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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorSans-Pola, Carla
dc.contributor.authorDanés Carreras, Immaculada
dc.contributor.authorBosch, Josep Àngel
dc.contributor.authorMarrero Álvarez, Patricia
dc.contributor.authorCortes Hernandez, Josefina
dc.contributor.authorAgustí, Antònia
dc.date.accessioned2023-06-15T05:48:11Z
dc.date.available2023-06-15T05:48:11Z
dc.date.issued2023-05-25
dc.identifier.citationSans-Pola C, Danés I, Bosch JÀ, Marrero-Álvarez P, Cortés J, Agustí A. Off-label use of rituximab in patients with systemic lupus erythematosus with extrarenal disease activity: a retrospective study and literature review. Front Med. 2023 May 25;10:1159794.
dc.identifier.issn2296-858X
dc.identifier.urihttps://hdl.handle.net/11351/9758
dc.descriptionEffectiveness; Rituximab; Systemic erythematosus lupus
dc.description.abstractIntroduction: Off-label rituximab is commonly used for patients with systemic lupus erythematosus (SLE) with extrarenal disease activity. Methods: The outcomes and tolerability of rituximab in adult patients with non-renal SLE treated at our hospital from 2013 to 2020 were described. Patients were followed-up until December 2021. Data were retrieved from electronic medical records. Response was classified into complete, partial or no response according to the Systemic Lupus Erythematosus Disease Activity Index 2000 (SLEDAI 2 K)-based definitions. Results: A total of 44 cycles were administered to 33 patients. Median age was 45 years and 97% were female. Median follow-up was 5.9 years (IQR 3.7–7.2). The most frequent symptoms that motivated rituximab use were thrombocytopenia (30.3%), arthritis (30.3%), neurological manifestations (24.2%) and cutaneous lupus (15.2%). After most treatment cycles a partial remission was achieved. The median SLEDAI-2 K score declined from 9 (IQR 5–13) to 1.5 (IQR 0–4) (p < 0.00001). The median number of flares significantly declined after receiving rituximab. Platelet counts significantly improved in patients with thrombocytopenia and patients with skin disorders or neurological manifestations also had a partial or complete response. Only 50% of patients with a predominant joint involvement had either a complete or a partial response. The median time to relapse after the first cycle was 1.6 years (95% CI, 0.6–3.1). Anti-dsDNA levels decreased significantly after rituximab from a median of 64.3 (IQR 12–373.9) to 32.7 (IQR 10–173), p = 0.00338. The most frequent adverse events were infusion-related reactions (18.2%) and infections (57.6%). All patients needed further treatment to maintain remission or to treat new flares. Conclusion: A partial or complete response was documented after most rituximab cycles in patients with non-renal SLE. Patients with thrombocytopenia, neurolupus, and cutaneous lupus had better response than those with a predominant joint involvement.
dc.language.isoeng
dc.publisherFrontiers Media
dc.relation.ispartofseriesFrontiers in Medicine;10
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceScientia
dc.subjectLupus eritematós sistèmic - Tractament
dc.subjectMedicaments antineoplàstics - Ús terapèutic
dc.subject.meshAntineoplastic Agents
dc.subject.mesh/therapeutic use
dc.subject.meshLupus Erythematosus, Systemic
dc.subject.mesh/drug therapy
dc.titleOff-label use of rituximab in patients with systemic lupus erythematosus with extrarenal disease activity: a retrospective study and literature review
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.3389/fmed.2023.1159794
dc.subject.decsantineoplásicos
dc.subject.decs/uso terapéutico
dc.subject.decslupus eritematoso sistémico
dc.subject.decs/farmacoterapia
dc.relation.publishversionhttps://doi.org/10.3389/fmed.2023.1159794
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Sans-Pola C, Danés I, Agustí A] Servei de Farmacologia Clínica, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Departament de Farmacologia, Terapèutica i Toxicologia, Universitat Autònoma de Barcelona, Bellaterra, Spain. Grup de Recerca de Farmacologia Clínica, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Vall d’Hebron Hospital Universitari, Barcelona, Spain. [Bosch JÀ] Departament de Medicina Interna, Universitat Autònoma de Barcelona, Bellaterra, Spain. [Marrero-Álvarez P] Servei de Farmàcia, Vall d’Hebron Hospital Universitari, Barcelona, Spain. [Cortés J] Servei de Medicina Interna, Vall d’Hebron Hospital Universitari, Barcelona, Spain
dc.identifier.pmid37305139
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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