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How comparable are rates of malignancies in patients with rheumatoid arthritis across the world? A comparison of cancer rates, and means to optimise their comparability, in five RA registries.
Askling, Johan; Berglind, Niklas; Franzen, Stefan; Frisell, Thomas; Garwood, Christopher; Greenberg, Jeffrey D; Ho, Meilien; Holmqvist, Marie; Horne, Laura; Inoue, Eisuke; Michaud, Kaleb; Nyberg, Fredrik; Pappas, Dimitrios A; Reed, George; Tanaka, Eiichi; Tran, Trung N; Verstappen, Suzanne M M; Yamanaka, Hisashi; Wesby-van Swaay, Eveline; Symmons, Deborah.
Afiliación
  • Askling J; Clinical Epidemiology Unit, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden Department of Rheumatology, Karolinska University Hospital, Stockholm, Sweden.
  • Berglind N; Biometric & Information Sciences, Global Medicines Development, AstraZeneca R&D, Mölndal, Sweden.
  • Franzen S; Biometric & Information Sciences, Global Medicines Development, AstraZeneca R&D, Mölndal, Sweden.
  • Frisell T; Clinical Epidemiology Unit, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden.
  • Garwood C; Arthritis Research UK Centre for Epidemiology, The University of Manchester, Manchester, UK.
  • Greenberg JD; NYU School of Medicine, New York, New York, USA Corrona LLC, Southborough, Massachusetts, USA.
  • Ho M; Clinical, Global Medicines Development, AstraZeneca R&D, Macclesfield, UK.
  • Holmqvist M; Clinical Epidemiology Unit, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden.
  • Horne L; Medical Evidence & Observational Research Centre, Global Medicines Development, AstraZeneca R&D, Wilmington, Delaware, USA.
  • Inoue E; Institute of Rheumatology, Tokyo Women's Medical University, Tokyo, Japan.
  • Michaud K; National Data Bank for Rheumatic Diseases, Wichita, Kansas, USA Department of Medicine, University of Nebraska Medical Center, Omaha, Nebraska, USA.
  • Nyberg F; Medical Evidence & Observational Research Centre, Global Medicines Development, AstraZeneca R&D, Mölndal, Sweden Occupational and Environmental Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
  • Pappas DA; Columbia University College of Physicians and Surgeons, New York, New York, USA.
  • Reed G; University of Massachusetts Medical School, Worcester, Massachusetts, USA.
  • Tanaka E; Institute of Rheumatology, Tokyo Women's Medical University, Tokyo, Japan.
  • Tran TN; MedImmune, Gaithersburg, Maryland, USA.
  • Verstappen SM; Arthritis Research UK Centre for Epidemiology, The University of Manchester, Manchester, UK.
  • Yamanaka H; Institute of Rheumatology, Tokyo Women's Medical University, Tokyo, Japan.
  • Wesby-van Swaay E; Patient Safety, GRAPSQA, Global Medicines Development, AstraZeneca R&D, Mölndal, Sweden.
  • Symmons D; Arthritis Research UK Centre for Epidemiology, The University of Manchester, Manchester, UK NIHR Manchester Musculoskeletal Biomedical Research Unit, Central Manchester NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, UK.
Ann Rheum Dis ; 75(10): 1789-96, 2016 Oct.
Article en En | MEDLINE | ID: mdl-26621482
BACKGROUND: The overall incidence of cancer in patients with rheumatoid arthritis (RA) is modestly elevated. The extent to which cancer rates in RA vary across clinical cohorts and patient subsets, as defined by disease activity or treatment is less known but critical for understanding the safety of existing and new antirheumatic therapies. We investigated comparability of, and means to harmonise, malignancy rates in five RA registries from four continents. METHODS: Participating RA registries were Consortium of Rheumatology Researchers of North America (CORRONA) (USA), Swedish Rheumatology Quality of Care Register (SRR) (Sweden), Norfolk Arthritis Register (NOAR) (UK), CORRONA International (several countries) and Institute of Rheumatology, Rheumatoid Arthritis (IORRA) (Japan). Within each registry, we analysed a main cohort of all patients with RA from January 2000 to last available data, and sensitivity analyses of sub-cohorts defined by disease activity, treatment change, prior comorbidities and restricted by calendar time or follow-up, respectively. Malignancy rates with 95% CIs were estimated, and standardised for age and sex, based on the distributions from a typical RA clinical trial programme population (fostamatinib). RESULTS: There was a high consistency in rates for overall malignancy excluding non-melanoma skin cancer (NMSC), for malignant lymphomas, but not for all skin cancers, across registries, in particular following age/sex standardisation. Standardised rates of overall malignancy excluding NMSC varied from 0.56 to 0.87 per 100 person-years. Within each registry, rates were generally consistent across sensitivity analyses, which differed little from the main analysis. CONCLUSION: In real-world RA populations, rates of both overall malignancy and of lymphomas are consistent.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Artritis Reumatoide / Sistema de Registros / Linfoma / Neoplasias Tipo de estudio: Etiology_studies / Incidence_studies / Prognostic_studies Límite: Aged / Female / Humans / Male / Middle aged País/Región como asunto: America do norte / Asia / Europa Idioma: En Revista: Ann Rheum Dis Año: 2016 Tipo del documento: Article País de afiliación: Suecia

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Artritis Reumatoide / Sistema de Registros / Linfoma / Neoplasias Tipo de estudio: Etiology_studies / Incidence_studies / Prognostic_studies Límite: Aged / Female / Humans / Male / Middle aged País/Región como asunto: America do norte / Asia / Europa Idioma: En Revista: Ann Rheum Dis Año: 2016 Tipo del documento: Article País de afiliación: Suecia