Division of Thoracic Surgery, Massachusetts General Hospital, Boston, Massachusetts; Codman Center for Clinical Effectiveness, Massachusetts General Hospital, Boston, Massachusetts.
Division of Thoracic Surgery, The University of Chicago Medicine & Biological Sciences, Chicago, Illinois.
Ann Thorac Surg. 2021 Apr;111(4):1125-1132. doi: 10.1016/j.athoracsur.2020.06.060. Epub 2020 Aug 25.
Clinical staging of lung cancer may not reliably predict nodal disease, and its accuracy in The Society of Thoracic Surgeons General Thoracic Surgery Database is not described.
Among anatomic pulmonary resections for stages I to III lung cancer with complete clinical and pathologic staging (2012-2017), the accuracy of invasive mediastinal staging (IMS) was compared with noninvasive mediastinal staging only. Accuracy, defined as concordance between clinical and pathologic nodal status, was examined using logistic regression to determine factors associated with clinical nodal (cN) accuracy. Variation in accuracy across centers was recorded and categorized.
We included 39,516 patients with stages I to III pulmonary cancer (adenocarcinoma, 66%; squamous, 23%; neuroendocrine, 5%; mixed, 3.3%; other, 2.4%), of whom 90.4% had cN0 disease. IMS was performed in 32.4%. The IMS group had more central tumors (14.8% vs 6.0%, P < .001) and cN1-2 (15.7% vs 6.8%, P < .001). Nodal accuracy was 79.8%. Although IMS had a lower nodal accuracy for cN0-2 disease (74.6% vs 82.6%, P < .001), IMS had higher accuracy when comparing patients with cN1-2 disease (53.9% vs 46.9%, P < .001). In multivariable analysis central tumors (odds ratio, 0.47; 95% confidence interval, 0.43-0.51) and >cN0 disease (odds ratio, 0.25; 95% confidence interval, 0.22-0.29) were associated with lower accuracy. Accuracy of IMS in the top 20 centers was 94.4% and in the bottom 20, 70.9%.
Staging accuracy in lung cancers selected for initial resection declines with >cN0 and central tumors. Noninvasive staging in tumors without cN involvement misses nearly 20% of cN1-2. Center-specific accuracy is a target for quality improvement.
肺癌的临床分期可能无法可靠地预测淋巴结疾病,并且在胸外科医师学会(STS)普通胸外科数据库中并未描述其准确性。
在 2012 年至 2017 年间进行的 I 期至 III 期肺癌解剖性肺切除术患者中,对有完整临床和病理分期的患者进行侵袭性纵隔分期(IMS)与仅进行非侵袭性纵隔分期的比较。使用逻辑回归确定与临床淋巴结(cN)准确性相关的因素,来检验准确性(定义为临床和病理淋巴结状态之间的一致性)。记录并分类了中心间准确性的差异。
我们纳入了 39516 例 I 期至 III 期肺癌患者(腺癌 66%,鳞癌 23%,神经内分泌癌 5%,混合癌 3.3%,其他 2.4%),其中 90.4%为 cN0 疾病。32.4%的患者进行了 IMS。与 IMS 组相比,非 IMS 组的中央型肿瘤(14.8%比 6.0%,P<0.001)和 cN1-2 疾病(15.7%比 6.8%,P<0.001)更多。淋巴结准确性为 79.8%。尽管 IMS 对 cN0-2 疾病的淋巴结准确性较低(74.6%比 82.6%,P<0.001),但对于 cN1-2 疾病患者,IMS 的准确性更高(53.9%比 46.9%,P<0.001)。多变量分析显示,中央型肿瘤(比值比,0.47;95%置信区间,0.43-0.51)和 >cN0 疾病(比值比,0.25;95%置信区间,0.22-0.29)与较低的准确性相关。前 20 名中心的 IMS 准确性为 94.4%,而最后 20 名中心的准确性为 70.9%。
选择初始切除的肺癌患者的分期准确性随着 >cN0 和中央型肿瘤而降低。无 cN 受累的肿瘤的非侵袭性分期会漏诊近 20%的 cN1-2 疾病。中心特异性准确性是质量改进的目标。