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EGFRMutationDraft, not yet medically reviewed

EGFR T790M

A change that often appears as a resistance mechanism after early-generation EGFR inhibitors.

Parent marker: EGFR

Not a diagnosis and not final medical advice. Must be reviewed by a doctor.

Clinical meaning

T790M was discussed as the reason earlier generation therapies stopped working. Third-generation inhibitors are designed to remain active at these changes.

How this finding appears in a report

Examination is often performed of new tissue or blood samples after progression.

When therapy stops working

After third-generation therapy, C797S alterations and non-EGFR mechanisms became part of re-examination.

What needs verification

  • Complete variant name as written in the laboratory report.
  • Examination methods and types of samples used.
  • Examination dates were compared with ongoing therapy.

Marker context: EGFR

A common EGFR mutation (exon 19 deletion, L858R) alters the way systemic therapy is selected in non-small-cell lung cancer. Other groups of mutations, including exon 20 insertions, are generally considered distinct and are often directed to other pathways, including clinical trials.

A negative result does not always mean absent

Test sensitivity differs by sample type and method. Results need to be read together with the pathology report and clinical condition.

Summary

Gen
EGFR
Variant
EGFR T790M
Alteration type
Mutation
Discussed in
Lung Cancer
Updated
2026-09-10

Other names in reports

T790M

Drugs discussed

Treatment categories

Clinical trials

Studies mentioning marker EGFR

Filtered from public study descriptions. Access status and site readiness remain unverified.

Next steps

These suggestions come from links between entries in TanyaKanker's database, not from a medical judgement. Each suggestion includes why it appears.

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