dc.contributor | Vall d'Hebron Barcelona Hospital Campus |
dc.contributor.author | Sans-Pola, Carla |
dc.contributor.author | Danés Carreras, Immaculada |
dc.contributor.author | Bosch, Josep Àngel |
dc.contributor.author | Marrero Álvarez, Patricia |
dc.contributor.author | Cortes Hernandez, Josefina |
dc.contributor.author | Agustí, Antònia |
dc.date.accessioned | 2023-06-15T05:48:11Z |
dc.date.available | 2023-06-15T05:48:11Z |
dc.date.issued | 2023-05-25 |
dc.identifier.citation | Sans-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.issn | 2296-858X |
dc.identifier.uri | https://hdl.handle.net/11351/9758 |
dc.description | Effectiveness; Rituximab; Systemic erythematosus lupus |
dc.description.abstract | Introduction: 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.iso | eng |
dc.publisher | Frontiers Media |
dc.relation.ispartofseries | Frontiers in Medicine;10 |
dc.rights | Attribution 4.0 International |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ |
dc.source | Scientia |
dc.subject | Lupus eritematós sistèmic - Tractament |
dc.subject | Medicaments antineoplàstics - Ús terapèutic |
dc.subject.mesh | Antineoplastic Agents |
dc.subject.mesh | /therapeutic use |
dc.subject.mesh | Lupus Erythematosus, Systemic |
dc.subject.mesh | /drug therapy |
dc.title | Off-label use of rituximab in patients with systemic lupus erythematosus with extrarenal disease activity: a retrospective study and literature review |
dc.type | info:eu-repo/semantics/article |
dc.identifier.doi | 10.3389/fmed.2023.1159794 |
dc.subject.decs | antineoplásicos |
dc.subject.decs | /uso terapéutico |
dc.subject.decs | lupus eritematoso sistémico |
dc.subject.decs | /farmacoterapia |
dc.relation.publishversion | https://doi.org/10.3389/fmed.2023.1159794 |
dc.type.version | info:eu-repo/semantics/publishedVersion |
dc.audience | Professionals |
dc.contributor.organismes | Institut 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.pmid | 37305139 |
dc.rights.accessrights | info:eu-repo/semantics/openAccess |