Dose escalation of imatinib after failure of standard dose in Korean patients with metastatic or unresectable gastrointestinal stromal tumor

Jpn J Clin Oncol. 2009 Feb;39(2):105-10. doi: 10.1093/jjco/hyn134. Epub 2008 Dec 3.

Abstract

Objective: We evaluated the results of imatinib dose escalation in patients with advanced gastrointestinal stromal tumors (GISTs) after disease progression on standard-dose imatinib.

Methods: Clinical data from patients with metastatic or unresectable GISTs whose dose of imatinib was increased after disease progression on imatinib 400 mg/day were retrospectively reviewed.

Results: The 24 patients studied had a median age of 52 years. Imatinib dosing was escalated to 600 mg/day in 12 patients, then to 800 mg/day in four patients. The other 12 patients had dose escalation directly to 800 mg/day. Two patients (8.3%) achieved a partial response, and seven (29.2%) had stable disease. Six-month progression-free and overall survival rates were 33.3 and 70.7%, respectively. Dose escalation to 600 or 800 mg/day was generally well tolerated.

Conclusion: Imatinib dose escalation is feasible and well tolerated in patients with advanced GIST who progress on standard-dose therapy, producing clinical benefit in approximately 37% of patients.

MeSH terms

  • Adult
  • Aged
  • Antineoplastic Agents / administration & dosage*
  • Antineoplastic Agents / toxicity
  • Asian People
  • Benzamides
  • DNA Mutational Analysis
  • Disease Progression
  • Female
  • Gastrointestinal Stromal Tumors / drug therapy*
  • Gastrointestinal Stromal Tumors / mortality
  • Humans
  • Imatinib Mesylate
  • Korea
  • Male
  • Middle Aged
  • Neoplasm Metastasis
  • Piperazines / administration & dosage*
  • Piperazines / toxicity
  • Proto-Oncogene Proteins c-kit / genetics
  • Pyrimidines / administration & dosage*
  • Pyrimidines / toxicity
  • Receptor, Platelet-Derived Growth Factor alpha / genetics
  • Retrospective Studies
  • Survival Rate
  • Treatment Failure

Substances

  • Antineoplastic Agents
  • Benzamides
  • Piperazines
  • Pyrimidines
  • Imatinib Mesylate
  • Proto-Oncogene Proteins c-kit
  • Receptor, Platelet-Derived Growth Factor alpha