Phase II evaluation of dibromodulcitol and actinomycin D, hydroxyurea, and cyclophosphamide in previously untreated patients with malignant melanoma

Invest New Drugs. 1987;5(3):293-7. doi: 10.1007/BF00175301.

Abstract

In this Eastern Cooperative Oncology Group (ECOG) phase II study, dibromodulcitol (DBD) and a combination of actinomycin D, hydroxyurea, and cyclophosphamide (AHC) were compared with methyl-CCNU, the current ECOG standard, in patients who had received no prior chemotherapy for disseminated malignant melanoma. The response rates were 6% (3/50) for AHC, 9% (3/34) for DBD, and 14% (7/49) for methyl-CCNU. Median survival times were 4, 5, and 6 months, respectively. Neither regimen appears to offer any advantage over methyl-CCNU as front-line therapy for patients with disseminated melanoma.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Antineoplastic Combined Chemotherapy Protocols / adverse effects
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Cyclophosphamide / administration & dosage
  • Dactinomycin / administration & dosage
  • Drug Evaluation
  • Female
  • Humans
  • Hydroxyurea / administration & dosage
  • Male
  • Melanoma / drug therapy*
  • Middle Aged
  • Mitolactol / adverse effects
  • Mitolactol / therapeutic use*
  • Semustine / therapeutic use

Substances

  • Semustine
  • Dactinomycin
  • Cyclophosphamide
  • Mitolactol
  • Hydroxyurea