Phase I-II trial of aclacinomycin A given in a four-consecutive-day schedule to patients with solid tumours. A South-East European Oncology Group (SEEOG) Study

Oncology. 1987;44(3):159-63. doi: 10.1159/000226469.

Abstract

Aclacinomycin A (ACM) in a daily dose of 30 mg/m2 was infused over 1 h on 4 consecutive days to 50 patients. Myelotoxicity was acceptable, nausea and vomiting was frequent, hair loss was mild. Grade 1-2 cardiac rhythm abnormalities were observed in 12% of the patients. Between days 1 and 4 the heart rate and the corrected Q-T interval increased while the amplitude of the T wave decreased significantly, cardiac contractility remained unchanged. In 24 evaluable breast cancer patients 1 complete remission (4%) and 2 partial remissions (8%) lasting for only 2-3 months were seen. None of the 8 patients suffering from ovarial cancer benefitted from ACM therapy.

MeSH terms

  • Aclarubicin
  • Adult
  • Aged
  • Antibiotics, Antineoplastic / administration & dosage*
  • Antibiotics, Antineoplastic / adverse effects
  • Antibiotics, Antineoplastic / therapeutic use
  • Bone Marrow / drug effects
  • Breast Neoplasms / drug therapy
  • Doxorubicin / therapeutic use
  • Drug Administration Schedule
  • Drug Evaluation
  • Electrocardiography
  • Female
  • Heart / drug effects
  • Humans
  • Male
  • Middle Aged
  • Naphthacenes / administration & dosage
  • Naphthacenes / adverse effects
  • Naphthacenes / therapeutic use
  • Neoplasms / drug therapy*
  • Ovarian Neoplasms / drug therapy

Substances

  • Antibiotics, Antineoplastic
  • Naphthacenes
  • Aclarubicin
  • Doxorubicin