Newly identified mutation in NSCLC suggests novel treatment option.
Genetic testing to identify potentially drug-targetable mutations is now the standard of care for NSCLC. In current practice, NSCLC tumors are screened for more than 50 potential genetic abnormalities, including EGFR mutations andALK or ROS1 translocations. However, approximately 40% to 50% of NSCLCs will not test positive for any of these known mutations.
To find novel NSCLC mutations, a research team led by Rebecca S. Heist, MD, MPH, Assistant Professor in Medicine, MGH Cancer Center, Massachusetts General Hospital, identified 54 never-smokers with NSCLC whose tumors tested negative for known driver mutations. Using an advanced form of genetic screening called next-generation sequencing (NGS), the researchers examined tumor samples from these patients to detect any other commonly occurring abnormalities.
Lung cancers that harbor specific genetic mutations can be highly sensitive to targeted therapies; said study co-author A. John Iafrate, MD, PhD, Associate Pathologist, Massachusetts General Hospital. The overall goal of our research is to find new genetic drivers in NSCLC that might lead to new targets for therapy.
Among the original group of 54 patients, 10 tumors exhibited a mutation called MET exon 14 skipping. The research team then tested a second group of tumor samples from 89 patients with NSCLC treated at the MGH Cancer Center. This group represented the full spectrum of NSCLC, with a range of disease stages (IA to IV), histology types (adenocarcinoma and squamous cell carcinoma), and smoking histories (0 to 60 pack years). Overall, 5.6% of cancers exhibited the MET exon 14 skipping abnormality.
Treatment with a MET inhibitor such as crizotinib is a promising strategy for patients with this mutation. As an example, Dr. Heist and colleagues described one patient with squamous cell lung carcinoma, extensive metastatic disease, andMET exon 14 skipping. After 4 weeks of twice daily treatment with crizotinib, the patient experienced near-complete resolution of a soft tissue mass around a lytic rib lesion, resolution of adrenal and liver lesions, and a decreased thrombus in the right main pulmonary artery. Now starting in the seventh month of treatment with crizotinib, the patient's initial response has been maintained.
Molecular testing for MET exon 14 skipping should be performed on all lung cancers because this alteration is targetable with currently available therapy, Dr. Iafrate said.Patients with this alteration appear to respond well to MET inhibition, including patients with NSCLC whose cancers do not exhibit any other known drug-targetable mutations.
Nate Pennell, a medical oncologist at the Cleveland Clinic and an Editor of The Oncologist commented, commented,The prevalence of MET exon 14 skipping mutations in approximately 5% of NSCLC cases which would make MET mutations the second most common actionable mutation in lung cancer after EGFR mutations. More importantly, these mutations are present in both smokers and nonsmokers, in both adenocarcinoma and squamous cell carcinoma, and appear to be responsive to already commercially available MET inhibitors, potentially broadening the exciting field of personalized medicine into a much broader segment of lung cancer patients than previously recognized.
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|Title Annotation:||non small cell lung cancer|
|Date:||Jul 31, 2016|
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