Science and Research

Survival benefit and toxicity profile of adjuvant icotinib for patients with EGFR mutation-positive non-small cell lung carcinoma: a retrospective study

BACKGROUND: Adjuvant epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) are increasing considered for the tailored management of resectable non-small cell lung cancer (NSCLC). This study aimed to analyze the survival and toxicity profile of patients with EGFR mutation-positive NSCLC treated with adjuvant icotinib. METHODS: This was a single-center retrospective study of patients with EGFR mutation-positive NSCLC who underwent R0 (microscopically margin-negative) resection and received adjuvant icotinib between November 2011 and December 2017. The outcomes included 2-year disease-free survival (DFS) rate, 3-year overall survival (OS) rates, DFS, OS, and adverse events (AEs). RESULTS: A total of 86 patients receiving adjuvant icotinib were included. Their mean age was 59.7±10.0 years, and 26 (30.2%) patients were male. The 2-year DFS rate was 86.7%, and the 3-year OS rate was 95.3% with adjuvant icotinib. DFS (P=0.044) and OS (P=0.003) are better in stage I/II disease than in stage III disease. There seems no differences in DFS and OS between patients with low or high preoperative CEA levels (cutoff of 5 ng/mL), patients with exon 19 or 21 EGFR mutation or patients with or without smoking history. The most common AEs with adjuvant icotinib were rash (83.7%) and diarrhea (19.8%). One (1.2%) patient-reported grade ≥3 AEs. No treatment-related death occurred. CONCLUSIONS: For patients with EGFR mutation-positive NSCLC, adjuvant icotinib might be associated with a promising survival benefit, with an acceptable toxicity profile.

  • Zeng, Z.
  • Yan, B.
  • Chen, Y.
  • Zhang, L.
  • Zhu, J.
  • Yang, F.
  • Wei, F.
  • Tam, T. C. C.
  • Kauffmann-Guerrero, D.
  • Soo, R. A.
  • Ren, X.
  • You, J.

Keywords

  • Non-small cell lung cancer (NSCLC)
  • adjuvant
  • epidermal growth factor receptor mutation (EGFR mutation)
  • icotinib
  • (available at http://dx.doi.org/10.21037/tlcr-20-1214). The authors have no
  • conflicts of interest to declare.
Publication details
DOI: 10.21037/tlcr-20-1214
Journal: Transl Lung Cancer Res
Pages: 2401-2410 
Number: 6
Work Type: Original
Location: CPC-M
Disease Area: LC
Partner / Member: LMU
Access-Number: 33489802

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