Clinical expression of leflunomide-induced pneumonitis

被引:58
作者
Chikura, Batsi [1 ]
Lane, Steven [2 ]
Dawson, Julie K. [3 ]
机构
[1] Royal Liverpool Univ Hosp, Liverpool L7 8XP, Merseyside, England
[2] Univ Liverpool, Dept Biostat, Liverpool L69 3BX, Merseyside, England
[3] St Helens Hosp, St Helens, England
关键词
Leflunomide-induced pneumonitis; Hypersensitivity pneumonitis; Interstitial lung disease; Delayed hypersensitivity; INTERSTITIAL LUNG-DISEASE; RHEUMATOID-ARTHRITIS; RISK-FACTORS; METHOTREXATE; THERAPY; DRUG; IMMUNOSUPPRESSION; TOXICITY; EFFICACY; INJURY;
D O I
10.1093/rheumatology/kep050
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives. To review all the current evidence of LEF-induced pneumonitis (LEIP) which will help rheumatologists recognize suspected cases of LEIP and to influence clinical guidelines. Methods. Thirty-two reported cases of LEIP (13 males and 19 females) were identified from a literature search and classified using Searles and McKendry's classification criteria. Their clinical characteristics were reviewed. Results. All patients had a history of either exposure to MTX or interstitial lung disease (ILD) or both and all patients had RA. Most patients (82%) had LEIP within the first 20 weeks of initiation of LEF. All patients who had a loading dose LEF and most patients with ILD developed LEIP early (within 12 weeks of exposure). Case mortality was 19%. Two patients had previous MTX-induced pneumonitis (MTX-P) prior to initiation of LEF; both died from LEIP. There was a high mortality in the following groups of patients: diffuse alveolar damage (DAD) on histological examination, pre-existing ILD and ground glass shadowing on high resolution computerised tomography (HRCT). Treatment with cholestyramine did not appear to alter clinical outcome. Conclusions. LEIP usually occurs within the first 20 weeks of initiation of LEF. Clinical features of patients who died were pre-existing ILD, ground glass shadowing on HRCT and DAD on histological examination, and these could be poor prognostic indicators. Patients need to be made aware of this rare complication. LEF should not be used in patients with previous MTX-P and should be used with caution in patients with ILD.
引用
收藏
页码:1065 / 1068
页数:4
相关论文
共 38 条
[1]  
Balakrishnan C, 2007, RHEUMATOLOGY, V46, P372, DOI 10.1093/rheumatology/kel373
[2]  
Bartram SA, 1998, ARTHRITIS RHEUM, V41, P1327, DOI 10.1002/1529-0131(199807)41:7<1327::AID-ART30>3.0.CO
[3]  
2-T
[4]  
Baughman RP, 2004, SARCOIDOSIS VASC DIF, V21, P43
[5]   Leflunomide as adjuvant treatment of dermatomyositis [J].
Boswell, J. Scott ;
Costner, Melissa I. .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2008, 58 (03) :403-406
[6]   PULMONARY-DISEASE DURING THE TREATMENT OF RHEUMATOID-ARTHRITIS WITH LOW-DOSE PULSE METHOTREXATE [J].
CARSON, CW ;
CANNON, GW ;
EGGER, MJ ;
WARD, JR ;
CLEGG, DO .
SEMINARS IN ARTHRITIS AND RHEUMATISM, 1987, 16 (03) :186-195
[7]   BSR/BHPR guideline for disease-modifying anti-rheumatic drug (DMARD) therapy in consultation with the British Association of Dermatologists [J].
Chakravarty, K. ;
McDonald, H. ;
Pullar, T. ;
Taggart, A. ;
Chalmers, R. ;
Oliver, S. ;
Mooney, J. ;
Somerville, M. ;
Bosworth, A. ;
Kennedy, T. .
RHEUMATOLOGY, 2008, 47 (06) :924-925
[8]   Variation of immunological response in methotrexate-induced pneumonitis [J].
Chikura, B. ;
Sathi, N. ;
Lane, S. ;
Dawson, J. K. .
RHEUMATOLOGY, 2008, 47 (11) :1647-1650
[9]   In vivo activity of leflunomide - Pharmacokinetic analyses and mechanism of immunosuppression [J].
Chong, ASF ;
Huang, W ;
Liu, W ;
Luo, JL ;
Shen, JK ;
Xu, W ;
Ma, LL ;
Blinder, L ;
Xiao, F ;
Xu, XL ;
Clardy, C ;
Foster, P ;
Williams, JA .
TRANSPLANTATION, 1999, 68 (01) :100-109
[10]  
Cohen S, 2001, ARTHRITIS RHEUM-US, V44, P1984, DOI 10.1002/1529-0131(200109)44:9<1984::AID-ART346>3.0.CO