Bott Matthew J, Patel Aalok P, Crabtree Traves D, Colditz Graham A, Kreisel Daniel, Krupnick A Sasha, Patterson G Alexander, Broderick Stephen, Meyers Bryan F, Puri Varun
Department of Surgery, Division of Cardiothoracic Surgery, Washington University School of Medicine, St. Louis, Missouri.
Department of Surgery, Division of Cardiothoracic Surgery, Washington University School of Medicine, St. Louis, Missouri.
Ann Thorac Surg. 2015 Dec;100(6):2048-53. doi: 10.1016/j.athoracsur.2015.05.100. Epub 2015 Aug 13.
A substantial proportion of patients with clinical stage I non-small cell lung cancer (NSCLC) have more advanced disease on final pathologic review. We studied potentially modifiable factors that may predict pathologic upstaging.
Data of patients with clinical stage I NSCLC undergoing resection were obtained from the National Cancer Database. Univariate and multivariate analyses were performed to identify variables that predict upstaging.
From 1998 to 2010, 55,653 patients with clinical stage I NSCLC underwent resection; of these, 9,530 (17%) had more advanced disease on final pathologic review. Of the 9,530 upstaged patients, 27% had T3 or T4 tumors, 74% had positive lymph nodes (n > 0), and 4% were found to have metastatic disease (M1). Patients with larger tumors (38 mm vs 29 mm, p < 0.001) and a delay greater than 8 weeks from diagnosis to resection were more likely to be upstaged. Upstaged patients also had more lymph nodes examined (10.9 vs 8.2, p < 0.001) and were more likely to have positive resection margins (10% vs 2%, p < 0.001). Median survival was lower in upstaged patients (39 months vs 73 months). Predictors of upstaging in multivariate regression analysis included larger tumor size, delay in resection greater 8 weeks, positive resection margins, and number of lymph nodes examined. There was a linear relationship between the number of lymph nodes examined and the odds of upstaging (1 to 3 nodes, odds ratio [OR] 2.01; >18 nodes OR 6.14).
Pathologic upstaging is a common finding with implications for treatment and outcomes in clinical stage I NSCLC. A thorough analysis of regional lymph nodes is critical to identify patients with more advanced disease.
相当一部分临床 I 期非小细胞肺癌(NSCLC)患者在最终病理检查时疾病分期更晚。我们研究了可能预测病理分期上调的潜在可改变因素。
从国家癌症数据库获取接受手术的临床 I 期 NSCLC 患者的数据。进行单因素和多因素分析以确定预测分期上调的变量。
1998 年至 2010 年,55653 例临床 I 期 NSCLC 患者接受了手术;其中,9530 例(17%)在最终病理检查时疾病分期更晚。在 9530 例分期上调的患者中,27%有 T3 或 T4 肿瘤,74%有阳性淋巴结(n>0),4%被发现有转移性疾病(M1)。肿瘤较大(38mm 对 29mm,p<0.001)以及从诊断到手术延迟超过 8 周的患者更有可能分期上调。分期上调的患者检查的淋巴结也更多(10.9 对 8.2,p<0.001),且更有可能有阳性手术切缘(10%对 2%,p<0.001)。分期上调患者的中位生存期较低(39 个月对 73 个月)。多因素回归分析中分期上调的预测因素包括肿瘤较大、手术延迟超过 8 周、阳性手术切缘以及检查的淋巴结数量。检查的淋巴结数量与分期上调的几率之间存在线性关系(1 至 3 个淋巴结,比值比[OR]2.01;>18 个淋巴结 OR 6.14)。
病理分期上调是临床 I 期 NSCLC 中常见的发现,对治疗和预后有影响。对区域淋巴结进行全面分析对于识别疾病分期更晚的患者至关重要。