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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Medical History, Lifestyle, Family History, and Occupational Risk Factors for Mantle Cell Lymphoma: The InterLymph Non-Hodgkin Lymphoma Subtypes Project</title><author><name sortKey="Smedby, Karin E" sort="Smedby, Karin E" uniqKey="Smedby K" first="Karin E." last="Smedby">Karin E. Smedby</name></author><author><name sortKey="Sampson, Joshua N" sort="Sampson, Joshua N" uniqKey="Sampson J" first="Joshua N." last="Sampson">Joshua N. Sampson</name></author><author><name sortKey="Turner, Jennifer J" sort="Turner, Jennifer J" uniqKey="Turner J" first="Jennifer J." last="Turner">Jennifer J. Turner</name></author><author><name sortKey="Slager, Susan L" sort="Slager, Susan L" uniqKey="Slager S" first="Susan L." last="Slager">Susan L. Slager</name></author><author><name sortKey="Maynadie, Marc" sort="Maynadie, Marc" uniqKey="Maynadie M" first="Marc" last="Maynadié">Marc Maynadié</name></author><author><name sortKey="Roman, Eve" sort="Roman, Eve" uniqKey="Roman E" first="Eve" last="Roman">Eve Roman</name></author><author><name sortKey="Habermann, Thomas M" sort="Habermann, Thomas M" uniqKey="Habermann T" first="Thomas M." last="Habermann">Thomas M. Habermann</name></author><author><name sortKey="Flowers, Christopher R" sort="Flowers, Christopher R" uniqKey="Flowers C" first="Christopher R." last="Flowers">Christopher R. Flowers</name></author><author><name sortKey="Berndt, Sonja I" sort="Berndt, Sonja I" uniqKey="Berndt S" first="Sonja I." last="Berndt">Sonja I. Berndt</name></author><author><name sortKey="Bracci, Paige M" sort="Bracci, Paige M" uniqKey="Bracci P" first="Paige M." last="Bracci">Paige M. Bracci</name></author><author><name sortKey="Hjalgrim, Henrik" sort="Hjalgrim, Henrik" uniqKey="Hjalgrim H" first="Henrik" last="Hjalgrim">Henrik Hjalgrim</name></author><author><name sortKey="Weisenburger, Dennis D" sort="Weisenburger, Dennis D" uniqKey="Weisenburger D" first="Dennis D." last="Weisenburger">Dennis D. Weisenburger</name></author><author><name sortKey="Morton, Lindsay M" sort="Morton, Lindsay M" uniqKey="Morton L" first="Lindsay M." last="Morton">Lindsay M. Morton</name></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">25174028</idno><idno type="pmc">4155462</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4155462</idno><idno type="RBID">PMC:4155462</idno><idno type="doi">10.1093/jncimonographs/lgu007</idno><date when="2014">2014</date><idno type="wicri:Area/Pmc/Corpus">001982</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">001982</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Medical History, Lifestyle, Family History, and Occupational Risk Factors for Mantle Cell Lymphoma: The InterLymph Non-Hodgkin Lymphoma Subtypes Project</title><author><name sortKey="Smedby, Karin E" sort="Smedby, Karin E" uniqKey="Smedby K" first="Karin E." last="Smedby">Karin E. Smedby</name></author><author><name sortKey="Sampson, Joshua N" sort="Sampson, Joshua N" uniqKey="Sampson J" first="Joshua N." last="Sampson">Joshua N. Sampson</name></author><author><name sortKey="Turner, Jennifer J" sort="Turner, Jennifer J" uniqKey="Turner J" first="Jennifer J." last="Turner">Jennifer J. Turner</name></author><author><name sortKey="Slager, Susan L" sort="Slager, Susan L" uniqKey="Slager S" first="Susan L." last="Slager">Susan L. Slager</name></author><author><name sortKey="Maynadie, Marc" sort="Maynadie, Marc" uniqKey="Maynadie M" first="Marc" last="Maynadié">Marc Maynadié</name></author><author><name sortKey="Roman, Eve" sort="Roman, Eve" uniqKey="Roman E" first="Eve" last="Roman">Eve Roman</name></author><author><name sortKey="Habermann, Thomas M" sort="Habermann, Thomas M" uniqKey="Habermann T" first="Thomas M." last="Habermann">Thomas M. Habermann</name></author><author><name sortKey="Flowers, Christopher R" sort="Flowers, Christopher R" uniqKey="Flowers C" first="Christopher R." last="Flowers">Christopher R. Flowers</name></author><author><name sortKey="Berndt, Sonja I" sort="Berndt, Sonja I" uniqKey="Berndt S" first="Sonja I." last="Berndt">Sonja I. Berndt</name></author><author><name sortKey="Bracci, Paige M" sort="Bracci, Paige M" uniqKey="Bracci P" first="Paige M." last="Bracci">Paige M. Bracci</name></author><author><name sortKey="Hjalgrim, Henrik" sort="Hjalgrim, Henrik" uniqKey="Hjalgrim H" first="Henrik" last="Hjalgrim">Henrik Hjalgrim</name></author><author><name sortKey="Weisenburger, Dennis D" sort="Weisenburger, Dennis D" uniqKey="Weisenburger D" first="Dennis D." last="Weisenburger">Dennis D. Weisenburger</name></author><author><name sortKey="Morton, Lindsay M" sort="Morton, Lindsay M" uniqKey="Morton L" first="Lindsay M." last="Morton">Lindsay M. Morton</name></author></analytic><series><title level="j">Journal of the National Cancer Institute. Monographs</title><idno type="ISSN">1052-6773</idno><idno type="eISSN">1745-6614</idno><imprint><date when="2014">2014</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><sec><title>Background</title><p>The etiology of mantle cell lymphoma (MCL), a distinctive subtype accounting for 2%–10% of all non-Hodgkin lymphoma, is not known.</p></sec><sec sec-type="methods"><title>Methods</title><p>We investigated associations with self-reported medical history, lifestyle, family history, and occupational risk factors in a pooled analysis of 557 patients with MCL and 13766 controls from 13 case–control studies in Europe, North America, and Australia. Odds ratios (ORs) and 95% confidence intervals (CIs) associated with each exposure were examined using multivariate logistic regression models.</p></sec><sec><title>Results</title><p>The median age of the MCL patients was 62 years and 76% were men. Risk of MCL was inversely associated with history of hay fever (OR = 0.63, 95% CI = 0.48 to 0.82), and the association was independent of other atopic diseases and allergies. A hematological malignancy among first-degree relatives was associated with a twofold increased risk of MCL (OR = 1.99, 95% CI = 1.39 to 2.84), which was stronger in men (OR = 2.21, 95% CI = 1.44 to 3.38) than women (OR = 1.61, 95% CI = 0.82 to 3.19). A modestly increased risk of MCL was also observed in association with ever having lived on a farm (OR = 1.40, 95% CI = 1.03 to 1.90). Unlike some other non-Hodgkin lymphoma subtypes, MCL risk was not statistically significantly associated with autoimmune disorders, tobacco smoking, alcohol intake, body mass index, or ultraviolet radiation.</p></sec><sec><title>Conclusions</title><p>The novel observations of a possible role for atopy and allergy and farm life in risk of MCL, together with confirmatory evidence of a familial link, suggest a multifactorial etiology of immune-related environmental exposures and genetic susceptibility. These findings provide guidance for future research in MCL etiology.</p></sec></div></front></TEI><pmc article-type="research-article"><pmc-comment>The publisher of this article does not allow downloading of the full text in XML form.</pmc-comment>
<front><journal-meta><journal-id journal-id-type="nlm-ta">J Natl Cancer Inst Monogr</journal-id><journal-id journal-id-type="iso-abbrev">J. Natl. Cancer Inst. Monographs</journal-id><journal-id journal-id-type="hwp">jncimono</journal-id><journal-id journal-id-type="publisher-id">jncmon</journal-id><journal-title-group><journal-title>Journal of the National Cancer Institute. Monographs</journal-title></journal-title-group><issn pub-type="ppub">1052-6773</issn><issn pub-type="epub">1745-6614</issn><publisher><publisher-name>Oxford University Press</publisher-name><publisher-loc>US</publisher-loc></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">25174028</article-id><article-id pub-id-type="pmc">4155462</article-id><article-id pub-id-type="doi">10.1093/jncimonographs/lgu007</article-id><article-categories><subj-group subj-group-type="heading"><subject>Article</subject></subj-group></article-categories><title-group><article-title>Medical History, Lifestyle, Family History, and Occupational Risk Factors for Mantle Cell Lymphoma: The InterLymph Non-Hodgkin Lymphoma Subtypes Project</article-title></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name><surname>Smedby</surname><given-names>Karin E.</given-names></name></contrib><contrib contrib-type="author"><name><surname>Sampson</surname><given-names>Joshua N.</given-names></name></contrib><contrib contrib-type="author"><name><surname>Turner</surname><given-names>Jennifer J.</given-names></name></contrib><contrib contrib-type="author"><name><surname>Slager</surname><given-names>Susan L.</given-names></name></contrib><contrib contrib-type="author"><name><surname>Maynadié</surname><given-names>Marc</given-names></name></contrib><contrib contrib-type="author"><name><surname>Roman</surname><given-names>Eve</given-names></name></contrib><contrib contrib-type="author"><name><surname>Habermann</surname><given-names>Thomas M.</given-names></name></contrib><contrib contrib-type="author"><name><surname>Flowers</surname><given-names>Christopher R.</given-names></name></contrib><contrib contrib-type="author"><name><surname>Berndt</surname><given-names>Sonja I.</given-names></name></contrib><contrib contrib-type="author"><name><surname>Bracci</surname><given-names>Paige M.</given-names></name></contrib><contrib contrib-type="author"><name><surname>Hjalgrim</surname><given-names>Henrik</given-names></name></contrib><contrib contrib-type="author"><name><surname>Weisenburger</surname><given-names>Dennis D.</given-names></name></contrib><contrib contrib-type="author"><name><surname>Morton</surname><given-names>Lindsay M.</given-names></name></contrib><aff id="AF0001"><bold>Affiliations of authors:</bold><institution>Unit of Clinical Epidemiology, Department of Medicine Solna, Karolinska Institutet, Karolinska University Hospital</institution>,<addr-line>Stockholm</addr-line>,<country>Sweden</country> (KES);<institution>Division of Cancer Epidemiology and Genetics, National Cancer Institute</institution>,<addr-line>National Institutes of Health, Bethesda, MD</addr-line> (JNS, SIB, LMM);<institution>Department of Histopathology, Douglass Hanly Moir Pathology, Macquarie Park</institution>, Australia The Australian, School of Advanced Medicine, Macquarie University, Sydney, Australia (JJT);<institution>Department of Health Sciences Research, Mayo Clinic</institution>,<addr-line>Rochester, MN</addr-line> (SLS, TMH);<institution>Biological Hematology Unit; CRB Ferdinand Cabanne, University Hospital of Dijon, Dijon, France, EA4184, University of Burgundy</institution>,<addr-line>Dijon</addr-line>,<country>France</country> (MM);<institution>Epidemiology and Cancer Statistics Group, Department of Health Sciences, University of York</institution>,<addr-line>York</addr-line>,<country>UK</country> (ER);<institution>Winship Cancer Institute, Emory University</institution>,<addr-line>Atlanta, GA</addr-line> (CRF);<institution>Department of Epidemiology and Biostatistics, University of California San Francisco</institution>,<addr-line>San Francisco, CA</addr-line> (PMB);<institution>Department of Epidemiology Research, Statens Serum Institut</institution>,<addr-line>Copenhagen</addr-line>,<country>Denmark</country> (HH);<institution>Department of Pathology, City of Hope National Medical Center</institution>,<addr-line>Duarte, CA</addr-line> (DDW).</aff></contrib-group><author-notes><corresp id="c1"><bold>Correspondence to:</bold> Karin E. Smedby, MD, PhD, Unit of Clinical Epidemiology, Department of Medicine, Solna, Karolinska Institutet, Karolinska University Hospital, Stockholm SE-171 76, Sweden (e-mail: <email>karin.ekstrom.smedby@ki.se</email>).</corresp></author-notes><pub-date pub-type="ppub"><month>8</month><year>2014</year></pub-date><pub-date pub-type="epub"><day>30</day><month>8</month><year>2014</year></pub-date><pub-date pub-type="pmc-release"><day>1</day><month>8</month><year>2015</year></pub-date><pmc-comment> PMC Release delay is 12 months and 0 days and was based on the
<volume>2014</volume><issue>48</issue><fpage>76</fpage><lpage>86</lpage><permissions><copyright-statement>Published by Oxford University Press 2014.</copyright-statement><copyright-year>2014</copyright-year></permissions><abstract><sec><title>Background</title><p>The etiology of mantle cell lymphoma (MCL), a distinctive subtype accounting for 2%–10% of all non-Hodgkin lymphoma, is not known.</p></sec><sec sec-type="methods"><title>Methods</title><p>We investigated associations with self-reported medical history, lifestyle, family history, and occupational risk factors in a pooled analysis of 557 patients with MCL and 13766 controls from 13 case–control studies in Europe, North America, and Australia. Odds ratios (ORs) and 95% confidence intervals (CIs) associated with each exposure were examined using multivariate logistic regression models.</p></sec><sec><title>Results</title><p>The median age of the MCL patients was 62 years and 76% were men. Risk of MCL was inversely associated with history of hay fever (OR = 0.63, 95% CI = 0.48 to 0.82), and the association was independent of other atopic diseases and allergies. A hematological malignancy among first-degree relatives was associated with a twofold increased risk of MCL (OR = 1.99, 95% CI = 1.39 to 2.84), which was stronger in men (OR = 2.21, 95% CI = 1.44 to 3.38) than women (OR = 1.61, 95% CI = 0.82 to 3.19). A modestly increased risk of MCL was also observed in association with ever having lived on a farm (OR = 1.40, 95% CI = 1.03 to 1.90). Unlike some other non-Hodgkin lymphoma subtypes, MCL risk was not statistically significantly associated with autoimmune disorders, tobacco smoking, alcohol intake, body mass index, or ultraviolet radiation.</p></sec><sec><title>Conclusions</title><p>The novel observations of a possible role for atopy and allergy and farm life in risk of MCL, together with confirmatory evidence of a familial link, suggest a multifactorial etiology of immune-related environmental exposures and genetic susceptibility. These findings provide guidance for future research in MCL etiology.</p></sec></abstract><counts><page-count count="11"></page-count></counts></article-meta></front></pmc></record>Pour manipuler ce document sous Unix (Dilib)
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