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dc.contributor.authorCostanza, Mary E.
dc.contributor.authorNathanson, L.
dc.contributor.authorSchoenfeld, David A.
dc.contributor.authorWolter, J.
dc.contributor.authorColsky, J.
dc.contributor.authorRegelson, W.
dc.contributor.authorCunningham, Timothy
dc.contributor.authorSedransk, N.
dc.date2022-08-11T08:11:05.000
dc.date.accessioned2022-08-23T17:32:59Z
dc.date.available2022-08-23T17:32:59Z
dc.date.issued1977-09-01
dc.date.submitted2007-07-30
dc.identifier.citation<p>Cancer. 1977 Sep;40(3):1010-5.</p>
dc.identifier.issn0008-543X (Print)
dc.identifier.doi10.1002/1097-0142(197709)40:3<1010::AID-CNCR2820400308>3.0.CO;2-C
dc.identifier.pmid332319
dc.identifier.urihttp://hdl.handle.net/20.500.14038/51071
dc.description.abstractThis report is the result of an Eastern Cooperative Oncology Group (ECOG) study. Four hundred and 15 patients with inoperable metastatic malignant melanoma, excluding those with cutaneous metastases only, were randomized to one of three drug treatments: DTIC alone, methyl-CCNU alone, or the combination DTIC plus methyl-CCNU. Responses were seen in 14% of DTIC patients (19/127), 15% of methyl-CCNU patients (18/119) and 14% of DTIC plus methyl-CCNU patients (18/122). Duration of response was the same (14 weeks) for all three treatment groups. There was no difference among the treatments in achieving complete responses. Survival was improved significantly for responders (50 weeks) compared with nonresponders (15 weeks) regardless of treatment regimen. Toxicities were generally tolerable. DTIC caused significantly more gastrointestinal toxicity than methyl-CCNU. Methyl-CCNU caused significantly more bone marrow toxicity than DTIC. There were three drug-related deaths. All occurred in patients on combination DTIC plus methyl-CCNU. Important pretreatment characteristics that favor response are ambulatory status, female, less than 50 years old, no prior chemotherapy and no liver or brain metastases. Patients with favorable characteristics combinations had a 30% response rate, while those with unfavorable characteristic combinations had only a 9% response rate.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=332319&dopt=Abstract">Link to article in PubMed</a></p>
dc.relation.urlhttps://doi.org/10.1002/1097-0142(197709)40:3<1010::AID-CNCR2820400308>3.0.CO;2-C
dc.subjectBrain Neoplasms
dc.subjectClinical Trials
dc.subjectDacarbazine
dc.subjectDrug Therapy, Combination
dc.subjectFemale
dc.subjectHumans
dc.subjectLiver Diseases
dc.subjectLiver Neoplasms
dc.subjectMale
dc.subjectMelanoma
dc.subjectNeoplasm Metastasis
dc.subjectNitrosourea Compounds
dc.subjectPrognosis
dc.subjectRemission, Spontaneous
dc.subjectSemustine
dc.subjectThrombocytopenia
dc.subjectTime Factors
dc.subjectTriazenes
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.subjectWomen's Studies
dc.titleResults with methyl-CCNU and DTIC in metastatic melanoma
dc.typeJournal Article
dc.source.journaltitleCancer
dc.source.volume40
dc.source.issue3
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/wfc_pp/84
dc.identifier.contextkey330320
html.description.abstract<p>This report is the result of an Eastern Cooperative Oncology Group (ECOG) study. Four hundred and 15 patients with inoperable metastatic malignant melanoma, excluding those with cutaneous metastases only, were randomized to one of three drug treatments: DTIC alone, methyl-CCNU alone, or the combination DTIC plus methyl-CCNU. Responses were seen in 14% of DTIC patients (19/127), 15% of methyl-CCNU patients (18/119) and 14% of DTIC plus methyl-CCNU patients (18/122). Duration of response was the same (14 weeks) for all three treatment groups. There was no difference among the treatments in achieving complete responses. Survival was improved significantly for responders (50 weeks) compared with nonresponders (15 weeks) regardless of treatment regimen. Toxicities were generally tolerable. DTIC caused significantly more gastrointestinal toxicity than methyl-CCNU. Methyl-CCNU caused significantly more bone marrow toxicity than DTIC. There were three drug-related deaths. All occurred in patients on combination DTIC plus methyl-CCNU. Important pretreatment characteristics that favor response are ambulatory status, female, less than 50 years old, no prior chemotherapy and no liver or brain metastases. Patients with favorable characteristics combinations had a 30% response rate, while those with unfavorable characteristic combinations had only a 9% response rate.</p>
dc.identifier.submissionpathwfc_pp/84
dc.contributor.departmentDepartment of Medicine, Division of Hematology/Oncology
dc.source.pages1010-5


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