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Gemcitabine and Cisplatin for Patients with Metastatic or Recurrent Esophageal Carcinoma: A Southwest Oncology Group Study

dc.contributor.authorUrba, Susan G.en_US
dc.contributor.authorChansky, Karien_US
dc.contributor.authorvan Veldhuizen, Peter J.en_US
dc.contributor.authorPluenneke, Robert E.en_US
dc.contributor.authorBenedetti, Jacqueline K.en_US
dc.contributor.authorMacdonald, John S.en_US
dc.contributor.authorAbbruzzese, James L.en_US
dc.date.accessioned2006-09-11T15:50:17Z
dc.date.available2006-09-11T15:50:17Z
dc.date.issued2004-01en_US
dc.identifier.citationUrba, Susan G.; Chansky, Kari; vanVeldhuizen, Peter J.; Pluenneke, Robert E.; Benedetti, Jacqueline K.; Macdonald, John S.; Abbruzzese, James L.; (2004). "Gemcitabine and Cisplatin for Patients with Metastatic or Recurrent Esophageal Carcinoma: A Southwest Oncology Group Study." Investigational New Drugs 22(1): 91-97. <http://hdl.handle.net/2027.42/45241>en_US
dc.identifier.issn0167-6997en_US
dc.identifier.issn1573-0646en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/45241
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=14707499&dopt=citationen_US
dc.description.abstractPurpose : Experimental data, both in vivo and in vitro , suggest that the combination of gemcitabine and cisplatin acts synergistically. Within the Southwest Oncology Group, we designed a Phase II trial to test this chemotherapy combination for patients with esophageal cancer. Experimental design : Patients with metastatic or recurrent esophageal cancer were treated with gemcitabine 1000 mg/m 2 on days 1, 8, and 15, and cisplatin 100 mg/m 2 on day 15. Cycles were repeated every 28 days. The statistical endpoint was overall survival. Results : Sixty-four eligible patients were accrued from 37 institutions. Twenty-six percent of patients had prior chemotherapy. The treatment was generally well-tolerated, with the most common toxicity being neutropenia in 31% of patients. All 64 patients have died. Survival at 3 months was 81%, and at 1 year was 20%. Median survival was 7.3 months. Conclusions : This regimen is tolerable palliative option for patients with metastatic esophageal cancer.en_US
dc.format.extent82314 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherKluwer Academic Publishers; Springer Science+Business Mediaen_US
dc.subject.otherMedicine & Public Healthen_US
dc.subject.otherPharmacology/Toxicologyen_US
dc.subject.otherOncologyen_US
dc.subject.otherEsophageal Canceren_US
dc.subject.otherChemotherapyen_US
dc.subject.otherGemcitabineen_US
dc.subject.otherCisplatinen_US
dc.titleGemcitabine and Cisplatin for Patients with Metastatic or Recurrent Esophageal Carcinoma: A Southwest Oncology Group Studyen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbsecondlevelRadiologyen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbsecondlevelChemical Engineeringen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumUniversity of Michigan Medical Center, Ann Arbor, MI, U.S.A.en_US
dc.contributor.affiliationotherSouthwest Oncology Group Statistical Center, Seattle, WA, U.S.Aen_US
dc.contributor.affiliationotherUniversity of Kansas Medical Center, Kansas City, MOen_US
dc.contributor.affiliationotherKansas City Community Clinical Oncology Program, Kansas City, MOen_US
dc.contributor.affiliationotherSouthwest Oncology Group Statistical Center, Seattle, WA, U.S.Aen_US
dc.contributor.affiliationotherSt Vincent's Comprehensive Cancer Center, New York, NY, U.S.Aen_US
dc.contributor.affiliationotherMD Anderson Cancer Center, Houston, TX, U.S.Aen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid14707499en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/45241/1/10637_2004_Article_5151120.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1023/B:DRUG.0000006179.20974.afen_US
dc.identifier.sourceInvestigational New Drugsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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