TY - JOUR
T1 - Smoking is the most significant modifiable lung cancer risk factor in systemic lupus erythematosus
AU - Bernatsky, Sasha
AU - Ramsey-Goldman, Rosalind
AU - Petri, Michelle
AU - Urowitz, Murray B.
AU - Gladman, Dafna D.
AU - Fortin, Paul R.
AU - Yelin, Edward H.
AU - Ginzler, Ellen
AU - Hanly, John G.
AU - Peschken, Christine
AU - Gordon, Caroline
AU - Nived, Ola
AU - Aranow, Cynthia
AU - Bae, Sang Cheol
AU - Isenberg, David
AU - Rahman, Anisur
AU - Hansen, James E.
AU - Pierre, Yvan St
AU - Clarke, Ann E.
N1 - Publisher Copyright:
Copyright © 2018 The Journal of Rheumatology. All rights reserved.
PY - 2018/3/1
Y1 - 2018/3/1
N2 - Objective. To assess lung cancer risk in systemic lupus erythematosus (SLE), relative to demographics, drug exposures, smoking, and disease activity. Methods.We analyzed data from 14 SLE cohorts. We calculated adjusted HR estimates for lung cancer in SLE, relative to demographics, smoking, time-dependent medication exposures, and cumulative disease activity [mean adjusted SLE Disease Activity Index (SLEDAI) scores]. This project was approved by the ethics boards of all participating institutions, including the Institutional Review Board of the McGill University Health Centre. The ethics approval number for the Cancer Risk study is GEN-06-031. Results. Within these 14 SLE cohorts, 49 incident lung cancers occurred. Among lung cancer cases, 59.0% were in the highest SLEDAI quartile at baseline versus 40.8% of lung cancer-free SLE controls. The vast majority (84.2%) of SLE lung cancer cases were ever-smokers at baseline, versus 40.1% of those without lung cancer. In adjusted models, the principal factors associated with lung cancer were ever smoking (at cohort entry) and current age. Estimated adjusted effects of all drugs were relatively imprecise, but did not point toward any drug exposures as strong lung cancer risk factors. Conclusion. We saw no clear evidence for drugs as a trigger for lung cancer risk in SLE, although drug risk estimates were relatively imprecise. Smoking may be the most significant modifiable lung cancer risk factor in SLE.
AB - Objective. To assess lung cancer risk in systemic lupus erythematosus (SLE), relative to demographics, drug exposures, smoking, and disease activity. Methods.We analyzed data from 14 SLE cohorts. We calculated adjusted HR estimates for lung cancer in SLE, relative to demographics, smoking, time-dependent medication exposures, and cumulative disease activity [mean adjusted SLE Disease Activity Index (SLEDAI) scores]. This project was approved by the ethics boards of all participating institutions, including the Institutional Review Board of the McGill University Health Centre. The ethics approval number for the Cancer Risk study is GEN-06-031. Results. Within these 14 SLE cohorts, 49 incident lung cancers occurred. Among lung cancer cases, 59.0% were in the highest SLEDAI quartile at baseline versus 40.8% of lung cancer-free SLE controls. The vast majority (84.2%) of SLE lung cancer cases were ever-smokers at baseline, versus 40.1% of those without lung cancer. In adjusted models, the principal factors associated with lung cancer were ever smoking (at cohort entry) and current age. Estimated adjusted effects of all drugs were relatively imprecise, but did not point toward any drug exposures as strong lung cancer risk factors. Conclusion. We saw no clear evidence for drugs as a trigger for lung cancer risk in SLE, although drug risk estimates were relatively imprecise. Smoking may be the most significant modifiable lung cancer risk factor in SLE.
KW - Lung cancer
KW - Systemic lupus erythematosus
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U2 - 10.3899/jrheum.170652
DO - 10.3899/jrheum.170652
M3 - Article
C2 - 29335347
AN - SCOPUS:85042724497
SN - 0315-162X
VL - 45
SP - 393
EP - 396
JO - Journal of Rheumatology
JF - Journal of Rheumatology
IS - 3
ER -