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dc.contributor.authorPanaccione, Remo
dc.contributor.authorAbreu, Maria T.
dc.contributor.authorLazariciu, Irina
dc.contributor.authorMundayat, Rajiv
dc.contributor.authorLawendy, Nervin
dc.contributor.authorSalese, Leonardo
dc.contributor.authorWoolcott, John C.
dc.contributor.authorSands, Bruce E.
dc.contributor.authorChaparro Sánchez, María 
dc.contributor.otherUAM. Departamento de Medicinaes_ES
dc.date.accessioned2023-02-20T12:52:27Z
dc.date.available2023-02-20T12:52:27Z
dc.date.issued2022-02-13
dc.identifier.citationAlimentary Pharmacology & Therapeutics 55.12 (2022): 1475-1591en_US
dc.identifier.issn0269-2813 (print)es_ES
dc.identifier.issn1365-2036 (online)es_ES
dc.identifier.urihttp://hdl.handle.net/10486/706448
dc.description.abstractTofacitinib is an oral Janus kinase inhibitor for the treatment of ulcerative colitis (UC). Aim:This post hoc analysis evaluated tofacitinib persistence in patients with UC in OCTAVE Open, an open-label, long-term extension study of patients receiving tofacitinib 5 or 10 mg twice daily. Methods: Kaplan-Meier estimates for tofacitinib drug survival and reasons for discontinuations were evaluated. Baseline factors were analysed as predictors of persistence. Results:This analysis included 603 patients: 280 entered OCTAVE Open with a clinical response (164 in remission and 116 not in remission), 220 were delayed responders, 75 were retreatment responders and 35 were dose escalation responders, treated for up to 7 years in OCTAVE Open. Of these, 118 (42.1%) responders, 121 (55.0%) delayed responders, 40 (53.3%) retreatment responders and 17 (48.6%) dose escalation responders discontinued tofacitinib with a median time to discontinuation of 5.6, 4.5, 4.0 and 4.4 years, respectively. The estimated 2- and 5-year drug survival rates in the responders (including patients in remission and not in remission) were 73.9% and 54.5%, respectively. Corresponding persistence values for delayed responders were 69.5% and 45.2%, for retreatment responders, 70.7% and 40.0%, and for dose escalation responders, 74.3% and 32.8%. ConclusionIn: OCTAVE Open, a high proportion of patients maintained tofacitinib treatment, with the median survival by group ranging from 4.0 to 5.6 years although these analyses are post hoc and limited by sample size. Further research should focus on factors to enhance persistence with tofacitinib treatment in patients with UCen_US
dc.description.sponsorshipThis study was sponsored by Pfizer. Medical writing support, under the guidance of the authors, was provided by Helen Findlow, PhD, CMC Connect, McCann Health Medical Communications and was funded by Pfizer Inc, New York, NY, USA in accordance with Good Publication Practice (GPP3) guidelines (Ann Intern Med. 2015;163:461–464)en_US
dc.format.extent11 pag.es_ES
dc.format.mimetypeapplication/pdfen_US
dc.language.isoengen_US
dc.publisherJohn Wiley & Sons, Ltden_US
dc.relation.ispartofAlimentary Pharmacology and Therapeuticsen_US
dc.rights© 2022 Pfizer Incen_US
dc.subject.otherTofacitiniben_US
dc.subject.otherulcerative colitisen_US
dc.titlePersistence of treatment in patients with ulcerative colitis who responded to tofacitinib therapy: data from the open-label, long-term extension study, OCTAVE openen_US
dc.typearticleen_US
dc.subject.ecienciaMedicinaes_ES
dc.relation.publisherversionhttps://doi.org/10.1111/apt.16848en_US
dc.identifier.doi10.1111/apt.16848es_ES
dc.identifier.publicationfirstpage1534es_ES
dc.identifier.publicationissue12es_ES
dc.identifier.publicationlastpage1544es_ES
dc.identifier.publicationvolume55es_ES
dc.type.versioninfo:eu-repo/semantics/publishedVersionen_US
dc.rights.ccReconocimiento – NoComercial – SinObraDerivadaes_ES
dc.rights.accessRightsopenAccessen_US
dc.facultadUAMFacultad de Medicinaes_ES
dc.institutoUAMInstituto de Investigación Sanitaria Hospital Universitario de La Princesa (IIS-Princesa)es_ES


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