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Breast cancer adjuvant chemotherapy dosing in obese patients

dc.contributor.authorGreenman, Christopher G.en_US
dc.contributor.authorJagielski, Christina H.en_US
dc.contributor.authorGriggs, Jennifer J.en_US
dc.date.accessioned2008-05-12T13:43:58Z
dc.date.available2009-06-01T20:08:52Zen_US
dc.date.issued2008-05-15en_US
dc.identifier.citationGreenman, Christopher G.; Jagielski, Christina H.; Griggs, Jennifer J. (2008). "Breast cancer adjuvant chemotherapy dosing in obese patients." Cancer 112(10): 2159-2165. <http://hdl.handle.net/2027.42/58590>en_US
dc.identifier.issn0008-543Xen_US
dc.identifier.issn1097-0142en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/58590
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=18338813&dopt=citationen_US
dc.description.abstractBACKGROUND Substantial variation in adjuvant breast cancer chemotherapy dosing in obese women suggests that there is uncertainty about optimal practices. The purpose of this study was to investigate variations in dose determinations in clinical trial protocols and publications over the last 3 decades as potential sources of this uncertainty. METHODS The National Cancer Institute database was used to identify protocols of breast cancer adjuvant chemotherapy conducted by cooperative groups between 1970–2000, and these protocols were then obtained directly from the cooperative groups. Dose determinations were categorized in each protocol and in published reports from each clinical trial. Fisher exact tests were used to compare the proportions of protocols that used full weight-based doses over time. RESULTS Protocol-specified chemotherapy dosing was obtained for all of 44 eligible trials. A significant increase was identified in the use of full weight-based doses in the later time period compared with the earlier ( P = .004; 2-sided Fisher exact test). A notable exception was 1 cooperative group that continues to require dose limitations for doxorubicin and cyclophosphamide in patients with a body surface area of more than 2.0 m 2 . Regardless of publication date, published reports of clinical trials rarely provide information on use of full or limited weight-based doses. CONCLUSIONS Variations in dose determinations among clinical trial protocols and lack of information on use of full weight-based doses in most publications are 2 likely sources of variation in chemotherapy dosing in obese women. Developing consensus and disseminating information on optimal chemotherapy dosing will likely reduce such variation and may improve survival among obese patients with breast cancer. Cancer 2008. © 2008 American Cancer Society.en_US
dc.format.extent148484 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherWiley Subscription Services, Inc., A Wiley Companyen_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherCancer Research, Oncology and Pathologyen_US
dc.titleBreast cancer adjuvant chemotherapy dosing in obese patientsen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelOncology and Hematologyen_US
dc.subject.hlbsecondlevelPublic Healthen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Internal Medicine-Hematology/Oncology, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartment of Internal Medicine-Hematology/Oncology, University of Michigan, Ann Arbor, Michigan ; Fax: (734) 763-7672 ; Department of Medicine, Hematology/Oncology, University of Michigan, 300 North Ingalls, 3A22, Ann Arbor, MI 48109en_US
dc.contributor.affiliationotherUniversity of Rochester, Rochester, New Yorken_US
dc.identifier.pmid18338813en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/58590/1/23416_ftp.pdf
dc.identifier.doihttp://dx.doi.org/10.1002/cncr.23416en_US
dc.identifier.sourceCanceren_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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