Results of a randomized study comparing DTIC with TIC mustard in malignant melanoma
Authors
Costanza, Mary E.Nathanson, L.
Costello, W. G.
Wolter, J.
Brunk, S. F.
Colsky, J.
Hall, T.
Oberfield, R. A.
Regelson, W.
UMass Chan Affiliations
Department of Medicine, Division of Hematology/OncologyDocument Type
Journal ArticlePublication Date
1976-04-01Keywords
Clinical TrialsDacarbazine
Drug Evaluation
Female
Humans
Imidazoles
Male
Melanoma
Nitrogen Mustard Compounds
effects
Prospective Studies
Triazenes
Life Sciences
Medicine and Health Sciences
Women's Studies
Metadata
Show full item recordAbstract
This prospective randomized Eastern Cooperative Oncology Group (ECOG) study (1071) was designed to compare a new and promising cytotoxic agent TIC Mustard (triazeno imidazole carboxamide mustard, NSC 82196) with DTIC (dimethyl triazeno imidazole carboxamide, NSC 45388) in the treatment of inoperable melanoma. One hundred and seventy-eight patients were randomized to receive either DTIC (150 mg/m2/day X 5) or TIC Mustard (800 mg/m2/day X 5). Of this group 145 patients were evaluable for tumor response at the completion of the study. Objective responses were seen in 15/79 (19.0%) DTIC patients and 4/66 (6.1%) TIC Mustard patients. Adjustment of crude response rates yielded final response rates of 18.2% for DTIC patients and 5.8% for TIC Mustard. These differences were significant at the p less than or equal to .03 level. Median response duration was 15 weeks for the DTIC responders and 4 weeks for the TIC Mustard responders. Responders and nonresponders did not differ significantly in any of the standard prognostic categories. However, responders had a significantly longer median survival (47.5 weeks) compared to that for nonresponders (17.8 weeks). Toxicity was tolerable for either drug and no deaths were ascribed to either. We conclude that TIC Mustard has limited usefulness in the treatment of malignant melanoma and is less effective than DTIC.Source
Cancer. 1976 Apr;37(4):1654-9.
DOI
10.1002/1097-0142(197604)37:4<1654::AID-CNCR2820370406>3.0.CO;2-BPermanent Link to this Item
http://hdl.handle.net/20.500.14038/51073PubMed ID
769936Related Resources
ae974a485f413a2113503eed53cd6c53
10.1002/1097-0142(197604)37:4<1654::AID-CNCR2820370406>3.0.CO;2-B