Tuberculosis and other opportunistic infections in tofacitinib-treated patients with rheumatoid arthritis

ObjectivesTo evaluate the risk of opportunistic infections (OIs) in patients with rheumatoid arthritis (RA) treated with tofacitinib.MethodsPhase II, III and long-term extension clinical trial data (April 2013 data-cut) from the tofacitinib RA programme were reviewed. OIs defined a priori included m...

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Published inAnnals of the rheumatic diseases Vol. 75; no. 6; pp. 1133 - 1138
Main Authors Winthrop, K L, Park, S-H, Gul, A, Cardiel, M H, Gomez-Reino, J J, Tanaka, Y, Kwok, K, Lukic, T, Mortensen, E, Ponce de Leon, D, Riese, R, Valdez, H
Format Journal Article
LanguageEnglish
Published England Elsevier Limited 01.06.2016
BMJ Publishing Group
SeriesExtended report
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Abstract ObjectivesTo evaluate the risk of opportunistic infections (OIs) in patients with rheumatoid arthritis (RA) treated with tofacitinib.MethodsPhase II, III and long-term extension clinical trial data (April 2013 data-cut) from the tofacitinib RA programme were reviewed. OIs defined a priori included mycobacterial and fungal infections, multidermatomal herpes zoster and other viral infections associated with immunosuppression. For OIs, we calculated crude incidence rates (IRs; per 100 patient-years (95% CI)); for tuberculosis (TB) specifically, we calculated rates stratified by patient enrolment region according to background TB IR (per 100 patient-years): low (≤0.01), medium (>0.01 to ≤0.05) and high (>0.05).ResultsWe identified 60 OIs among 5671 subjects; all occurred among tofacitinib-treated patients. TB (crude IR 0.21, 95% CI of (0.14 to 0.30)) was the most common OI (n=26); median time between drug start and diagnosis was 64 weeks (range 15–161 weeks). Twenty-one cases (81%) occurred in countries with high background TB IR, and the rate varied with regional background TB IR: low 0.02 (0.003 to 0.15), medium 0.08 (0.03 to 0.21) and high 0.75 (0.49 to 1.15). In Phase III studies, 263 patients diagnosed with latent TB infection were treated with isoniazid and tofacitinib concurrently; none developed TB. For OIs other than TB, 34 events were reported (crude IR 0.25 (95% CI 0.18 to 0.36)).ConclusionsWithin the global tofacitinib RA development programme, TB was the most common OI reported but was rare in regions of low and medium TB incidence. Patients who screen positive for latent TB can be treated with isoniazid during tofacitinib therapy.
AbstractList Objectives To evaluate the risk of opportunistic infections (OIs) in patients with rheumatoid arthritis (RA) treated with tofacitinib. Methods Phase II, III and long-term extension clinical trial data (April 2013 data-cut) from the tofacitinib RA programme were reviewed. OIs defined a priori included mycobacterial and fungal infections, multidermatomal herpes zoster and other viral infections associated with immunosuppression. For OIs, we calculated crude incidence rates (IRs; per 100 patient-years (95% CI)); for tuberculosis (TB) specifically, we calculated rates stratified by patient enrolment region according to background TB IR (per 100 patient-years): low (â[per thousand]¤0.01), medium (>0.01 to â[per thousand]¤0.05) and high (>0.05). Results We identified 60 OIs among 5671 subjects; all occurred among tofacitinib-treated patients. TB (crude IR 0.21, 95% CI of (0.14 to 0.30)) was the most common OI (n=26); median time between drug start and diagnosis was 64 weeks (range 15-161 weeks). Twenty-one cases (81%) occurred in countries with high background TB IR, and the rate varied with regional background TB IR: low 0.02 (0.003 to 0.15), medium 0.08 (0.03 to 0.21) and high 0.75 (0.49 to 1.15). In Phase III studies, 263 patients diagnosed with latent TB infection were treated with isoniazid and tofacitinib concurrently; none developed TB. For OIs other than TB, 34 events were reported (crude IR 0.25 (95% CI 0.18 to 0.36)). Conclusions Within the global tofacitinib RA development programme, TB was the most common OI reported but was rare in regions of low and medium TB incidence. Patients who screen positive for latent TB can be treated with isoniazid during tofacitinib therapy.
To evaluate the risk of opportunistic infections (OIs) in patients with rheumatoid arthritis (RA) treated with tofacitinib.OBJECTIVESTo evaluate the risk of opportunistic infections (OIs) in patients with rheumatoid arthritis (RA) treated with tofacitinib.Phase II, III and long-term extension clinical trial data (April 2013 data-cut) from the tofacitinib RA programme were reviewed. OIs defined a priori included mycobacterial and fungal infections, multidermatomal herpes zoster and other viral infections associated with immunosuppression. For OIs, we calculated crude incidence rates (IRs; per 100 patient-years (95% CI)); for tuberculosis (TB) specifically, we calculated rates stratified by patient enrolment region according to background TB IR (per 100 patient-years): low (≤0.01), medium (>0.01 to ≤0.05) and high (>0.05).METHODSPhase II, III and long-term extension clinical trial data (April 2013 data-cut) from the tofacitinib RA programme were reviewed. OIs defined a priori included mycobacterial and fungal infections, multidermatomal herpes zoster and other viral infections associated with immunosuppression. For OIs, we calculated crude incidence rates (IRs; per 100 patient-years (95% CI)); for tuberculosis (TB) specifically, we calculated rates stratified by patient enrolment region according to background TB IR (per 100 patient-years): low (≤0.01), medium (>0.01 to ≤0.05) and high (>0.05).We identified 60 OIs among 5671 subjects; all occurred among tofacitinib-treated patients. TB (crude IR 0.21, 95% CI of (0.14 to 0.30)) was the most common OI (n=26); median time between drug start and diagnosis was 64 weeks (range 15-161 weeks). Twenty-one cases (81%) occurred in countries with high background TB IR, and the rate varied with regional background TB IR: low 0.02 (0.003 to 0.15), medium 0.08 (0.03 to 0.21) and high 0.75 (0.49 to 1.15). In Phase III studies, 263 patients diagnosed with latent TB infection were treated with isoniazid and tofacitinib concurrently; none developed TB. For OIs other than TB, 34 events were reported (crude IR 0.25 (95% CI 0.18 to 0.36)).RESULTSWe identified 60 OIs among 5671 subjects; all occurred among tofacitinib-treated patients. TB (crude IR 0.21, 95% CI of (0.14 to 0.30)) was the most common OI (n=26); median time between drug start and diagnosis was 64 weeks (range 15-161 weeks). Twenty-one cases (81%) occurred in countries with high background TB IR, and the rate varied with regional background TB IR: low 0.02 (0.003 to 0.15), medium 0.08 (0.03 to 0.21) and high 0.75 (0.49 to 1.15). In Phase III studies, 263 patients diagnosed with latent TB infection were treated with isoniazid and tofacitinib concurrently; none developed TB. For OIs other than TB, 34 events were reported (crude IR 0.25 (95% CI 0.18 to 0.36)).Within the global tofacitinib RA development programme, TB was the most common OI reported but was rare in regions of low and medium TB incidence. Patients who screen positive for latent TB can be treated with isoniazid during tofacitinib therapy.CONCLUSIONSWithin the global tofacitinib RA development programme, TB was the most common OI reported but was rare in regions of low and medium TB incidence. Patients who screen positive for latent TB can be treated with isoniazid during tofacitinib therapy.
ObjectivesTo evaluate the risk of opportunistic infections (OIs) in patients with rheumatoid arthritis (RA) treated with tofacitinib.MethodsPhase II, III and long-term extension clinical trial data (April 2013 data-cut) from the tofacitinib RA programme were reviewed. OIs defined a priori included mycobacterial and fungal infections, multidermatomal herpes zoster and other viral infections associated with immunosuppression. For OIs, we calculated crude incidence rates (IRs; per 100 patient-years (95% CI)); for tuberculosis (TB) specifically, we calculated rates stratified by patient enrolment region according to background TB IR (per 100 patient-years): low (≤0.01), medium (>0.01 to ≤0.05) and high (>0.05).ResultsWe identified 60 OIs among 5671 subjects; all occurred among tofacitinib-treated patients. TB (crude IR 0.21, 95% CI of (0.14 to 0.30)) was the most common OI (n=26); median time between drug start and diagnosis was 64 weeks (range 15–161 weeks). Twenty-one cases (81%) occurred in countries with high background TB IR, and the rate varied with regional background TB IR: low 0.02 (0.003 to 0.15), medium 0.08 (0.03 to 0.21) and high 0.75 (0.49 to 1.15). In Phase III studies, 263 patients diagnosed with latent TB infection were treated with isoniazid and tofacitinib concurrently; none developed TB. For OIs other than TB, 34 events were reported (crude IR 0.25 (95% CI 0.18 to 0.36)).ConclusionsWithin the global tofacitinib RA development programme, TB was the most common OI reported but was rare in regions of low and medium TB incidence. Patients who screen positive for latent TB can be treated with isoniazid during tofacitinib therapy.
To evaluate the risk of opportunistic infections (OIs) in patients with rheumatoid arthritis (RA) treated with tofacitinib. Phase II, III and long-term extension clinical trial data (April 2013 data-cut) from the tofacitinib RA programme were reviewed. OIs defined a priori included mycobacterial and fungal infections, multidermatomal herpes zoster and other viral infections associated with immunosuppression. For OIs, we calculated crude incidence rates (IRs; per 100 patient-years (95% CI)); for tuberculosis (TB) specifically, we calculated rates stratified by patient enrolment region according to background TB IR (per 100 patient-years): low (≤0.01), medium (>0.01 to ≤0.05) and high (>0.05). We identified 60 OIs among 5671 subjects; all occurred among tofacitinib-treated patients. TB (crude IR 0.21, 95% CI of (0.14 to 0.30)) was the most common OI (n=26); median time between drug start and diagnosis was 64 weeks (range 15-161 weeks). Twenty-one cases (81%) occurred in countries with high background TB IR, and the rate varied with regional background TB IR: low 0.02 (0.003 to 0.15), medium 0.08 (0.03 to 0.21) and high 0.75 (0.49 to 1.15). In Phase III studies, 263 patients diagnosed with latent TB infection were treated with isoniazid and tofacitinib concurrently; none developed TB. For OIs other than TB, 34 events were reported (crude IR 0.25 (95% CI 0.18 to 0.36)). Within the global tofacitinib RA development programme, TB was the most common OI reported but was rare in regions of low and medium TB incidence. Patients who screen positive for latent TB can be treated with isoniazid during tofacitinib therapy.
Author Mortensen, E
Valdez, H
Winthrop, K L
Gomez-Reino, J J
Gul, A
Tanaka, Y
Riese, R
Lukic, T
Cardiel, M H
Ponce de Leon, D
Park, S-H
Kwok, K
AuthorAffiliation 3 Istanbul Faculty of Medicine , Istanbul University , Istanbul , Turkey
5 Hospital Clínico Universitario de Santiago , Santiago de Compostela , Spain
7 Pfizer Inc , New York, New York , USA
2 Division of Rheumatology, Department of Internal Medicine , Seoul St. Mary's Hospital, The Catholic University of Korea , Seoul , South Korea
6 University of Occupational and Environmental Health , Kitakyushu , Japan
9 Pfizer Inc , Lima , Peru
4 Centro de Investigación Clínica de Morelia SC , Morelia , Mexico
1 Oregon Health and Science University , Portland, Oregon , USA
8 Pfizer Inc , Collegeville , Pennsylvania, USA
10 Pfizer Inc , Groton , Connecticut, USA
AuthorAffiliation_xml – name: 5 Hospital Clínico Universitario de Santiago , Santiago de Compostela , Spain
– name: 2 Division of Rheumatology, Department of Internal Medicine , Seoul St. Mary's Hospital, The Catholic University of Korea , Seoul , South Korea
– name: 9 Pfizer Inc , Lima , Peru
– name: 3 Istanbul Faculty of Medicine , Istanbul University , Istanbul , Turkey
– name: 7 Pfizer Inc , New York, New York , USA
– name: 6 University of Occupational and Environmental Health , Kitakyushu , Japan
– name: 4 Centro de Investigación Clínica de Morelia SC , Morelia , Mexico
– name: 8 Pfizer Inc , Collegeville , Pennsylvania, USA
– name: 1 Oregon Health and Science University , Portland, Oregon , USA
– name: 10 Pfizer Inc , Groton , Connecticut, USA
Author_xml – sequence: 1
  givenname: K L
  surname: Winthrop
  fullname: Winthrop, K L
  email: Winthrop@ohsu.edu
  organization: Oregon Health and Science University, Portland, Oregon, USA
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  givenname: S-H
  surname: Park
  fullname: Park, S-H
  email: Winthrop@ohsu.edu
  organization: Division of Rheumatology, Department of Internal Medicine, Seoul St. Mary's Hospital, The Catholic University of Korea, Seoul, South Korea
– sequence: 3
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  surname: Gul
  fullname: Gul, A
  email: Winthrop@ohsu.edu
  organization: Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey
– sequence: 4
  givenname: M H
  orcidid: 0000-0002-2731-9180
  surname: Cardiel
  fullname: Cardiel, M H
  email: Winthrop@ohsu.edu
  organization: Centro de Investigación Clínica de Morelia SC, Morelia, Mexico
– sequence: 5
  givenname: J J
  surname: Gomez-Reino
  fullname: Gomez-Reino, J J
  email: Winthrop@ohsu.edu
  organization: Hospital Clínico Universitario de Santiago, Santiago de Compostela, Spain
– sequence: 6
  givenname: Y
  surname: Tanaka
  fullname: Tanaka, Y
  email: Winthrop@ohsu.edu
  organization: University of Occupational and Environmental Health, Kitakyushu, Japan
– sequence: 7
  givenname: K
  surname: Kwok
  fullname: Kwok, K
  email: Winthrop@ohsu.edu
  organization: Pfizer Inc, New York, New York, USA
– sequence: 8
  givenname: T
  surname: Lukic
  fullname: Lukic, T
  email: Winthrop@ohsu.edu
  organization: Pfizer Inc, New York, New York, USA
– sequence: 9
  givenname: E
  surname: Mortensen
  fullname: Mortensen, E
  email: Winthrop@ohsu.edu
  organization: Pfizer Inc, Collegeville, Pennsylvania, USA
– sequence: 10
  givenname: D
  surname: Ponce de Leon
  fullname: Ponce de Leon, D
  email: Winthrop@ohsu.edu
  organization: Pfizer Inc, Lima, Peru
– sequence: 11
  givenname: R
  surname: Riese
  fullname: Riese, R
  email: Winthrop@ohsu.edu
  organization: Pfizer Inc, Groton, Connecticut, USA
– sequence: 12
  givenname: H
  surname: Valdez
  fullname: Valdez, H
  email: Winthrop@ohsu.edu
  organization: Pfizer Inc, New York, New York, USA
BackLink https://www.ncbi.nlm.nih.gov/pubmed/26318385$$D View this record in MEDLINE/PubMed
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Issue 6
Keywords DMARDs (synthetic)
Infections
Treatment
Tuberculosis
Rheumatoid Arthritis
Language English
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Snippet ObjectivesTo evaluate the risk of opportunistic infections (OIs) in patients with rheumatoid arthritis (RA) treated with tofacitinib.MethodsPhase II, III and...
To evaluate the risk of opportunistic infections (OIs) in patients with rheumatoid arthritis (RA) treated with tofacitinib. Phase II, III and long-term...
Objectives To evaluate the risk of opportunistic infections (OIs) in patients with rheumatoid arthritis (RA) treated with tofacitinib. Methods Phase II, III...
To evaluate the risk of opportunistic infections (OIs) in patients with rheumatoid arthritis (RA) treated with tofacitinib.OBJECTIVESTo evaluate the risk of...
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SubjectTerms Antirheumatic Agents - adverse effects
Antirheumatic Agents - therapeutic use
Arthritis, Rheumatoid - drug therapy
Arthritis, Rheumatoid - epidemiology
Arthritis, Rheumatoid - immunology
Clinical and Epidemiological Research
Clinical Trials as Topic
Cytomegalovirus
Herpes viruses
Humans
Immunocompromised Host
Immunosuppressive Agents - adverse effects
Immunosuppressive Agents - therapeutic use
Incidence
Infections
Janus Kinase 3 - antagonists & inhibitors
Kinases
Opportunistic Infections - chemically induced
Opportunistic Infections - epidemiology
Opportunistic Infections - immunology
Patients
Piperidines - adverse effects
Piperidines - therapeutic use
Pneumonia
Protein Kinase Inhibitors - adverse effects
Protein Kinase Inhibitors - therapeutic use
Pyrimidines - adverse effects
Pyrimidines - therapeutic use
Pyrroles - adverse effects
Pyrroles - therapeutic use
Regions
Rheumatoid arthritis
Risk Assessment
Steroids
Tuberculosis
Tuberculosis - chemically induced
Tuberculosis - epidemiology
Tuberculosis - immunology
Tumor necrosis factor-TNF
Viral infections
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Title Tuberculosis and other opportunistic infections in tofacitinib-treated patients with rheumatoid arthritis
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