Randomized Phase II Study of 3 Months or 2 Years of Adjuvant Afatinib in Patients With Surgically Resected Stage

Joel W Neal1, Daniel B Costa2, Alona Muzikansky3

  • 1Stanford Cancer Institute, Stanford, CA.

Insights

Adjuvant therapy with epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) may delay recurrence in non-small-cell lung cancer. A 2-year afatinib course showed a trend toward improved recurrence-free survival compared to 3 months, but did not meet the primary endpoint.

Area of Science:

  • Oncology
  • Pharmacology

Background:

  • Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) are investigated for adjuvant therapy in resected non-small-cell lung cancer (NSCLC).
  • The optimal duration of adjuvant EGFR TKI therapy to prevent cancer recurrence remains undetermined.

Purpose of the Study:

  • To compare the efficacy of 3 months versus 2 years of adjuvant afatinib in patients with resected EGFR-mutant NSCLC.
  • To assess the recurrence rate at 2 years following different durations of adjuvant afatinib treatment.

Main Methods:

  • A randomized phase II study enrolled 45 patients with completely resected stage IA-IIIB EGFR-mutant NSCLC.
  • Patients received either 3 months or 2 years of adjuvant afatinib (30 mg daily).
  • Recurrence rates at 2 years were the primary endpoint, with imaging every 6 months for 3 years.

Main Results:

  • The 2-year recurrence-free survival (RFS) rates were 70% for 3 months of afatinib and 81% for 2 years (P = .55).
  • Median RFS was 42.8 months versus 58.6 months, respectively.
  • Early drug discontinuation was higher in the 2-year group (59% vs 4%).

Conclusions:

  • Two years of adjuvant afatinib showed a trend towards improved RFS compared to 3 months in resected EGFR-mutant NSCLC, but did not meet the primary endpoint target.
  • Underaccrual and early discontinuation in the 2-year arm likely impacted results.
  • The optimal duration of adjuvant EGFR TKI therapy requires further investigation, especially with newer agents like osimertinib.

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