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Etiologic heterogeneity among non-Hodgkin lymphoma subtypes: the InterLymph Non-Hodgkin Lymphoma Subtypes Project.

Authors :
Morton LM
Slager SL
Cerhan JR
Wang SS
Vajdic CM
Skibola CF
Bracci PM
de Sanjosé S
Smedby KE
Chiu BC
Zhang Y
Mbulaiteye SM
Monnereau A
Turner JJ
Clavel J
Adami HO
Chang ET
Glimelius B
Hjalgrim H
Melbye M
Crosignani P
di Lollo S
Miligi L
Nanni O
Ramazzotti V
Rodella S
Costantini AS
Stagnaro E
Tumino R
Vindigni C
Vineis P
Becker N
Benavente Y
Boffetta P
Brennan P
Cocco P
Foretova L
Maynadié M
Nieters A
Staines A
Colt JS
Cozen W
Davis S
de Roos AJ
Hartge P
Rothman N
Severson RK
Holly EA
Call TG
Feldman AL
Habermann TM
Liebow M
Blair A
Cantor KP
Kane EV
Lightfoot T
Roman E
Smith A
Brooks-Wilson A
Connors JM
Gascoyne RD
Spinelli JJ
Armstrong BK
Kricker A
Holford TR
Lan Q
Zheng T
Orsi L
Dal Maso L
Franceschi S
La Vecchia C
Negri E
Serraino D
Bernstein L
Levine A
Friedberg JW
Kelly JL
Berndt SI
Birmann BM
Clarke CA
Flowers CR
Foran JM
Kadin ME
Paltiel O
Weisenburger DD
Linet MS
Sampson JN
Source :
Journal of the National Cancer Institute. Monographs [J Natl Cancer Inst Monogr] 2014 Aug; Vol. 2014 (48), pp. 130-44.
Publication Year :
2014

Abstract

Background: Non-Hodgkin lymphoma (NHL) comprises biologically and clinically heterogeneous subtypes. Previously, study size has limited the ability to compare and contrast the risk factor profiles among these heterogeneous subtypes.<br />Methods: We pooled individual-level data from 17 471 NHL cases and 23 096 controls in 20 case-control studies from the International Lymphoma Epidemiology Consortium (InterLymph). We estimated the associations, measured as odds ratios, between each of 11 NHL subtypes and self-reported medical history, family history of hematologic malignancy, lifestyle factors, and occupation. We then assessed the heterogeneity of associations by evaluating the variability (Q value) of the estimated odds ratios for a given exposure among subtypes. Finally, we organized the subtypes into a hierarchical tree to identify groups that had similar risk factor profiles. Statistical significance of tree partitions was estimated by permutation-based P values (P NODE).<br />Results: Risks differed statistically significantly among NHL subtypes for medical history factors (autoimmune diseases, hepatitis C virus seropositivity, eczema, and blood transfusion), family history of leukemia and multiple myeloma, alcohol consumption, cigarette smoking, and certain occupations, whereas generally homogeneous risks among subtypes were observed for family history of NHL, recreational sun exposure, hay fever, allergy, and socioeconomic status. Overall, the greatest difference in risk factors occurred between T-cell and B-cell lymphomas (P NODE < 1.0×10(-4)), with increased risks generally restricted to T-cell lymphomas for eczema, T-cell-activating autoimmune diseases, family history of multiple myeloma, and occupation as a painter. We further observed substantial heterogeneity among B-cell lymphomas (P NODE < 1.0×10(-4)). Increased risks for B-cell-activating autoimmune disease and hepatitis C virus seropositivity and decreased risks for alcohol consumption and occupation as a teacher generally were restricted to marginal zone lymphoma, Burkitt/Burkitt-like lymphoma/leukemia, diffuse large B-cell lymphoma, and/or lymphoplasmacytic lymphoma/Waldenström macroglobulinemia.<br />Conclusions: Using a novel approach to investigate etiologic heterogeneity among NHL subtypes, we identified risk factors that were common among subtypes as well as risk factors that appeared to be distinct among individual or a few subtypes, suggesting both subtype-specific and shared underlying mechanisms. Further research is needed to test putative mechanisms, investigate other risk factors (eg, other infections, environmental exposures, and diet), and evaluate potential joint effects with genetic susceptibility.<br /> (Published by Oxford University Press 2014.)

Details

Language :
English
ISSN :
1745-6614
Volume :
2014
Issue :
48
Database :
MEDLINE
Journal :
Journal of the National Cancer Institute. Monographs
Publication Type :
Academic Journal
Accession number :
25174034
Full Text :
https://doi.org/10.1093/jncimonographs/lgu013