Bronchoscopy Unit, Pulmonology Department, Hospital Germans Trias i Pujol, Badalona, Spain; Pulmonology Department, Hospital Universitari Mútua Terrassa, University of Barcelona, Terrassa, Spain.
Bronchoscopy Unit, Pulmonology Department, Hospital Germans Trias i Pujol, Badalona, Spain; Medicine Department, Universitat Autònoma de Barcelona, Cerdanyola, Spain.
Ann Thorac Surg. 2018 Aug;106(2):398-403. doi: 10.1016/j.athoracsur.2018.02.088. Epub 2018 Apr 6.
To evaluate the accuracy of systematic mediastinal staging by endobronchial ultrasound transbronchial needle aspiration (EBUS-TBNA) (sampling of all visible nodes measuring ≥5 mm from stations N3 to N1 regardless of their positron emission tomography/computed tomography [PET/CT] features) and compare this staging approach with targeted EBUS-TBNA staging (sampling only 18F-fluorodeoxyglucose [FDG]-avid nodes) in patients with N2 non-small cell lung cancer on PET/CT.
Retrospective study of 107 patients who underwent systematic EBUS-TBNA mediastinal staging. The results were compared with those of a hypothetical scenario where only FDG-avid nodes on PET/CT would be sampled.
Systematic EBUS-TBNA sampling demonstrated N3 disease in 3 patients, N2 disease in 60 (42 single-station or N2a, 18 multiple-station or N2b) and N0/N1 disease in 44. Of these 44, 7 underwent mediastinoscopy, which did not show mediastinal disease; 6 of the 7 proceeded to lung resection, which also showed no mediastinal disease. Thirty-four N0/N1 patients after EBUS-TBNA underwent lung resection directly: N0/N1 was found in 30 and N2 in 4 (1 N2b with a PET/CT showing N2a disease, 3 N2a). Sensitivity, specificity, negative predictive value, positive predictive value, and overall accuracy of systematic EBUS-TBNA were 94%, 100%, 90%, 100% and 96%, respectively. Compared with targeted EBUS-TBNA, systematic EBUS-TBNA sampling provided additional important clinical information in 14 cases (13%): 3 N3 cases would have passed unnoticed, and 11 N2b cases would have been staged as N2a.
In clinical practice, systematic sampling of the mediastinum by EBUS-TBNA, regardless of PET/CT features, is to be recommended over targeted sampling.
评估经支气管超声内镜引导下针吸活检术(EBUS-TBNA)(系统纵隔分期,对所有可见淋巴结进行取样,无论其正电子发射断层扫描/计算机断层扫描[PET/CT]特征如何,从 N3 到 N1 站的测量值均≥5mm)的准确性,并将这种分期方法与针对 PET/CT 上 N2 非小细胞肺癌的靶向 EBUS-TBNA 分期(仅取样 18F-氟脱氧葡萄糖[FDG]-活性淋巴结)进行比较。
回顾性研究了 107 例接受系统 EBUS-TBNA 纵隔分期的患者。结果与假设情况进行了比较,即在 PET/CT 上仅取样 FDG-活性淋巴结。
系统 EBUS-TBNA 取样显示 3 例 N3 疾病,60 例 N2 疾病(42 例单站或 N2a,18 例多站或 N2b),44 例 N0/N1 疾病。其中 7 例接受纵隔镜检查,未见纵隔疾病;7 例中 6 例行肺切除术,亦未见纵隔疾病。34 例 EBUS-TBNA 后 N0/N1 患者直接行肺切除术:30 例为 N0/N1,4 例为 N2(1 例 PET/CT 显示 N2a 疾病,3 例 N2a)。系统 EBUS-TBNA 的敏感性、特异性、阴性预测值、阳性预测值和总准确率分别为 94%、100%、90%、100%和 96%。与靶向 EBUS-TBNA 相比,系统 EBUS-TBNA 取样在 14 例(13%)中提供了额外的重要临床信息:3 例 N3 病例将被忽略,11 例 N2b 病例将被分期为 N2a。
在临床实践中,建议采用 EBUS-TBNA 对纵隔进行系统取样,而不考虑 PET/CT 特征,而不是采用靶向取样。