Phase II study of N-methylformamide, spirogermanium, and 4-demethoxydaunorubicin in the treatment of non-small cell lung cancer (EST 3583): an Eastern Cooperative Oncology Group study

Med Pediatr Oncol. 1989;17(3):197-201. doi: 10.1002/mpo.2950170306.

Abstract

One hundred forty-four patients with non-small cell lung cancer, the majority (72%) of whom had received previous chemotherapy, were evaluable in this randomized phase II study of N-methylformamide (N-MF), spirogermanium, and 4-demethoxydaunorubicin. There were two partial responses, one each with spirogermanium and 4-demethoxydaunorubicin. There were eight life-threatening complications (mostly hematologic) and two lethal complications (N-MF, hematologic; 4-demethoxydaunorubicin, gastrointestinal). The overall survival ranged from 9 days to 533 days with a median of 17.6 weeks. The following factors were associated with poor survival: Poor initial performance status, prior weight loss, presence of liver or subcutaneous metastases.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Aged
  • Antineoplastic Agents / adverse effects
  • Antineoplastic Agents / therapeutic use*
  • Carcinoma, Non-Small-Cell Lung / drug therapy*
  • Drug Evaluation
  • Female
  • Formamides / adverse effects
  • Formamides / therapeutic use*
  • Germanium / adverse effects
  • Germanium / therapeutic use*
  • Humans
  • Idarubicin / therapeutic use*
  • Lung Neoplasms / drug therapy*
  • Male
  • Middle Aged
  • Organometallic Compounds / adverse effects
  • Organometallic Compounds / therapeutic use*
  • Prognosis
  • Random Allocation
  • Remission Induction
  • Spiro Compounds / adverse effects
  • Spiro Compounds / therapeutic use*

Substances

  • Antineoplastic Agents
  • Formamides
  • Organometallic Compounds
  • Spiro Compounds
  • Germanium
  • spirogermanium
  • methylformamide
  • Idarubicin