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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorMartínez Cutillas, Julio
dc.contributor.authorAlerany Pardo, Carme
dc.contributor.authorFerrer Artola, Ana Maria
dc.contributor.authorLópez Hernández, Andrés
dc.contributor.authorBosch Gil, Jose Angel
dc.contributor.authorDanés, Imma
dc.contributor.authorAgustí, Antònia
dc.contributor.authorVallano, Antonio
dc.contributor.authorCortes Hernandez, Josefina
dc.date.accessioned2025-01-27T11:38:13Z
dc.date.available2025-01-27T11:38:13Z
dc.date.issued2013-09
dc.identifier.citationDanés I, Agustí A, Vallano A, Martínez J, Alerany C, Ferrer A, et al. Available evidence and outcome of off-label use of rituximab in clinical practice. Eur J Clin Pharmacol. 2013 Sep;69(9):1689–99.
dc.identifier.issn1879-0828
dc.identifier.urihttps://hdl.handle.net/11351/12496
dc.descriptionOutcomes; Label; Rituximab
dc.description.abstractPurpose To analyze the therapeutic indications for off-label use of rituximab, the available evidence for its use, the outcomes, and the cost. Methods This was a retrospective analysis of patients treated with rituximab for off-label indications from January 2007 to December 2009 in two tertiary hospitals. Information on patient characteristics, medical conditions, and therapeutic responses was collected from medical records. Available evidence for the efficacy of rituximab in each condition was reviewed, and the cost of treatment was calculated. Results A total of 101 cases of off-label rituximab use were analyzed. The median age of the patients involved was 53 [interquartile range (IQR) 37.5–68.0] years; 55.4 % were women. The indications for prescribing rituximab were primarily hematological diseases (46 %), systemic connective tissue disorders (27 %), and kidney diseases (20 %). Available evidence supporting rituximab treatment for these indications mainly came from individual cohort studies (53.5 % of cases) and case series (25.7 %). The short-term outcome (median 3 months, IQR 2–4 months) was a complete response in 38 % of cases and partial response in 32.6 %. The highest short-term responses were observed for systemic lupus erythematosus and membranous glomerulonephritis, and the lowest was for neuromyelitis optica, idiopathic thrombocytopenic purpura, and miscellaneous indications. Some response was maintained in long-term follow-up (median 23 months IQR 12–30 months) in 69.2 % of patients showing a short-term response. Median cost per patient was € 5,187.5 (IQR € 5,187.5–7,781.3). Conclusions In our study, off-label rituximab was mainly used for the treatment of hematological, kidney, and systemic connective tissue disorders, and the response among our patient cohort was variable depending on the specific disease. The level of evidence supporting the use of rituximab for these indications was low and the cost was very high. We conclude that more clinical trials on the off-label use of rituximab are needed, although these may be difficult to conduct in some rare diseases. Data from observational studies may provide useful information to assist prescribing in clinical practice.
dc.language.isoeng
dc.publisherSpringer
dc.relation.ispartofseriesEuropean Journal of Clinical Pharmacology;69(9)
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceScientia
dc.subjectRonyons - Malalties - Tractament
dc.subjectSang - Malalties - Tractament
dc.subjectAnticossos monoclonals - Ús terapèutic
dc.subjectAvaluació de resultats (Assistència sanitària)
dc.subjectMedicaments - Prescripció
dc.subject.meshTreatment Outcome
dc.subject.meshOff-Label Use
dc.subject.meshAntibodies, Monoclonal, Murine-Derived
dc.subject.meshHematologic Diseases
dc.subject.meshKidney Diseases
dc.titleAvailable evidence and outcome of off-label use of rituximab in clinical practice
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1007/s00228-013-1518-4
dc.subject.decsresultado del tratamiento
dc.subject.decsprescripción en indicaciones no aprobadas
dc.subject.decsanticuerpos monoclonales de origen murino
dc.subject.decsenfermedades hematológicas
dc.subject.decsenfermedades renales
dc.relation.publishversionhttps://doi.org/10.1007/s00228-013-1518-4
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Danés I] Servei de Farmacologia Clínica, Fundació Institut Català de Farmacologia, Barcelona, Spain. Servei de Farmacologia Clínica, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Departament de Farmacologia Terapèutica i Toxicologia, Universitat Autònoma de Barcelona, Bellaterra, Spain. [Agustí A] Servei de Farmacologia Clínica, Fundació Institut Català de Farmacologia, Barcelona, Spain. Departament de Farmacologia Terapèutica i Toxicologia, Universitat Autònoma de Barcelona, Bellaterra, Spain. [Vallano A] Clinical Pharmacology Service, Bellvitge Biomedical Research Institute (IDIBELL), Hospital Universitari de Bellvitge, Hospitalet de Llobregat, Barcelona, Spain Department of Pathology and Experimental Therapeutics, Universitat de Barcelona, Hospitalet de Llobregat, Barcelona, Spain. [Martínez J, Alerany C] Servei de Farmàcia, Vall d’Hebron Hospital Universitari, Barcelona, Spain. [Ferrer A] Pharmacy Service, Hospital Universitari de Bellvitge, Hospitalet de Llobregat, Barcelona, Spain. [López A] Servei d’Hematologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain. [Cortés-Hernández J] Servei de Medicina Interna, Vall d’Hebron Hospital Universitari, Barcelona, Spain. [Bosch JA] Servei de Medicina Interna, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain
dc.identifier.pmid23700188
dc.identifier.wos000343807000012
dc.rights.accessrightsinfo:eu-repo/semantics/restrictedAccess


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