医学
危险系数
肺癌
解剖(医学)
淋巴结
比例危险模型
置信区间
纵隔淋巴结
内科学
肿瘤科
外科
队列
癌症
泌尿科
转移
作者
P. Thomas,Cesare Braggio,Alex Fourdrain,Matthieu Vasse,Geoffrey Brioude,Delphine Trousse,David Boulate,Jean‐Philippe Dales,C. Doddoli,Pascale Tomasini,Xavier Benoît D’Journo,Laurent Greillier
标识
DOI:10.1093/ejcts/ezae438
摘要
Abstract OBJECTIVES To evaluate the impact of a quality improvement initiative on intraoperative lymph node (LN) dissection adequacy. METHODS A single-centre cohort of 781 naïve patients who underwent resection of non-small cell lung cancer with pathological LN involvement and survived beyond 90 days was reviewed. LN dissection metrics were compared before and after the implementation of a quality improvement initiative. Quality metrics (QM) were: QM1 (≥10 LN examined), QM2 (≥3 intrapulmonary and hilar LN, ≥ 3 mediastinal stations, including station 7 in all cases), and QM3 (combination of QM1 and QM2). RESULTS The proportion of patients meeting QM1 did not differ significantly between the pre- (87.8%) and post-implementation (89.1%) periods. However, meeting QM2 and QM3 significantly improved from 79.5% to 88.6% (P = 0.001), and 76.2% to 84.4% (P = 0.007), respectively. Cox proportional hazard regression model for disease-free survival showed that patients operated on after the implementation of the quality improvement initiative exhibited better disease-free survival compared to those operated on before [adjusted hazard ratio (aHR): 0.73; 95% confidence interval (CI) 0.59–0.90; P = 0.003]. Nevertheless, none of these quality metrics influenced long-term outcomes. In contrast, adjuvant chemotherapy (aHR: 0.55; 95% CI 0.43–0.71; P < 0.001) was associated with improved disease-free survival. In case of metastatic progression, immunotherapy improved overall survival (hazard ratio: 0.54; 95% CI 0.37–0.77; P = 0.0003). CONCLUSIONS Utilizing transparent data and collaborative feedback were effective to enhance the quality of nodal assessment in lung cancer surgery. Overall, long-term outcomes for patients with lymph node involvement was primarily associated with disease burden, adjuvant chemotherapy, and rescue immunotherapy. IRB approval number CERC-SFCTCV-2024-04-30_34750 on 30 April 2024.
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