Scientific activity

• Member of the Spanish Society of Pediatric Haematology and Oncology ALL treatment protocol development committee (SEHOP/ALL 2013).
• Coordination of the SEHOP chronic myeloid leukaemia working group.
• Member of the Spanish Society of Pediatric Haematology and Oncology committee for the treatment and diagnosis of falciform cell anaemia (SEHOP/ECF 2010).

Publications

• Maude SL., Laetsch TW., Buechner J., Rives S., Boyer M., Bittencourt H., Bader P, Verneris MR., Stefanski HE., Myers GD., Qayed M., De Moerloose B., Hiramatsu H., Schlis K., Davis KL., et al. Tisagenlecleucel in Children and Young Adults with B-Cell Lymphoblastic Leukemia. Infusion of tisagenlecleucel in a planned analysis in 75 patients with lymphoblastic leukemia. The general remission rate in 3 months was 81%. New England Journal of Medicine, 2018; 378(5):439-448. doi: 10.1056/NEJMoa1709866.
• Alonso-Saladrigues A., Català A., Berrueco R., Camós M., Torrebadell M., Rives S.: Aplastic crisis secondary to parvovirus B19 infection as the first manifestation of an undiagnosed hereditary spherocytosis: report of a pediatric series of spanish patients. Journal of Pediatric Hematology/Oncology, 2016 January; 38 (1): 81-2
• Bautista F., Gallego S., Cañete A., Mora J., Diaz de Heredia C., Cruz O., Fernández J.M., Rives S., Madero L., Castel V., Cela M.E., Ramírez G., Sábado C., Acha T., Astigarraga I., Sastre A., Una Muñoz, Guibelalde M., Moreno L. Landscape of early clinical trials for childhood and adolescence cancer in Spain. Clinical and Translational Oncology, 2015 October 21. E-pub ahead of print.
• Berrueco R., Alonso-Saladrigues A., Martorell-Sampol L., Català-Temprano A., Ruiz-Llobet A., Toll T., Torrebadell M., Naudó M., Camós M., Rives S. Outcome and toxicities associated to chemotherapy in children with acute lymphoblastic leukemia and Gilbert syndrome. Usefulness of UGT1A1 mutational screening. Pediatric Blood & Cancer, 2015 62: 1195-201. 
• Bento C., Percy M.J., Gardie B., Maia T.M., van Wijk R., Perrotta S., Ragione F.D., Almeida H., Rossi C., Girodon F., Aström M., Neuman D., Schnittger S., Landin B., Minkov M., Randi M.L., Casadevall N., et al. Genetic basis of congenital erythrocytosis: mutation update and online databases. Human Mutation, 2014; 35: 15-26.
• Rives S., Camós M., Estella J., Gómez P., Moreno M.J., Vivanco J.L., Melo M., Fernández-Delgado R., Verdeguer A., Fernández-Teijeiro A., Lendínez F., López-Almaraz R., Uriz J.J., Badell I. Spanish Paediatric Haemato-Oncology Group (SHOP/SEHOP). Longer follow-up confirms major improvement in outcome in children and adolescents with Philadelphia chromosome acute lymphoblastic leukaemia treated with continuous imatinib and haematopoietic stem cell transplantation. Results from the Spanish Cooperative Study. SHOP/ALL-2005. British Journal of Haematology, 2013; 162: 419-21.

See more publications