본문으로 건너뛰기
← 뒤로

Real-World Outcomes of Sequential Afatinib and Osimertinib Versus Afatinib and Chemotherapy in EGFR-Mutant NSCLC: Taiwan Multicenter GIANT Study.

Targeted oncology 2026 Vol.21(2) p. 213-226

Ko HW, Liao YT, Liang SK, Huang YH, Lin YC, Liu PC, Wang CC, Tsai JS, Chen YM, Shih JY, Yang TY, Yang CT

📝 환자 설명용 한 줄

[BACKGROUND] The optimal treatment strategy for epidermal growth factor receptor (EGFR)-mutated advanced non-small cell lung cancer (NSCLC)-sequential tyrosine kinase inhibitor (TKI) monotherapies ver

🔬 핵심 임상 통계 (초록에서 자동 추출 — 원문 검증 권장)
  • 표본수 (n) 303
  • p-value p < 0.001
  • 95% CI 30.3-34.5
  • 연구 설계 cohort study

이 논문을 인용하기

BibTeX ↓ RIS ↓
APA Ko HW, Liao YT, et al. (2026). Real-World Outcomes of Sequential Afatinib and Osimertinib Versus Afatinib and Chemotherapy in EGFR-Mutant NSCLC: Taiwan Multicenter GIANT Study.. Targeted oncology, 21(2), 213-226. https://doi.org/10.1007/s11523-026-01203-6
MLA Ko HW, et al.. "Real-World Outcomes of Sequential Afatinib and Osimertinib Versus Afatinib and Chemotherapy in EGFR-Mutant NSCLC: Taiwan Multicenter GIANT Study.." Targeted oncology, vol. 21, no. 2, 2026, pp. 213-226.
PMID 41862776

Abstract

[BACKGROUND] The optimal treatment strategy for epidermal growth factor receptor (EGFR)-mutated advanced non-small cell lung cancer (NSCLC)-sequential tyrosine kinase inhibitor (TKI) monotherapies versus upfront combination therapies-remains debated.

[OBJECTIVE] The Giotrif In Advanced NSCLC Taiwan (GIANT) study evaluated the real-world outcomes of sequential afatinib-based strategies.

[PATIENTS AND METHODS] This multicenter retrospective cohort study included 733 treatment-naïve patients with American Joint Committee on Cancer stage IIIB-IV NSCLC harboring Del19 or L858R EGFR mutations who received first-line afatinib across seven major Taiwanese medical centers between 2016 and 2024. Patients were stratified by second-line therapy into two groups: afatinib-osimertinib (n = 303) and afatinib-chemotherapy/other lines (n = 430). The primary outcome was overall survival (OS).

[RESULTS] Sequential afatinib-osimertinib therapy achieved a median OS of 55 months (95% confidence interval [CI] 53.2-66.4) compared to 32.3 months (95% CI 30.3-34.5) with alternative strategies (adjusted hazard ratio 0.43, p < 0.001). Survival benefits were consistent across EGFR mutations and brain metastasis statuses.

[CONCLUSION] Sequential afatinib-to-osimertinib therapy achieved remarkable OS exceeding 55 months in real-world practice, with outcomes appearing competitive with contemporary combination strategies. These findings support sequential TKI therapy as a durable and effective alternative that warrants prospective validation.

MeSH Terms

Humans; Afatinib; Carcinoma, Non-Small-Cell Lung; Female; Male; Lung Neoplasms; Taiwan; Aniline Compounds; Middle Aged; Acrylamides; Aged; Retrospective Studies; ErbB Receptors; Mutation; Antineoplastic Combined Chemotherapy Protocols; Adult; Treatment Outcome; Indoles; Pyrimidines