Multi-centre Phase II trial of the polyamine synthesis inhibitor SAM486A (CGP48664) in patients with metastatic melanoma

Invest New Drugs. 2005 Jun;23(3):253-6. doi: 10.1007/s10637-005-6734-z.

Abstract

Purpose: To determine the activity and tolerability of SAM496A, an inhibitor of S-adenosylmethionine decarboxylase (SAMDC), in patients with metastatic melanoma who had not received prior chemotherapy. Selected patients were offered participation in two sub-studies examining early changes in tumor metabolism with FDG-PET and changes in tumor polyamine content.

Patients and methods: Fifteen patients with measurable metastatic melanoma, normal cardiac function, and no known CNS metastases were eligible and received SAM486A by 1-hour IV infusion daily for 5 days every 3 weeks. Response was assessed by SWOG criteria.

Results: No patient had a confirmed partial response. Fatigue/lethargy, myalgia and neutropenia were the main toxicities but no febrile neutropenia or grade 4 non-hematological toxicity occurred. Five patients had PET scans pre-treatment and on days 8-12 of cycle 1. No patient had reduction of tumor metabolism. Serial biopsy in one patient showed alterations in polyamines consistent with SAMDC inhibition.

Conclusions: Using the present dose and schedule of administration, SAM486A does not have significant therapeutic potential in patients with metastatic melanoma.

Publication types

  • Clinical Trial
  • Clinical Trial, Phase II
  • Multicenter Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosylmethionine Decarboxylase / antagonists & inhibitors*
  • Adult
  • Aged
  • Amidines / adverse effects
  • Amidines / therapeutic use*
  • Antineoplastic Agents / adverse effects
  • Antineoplastic Agents / therapeutic use*
  • Female
  • Fluorodeoxyglucose F18
  • Humans
  • Indans / adverse effects
  • Indans / therapeutic use*
  • Karnofsky Performance Status
  • Male
  • Melanoma / diagnostic imaging
  • Melanoma / drug therapy*
  • Melanoma / pathology*
  • Middle Aged
  • Neoplasm Metastasis
  • Positron-Emission Tomography
  • Radiopharmaceuticals

Substances

  • Amidines
  • Antineoplastic Agents
  • Indans
  • Radiopharmaceuticals
  • Fluorodeoxyglucose F18
  • 4-amidinoindan-1-one 2'-amidinohydrazone
  • Adenosylmethionine Decarboxylase