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Small cell transformation in crizotinib-resistant ROS1-rearranged non-small cell lung cancer with retention of ROS1 fusion: A case report.

Abstract
C-ros oncogene 1 receptor tyrosine kinase (ROS1) rearrangement has been detected in patients with advanced non-small cell lung cancer (NSCLC). Although ROS1 tyrosine kinase inhibitors (TKIs) provide a survival benefit for patients with ROS1-rearranged advanced NSCLC, subsequent therapy remains limited. Small cell transformation is an important mechanism of drug resistance in epidermal growth factor receptor-mutant NSCLC. However, its significance in mediating ROS1 resistance has not been determined yet. Here, we present the case of a 63-year-old man with ROS1-rearranged advanced NSCLC who had disease progression with small cell transformation of the mediastinal lymph node after 8 months of treatment with crizotinib. More importantly, fluorescence in situ hybridization of post-progression tumor biopsy demonstrated retention of ROS1 rearrangement. Tissue biopsy remains indispensable for patients who acquire resistance to ROS1 TKIs.
AuthorsChi-Hao Wu, Po-Lan Su, Che-Wei Hsu, Chang-Yao Chu, Chien-Chung Lin
JournalThoracic cancer (Thorac Cancer) Vol. 12 Issue 22 Pg. 3068-3071 (11 2021) ISSN: 1759-7714 [Electronic] Singapore
PMID34623764 (Publication Type: Case Reports)
Copyright© 2021 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd.
Chemical References
  • Protein Kinase Inhibitors
  • Proto-Oncogene Proteins
  • Crizotinib
  • Protein-Tyrosine Kinases
  • ROS1 protein, human
Topics
  • Carcinoma, Non-Small-Cell Lung (drug therapy, genetics, pathology)
  • Cell Transformation, Neoplastic (genetics)
  • Crizotinib (therapeutic use)
  • Drug Resistance, Neoplasm (genetics)
  • Gene Rearrangement
  • Humans
  • Lung Neoplasms (drug therapy, genetics, pathology)
  • Male
  • Middle Aged
  • Protein Kinase Inhibitors (therapeutic use)
  • Protein-Tyrosine Kinases (genetics)
  • Proto-Oncogene Proteins (genetics)
  • Small Cell Lung Carcinoma (drug therapy, genetics, pathology)

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