Lung cancer
ICD-10 C34 · ICD-11 2C25.Z

Treatment of Advanced or Metastatic NSCLC with EGFR S768I, L861Q, or G719X Mutation

Clinical Scenario

This protocol addresses patients with advanced or metastatic non-small cell lung cancer (NSCLC) whose tumours carry one or more of the uncommon EGFR point mutations: S768I, L861Q, and/or G719X. These variants represent approximately 10% of EGFR mutations observed in NSCLC, forming a molecularly distinct subgroup with specific first-line treatment guidance.

Treatment Approach

For patients in this molecular subgroup, first-line EGFR-directed targeted therapy is the recommended approach. Guideline panels have designated both preferred and other recommended agents — the full selection criteria, agent ranking, and treatment algorithm are available in the structured protocol.

Complete regimen details, agent selection, and sequencing are in the full protocol.

Instant Access to Structured Evidence-Based Regimens

References

Other less common EGFR mutations (approximately 10% of EGFR mutations observed in patients with NSCLC) include S768I, L861Q, and/or G719X.

The Panel recommends afatinib or osimertinib as preferred first-line therapy options for patients with advanced or metastatic NSCLC with EGFR S768I, L861Q, and/or G719X mutations.

Dacomitinib, erlotinib, and gefitinib are other recommended first-line treatment options.

View source ↗