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Rare GCC2-ALK fusion G13:A20 detected by next generation sequencing in non-small cell lung cancer patients and treatment response.
Qin, Jing; Zeng, Daxiong; Xie, Fajun; Yu, Ruoying; Wu, Xue; Liu, Kaihua; Shao, Yang W; Lu, Hongyang; Jiang, Junhong.
Afiliação
  • Qin J; Department of Thoracic Medical Oncology, Zhejiang Cancer Hospital, Hangzhou 310022, China.
  • Zeng D; Department of Respiratory Medicine, The First Affiliated Hospital of Soochow University, Suzhou 215006, China.
  • Xie F; Department of Thoracic Medical Oncology, Zhejiang Cancer Hospital, Hangzhou 310022, China.
  • Yu R; Translational Medicine Research Institute, Geneseeq Technology Inc., Toronto, Ontario, Canada.
  • Wu X; Translational Medicine Research Institute, Geneseeq Technology Inc., Toronto, Ontario, Canada.
  • Liu K; Nanjing Geneseeq Technology Inc., Nanjing 210032, China.
  • Shao YW; Translational Medicine Research Institute, Geneseeq Technology Inc., Toronto, Ontario, Canada.
  • Lu H; Department of Thoracic Medical Oncology, Zhejiang Cancer Hospital, Hangzhou 310022, China.
  • Jiang J; Department of Respiratory Medicine, The First Affiliated Hospital of Soochow University, Suzhou 215006, China.
Transl Cancer Res ; 8(5): 2187-2191, 2019 Sep.
Article em En | MEDLINE | ID: mdl-35116968
ABSTRACT
Two patients with rare GCC2-ALK fusion G13A20 which were found in Chinese population by next generation sequencing (NGS) developed resistant to crizotinib with a prolonged progression-free survival (PFS). Both patients showed unfavorable response to subsequent second or third generation tyrosine kinase inhibitors (TKIs) treatment with shorten PFS. In conclusion, non-small cell lung cancer (NSCLC) patients with rare GCC2-ALK fusion G13A20 may be optimal candidates for crizotinib as front-line therapy and may have a high possibility to exhibit unsatisfactory response to subsequent second or third generation TKIs target therapy after acquiring resistance to crizotinib.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Transl Cancer Res Ano de publicação: 2019 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Transl Cancer Res Ano de publicação: 2019 Tipo de documento: Article País de afiliação: China