4.7 Article

Cancer risk in systemic lupus: An updated international multi-centre cohort study

期刊

JOURNAL OF AUTOIMMUNITY
卷 42, 期 -, 页码 130-135

出版社

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.jaut.2012.12.009

关键词

Systemic lupus erythematosus; Epidemiology; Treatment; Disease activity

资金

  1. Canadian Institutes of Health Research/Arthritis Society [RG06/092]
  2. National Institutes of Health (NIH) [1R03CA128052-01]
  3. NIH/NIAMS [P60 2 AR30692, P60 AR053308, R01 5R01AR56476-9]
  4. NIH [R01 AR43727]
  5. Department of Education, Universities and Research of the Basque Government
  6. Singer Family Fund for Lupus Research
  7. Alliance for Lupus Research
  8. Kirkland Scholar Award
  9. Korea Healthcare technology R&D Project, Ministry for Health and Welfare, Republic of Korea [A120404]

向作者/读者索取更多资源

Objective: To update estimates of cancer risk in SLE relative to the general population. Methods: A multisite international SLE cohort was linked with regional tumor registries. Standardized incidence ratios (SIRs) were calculated as the ratio of observed to expected cancers. Results: Across 30 centres, 16,409 patients were observed for 121,283 (average 7.4) person years. In total, 644 cancers occurred. Some cancers, notably hematologic malignancies, were substantially increased (SIR 3.02, 95% confidence interval, CI, 2.48, 3.63), particularly non-Hodgkin's lymphoma, NHL (SIR 4.39, 95% CI 3.46, 5.49) and leukemia. In addition, increased risks of cancer of the vulva (SIR 3.78, 95% CI 1.52, 7.78), lung (SIR 1.30, 95% CI 1.04, 1.60), thyroid (SIR 1.76, 95% CI 1.13, 2.61) and possibly liver (SIR 1.87, 95% CI 0.97, 3.27) were suggested. However, a decreased risk was estimated for breast (SIR 0.73, 95% CI 0.61-0.88), endometrial (SIR 0.44, 95% CI 0.23-0.77), and possibly ovarian cancers (0.64, 95% Cl 0.34-1.10). The variability of comparative rates across different cancers meant that only a small increased risk was estimated across all cancers (SIR 1.14, 95% CI 1.05, 1.23). Conclusion: These data estimate only a small increased risk in SLE (versus the general population) for cancer over-all. However, there is clearly an increased risk of NHL and cancers of the vulva, lung, thyroid, and possibly liver. It remains unclear to what extent the association with NHL is mediated by innate versus exogenous factors. Similarly, the etiology of the decreased breast, endometrial, and possibly ovarian cancer risk is uncertain, though investigations are ongoing. (C) 2013 Elsevier Ltd. All rights reserved.

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