Leukaemia and Paediatric Haematology Disorders
Research Program
Leaders
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Pablo Menéndez Buján
Where we are
SJD Barcelona Children's Hospital
Related websites
Our group carries out translational research with the aim of applying the advances made in biological diagnosis to healthcare practice and the use of the most innovative treatments in paediatric patients with blood disorders. Since its creation in 2012, our group has obtained uninterrupted funding for competitive and non-competitive calls for public and private aid.
We participate as a clinical group associated with the Hereditary Cancer and Related Syndromes Group in the Centre for Biomedical Network Research on Rare Diseases (CIBERER). The Hereditary Red Blood Cell Disorders Unit, which is part of both SJD Barcelona Children's Hospital and Hospital de la Santa Creu i Sant Pau, will shortly be recognised as a Reference Centre-Service Unit (RCSU).
We have been a consolidated AGAUR research group (Government of Catalonia, references 2014 SGR 1398 and 2017 SGR 1672) since 2014.
Desarrollo de una nueva terapia CAR-T dirigida a CD1a para el tratamiento de leucemias/linfomas de células T CD1a+
Investigador principal: Susana Rives Solà
Convocatoria: proyectos colaboración público-privada
Código: CPP2021-008508
Año inicio: 2022
Año finalización: 2025
Financiador: Ministerio de Ciencia e innovación, Agencia Estatal de investigación
Importe concedido: 510.821,00 €
Proyecto CPPC2021-008508 financiado por MICIN/AEI/10.13039/501100011033 y por la Unión Europea NextGenerationEU/PRTR

Research lines
- Acute lymphoblastic leukaemia (ALL).
- Acute myeloblastic leukaemia (AML).
- Bone marrow failure and myelodysplastic syndromes.
- Red blood cell disorders.
- Alterations in haemostasis.
- Immunotherapy and cell therapy.
- Prevention of toxicity secondary to leukaemia treatment.
Scientific objectives
- To consolidate our group as a CIBER associated clinical group and define the current situation of paediatric haematology diseases in the context of those considered as "rare diseases".
- To promote cooperative strategies to advance biological diagnosis and follow-up of minimal residual disease (MRD) in cases of acute leukaemias and other paediatric haematology disorders. To design and implement new techniques and internal/external quality controls.
- To analyse new biomarkers of potential diagnostic, prognostic and therapeutic utility in high-risk paediatric leukaemias.
- To promote the applicability of new therapies in paediatric patients by conducting clinical trials. To consolidate the experience of our group in the use of cell therapy with combination antiretroviral therapy (cART) and haematopoietic progenitor transplantation.
- To study the biological and clinical factors that could help prevent or alleviate toxicity secondary to leukaemia therapy.
- To apply photonics to the diagnosis and monitoring of red blood cell disorders.
- To study the risk factors associated with chemotherapy-induced thrombosis in paediatric ALL and establish preventive measures.
- To establish genomic precision diagnosis using next-generation sequencing techniques to different paediatric haematology disorders.
Area/Field of expertise
We conduct translational research aimed at the rapid "bench-to-bedside" application of diagnostic and therapeutic innovations relevant to leukaemia and other haematology disorders. Our group includes haematologists, paediatric haematology-oncologists, biologists and lab technicians, with recognised expertise in the diagnosis and treatment of children with haematology disorders. With this multidisciplinary team, we can provide a comprehensive approach to the real problems of patients and conduct research that is readily transmitted to clinical practice.
Since its creation, our group has established itself within the main clinical and biological coordination positions in the area of paediatric haematology disorders. This has enabled us to represent the Spanish group in major international cooperative groups and participate in national and international cooperation projects.
Over the past few years, we have incorporated diagnostic and therapeutic tools and consolidated the harvesting of blood samples in our biobank. This has led to the establishing of the hospital as a reference centre for research into childhood leukaemia and other blood disorders. We deploy various methodologies including complete biological diagnosis and close monitoring of minimal residual disease in acute leukaemia (morphology, flow cytometry, molecular biology, including next-generation sequencing, lymphoid clonality testing, etc.). The incorporation of global haemostasis assays, such as the thrombin generation assay, will enable us to establish normal values and standardise their use in the paediatric population.
This year, the integrated HSJD-HSP unit was granted RSCU accreditation in hereditary RBC disorders.
Group members
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Investigador pre-doc
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Investigador pre-doc
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Investigador pre-doc
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Montserrat Torrebadell Burriel
Investigador
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Investigador
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Investigador
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Investigador
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Investigador
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Investigador pre-doc
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Técnico
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Técnico
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Investigador
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Investigador
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Investigador
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Técnico
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Investigador
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Investigador
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Investigador
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Investigador
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Investigador
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Investigador
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Investigador post-doc
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Investigador
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Investigador
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Investigador
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Joana Bernabeu López
Técnico
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Gestión
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Jefe de Grupo
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Gestión
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Pablo Menéndez Buján
Jefe de Grupo
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Marcel Arias Badia
Investigador
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Investigador
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Investigador post-doc
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Investigador
Last Publications
- Nafria-Escalera B, Claverol J, Cubells M, Llanos C, Solé L, Sans E, López S, Català-Mora J, Rives-Solà S, Morales-La Madrid A, Pineda M, Garcia-Cazorla A, Nascimento-Osorio A, Morales-Ballús M, Roe D, Fortuny-Guasch C and Phillips B Cross-border access to clinical trials: participation of pediatric patients and language inclusion PEDIATRIC RESEARCH . : .
- Vatovec T, Neehus AL, Jackson KJL, Avery DT, Bagaric I, Erazo L, Arango-Franco CA, Ogishi M, Ahmed SF, Cederholm A, Russell AJ, Della Mina E, Al-Rifai D, Bull R, Buetow L, Sobrino S, Zhang A, Wahlster L, Michelet M, Parvaneh N, Peel J, Barzaghi F, Leardini D, Philippot Q, Saettini F, Dutrieux J, de Muylder B, Vendemini F, Baccelli F, Català-Temprano A, Gambineri E, Veltroni M, Pandiarajan V, Aguilar Y, Haerynck F, Elliott M, Turville S, Brillot F, Khan T, Consonni F, Berteloot L, Sewell WA, Rao G, Largeaud L, Conti F, Roullion C, Masson C, Pegoraro F, Ye T, Joubran S, Villalpando E, Bessot B, Seeleuthner Y, Le Voyer T, Rosain J, Li H, Janda Z, Muratore E, Soudée C, Delabesse E, Goulvestre C, Shahrooei M, Puel A, André I, Bole-Feysot C, Abel L, Erlacher M, Béziat V, Lagresle-Peyrou C, Cheynier R, Six E, Marr N, Pasquet M, Alsina L, Goodnow CC, Landegren N, Aiuti A, Zhang P, Masetti R, Huang DT, Ma CS, Casanova JL, Sankaran VG, Bustamante J, Tangye SG and Bohlen J Somatic deficiency of the human E3 ubiquitin ligase CBL in leukocytes impairs B cell but not T cell development and function NATURE IMMUNOLOGY . : .
- Mikkelsen, T, Helenius, M, Ampatzidou, M, Attarbaschi, A, Andres-Jensen, L, Borkhardt, A, Conde N, Escherich, G, Hagleitner, MM, Halsey, C, Josephs-Spaulding, J, Lundgren, L, Pehn, S, Polychronopoulou, S, Stoltze, U, Toksvang, LN, Wahlberg, A, Junk, SV and Schmiegelow, K Role of common host genome variants in Childhood Acute Lymphoblastic Leukemia. LEUKEMIA . 40(1): 3-24.
Projects
- Project name:
- Ensayo clínico fase Ib multicéntrico, exploratorio, abierto, no-aleatorizado y prospectivo, basket trial, con células CAR-T anti-CD19 (ARI-0001) en pacientes pediátricos con enfermedades autoinmunes sistémicas.
- Leader
- Jordi Antón López, Susana Rives Solà
- Funding entities:
- Instituto de Salud Carlos III (ISCIII)
- Code
- ICI25/00025
- Starting - finishing date:
- 2026 - 2029
- Project name:
- ADVANCED THERAPIES (RICORS-TERAV)
- Leader
- Susana Rives Solà
- Funding entities:
- Instituto de Salud Carlos III (ISCIII)
- Code
- RD24/0014/0006
- Starting - finishing date:
- 2025 - 2027
- Project name:
- Tratamiento y prevención de la coagulopatía intravascular localizada en malformaciones venosas y linfáticas de bajo flujo en pacientes pediátricos. Uso de enoxaparina durante intervencionismo percutáneo
- Leader
- Eulalia Baselga Torres, Ruben Berrueco Moreno
- Funding entities:
- Instituto de Salud Carlos III (ISCIII)
- Code
- PI24/00803
- Starting - finishing date:
- 2025 - 2027
Theses
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Estudi de nous biomarcadors en pacients amb leucèmia pediàtrica d´alt risc
- Author
- Esperanza Cebollada, Elena
- Institution
- UNIVERSIDAD DE BARCELONA
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Estudi de factors clínics i biològics associats a toxicitat en el tractament de la leucèmia limfoblàstica aguda pediàtrica.
- Author
- Mesegue Meda, Montserrat
- Institution
- UNIVERSIDAD DE BARCELONA
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Estudi del perfil d'expressió de les histones deacetilasa (HDAC) en pacients pediàtrics amb leucèmia aguda
- Author
- Vega García, Nerea
- Institution
- UNIVERSIDAD DE BARCELONA
News
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Sant Joan de Déu coordinates the European project ARI-chALL to promote a new clinical trial in pediatric leukemia
Sant Joan de Déu coordinates the European project ARI-chALL, an international initiative that promotes a new clinical trial with the aim of identifying a treatment for children with acute lymphoblastic leukemia (ALL) in first relapse through the CAR-T ARI-0001 therapy.
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Genetic events that could trigger leukemia in patients with a rare genetic disorder are deciphered
The study has been carried out thanks to advanced models of this genetic disorder generated by the researchers, which are presented as a key tool in its investigation.
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The Josep Carreras Foundation and Sant Joan de Déu Create a Childhood Leukemia Research Program Worth Over 10 Million Euros
The Josep Carreras Foundation (FJC), the Josep Carreras Leukemia Research Institute (IJC), and the Sant Joan de Déu Research Institute (IRSJD) have agreed to develop a joint research program on childhood leukemia valued at over 10 million euros.
More activities
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Defensa tesi doctoral: Elena Esperanza Cebollada
Auditori Plaza, Hospital Sant Joan de Déu · Online
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Defensa tesi doctoral: Montserrat Mesegué Medà
Auditori Plaza, Hospital Sant Joan de Déu · Online
SJD Barcelona Children's Hospital