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    Recurrence and Risk Factors for Postoperative Recurrence in Patients with Completely Resected Stage IA2 and IA3 EGFR-Mutated Lung Adenocarcinoma

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    https://www.riss.kr/link?id=T17568038

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    Introduction: Data on recurrence risk in patients with stage IA EGFR-mutated non-small cell lung cancer (NSCLC) remain limited. We investigated long-term recurrence outcomes and risk factors in patients with completely resected stage IA2–IA3 EGFR-mutated NSCLC.
    Methods: This multicenter retrospective cohort study included patients from 12 academic institutions in South Korea who underwent curative-intent resection for stage IA2–IA3 EGFR-mutated NSCLC between 2010 and 2017. Recurrence-free survival (RFS), overall survival, and risk factors for recurrence were evaluated using Cox proportional hazards regression analyses.
    Results: A total of 314 patients were included, with a median follow-up of 79.3 months. Disease recurrence occurred in 50 patients (15.9%). The 5-year RFS(define at first use) rates were 90.1% for stage IA2 and 86.4% for stage IA3 disease, with no significant difference between the 2 stages (P = 0.129). In the multivariable analysis, a consolidation-to-tumor ratio (CTR) ≥ 0.5 (hazard ratio [HR], 5.274; 95% confidence interval [CI], 1.608–17.292; P = 0.006) and poor histological differentiation (HR, 3.401; 95% CI, 1.328–8.709; P = 0.011) were independently associated with recurrence. Age ≥ 65 years was the only independent predictor of mortality (HR, 5.027; 95% CI, 2.354–10.734; P 〈 0.001).
    Conclusions: Patients with completely resected stage IA2–IA3 EGFR-mutated NSCLC had favorable long-term outcomes, although recurrence occurred in approximately one-sixth of patients. A CTR of ≥ 0.5 and poor histological differentiation were independently associated with recurrence. These factors may help identify patients who could benefit from consideration of adjuvant treatment.
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    Introduction: Data on recurrence risk in patients with stage IA EGFR-mutated non-small cell lung cancer (NSCLC) remain limited. We investigated long-term recurrence outcomes and risk factors in patients with completely resected stage IA2–IA3 EGF...

    Introduction: Data on recurrence risk in patients with stage IA EGFR-mutated non-small cell lung cancer (NSCLC) remain limited. We investigated long-term recurrence outcomes and risk factors in patients with completely resected stage IA2–IA3 EGFR-mutated NSCLC.
    Methods: This multicenter retrospective cohort study included patients from 12 academic institutions in South Korea who underwent curative-intent resection for stage IA2–IA3 EGFR-mutated NSCLC between 2010 and 2017. Recurrence-free survival (RFS), overall survival, and risk factors for recurrence were evaluated using Cox proportional hazards regression analyses.
    Results: A total of 314 patients were included, with a median follow-up of 79.3 months. Disease recurrence occurred in 50 patients (15.9%). The 5-year RFS(define at first use) rates were 90.1% for stage IA2 and 86.4% for stage IA3 disease, with no significant difference between the 2 stages (P = 0.129). In the multivariable analysis, a consolidation-to-tumor ratio (CTR) ≥ 0.5 (hazard ratio [HR], 5.274; 95% confidence interval [CI], 1.608–17.292; P = 0.006) and poor histological differentiation (HR, 3.401; 95% CI, 1.328–8.709; P = 0.011) were independently associated with recurrence. Age ≥ 65 years was the only independent predictor of mortality (HR, 5.027; 95% CI, 2.354–10.734; P 〈 0.001).
    Conclusions: Patients with completely resected stage IA2–IA3 EGFR-mutated NSCLC had favorable long-term outcomes, although recurrence occurred in approximately one-sixth of patients. A CTR of ≥ 0.5 and poor histological differentiation were independently associated with recurrence. These factors may help identify patients who could benefit from consideration of adjuvant treatment.

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    목차 (Table of Contents)

    • Introduction∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙1
    • Methods∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙3
    • Introduction∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙1
    • Methods∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙3
    • Results∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙7
    • Discussion∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙20
    • Conclusion∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙24
    • References∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙25
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