Tofacitinib, an oral Janus kinase inhibitor, in patients from Mexico with rheumatoid arthritis: Pooled efficacy and safety analyses from Phase 3 and LTE studies [Tofacitinib, un inhibidor oral de la cinasa Janus, en pacientes Mexicanos con Artritis Reumatoide: análisis de eficacia y seguridad de estudios fase 3 y de extensión a largo plazo]
Article
Overview
Research
Identity
Additional Document Info
View All
Overview
abstract
Objectives: Tofacitinib is an oral Janus kinase inhibitor for the treatment of rheumatoid arthritis (RA). We characterized efficacy and safety of tofacitinib in Mexican patients from RA Phase 3 and long-term extension (LTE) studies. Methods: Data from Mexican patients with RA and an inadequate response to disease-modifying antirheumatic drugs (DMARDs) were taken from four Phase 3 studies (pooled across studies) and one open-label LTE study of tofacitinib. Patients received tofacitinib 5 or 10 mg twice daily, adalimumab (one Phase 3 study) or placebo (four Phase 3 studies) as monotherapy or in combination with conventional synthetic DMARDs. Efficacy up to Month 12 (Phase 3) and Month 36 (LTE) was assessed by American College of Rheumatology 20/50/70 response rates, Disease Activity Score (erythrocyte sedimentation rate), and Health Assessment Questionnaire-Disability Index. Safety, including incidence rates (IRs; patients with events/100 patient-years) for adverse events (AEs) of special interest, was assessed throughout the studies. Results: 119 and 212 Mexican patients were included in the Phase 3 and LTE analyses, respectively. Tofacitinib-treated patients in Phase 3 had numerically greater improvements in efficacy responses versus placebo at Month 3. Efficacy was sustained in Phase 3 and LTE studies. IRs for AEs of special interest were similar to those with tofacitinib in the global and Latin American RA populations. Conclusions: In Mexican patients from the tofacitinib global RA program, tofacitinib efficacy was demonstrated up to Month 12 in Phase 3 studies and Month 36 in the LTE study, with a safety profile consistent with tofacitinib global population. © 2017 Elsevier España, S.L.U. and Sociedad Española de Reumatología y Colegio Mexicano de Reumatología
publication date
funding provided via
published in
Research
keywords
Efficacy; Janus kinase; Mexico; Rheumatoid arthritis; Safety adalimumab; chloroquine; disease modifying antirheumatic drug; glucocorticoid; hemoglobin; leflunomide; methotrexate; placebo; salazosulfapyridine; tofacitinib; antirheumatic agent; Janus kinase inhibitor; piperidine derivative; pyrimidine derivative; pyrrole derivative; tofacitinib; abdominal pain; adult; aged; anemia; Article; chronic obstructive lung disease; combination drug therapy; controlled study; diarrhea; disease activity score; dose response; drug dose comparison; drug efficacy; drug fatality; drug safety; drug withdrawal; erythrocyte sedimentation rate; falling; female; gastritis; Health Assessment Questionnaire; hemoglobin blood level; herpes zoster; human; infection; influenza; liver failure; lung metastasis; lymphocyte count; lymphocytopenia; major clinical study; male; Mexican; Mexico; monotherapy; nausea; neutrophil count; pharyngitis; respiratory failure; rheumatoid arthritis; rhinopharyngitis; sepsis; side effect; synovial sarcoma; tonsillitis; tooth fracture; tuberculosis; upper respiratory tract infection; urinary tract infection; vomiting; drug administration; longitudinal study; meta analysis; middle aged; oral drug administration; phase 3 clinical trial (topic); randomized controlled trial (topic); rheumatoid arthritis; treatment outcome; very elderly; Administration, Oral; Adult; Aged; Aged, 80 and over; Antirheumatic Agents; Arthritis, Rheumatoid; Clinical Trials, Phase III as Topic; Drug Administration Schedule; Drug Therapy, Combination; Female; Humans; Janus Kinase Inhibitors; Longitudinal Studies; Male; Mexico; Middle Aged; Piperidines; Pyrimidines; Pyrroles; Randomized Controlled Trials as Topic; Treatment Outcome
Identity
Digital Object Identifier (DOI)
PubMed ID
Additional Document Info
start page
end page
volume
issue