation before the age of three (median: 18 months). Indications for chelation were a serum ferritin ≥ 500 ng/mL (median: 1340 ng/mL) and more than 10 transfusions. Deferasirox was the most frequently used chelator (63%), followed by deferoxamine (35%). Chelation was associated with a significant reduction in serum ferritin levels (-11% per year; p < 0.001). At 5-6 years of age, ferritin level was available for 28 patients: 43% had levels < 500 ng/mL, and none exceeded 2000 ng/mL. Liver iron concentration was assessed in 31/64 patients (48%) at a median age of 3.2 years; 45% showed severe overload at first evaluation. Among 22 patients who underwent cardiac magnetic resonance, no myocardial iron overload was detected. These real-world data support the feasibility, tolerability, and effectiveness of chelation in transfusion-dependent DBAS patients under 3 years, allowing prevention of cardiac iron overload. Although derived from DBAS, these findings may inform the management of iron overload in infants and toddlers with other transfusion-dependent anemias and support development of age-specific chelation strategies.

Indexed as

Anemia, Diamond-BlackfanIron Chelating AgentsIron OverloadChild, PreschoolDeferasiroxDeferoxamineErythrocyte TransfusionFemaleFerritinsFranceHumansInfantIronItalyLiverMaleDeferasiroxDeferoxamineFerritinsIronIron Chelating AgentsDiamond–Blackfan Anemia Syndromeearly iron chelationiron overload

Identifiers

PMID42108919
PMCPMC13331634

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Registered trials

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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.