Lung cancer in systemic lupus erythematosus

J. Bin, S. Bernatsky*, C. Gordon, J. F. Boivin, E. Ginzler, D. Gladman, P. R. Fortin, M. Urowitz, S. Manzi, D. Isenberg, A. Rahman, M. Petri, O. Nived, G. Sturfeldt, R. Ramsey-Goldman, A. E. Clarke

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

51 Scopus citations

Abstract

Background: Evidence points to a link between systemic lupus erythematosus (SLE) and an increased risk of lung cancer. Our objective was to provide a brief report of the lung cancer cases from an SLE cohort, with respect to demographics, histology, and exposures to smoking and immunosuppressive medications. Methods: Data were obtained from a multi-site international cohort study of over 9500 SLE patients from 23 centres. Cancer cases were ascertained through linkage with regional tumor registries. Results: We analyzed information on histology subtype for 30 lung cancer cases that had occurred across five countries. Most (75%) of these 30 cases were female, with a median age of 61 (range 27-91) years. In eight cases, the histological type was not specified. In the remainder, the most common histological type reported was adenocarcinoma (N = 8; two of the adenocarcinomas were bronchoalveolar carcinoma) followed by small cell carcinoma (N = 6), and squamous cell carcinoma (N = 6) with one case each of large cell carcinoma and carcinoid tumor. Most (71%) of the lung cancer cases were smokers; only the minority (20%) had been previously exposed to immunosuppressive agents. Conclusions: The histological distribution of the lung cancers from the SLE sample appeared similar to that of lung cancer patients in the general population, though the possibility of a higher proportion of more uncommon tumors (such as bronchoalveolar and carcinoid) cannot be excluded. A large proportion of the cancer cases were smokers, which is also not surprising. However, only a minority appeared to have been exposed to immunosuppressive agents. A large case-cohort study currently in progress should help shed light on the relative importance of these exposures in lung cancer risk for SLE patients.

Original languageEnglish (US)
Pages (from-to)303-306
Number of pages4
JournalLung Cancer
Volume56
Issue number3
DOIs
StatePublished - Jun 2007

Funding

Support: S. Bernatsky: Canadian Institutes of Health Research [CIHR] Junior Investigator Award; Fonds de la Recherche en Santé du Québec (FRSQ); Lupus Canada Fellowship; Canadian Arthritis Network Scholar Award. C. Gordon: Financial support for the Birmingham UK lupus cohort was provided by Lupus UK and the Wellcome Trust Clinical Research Facility. P.R. Fortin: Arthritis Centre of Excellence University of Toronto, Arthritis & Autoimmunity Research Centre, University Health Network, Lupus Canada; Investigator Award The Arthritis Society (TAS)/CIHR. M. Petri: The Hopkins Lupus Cohort is supported by NIH AR437337 and the Johns Hopkins University Clinical Research Centre M01-RR00052. O. Nived and G. Sturfeldt: Swedish Medical Research Council #13489. R. Ramsey-Goldman: Arthritis Foundation, Clinical Science Grant, Arthritis Foundation Greater Chicago Chapter NIH RO-3 CA 110904, AR 02138, AR 48098; Lupus Foundation of Illinois Chapter Grant. A.E. Clarke: Singer Family Fund for Lupus Research; FRSQ National Scholar Award; TAS 99-105; CIHR MOP-57816, MOP-62817, MOP-74630; National Cancer Institute of Canada 013135.

Keywords

  • Lung cancer
  • SLE
  • Systemic lupus erythematosus

ASJC Scopus subject areas

  • Oncology
  • Pulmonary and Respiratory Medicine
  • Cancer Research

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