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

Identifieur interne : 000105 ( Main/Exploration ); précédent : 000104; suivant : 000106

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

Auteurs : K L Winthrop [États-Unis] ; S-H Park [Corée du Sud] ; A. Gul [Turquie] ; M H Cardiel [Mexique] ; J J Gomez-Reino [Espagne] ; Y. Tanaka [Japon] ; K. Kwok [États-Unis] ; T. Lukic [États-Unis] ; E. Mortensen [États-Unis] ; D. Ponce De Leon [Pérou] ; R. Riese [États-Unis] ; H. Valdez [États-Unis]

Source :

RBID : PMC:4893093

Abstract

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 (≤0.01), medium (>0.01 to ≤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.


Url:
DOI: 10.1136/annrheumdis-2015-207319
PubMed: 26318385
PubMed Central: 4893093


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<addr-line>Collegeville</addr-line>
, Pennsylvania,
<country>USA</country>
</nlm:aff>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea># see nlm:aff country strict</wicri:regionArea>
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<name sortKey="Ponce De Leon, D" sort="Ponce De Leon, D" uniqKey="Ponce De Leon D" first="D" last="Ponce De Leon">D. Ponce De Leon</name>
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,
<addr-line>Lima</addr-line>
,
<country>Peru</country>
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<country xml:lang="fr">Pérou</country>
<wicri:regionArea># see nlm:aff country strict</wicri:regionArea>
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<institution>Pfizer Inc</institution>
,
<addr-line>Groton</addr-line>
, Connecticut,
<country>USA</country>
</nlm:aff>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea># see nlm:aff country strict</wicri:regionArea>
</affiliation>
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<name sortKey="Valdez, H" sort="Valdez, H" uniqKey="Valdez H" first="H" last="Valdez">H. Valdez</name>
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<addr-line>New York, New York</addr-line>
,
<country>USA</country>
</nlm:aff>
<country xml:lang="fr">États-Unis</country>
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<div type="abstract" xml:lang="en">
<sec>
<title>Objectives</title>
<p>To evaluate the risk of opportunistic infections (OIs) in patients with rheumatoid arthritis (RA) treated with tofacitinib.</p>
</sec>
<sec>
<title>Methods</title>
<p>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).</p>
</sec>
<sec>
<title>Results</title>
<p>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)).</p>
</sec>
<sec>
<title>Conclusions</title>
<p>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.</p>
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<li>Corée du Sud</li>
<li>Espagne</li>
<li>Japon</li>
<li>Mexique</li>
<li>Pérou</li>
<li>Turquie</li>
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