Pediatric, elderly, and emerging adult-onset peaks in Burkitt's lymphoma incidence diagnosed in four continents, excluding Africa
Burkitt's lymphoma (BL) in the general population and immunosuppressed persons with AIDS in the United States was characterized by three age‐specific incidence peaks near 10, 40, and 70 years. We hypothesized that BL from different geographical areas may exhibit pediatric, adult, and elderly ag...
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Published in: | American journal of hematology Vol. 87; no. 6; pp. 573 - 578 |
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Main Authors: | , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Hoboken
Wiley Subscription Services, Inc., A Wiley Company
01-06-2012
Wiley-Liss Wiley Subscription Services, Inc |
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Online Access: | Get full text |
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Summary: | Burkitt's lymphoma (BL) in the general population and immunosuppressed persons with AIDS in the United States was characterized by three age‐specific incidence peaks near 10, 40, and 70 years. We hypothesized that BL from different geographical areas may exhibit pediatric, adult, and elderly age incidence peaks. We investigated this hypothesis using data on 3,403 cases obtained from the International Agency for Research on Cancer (1963–2002). Data from Africa were sparse or incomplete, and thus were excluded. Age‐standardized rates (ASRs) and age‐specific incidence rates were calculated, supplemented with the calculations performed using age–period–cohort (APC) models. The ASR rose 5.3% (95% confidence interval [CI], 5.0–5.6) per year in males and 4.6% (95% CI, 4.5–4.8) in females. The ASR increased gradually in children, steeply in adults and most rapidly in the elderly both in males and in females. Overall, BL male/female ASR ratio was 2.5, but it declined from 3.1 (95% CI, 3.0–3.3) for pediatric BL to 2.3 (95% CI, 2.2–2.4) for adult BL and 1.5 (95% CI, 1.4–1.6) for elderly BL. Age‐specific incidence peaks occurred near 10 and 70 years in all regions and periods. A peak near 40 years of age emerged in the mid‐1990s, particularly in men. Findings using APC models confirmed those based on the standard analyses. Our findings, based on the international BL cases, support our hypothesis that BL is multimodal and that BL peaks at different ages may be clues to differences in the etiology and/or biology of BL at those ages. Am. J. Hematol. 87:573–578, 2012. © 2012 Wiley Periodicals, Inc. |
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Bibliography: | ark:/67375/WNG-5ZZL77FQ-2 Division of Cancer Epidemiology and Genetics Department of Health and Human Services ArticleID:AJH23187 National Cancer Institute istex:E623C22B9DFA45E4C422576EFB0E7B61BEFA4C63 Conflict of interest: Nothing to report National Institutes of Health ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 0361-8609 1096-8652 |
DOI: | 10.1002/ajh.23187 |