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dc.contributor.authorHolmes, Michelle Den_US
dc.contributor.authorOlsson, Henriken_US
dc.contributor.authorPawitan, Yudien_US
dc.contributor.authorHolm, Johannaen_US
dc.contributor.authorLundholm, Ceciliaen_US
dc.contributor.authorAndersson, Therese M-Len_US
dc.contributor.authorAdami, Hans-Oloven_US
dc.contributor.authorAskling, Johanen_US
dc.contributor.authorSmedby, Karin Ekströmen_US
dc.date.accessioned2014-07-07T17:01:57Z
dc.date.issued2014en_US
dc.identifier.citationHolmes, Michelle D, Henrik Olsson, Yudi Pawitan, Johanna Holm, Cecilia Lundholm, Therese M-L Andersson, Hans-Olov Adami, Johan Askling, and Karin Ekström Smedby. 2014. “Aspirin intake and breast cancer survival – a nation-wide study using prospectively recorded data in Sweden.” BMC Cancer 14 (1): 391. doi:10.1186/1471-2407-14-391. http://dx.doi.org/10.1186/1471-2407-14-391.en
dc.identifier.issn1471-2407en
dc.identifier.urihttp://nrs.harvard.edu/urn-3:HUL.InstRepos:12406576
dc.description.abstractBackground: Aspirin (ASA) use has been associated with improved breast cancer survival in several prospective studies. Methods: We conducted a nested case–control study of ASA use after a breast cancer diagnosis among women using Swedish National Registries. We assessed prospectively recorded ASA exposure during several different time windows following cancer diagnosis using conditional logistic regression with breast cancer death as the main outcome. Within each six-month period of follow-up, we categorized dispensed ASA doses into three groups: 0, less than 1, and 1 or more daily doses. Results: We included 27,426 women diagnosed with breast cancer between 2005 and 2009; 1,661 died of breast cancer when followed until Dec 31, 2010. There was no association between ASA use and breast cancer death when exposure was assessed either shortly after diagnosis, or 3–12 months before the end of follow-up. Only during the period 0–6 months before the end of follow-up was ASA use at least daily compared with non-use associated with a decreased risk of breast cancer death: HR (95% CI) = 0.69 (0.56-0.86). However, in the same time-frame, those using ASA less than daily had an increased risk of breast cancer death: HR (95% CI) = 1.43 (1.09-1.87). Conclusions: Contrary to other studies, we did not find that ASA use was associated with a lower risk of death from breast cancer, except when assessed short term with no delay to death/end of follow-up, which may reflect discontinuation of ASA during terminal illness.en
dc.language.isoen_USen
dc.publisherBioMed Centralen
dc.relation.isversionofdoi:10.1186/1471-2407-14-391en
dc.relation.hasversionhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC4065077/pdf/en
dash.licenseLAAen_US
dc.subjectAspirinen
dc.subjectBreast neoplasmsen
dc.subjectSurvivalen
dc.subjectProspective studyen
dc.subjectSwedenen
dc.subjectRegistriesen
dc.titleAspirin intake and breast cancer survival – a nation-wide study using prospectively recorded data in Swedenen
dc.typeJournal Articleen_US
dc.description.versionVersion of Recorden
dc.relation.journalBMC Canceren
dash.depositing.authorHolmes, Michelle Den_US
dc.date.available2014-07-07T17:01:57Z
dc.identifier.doi10.1186/1471-2407-14-391*
dash.contributor.affiliatedHolmes, Michelle
dash.contributor.affiliatedAdami, Hans-Olov


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