MET amplification (gene copy number)
MET amplification means extra copies of the MET gene, either as a primary driver in a few lung cancers or as the escape route after EGFR inhibitors. No label yet selects on it; trials define it by FISH ratio or copy number.
Overview
MET amplification is scored by FISH as MET/CEP7 ratio (high-level at 5 or more in the Camidge classification, or 2 or more with mean copies of 10 or more) or by sequencing as gene copy number (GCN 10 or more is the common trial threshold). It occurs de novo in 1 to 4 percent of NSCLC and arises in 5 to 20 percent of EGFR-mutant cancers progressing on osimertinib, the setting of the MARIPOSA-2 and the SAVANNAH trial of osimertinib plus savolitinib (NCT03778229). No approval names MET amplification as the selection criterion; amivantamab is approved on EGFR status rather than MET, and capmatinib's label covers exon 14 skipping only.
- Target · the protein and the cell it sits on
- Drug · antibody, small molecule, cell or radioligand
- Effect · signal, damage or kill
In plain words · A receptor that is either mutated in some lung cancers or amplified as an escape route when other lung cancer drugs fail.
MET amplification on your report does not yet open an approved treatment on its own. If your lung cancer is EGFR-mutant and grew on osimertinib, it is the reason trials combine a MET inhibitor with the EGFR drug, and your team may discuss those trials or amivantamab, which is approved on EGFR status.
Written only from the label or guideline text cited on this page. Not medical advice; your own report and the reading your team gives it come first.
MET/CEP7 ratio by FISH (high-level 5 or more) or MET gene copy number by sequencing (trial thresholds of 6 or 10 copies); no label defines a threshold.
“MET amplification (bypass resistance)”
SAVANNAH trial (NCT03778229): MET overexpression and/or amplification defined by IHC 90 percent 3+ or FISH 10 or more copiesNo approval uses this readout as a threshold. It is defined by SAVANNAH: osimertinib plus savolitinib in MET-amplified or overexpressed EGFR-mutant NSCLC after osimertinib (ClinicalTrials.gov NCT03778229).
Matched on the name and aliases of the readout in the title, setting and summary of each trial; a match is a mention, not proof the readout was an entry criterion.
- NCT02864992 · 2023Tepotinib Phase II in NSCLC Harboring MET Alterations (VISION)
- NCT02414139 · 2020GEOMETRY mono-1
- NCT07196644A Study to Assess Adverse Events and Change in Disease Activity in Participants 12 Years of Age or Older With Locally Advanced or Metastatic Solid Tumors That Harbor MET Amplification Receiving Intravenously Infused Telisotuzumab Adizutecan
- NCT06829459A Study to Evaluate the Efficacy and Safety of Glumetinib Combined With Osimertinib Mesylate Versus Platinum-based Doublet Chemotherapy in N
- NCT07109531ASKC202 Combined With Limertinib Versus Platinum-based Chemotherapy in Treatment of Locally Advanced or Metastatic NSCLC With MET Amplification/Overexpression After Failure of EGFR-TKI Therapy
- NCT06343064Vebreltinib Plus PLB1004 in EGFR-mutated, Advanced NSCLC With MET Amplification or MET Overexpression Following EGFR-TKI
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