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EGFRMutationDraft, not yet medically reviewed

EGFR L858R

A point mutation in exon 21 that, together with exon 19 deletion, is among the most commonly discussed EGFR groups.

Parent marker: EGFR

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

Clinical meaning

This group is generally discussed with third generation EGFR inhibitors in advanced disease. The final selection still considers the patient's condition and therapy history.

How this finding appears in a report

Usually reported together with exon 19 deletion in a sequencing panel.

When therapy stops working

Frequently sought resistance mechanisms include T790M, C797S, MET amplification, and histological transformation.

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 L858R (exon 21)
Alteration type
Mutation
Discussed in
Lung Cancer
Updated
2026-09-10

Other names in reports

L858R, exon 21 mutation

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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