A prospective, randomized controlled trial of megestrol acetate among high-risk patients with resected malignant melanoma

Am J Clin Oncol. 1989 Apr;12(2):152-5. doi: 10.1097/00000421-198904000-00013.

Abstract

In light of some evidence that hormonal factors may impact on malignant melanoma, we performed a randomized trial of megestrol acetate versus observation among 67 patients with high-risk resected stage I or stage II (nodal) malignant melanoma. Following stratification by relevant prognostic factors, we observed a statistical significance in survival advantage for megestrol acetate that approached 7.6 versus 2.6 years, median survival; two-sided log rank p = 0.06. Disease-free survival was also greater for patients who received this hormonal therapy (3.4 versus 1.1 years, median disease-free survival), but the difference was not statistically significant (two-sided log rank p = 0.20). The most noteworthy side effects were weight gain (median 6-month gain of 8.2 kg) and impotence. Fully recognizing the hazards of limited sample analyses and the need for confirmatory trials, our findings suggest a possible role for megestrol acetate as adjuvant therapy for selected patients with malignant melanoma.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Female
  • Follow-Up Studies
  • Humans
  • Male
  • Megestrol / adverse effects
  • Megestrol / analogs & derivatives*
  • Megestrol / therapeutic use
  • Megestrol Acetate
  • Melanoma / drug therapy
  • Melanoma / surgery*
  • Middle Aged
  • Neoplasm Recurrence, Local
  • Prognosis
  • Prospective Studies
  • Random Allocation
  • Risk Factors
  • Time Factors
  • Weight Gain

Substances

  • Megestrol
  • Megestrol Acetate