Dramatic response to high-dose icotinib in a lung adenocarcinoma patient after erlotinib failure

Lung Cancer. 2014 Feb;83(2):305-7. doi: 10.1016/j.lungcan.2013.12.002. Epub 2013 Dec 12.

Abstract

Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI) retreatment is rarely administered for non-small cell lung cancer (NSCLC) patients who did not respond to previous TKI treatment. A high dose of TKI may overcome resistance to the standard dose of TKI and have different effectiveness toward cancer compared with the standard dose of TKI. This manuscript describes a dramatic and durable response to high-dose icotinib in a NSCLC patient who did not respond to a previous standard dose of erlotinib. The treatment extended the life of the patient for one additional year. A higher dose of icotinib deserves further study not only for patients whose therapy failed with the standard dose of TKI but also for newly diagnosed NSCLC patients with a sensitive mutation. Serial mutation testing during disease development is necessary for analysis and evaluation of EGFR TKI treatment.

Keywords: Epidermal growth factor receptor; High dose; Icotinib; Mutation; Non-small cell lung cancer; Tyrosine kinase inhibitor.

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adenocarcinoma / drug therapy*
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Cisplatin / administration & dosage
  • Cisplatin / adverse effects
  • Crown Ethers / administration & dosage*
  • Crown Ethers / adverse effects
  • Docetaxel
  • Drug Dosage Calculations
  • ErbB Receptors / antagonists & inhibitors
  • ErbB Receptors / genetics
  • Erlotinib Hydrochloride
  • Fatal Outcome
  • Humans
  • Lung Neoplasms / drug therapy*
  • Male
  • Middle Aged
  • Mutation / genetics
  • Neoplasm Staging
  • Quinazolines / administration & dosage*
  • Quinazolines / adverse effects
  • Remission Induction
  • Salvage Therapy
  • Taxoids / administration & dosage
  • Taxoids / adverse effects
  • Treatment Failure

Substances

  • Crown Ethers
  • Quinazolines
  • Taxoids
  • Docetaxel
  • icotinib
  • Erlotinib Hydrochloride
  • EGFR protein, human
  • ErbB Receptors
  • Cisplatin