Phase II study of mitolactol in metastatic malignant melanoma

M. A. Simmonds, Allan Lipton, Harold Harvey, N. Ellison, D. S. White

Research output: Contribution to journalArticle

3 Scopus citations

Abstract

The Central Pennsylvania Oncology Group conducted a phase II study of mitolactol in advanced metastatic melanoma to determine the overall survival rate and duration of response to this agent. The starting dose was 100 mg/m2/day orally. If no hematologic toxicity was noted on weekly blood cell counts, the dose was increased to 130 mg/m2/day on Day 35, and, if still tolerated, to 160 mg/m2/day on Day 70. Six of 25 evaluable patients (24%) had objective partial response. The median duration of response was 20 weeks, with a range of 10-66 weeks. The median survival from date of entry in this study was 21 weeks in responding or stable patients compared to 7 weeks in nonresponders. Hematologic toxicity was the dose-limiting factor. This study shows that mitolactol has moderate activity against advanced melanoma, and the drug deserves further study in combination with nonmyelotoxic drugs.

Original languageEnglish (US)
Pages (from-to)65-67
Number of pages3
JournalCancer Treatment Reports
Volume69
Issue number1
StatePublished - Mar 13 1985

All Science Journal Classification (ASJC) codes

  • Oncology
  • Cancer Research

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    Simmonds, M. A., Lipton, A., Harvey, H., Ellison, N., & White, D. S. (1985). Phase II study of mitolactol in metastatic malignant melanoma. Cancer Treatment Reports, 69(1), 65-67.