TY - JOUR
T1 - Leflunomide-induced interstitial lung disease
T2 - Prevalence and risk factors in Japanese patients with rheumatoid arthritis
AU - Sawada, Tetsuji
AU - Inokuma, Shigeko
AU - Sato, Takeo
AU - Otsuka, Takeshi
AU - Saeki, Yukihiko
AU - Takeuchi, Tsutomu
AU - Matsuda, Takemasa
AU - Takemura, Tamiko
AU - Sagawa, Akira
PY - 2009/9
Y1 - 2009/9
N2 - Objective: The possible link between LEF and interstitial lung disease (ILD) has evoked increasing concern. The aim of the present study was to elucidate the prevalence and risk factors for newly developed and/or exacerbated ILD, based on post-marketing surveillance data, in which all RA patients receiving LEF were pre-registered and monitored for 24 weeks in Japan. Methods: We analysed data from a cohort of 5054 RA patients who were prescribed LEF since its launch in September 2003 in Japan. Multivariable logistic analysis was performed to identify the risk factors for newly developed and/or exacerbation of ILD. Results: Sixty-one (1.2%) of 5054 RA patients who received LEF were reported to have development and/or exacerbation of ILD as an adverse drug reaction to LEF, judged by the attending physicians. Multivariable logistic regression analysis identified pre-existing ILD [odds ratio (OR) 8.17; 95% CI 4.63, 14.4], cigarette smoking (3.12; 95% CI 1.73, 5.60), a low body weight (<40 kg vs >50 kg) (2.91; 95% CI 1.15, 7.37) and the use of a loading dose (3.97; 95% CI 1.22, 12.9) as independent risk factors for LEF-induced ILD. Conclusions: Pre-existing ILD was the most important risk factor for LEF-induced ILD. We suggest that LEF should not be prescribed for RA patients complicated with ILD.
AB - Objective: The possible link between LEF and interstitial lung disease (ILD) has evoked increasing concern. The aim of the present study was to elucidate the prevalence and risk factors for newly developed and/or exacerbated ILD, based on post-marketing surveillance data, in which all RA patients receiving LEF were pre-registered and monitored for 24 weeks in Japan. Methods: We analysed data from a cohort of 5054 RA patients who were prescribed LEF since its launch in September 2003 in Japan. Multivariable logistic analysis was performed to identify the risk factors for newly developed and/or exacerbation of ILD. Results: Sixty-one (1.2%) of 5054 RA patients who received LEF were reported to have development and/or exacerbation of ILD as an adverse drug reaction to LEF, judged by the attending physicians. Multivariable logistic regression analysis identified pre-existing ILD [odds ratio (OR) 8.17; 95% CI 4.63, 14.4], cigarette smoking (3.12; 95% CI 1.73, 5.60), a low body weight (<40 kg vs >50 kg) (2.91; 95% CI 1.15, 7.37) and the use of a loading dose (3.97; 95% CI 1.22, 12.9) as independent risk factors for LEF-induced ILD. Conclusions: Pre-existing ILD was the most important risk factor for LEF-induced ILD. We suggest that LEF should not be prescribed for RA patients complicated with ILD.
KW - Adverse drug reaction
KW - Interstitial lung disease
KW - Leflunomide
KW - Loading dose
KW - Rheumatoid arthritis
KW - Risk factor
KW - Smoking
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U2 - 10.1093/rheumatology/kep052
DO - 10.1093/rheumatology/kep052
M3 - Article
C2 - 19321513
AN - SCOPUS:70349785354
SN - 1462-0324
VL - 48
SP - 1069
EP - 1072
JO - Rheumatology and Rehabilitation
JF - Rheumatology and Rehabilitation
IS - 9
ER -