Eltrombopag for Bone Marrow Failure in Fanconi Anemia: Results From the Phase II Clinical Trial FANCREV

Eltrombopag stimulates hematopoiesis in aplastic anemia, and preclinical studies suggest it promotes DNA repair in Fanconi Anemia (FA) hematopoietic stem cells. We conducted a clinical trial to explore its safety and efficacy in bone marrow failure due to FA. Eltrombopag was administered to 8 pediatric patients with one or more significant cytopenias. After 6 months, those who achieved at least a partial response in peripheral blood continued treatment for 6 additional months. Median age was 7 years (4-12), one patient had somatic mosaicism in bone marrow, and two had been treated by gene therapy (GT). At 6 months, three patients (37.5%) achieved a response, persisting in one at 12 months. The three patients with either somatic mosaicism or with GT-corrected cells showed an enhanced increase of corrected cells. One patient required dose modifications due to gastrointestinal intolerance and two because of hepatobiliary laboratory toxicity. No clonal evolution was observed by conventional cytogenetics, but a patient developed a transient somatic variant in RUNX1. In conclusion, eltrombopag did not mediate clinically relevant responses, although a possible impact of dose reductions and treatment duration must be considered. The increase of gene-corrected cells suggests it promoted a proliferative advantage over uncorrected ones. Www.clinicaltrials.gov #NCT06045052.

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Publication Details

Journal
European Journal Of Haematology
Published
2025-07-16
DOI
https://doi.org/10.1111/ejh.70007
Citations
1
Primary Topic
Acute Myeloid Leukemia Research
Type
article
Field-Weighted Citation Impact
1.77

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article

Eltrombopag for Bone Marrow Failure in Fanconi Anemia: Results From the Phase II Clinical Trial FANCREV

Almudena Galán, Juan A. Bueren, María Solsona, Albert Català et al.
1 citations
European Journal Of Haematology
Acute Myeloid Leukemia Research
1.77
article

Eltrombopag for Bone Marrow Failure in Fanconi Anemia: Results From the Phase II Clinical Trial FANCREV

Almudena Galán, Juan A. Bueren, María Solsona, Albert Català, Alejandro Sanz, Elena Sebastián, Silvia Martín‐Prado, Susana Navarro, Jesús González de Pablo, Josune Zubicaray, Lise Larcher, Nagore García de Andoín, Julián Sevilla, Paula Rı́o, Jean Soulier, June Iriondo, Jose Javier Uriz, Jordi Surrallés, Jonathan D. Schwartz, Eileen Nicoletti, José Manuel Vagace, Ana M. Gómez, María Roser Pujol, Ana de la Cruz
article en
1 citations

Abstract

Eltrombopag stimulates hematopoiesis in aplastic anemia, and preclinical studies suggest it promotes DNA repair in Fanconi Anemia (FA) hematopoietic stem cells. We conducted a clinical trial to explore its safety and efficacy in bone marrow failure due to FA. Eltrombopag was administered to 8 pediatric patients with one or more significant cytopenias. After 6 months, those who achieved at least a partial response in peripheral blood continued treatment for 6 additional months. Median age was 7 years (4-12), one patient had somatic mosaicism in bone marrow, and two had been treated by gene therapy (GT). At 6 months, three patients (37.5%) achieved a response, persisting in one at 12 months. The three patients with either somatic mosaicism or with GT-corrected cells showed an enhanced increase of corrected cells. One patient required dose modifications due to gastrointestinal intolerance and two because of hepatobiliary laboratory toxicity. No clonal evolution was observed by conventional cytogenetics, but a patient developed a transient somatic variant in RUNX1. In conclusion, eltrombopag did not mediate clinically relevant responses, although a possible impact of dose reductions and treatment duration must be considered. The increase of gene-corrected cells suggests it promoted a proliferative advantage over uncorrected ones. Www.clinicaltrials.gov #NCT06045052.

European Journal Of HaematologyVol. 115(4)
Universitat Autònoma de Barcelona (ES), Centre National de la Recherche Scientifique (FR), Foundation for Biomedical Research (US), Hospital Sant Joan de Déu Barcelona (ES), Inserm (FR), Université Paris Cité (FR), Assistance Publique – Hôpitaux de Paris (FR), Biogipuzkoa Health Research Institute (ES), Centre for Biomedical Network Research on Rare Diseases (ES), Hospital Infantil Universitario Niño Jesús (ES), Centro de Implantología Cirugía Oral y Maxilofacial (ES), Hôpital Saint-Louis (FR), Sunesis (United States) (US)
European Commission, Instituto de Salud Carlos III
Good health and well-being
Openalex Percentile: Top 14%
Acute Myeloid Leukemia Research
1.77
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