TY - JOUR
T1 - Pneumocystis jirovecii pneumonia associated with etanercept treatment in patients with rheumatoid arthritis
T2 - A retrospective review of 15 cases and analysis of risk factors
AU - Tanaka, Michi
AU - Sakai, Ryoko
AU - Koike, Ryuji
AU - Komano, Yukiko
AU - Nanki, Toshihiro
AU - Sakai, Fumikazu
AU - Sugiyama, Haruhito
AU - Matsushima, Hidekazu
AU - Kojima, Toshihisa
AU - Ohta, Shuji
AU - Ishibe, Yoji
AU - Sawabe, Takuya
AU - Ota, Yasuhiro
AU - Ohishi, Kazuhisa
AU - Miyazato, Hajime
AU - Nonomura, Yoshinori
AU - Saito, Kazuyoshi
AU - Tanaka, Yoshiya
AU - Nagasawa, Hayato
AU - Takeuchi, Tsutomu
AU - Nakajima, Ayako
AU - Ohtsubo, Hideo
AU - Onishi, Makoto
AU - Goto, Yoshinori
AU - Dobashi, Hiroaki
AU - Miyasaka, Nobuyuki
AU - Harigai, Masayoshi
N1 - Funding Information:
interest for the other authors regarding this article. This work was supported by Grants-in-Aid for Scientific Research (KAKENHI) from the Japan Society for the Promotion of Science to R.K. (#19590530), M.H. (#20390158) and M.T. (#23590171), and by Grants-in-Aid from the Ministry of Health, Labour and Welfare, Japan (H19-meneki-ippan-009 to M.N. and M.H. and H22-meneki-ippann-001 to T.T. and M.H.). This work was also supported by the Global Center of Excellence (GCOE) program, ‘International Research Center for Molecular Science in Tooth and Bone Diseases’.
PY - 2012/11
Y1 - 2012/11
N2 - Objectives The association of anti-tumor necrosis factor therapy with opportunistic infections in rheumatoid arthritis (RA) patients has been reported. The goal of this study was to clarify the clinical characteristics and the risk factors of RA patients who developed Pneumocystis jirovecii pneumonia (PCP) during etanercept therapy. Methods We conducted a multicenter, case-control study in which 15 RA patients who developed PCP were compared with 74 RA patients who did not develop PCP during etanercept therapy. Results PCP developed within 26 weeks following the first injection of etanercept in 86.7% of the patients. All PCP patients presented with a rapid and severe clinical course and the overall mortality was 6.7%. Independent risk factors were identified using multivariate analysis and included age ≥65 years [hazard ratio (HR) 3.35, p = 0.037], coexisting lung disease (HR 4.48, p = 0.009), and concomitant methotrexate treatment (HR 4.68, p = 0.005). In patients having a larger number of risk factors, the cumulative probability of developing PCP was significantly higher (p<0.001 for patients with two or more risk factors vs. those with no risk factor, and p = 0.001 for patients with one risk factor vs. those with no risk factor). Conclusion Physicians must consider the possibility of PCP developing during etanercept therapy in RA patients, particularly if one or more risk factors are present.
AB - Objectives The association of anti-tumor necrosis factor therapy with opportunistic infections in rheumatoid arthritis (RA) patients has been reported. The goal of this study was to clarify the clinical characteristics and the risk factors of RA patients who developed Pneumocystis jirovecii pneumonia (PCP) during etanercept therapy. Methods We conducted a multicenter, case-control study in which 15 RA patients who developed PCP were compared with 74 RA patients who did not develop PCP during etanercept therapy. Results PCP developed within 26 weeks following the first injection of etanercept in 86.7% of the patients. All PCP patients presented with a rapid and severe clinical course and the overall mortality was 6.7%. Independent risk factors were identified using multivariate analysis and included age ≥65 years [hazard ratio (HR) 3.35, p = 0.037], coexisting lung disease (HR 4.48, p = 0.009), and concomitant methotrexate treatment (HR 4.68, p = 0.005). In patients having a larger number of risk factors, the cumulative probability of developing PCP was significantly higher (p<0.001 for patients with two or more risk factors vs. those with no risk factor, and p = 0.001 for patients with one risk factor vs. those with no risk factor). Conclusion Physicians must consider the possibility of PCP developing during etanercept therapy in RA patients, particularly if one or more risk factors are present.
KW - Anti-TNF therapy
KW - Etanercept
KW - Opportunistic infection
KW - Pneumocystis jirovecii pneumonia
KW - Rheumatoid arthritis
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U2 - 10.1007/s10165-012-0615-z
DO - 10.1007/s10165-012-0615-z
M3 - Review article
C2 - 22354637
AN - SCOPUS:84870319550
SN - 1439-7595
VL - 22
SP - 849
EP - 858
JO - Modern rheumatology
JF - Modern rheumatology
IS - 6
ER -