Hematologic Landscape of Adult Patients With Diamond‐Blackfan Anemia Syndrome

Information about Diamond-Blackfan anemia syndrome (DBAS), a ribosomopathy associated with anemia, congenital anomalies and cancer predisposition is limited in adults. Using the French DBAS registry, 235 adult patients with DBAS were analyzed for hematological outcomes. At last follow-up, anemia, neutropenia, thrombocytopenia, and pancytopenia affected respectively 78%, 31%, 15%, and 11% of the patients. There was no severe aplastic anemia outside of clonal evolution. Among patients without DBAS-specific treatment (e.g., steroids or red blood cell transfusions), the incidence of anemia, neutropenia, and thrombocytopenia was 52%, 35%, and 10%, highlighting that treatment independence does not mean hematologic remission. Four patients developed myelodysplastic syndrome (MDS) or acute myeloid leukemia (AML), all associated with poor-risk features and dismal outcomes. Observed to expected ratios were 155 for MDS and 55.4 for AML, confirming a major risk-excess despite stringent criteria for MDS diagnosis. With a median follow-up of 32.2 years (IQR 26-44), overall survival (OS) was 98.0% (95% CI, 95.8-100), 90.6% (95% CI, 84.2-97.5), and 70.7% (95% CI, 57.3-87.2) at 30, 40, and 50 years respectively. Solid and hematologic cancers were the main cause of death. This study demonstrates, in a large cohort of adults with DBAS, that cytopenias beyond anemia are frequent and persistent. Myeloid neoplasms occur with a high incidence and dismal outcomes. These findings highlight the need for risk stratification, tailored surveillance, and optimized therapeutic strategies in this vulnerable population.

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Publication Details

Journal
American Journal of Hematology
Published
2026-01-07
DOI
https://doi.org/10.1002/ajh.70197
Primary Topic
RNA modifications and cancer
Type
article
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article

Hematologic Landscape of Adult Patients With Diamond‐Blackfan Anemia Syndrome

Laurence Sanhès, Nicolas Lecornec, Pierre Fenaux, Stanislas Nimubona et al.
American Journal of Hematology
RNA modifications and cancer
article

Hematologic Landscape of Adult Patients With Diamond‐Blackfan Anemia Syndrome

Laurence Sanhès, Nicolas Lecornec, Pierre Fenaux, Stanislas Nimubona, Flore Sicre de Fontbrune, Loïc Garçon, Isabelle J. Marié, K. Delavigne, Marie‐Pierre Ledoux, E C deConinck, Thierry Leblanc, Isabelle Brindel, Pierre Cougoul, J DALLE, L. Terriou, R. Pefault De Latour, Edouard Forcade, G Leverger, M. de Montalembert, Lydie Da Costa, Étienne Daguindau, Shanti Amé
article en

Abstract

Information about Diamond-Blackfan anemia syndrome (DBAS), a ribosomopathy associated with anemia, congenital anomalies and cancer predisposition is limited in adults. Using the French DBAS registry, 235 adult patients with DBAS were analyzed for hematological outcomes. At last follow-up, anemia, neutropenia, thrombocytopenia, and pancytopenia affected respectively 78%, 31%, 15%, and 11% of the patients. There was no severe aplastic anemia outside of clonal evolution. Among patients without DBAS-specific treatment (e.g., steroids or red blood cell transfusions), the incidence of anemia, neutropenia, and thrombocytopenia was 52%, 35%, and 10%, highlighting that treatment independence does not mean hematologic remission. Four patients developed myelodysplastic syndrome (MDS) or acute myeloid leukemia (AML), all associated with poor-risk features and dismal outcomes. Observed to expected ratios were 155 for MDS and 55.4 for AML, confirming a major risk-excess despite stringent criteria for MDS diagnosis. With a median follow-up of 32.2 years (IQR 26-44), overall survival (OS) was 98.0% (95% CI, 95.8-100), 90.6% (95% CI, 84.2-97.5), and 70.7% (95% CI, 57.3-87.2) at 30, 40, and 50 years respectively. Solid and hematologic cancers were the main cause of death. This study demonstrates, in a large cohort of adults with DBAS, that cytopenias beyond anemia are frequent and persistent. Myeloid neoplasms occur with a high incidence and dismal outcomes. These findings highlight the need for risk stratification, tailored surveillance, and optimized therapeutic strategies in this vulnerable population.

American Journal of HematologyVol. 101(4)
Hôpital Necker-Enfants Malades (FR), Inserm (FR), Université Paris Cité (FR), Université de Lille (FR), Institut Gustave Roussy (FR), Saint Louis University Hospital (US), Sorbonne Université (FR), Institut Necker Enfants Malades (FR), Hôpital Armand-Trousseau (FR), Centre Hospitalier Universitaire de Besançon (FR), Centre Hospitalier de Perpignan (FR), Institut de Cancérologie Strasbourg (FR), Lille’s Cardiology Hospital (FR), Institut universitaire du cancer de Toulouse Oncopole (FR), Laboratoire National de Référence (MA), Hôpital Cardiologique du Haut-Lévêque (FR), Hôpital Robert-Debré (FR), Hôpital Privé Jean Mermo (FR), Hôpital Saint-Louis (FR), Centre Hospitalier Universitaire de Rennes (FR), Bicêtre Hospital (FR), Université de Picardie Jules Verne (FR)
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RNA modifications and cancer
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