Authors
Costanza, Mary E.Nathanson, L.
Schoenfeld, David A.
Wolter, J.
Colsky, J.
Regelson, W.
Cunningham, Timothy
Sedransk, N.
UMass Chan Affiliations
Department of Medicine, Division of Hematology/OncologyDocument Type
Journal ArticlePublication Date
1977-09-01Keywords
Brain NeoplasmsClinical Trials
Dacarbazine
Drug Therapy, Combination
Female
Humans
Liver Diseases
Liver Neoplasms
Male
Melanoma
Neoplasm Metastasis
Nitrosourea Compounds
Prognosis
Remission, Spontaneous
Semustine
Thrombocytopenia
Time Factors
Triazenes
Life Sciences
Medicine and Health Sciences
Women's Studies
Metadata
Show full item recordAbstract
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.Source
Cancer. 1977 Sep;40(3):1010-5.
DOI
10.1002/1097-0142(197709)40:3<1010::AID-CNCR2820400308>3.0.CO;2-CPermanent Link to this Item
http://hdl.handle.net/20.500.14038/51071PubMed ID
332319Related Resources
ae974a485f413a2113503eed53cd6c53
10.1002/1097-0142(197709)40:3<1010::AID-CNCR2820400308>3.0.CO;2-C