Two are better than one on progression through MET mechanism for EGFR+ NSCLC patients
Recent years have borne witness to the development of numerous acquired resistances to epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitors (TKIs) treatment for patients with EGFR-mutated non-small cell lung cancer (NSCLC). Mechanism of resistant includes EGFR T790M, MET gene amplification (1,2), transformation to small cell lung cancer and others. Approximately 5 to 26 percent of these acquired modifications occur due to dysregulation of the mesenchymal-epithelial transition factor (MET) either by amplification or overexpression patterns. Previous studies have failed to show efficacy of adding MET inhibitors to EGFR-TKI therapies upon progression (3).
Wu et al. reports in this journal that adding capmatinib to gefitinib yielded an overall ORR of 27% while a 47% ORR was reported among patients with high MET amplification (≥6 gene copies). In addition, previous reports (3), have also reported results in the same direction. Therefore, the main challenge is patient’s selection, namely optimizing precision cancer care in lung cancer.
Currently, upon progression on EGFR-TKI therapy, the most common practice is seeking only for EGFR T790M sub-mutation (4), while the presented study clearly indicates the need for widening the scope of the diagnostic approach. This study showed that MET profiling should be included for all EGFR T790M negatives reaching progression.
Moreover, the next open question would be: what is the best MET biomarker and the appropriate method of analysis? Should we use protein-based analysis by IHC, Mass Spectrometry, RNA expression levels, DNA gene amplification levels or DNA mutations found in MET? Wu et al. evaluated both MET gene amplification by FISH seeing a positive correlation, while negative for IHC. Therefore, standardization should be performed in order to better select the patients who may benefit from MET blockade on top of EGFR TKI therapy.
The efficacy of capmatinib plus gefitinib was examined by Wu et al. in total of 161 patients. The final dose for the phase II study was capmatinib 400 mg BID plus gefitinib 250 mg QD. The highest efficacy with ORR of 47% was seen in patients with high MET gene amplified tumors (MET gene copy number ≥6). Interestingly, capmatinib shows also an effect of restoring sensitivity to erlotinib and promotes apoptosis by hepatocyte growth factor pathway in NSCLC models with erlotinib-resistant (5).
In summary MET gene amplification is an escape mechanism from EGFR related therapy. Therefore, its profiling is crucial on disease progression and particularly when the T790M mutation is negative. Clinical studies should invest in their companion diagnostic, probably aimed to profile amplifications or skip mutations rather than just IHC, however further cross validation in this matter needs to be performed.
Acknowledgements
None.
Footnote
Conflicts of Interest: The authors have no conflicts of interest to declare.
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