Clinical stage-specific prognostic impact of adequate lymphadenectomy in early-stage lung cancer

医学 倾向得分匹配 淋巴结切除术 危险系数 阶段(地层学) 癌胚抗原 内科学 围手术期 肺癌 淋巴结 肿瘤科 比例危险模型 多元分析 胃肠病学 辅助治疗 癌症 外科 置信区间 古生物学 生物
作者
Chia-Yih Liu,Ko-Han Lin,Hui‐Mei Chen,Lei‐Chi Wang,Yi‐Chen Yeh,Po‐Kuei Hsu,Chien‐Sheng Huang,Chih‐Cheng Hsieh,Han-Shui Hsu
出处
期刊:European Journal of Cardio-Thoracic Surgery [Oxford University Press]
标识
DOI:10.1093/ejcts/ezaf083
摘要

Abstract and keywords OBJECTIVES To assess the prognostic impact of adequate lymphadenectomy and determine the optimal nodal assessment for different clinical stages of lung cancer. METHODS We retrospectively reviewed 1214 patients with clinical stage I–III non-small cell lung cancer who had preoperative PET/CT and curative surgery (2006–2017). Patients were categorized based on whether they had adequate [R0] or inadequate lymphadenectomy [R(un)]. Propensity score matching was conducted to minimize bias. Primary end-points were recurrence-free survival (RFS), overall survival (OS), and cancer-specific survival (CSS). Secondary end-points included outcomes stratified by clinical stages. RESULTS Multivariate Cox analysis identified preoperative carcinoembryonic antigen level, tumour size, uptake of tumour on PET/CT, R(un) (Hazard ratio (HR)= 2.16; p < 0.001), angiolymphatic invasion, lymph node involvement, and postoperative adjuvant therapy as independent predictors of RFS. The matched cohort included 440 R0 and 440 R(un) patients, with a median follow-up of 94 months. Significant differences were found in 10-year RFS (77.2% vs 61.3%, p < 0.001), OS (75.8% vs 64.3%, p < 0.001) and CSS (83.8% vs 74.2%, p < 0.001). Despite longer operative time for R0 (210 vs 195 min, p = 0.008), perioperative complications, hospital stay length, and blood loss were similar. Subgroup analysis showed R(un) as an independent predictor of RFS in clinical stages IA3 (HR = 2.53, p = 0.001), IB (HR = 1.71, p = 0.046), and II (HR = 2.44, p < 0.001), but not in IA1 or IA2. R0 had significantly better RFS than R(un) in matched cohort of stages IA3 (p = 0.003), IB (p = 0.001), and II (p = 0.001). CONCLUSIONS Adequate lymph node assessment improves prognosis in patients with clinical stages ≥ IA3. A uniform nodal assessment approach should be reconsidered for different clinical stages.
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