Division of General Internal Medicine, Icahn School of Medicine at Mount Sinai, New York, NY.
Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
Chest. 2014 Dec;146(6):1619-1626. doi: 10.1378/chest.14-0204.
Visceral pleural invasion (VPI) may impact non-small cell lung cancer (NSCLC) survival. However, previous studies are mixed as to whether VPI is an independent prognostic factor in early-stage cancers and whether its effect is size dependent. In the current American Joint Committee on Cancer (AJCC) staging system, VPI leads to upstaging of cancers < 3 cm but not of those 3 to 7 cm in size.
Using the Surveillance, Epidemiology, and End Results (SEER) registry, we identified 16,315 patients with stage I-II NSCLC treated with lobectomy. We used the Kaplan-Meier method and Cox regression to assess the association of VPI with lung cancer-specific (primary outcome) and overall survival. Based on these results, we created a revised VPI staging classification.
Overall, 3,389 patients (21%) had VPI. Kaplan-Meier analysis stratified by tumor size showed worse cancer-specific survival in patients with VPI (P < .0001). VPI was independently associated with decreased lung cancer-specific survival (hazard ratio, 1.38; 95% CI, 1.29-1.47) after controlling for tumor size and other confounders; this effect was not size dependent. In our revised classification, tumors < 7 cm with VPI were upstaged to the next T category.
VPI is a prevalent finding associated with worse prognosis in early-stage lung cancer, even among patients with tumors > 3 cm, a factor not captured in the current staging system. Patients with VPI may be considered candidates for more aggressive treatment.
内脏胸膜侵犯(VPI)可能影响非小细胞肺癌(NSCLC)的生存。然而,先前的研究对于 VPI 是否是早期癌症的独立预后因素以及其影响是否与肿瘤大小有关存在分歧。在目前的美国癌症联合委员会(AJCC)分期系统中,VPI 导致<3cm 的癌症分期升级,但不影响 3 至 7cm 大小的癌症。
我们使用监测、流行病学和最终结果(SEER)登记处,确定了 16315 例接受肺叶切除术治疗的 I-II 期 NSCLC 患者。我们使用 Kaplan-Meier 方法和 Cox 回归评估 VPI 与肺癌特异性(主要结局)和总生存的相关性。根据这些结果,我们创建了一个修订的 VPI 分期分类。
总体而言,3389 例(21%)患者存在 VPI。按肿瘤大小分层的 Kaplan-Meier 分析显示,VPI 患者的肺癌特异性生存率更差(P<.0001)。在控制肿瘤大小和其他混杂因素后,VPI 与肺癌特异性生存率降低独立相关(风险比,1.38;95%CI,1.29-1.47);这种影响与肿瘤大小无关。在我们的修订分类中,<7cm 且存在 VPI 的肿瘤被升级到下一个 T 分期。
VPI 是一种常见的发现,与早期肺癌的预后更差相关,即使在肿瘤>3cm 的患者中也是如此,这是当前分期系统中未捕捉到的因素。存在 VPI 的患者可能被认为是更积极治疗的候选者。