Non-Hodgkin's lymphoma in systemic lupus erythematosus

被引:90
作者
Bernatsky, S
Ramsey-Goldman, R
Rajan, R
Boivin, JF
Joseph, L
Lachance, S
Cournoyer, D
Zoma, A
Manzi, S
Ginzler, E
Urowitz, M
Gladman, D
Fortin, PR
Edworthy, S
Barr, S
Gordon, C
Bae, SC
Sibley, J
Steinsson, K
Nived, O
Sturfelt, G
St Pierre, Y
Clarke, A
机构
[1] Montreal Gen Hosp, Div Clin Epidemiol, Montreal, PQ H3G 1A4, Canada
[2] Northwestern Univ, Div Rheumatol, Chicago, IL 60611 USA
[3] Montreal Gen Hosp, Dept Oncol, Montreal, PQ H3G 1A4, Canada
[4] McGill Univ, Dept Epidemiol & Biostat, Montreal, PQ, Canada
[5] Univ Pittsburgh, Sch Med, Pittsburgh, PA USA
[6] Univ Pittsburgh, Grad Sch Publ Hlth, Pittsburgh, PA USA
[7] SUNY Downstate Med Ctr, Brooklyn, NY 11203 USA
[8] Univ Toronto, Univ Hlth Network, Toronto Western Div, Toronto, ON, Canada
[9] Univ Calgary, Calgary, AB, Canada
[10] Univ Birmingham, Dept Rheumatol, Birmingham, W Midlands, England
[11] Hanyang Univ, Hosp Rheumat Dis, Dept Internal Med, Div Rheumatol, Seoul 133791, South Korea
[12] Royal Univ Hosp, Dept Rheumatol, Saskatoon, SK S7N 0W8, Canada
[13] Univ Hosp, Landspitalinn, Dept Rheumatol, Reykjavik, Iceland
[14] Univ Hosp, Landspitalinn, Ctr Rheumatol Res, Reykjavik, Iceland
[15] Univ Lund Hosp, Dept Rheumatol, S-22185 Lund, Sweden
[16] Montreal Gen Hosp, Div Clin Immunol Allergy, Montreal, PQ H3G 1A4, Canada
关键词
D O I
10.1136/ard.2004.034504
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Recent evidence supports an association between systemic lupus erythematosus (SLE) and non-Hodgkin's lymphoma (NHL). Objectives: To describe demographic factors, subtypes, and survival of patients with SLE who develop NHL. Methods: A multi-site cohort of 9547 subjects with definite SLE was assembled. Subjects at each centre were linked to regional tumour registries to determine cancer cases occurring after SLE diagnosis. For the NHL cases ascertained, descriptive statistics were calculated, and NHL subtype frequency and median survival time of patients determined. Results: 42 cases of NHL occurred in the patients with SLE during the 76 948 patient-years of observation. The median age of patients at NHL diagnosis was 57 years. Thirty six (86%) of the 42 patients developing NHL were women, reflecting the female predominance of the cohort. In the patients, aggressive histological subtypes appeared to predominate, with the most commonly identified NHL subtype being diffuse large B cell ( 11 out of 21 cases for which histological subtype was available). Twenty two of the patients had died a median of 1.2 years after lymphoma diagnosis. Conclusions: These data suggest aggressive disease in patients with SLE who develop NHL. Continuing work should provide further insight into the patterns of presentation, prognosis, and aetiology of NHL in SLE.
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收藏
页码:1507 / 1509
页数:3
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