Haematopoietic malignancies in rheumatoid arthritis:: lymphoma risk and characteristics after exposure to tumour necrosis factor antagonists

被引:302
作者
Askling, J
Fored, CM
Baecklund, E
Brandt, L
Backlin, C
Ekbom, A
Sundström, C
Bertilsson, L
Cöster, L
Geborek, P
Jacobsson, LT
Lindblad, S
Lysholm, J
Rantapää-Dahlqvist, S
Saxne, T
Klareskog, L
Feltelius, N
机构
[1] Karolinska Univ Hosp, Clin Epidemiol Unit, Dept Med, Stockholm, Sweden
[2] Karolinska Univ Hosp, Rheumatol Unit, Dept Med, Stockholm, Sweden
[3] Univ Uppsala Hosp, Dept Rheumatol, Uppsala, Sweden
[4] Uppsala Univ, Rudbeck Lab, Dept Genet & Pathol, Uppsala, Sweden
[5] Sahlgrens Univ Hosp, Dept Rheumatol, Gothenburg, Sweden
[6] Linkoping Univ Hosp, Dept Rheumatol, S-58185 Linkoping, Sweden
[7] Univ Lund Hosp, Dept Rheumatol, S-22185 Lund, Sweden
[8] Malmo Univ Hosp, Dept Rheumatol, Malmo, Sweden
[9] Falu Cty Hosp, Dept Rheumatol, Falun, Sweden
[10] Univ Hosp, Dept Rheumatol, Umea, Sweden
[11] Med Prod Agcy, Uppsala, Sweden
关键词
D O I
10.1136/ard.2004.033241
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Patients with rheumatoid arthritis ( RA) are at increased risk of malignant lymphomas, and maybe also of leukaemia and multiple myeloma. The effect of tumour necrosis factor (TNF) antagonists on lymphoma risk and characteristics is unclear. Objective: To assess expected rates and relative risks of haematopoietic malignancies, especially those associated with TNF antagonists, in large population based cohorts of patients with RA. Methods: A population based cohort study was performed of patients with RA ( one prevalent cohort (n = 53 067), one incident cohort ( n = 3703), and one TNF antagonist treated cohort 1999 through 2003 ( n = 4160)), who were linked with the Swedish Cancer Register. Additionally, the lymphoma specimens for the 12 lymphomas occurring in patients with RA exposed to TNF antagonists in Sweden 1999 through 2004 were reviewed. Results: Study of almost 500 observed haematopoietic malignancies showed that prevalent and incident patients with RA were at increased risk of lymphoma ( SIR = 1.9 and 2.0, respectively) and leukaemia ( SIR = 2.1 and 2.2, respectively) but not of myeloma. Patients with RA treated with TNF antagonists had a tripled lymphoma risk ( SIR = 2.9) compared with the general population. After adjustment for sex, age, and disease duration, the lymphoma risk after exposure to TNF antagonists was no higher than in the other RA cohorts. Lymphomas associated with TNF antagonists had characteristics similar to those of other RA lymphomas. Conclusion: Overall, patients with RA are at equally increased risks for lymphomas and leukaemias. Patients with RA treated with TNF antagonists did not have higher lymphoma risks than other patients with RA. Prolonged observation is needed to determine the long term effects of TNF antagonists on lymphoma risk.
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页码:1414 / 1420
页数:7
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