Clinical status and optimal use of amifostine

Oncology (Williston Park). 1999 Jan;13(1):47-59; discussion 63, 67.

Abstract

Amifostine (Ethyol) is an analog of cysteamine that selectively protects normal tissues in multiple organ systems against the toxic effects of radiation and various cytotoxic drugs while preserving the antitumor effects of these therapies. Amifostine was evaluated in a multicenter, multinational phase III clinical trial that enrolled women with stage III/IV ovarian cancer. Its effects have also been studied using normal human bone marrow and human breast cancer cells, as well as leukemia cells. Additional clinical trials have shown that amifostine can protect normal tissues from the toxic effects of alkylating agents, organoplatinums, anthracyclines, taxanes, and radiation. Other laboratory and clinical investigations indicate a potential role for this cytoprotective agent in the treatment of the ineffective hematopoiesis characteristic of the myelodysplastic syndromes.

Publication types

  • Review

MeSH terms

  • Amifostine / pharmacokinetics
  • Amifostine / therapeutic use*
  • Animals
  • Antineoplastic Agents / therapeutic use
  • Bone Marrow Cells / cytology
  • Bone Marrow Cells / drug effects
  • Bone Marrow Cells / radiation effects
  • Clinical Trials, Phase III as Topic
  • Drug Therapy, Combination
  • Female
  • Humans
  • Leukemia / drug therapy
  • Leukemia / pathology
  • Leukemia / radiotherapy
  • Multicenter Studies as Topic
  • Ovarian Neoplasms / drug therapy
  • Ovarian Neoplasms / pathology
  • Ovarian Neoplasms / radiotherapy
  • Radiation Injuries / prevention & control*
  • Radiation-Protective Agents / pharmacokinetics
  • Radiation-Protective Agents / therapeutic use*
  • Tumor Cells, Cultured / drug effects
  • Tumor Cells, Cultured / pathology
  • Tumor Cells, Cultured / radiation effects

Substances

  • Antineoplastic Agents
  • Radiation-Protective Agents
  • Amifostine