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Updated: Mar 25, 2026

Next Generation Sequencing for the Detection of Actionable Mutations in Solid and Liquid Tumors
Published on: September 20, 2016
A never-smoker lung adenocarcinoma patient with a MET exon 14 mutation (D1028N) and a rapid partial response after
Linda Mahjoubi1,2, Anas Gazzah3,4, Benjamin Besse5
1Drug development Department (DITEP), Gustave Roussy, 114 rue Edouard Vaillant, 94805, Villejuif, France. linda.mahjoubi@gustaveroussy.fr.
Abstract:
During the past decade, the treatment of lung adenocarcinomas has been revolutionized with novel molecular targeted therapies. We describe a case of clinical activity of crizotinib in a female patient with a lung adenocarcinoma displaying a MET exon 14 donor splice site mutation (D1028N) detected using next generation sequencing. Within 5 weeks of crizotinib therapy, a partial response was observed in this 67 year-old woman. Further clinical trials of crizotinib are needed for non-small cell lung cancer exhibiting MET mutations.
Insights
Crizotinib shows clinical activity in a patient with lung adenocarcinoma harboring a MET exon 14 splice site mutation. This targeted therapy resulted in a partial response, highlighting its potential for non-small cell lung cancer.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Lung adenocarcinoma treatment has advanced with molecular targeted therapies.
- Next-generation sequencing enables precise identification of actionable mutations.
Observation:
- A 67-year-old female patient with lung adenocarcinoma was treated with crizotinib.
- The patient's tumor harbored a MET exon 14 donor splice site mutation (D1028N).
Findings:
- Crizotinib therapy demonstrated clinical activity in this patient.
- A partial response was observed within 5 weeks of treatment initiation.
Implications:
- Crizotinib shows promise for treating non-small cell lung cancer with MET mutations.
- Further clinical trials are warranted to confirm efficacy and safety.
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