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Treatment options for muscle-invasive urothelial cancer for patients who were not eligible for cystectomy or neoadjuvant chemotherapy with methotrexate, vinblastine, doxorubicin, and cisplatin

dc.contributor.authorHigano, Celestia S.en_US
dc.contributor.authorTangen, Catherine M.en_US
dc.contributor.authorSakr, Wael A.en_US
dc.contributor.authorFaulkner, Jamesen_US
dc.contributor.authorRivkin, Saul E.en_US
dc.contributor.authorMeyers, Frederick J.en_US
dc.contributor.authorHussain, Maha H. A.en_US
dc.contributor.authorBaker, Laurence H.en_US
dc.contributor.authorRussell, Kenneth J.en_US
dc.contributor.authorCrawford, E. Daviden_US
dc.date.accessioned2008-05-12T13:44:11Z
dc.date.available2009-06-01T20:08:52Zen_US
dc.date.issued2008-05-15en_US
dc.identifier.citationHigano, Celestia S.; Tangen, Catherine M.; Sakr, Wael A.; Faulkner, James; Rivkin, Saul E.; Meyers, Frederick J.; Hussain, Maha; Baker, Laurence H.; Russell, Kenneth J.; Crawford, E. David (2008). "Treatment options for muscle-invasive urothelial cancer for patients who were not eligible for cystectomy or neoadjuvant chemotherapy with methotrexate, vinblastine, doxorubicin, and cisplatin." Cancer 112(10): 2181-2187. <http://hdl.handle.net/2027.42/58591>en_US
dc.identifier.issn0008-543Xen_US
dc.identifier.issn1097-0142en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/58591
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=18404692&dopt=citationen_US
dc.description.abstractBACKGROUND. Many patients with invasive urothelial cell cancer are poor candidates for cisplatin-based chemotherapy, and many are high risk for cystectomy. Southwest Oncology Group Trial 8733 was designed to address treatment for such patients. METHODS. Eligible patients had primary or recurrent muscle-invasive disease with transitional cell or squamous cell histology, a performance status from 0 to 2, no extrapelvic disease, a life expectancy >3 months, and adequate hematologic function. The treating clinician assigned patients to operable or inoperable groups. All patients received 2 cycles of 5-fluorouracil (5-FU) at a dose of 1000mg/m 2 per day × 4 starting concurrently with radiation at a dose of 200 centigrays per day × 10 each cycle. After 2 cycles, operable patients with positive biopsies underwent cystectomy, and patients with negative biopsies received a third cycle of chemoradiotherapy. Patients in the inoperable group received 3 cycles without interim biopsy. RESULTS. Eighteen of 24 eligible patients in the operable group were evaluable for response. Five patients had a complete response (CR), 9 patients had stable disease, 1 patient had progressive disease, and 3 patients were not assessable. The median progression-free survival was 10 months (95% confidence interval [95% CI], 4–14 months), and the median overall survival was 18 months (95% CI, 7–28 months). In the inoperable group, 35 of 37 eligible patients were evaluable for response with 17 CRs (49%; 95% CI, 31%–66%). The median progression-free survival was 13 months (95% CI, 10–17 months), and the median overall survival was 20 months (95% CI, 11–53 months). There were no episodes of grade 4 toxicity. CONCLUSIONS. In the current study, the combination of 5-FU and radiation was found to be tolerated well by patients with numerous comorbidities who could not tolerate cisplatin-based therapy or cystectomy. Cancer 2008. © 2008 American Cancer Society.en_US
dc.format.extent168083 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.titleTreatment options for muscle-invasive urothelial cancer for patients who were not eligible for cystectomy or neoadjuvant chemotherapy with methotrexate, vinblastine, doxorubicin, and cisplatinen_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, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationotherDepartment of Medicine, Division of Oncology, University of Washington, Seattle, Washington ; Fax: (210) 677-0006 ; Southwest Oncology Group (SWOG-8733), Operations Office, 14980 Omicron Drive, San Antonio, TX 78245-3217en_US
dc.contributor.affiliationotherSouthwest Oncology Group Statistical Center, Seattle, Washingtonen_US
dc.contributor.affiliationotherDepartment of Pathology, Wayne State University Medical Center, Detroit, Michiganen_US
dc.contributor.affiliationotherSouthwest Oncology Group Statistical Center, Seattle, Washingtonen_US
dc.contributor.affiliationotherPuget Sound Oncology Consortium, Seattle, Washingtonen_US
dc.contributor.affiliationotherDepartment of Internal Medicine, University of California at Davis, Sacramento, Californiaen_US
dc.contributor.affiliationotherDepartment of Internal Medicine, Division of Hematology/Oncology, Wayne State University Medical Center, Detroit, Michiganen_US
dc.contributor.affiliationotherDepartment of Radiation Oncology, University of Washington, Seattle, Washingtonen_US
dc.contributor.affiliationotherDepartment of Surgery, University of Colorado Health Sciences Center, Denver, Coloradoen_US
dc.identifier.pmid18404692en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/58591/1/23420_ftp.pdf
dc.identifier.doihttp://dx.doi.org/10.1002/cncr.23420en_US
dc.identifier.sourceCanceren_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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