Division of Thoracic Surgery, Keck School of Medicine, The University of Southern California, Los Angeles, CA, USA.
Keck School of Medicine, The University of Southern California, Los Angeles, CA, USA.
Eur J Cardiothorac Surg. 2022 Jun 15;62(1). doi: 10.1093/ejcts/ezab498.
Visceral pleural invasion (VPI) guidelines, for tumours ≤4 cm are ambiguous. Non-small-cell lung cancers (NSCLCs) 3 to ≤4 cm are assigned the T2a designation. Similarly, any tumours with VPI, smaller than 3 cm, are upstaged and also assigned the same T2a designation. We hypothesized that adjuvant chemotherapy would significantly improve 5-year survival for NSCLC ≤4 cm with VPI.
The National Cancer Database was queried from 2010 to 2016 for cases of NSCLC with clinical stage I disease, ≤4 cm, who subsequently underwent surgical resection. These stage I NSCLCs were stratified according to clinical tumour sizes (0 to ≤1, 1 to ≤2, 2 to ≤3 and 3 to ≤4 cm). This cohort was then divided into groups with and without VPI and further split based on the administration of adjuvant chemotherapy. Kaplan-Meier analysis was used to calculate 5-year overall survival (OS) for patients categorized by tumour size, VPI status, and receipt of adjuvant chemotherapy. Multivariable Cox regression adjusting for tumour size and VPI status was used to determine associations between use of adjuvant chemotherapy and OS.
A total of 61 454 patients with NSCLC and clinical tumour sizes <4 cm were identified and grouped based on size along with VPI and adjuvant chemotherapy. The 5-year OS for combined tumour sizes without VPI was higher than for patients with VPI (66.2% vs 59.5%, P < 0.001). The OS for tumour size (0 to ≤1, 1 to ≤2, 2 to ≤3 and 3 to ≤4 cm) was lower for patients with VPI regardless of size (all P ≤ 0.010). When all tumour sizes were combined, patients with VPI who received adjuvant chemotherapy had an improved 5-year OS compared to patients without adjuvant chemotherapy (65.5% vs 58.8%, P < 0.001). When cohorts were created by tumour size, only VPI tumours 3 to ≤4 cm had a statistically significant increase in 5-year OS for patients receiving adjuvant chemotherapy (68.8% vs 49.9%, P < 0.001). On multivariable Cox regression for OS, adjuvant chemotherapy was associated with significantly longer 5-year OS in tumour size 3 to ≤4 (hazard ratio = 0.62, 95% confidence interval 0.46-0.83, P = 0.001).
VPI remains a poor prognostic factor in clinically node-negative, T2a or less, NSCLC patients. Guidelines recommend considering chemotherapy for high-risk T2aN0, margin-negative patients-including those patients with VPI. Based on the analysis, adjuvant chemotherapy should be considered specifically for 3 to ≤4 cm with VPI due to an observed 5-year OS advantage.
对于直径≤4cm 的肿瘤,内脏胸膜侵犯(VPI)指南存在模糊性。直径为 3 至≤4cm 的非小细胞肺癌(NSCLC)被归类为 T2a 期。同样,任何 VPI 小于 3cm 的肿瘤,都会被升级,并被归类为相同的 T2a 期。我们假设辅助化疗会显著提高 VPI 直径≤4cm 的 NSCLC 的 5 年生存率。
从 2010 年到 2016 年,我们在国家癌症数据库中查询了接受手术切除的临床 I 期疾病、直径≤4cm 的 NSCLC 病例。这些 I 期 NSCLC 按临床肿瘤大小(0 至≤1、1 至≤2、2 至≤3 和 3 至≤4cm)分层。然后,将这些队列分为有 VPI 和无 VPI 两组,并根据是否接受辅助化疗进一步细分。采用 Kaplan-Meier 分析计算按肿瘤大小、VPI 状态和接受辅助化疗分类的患者的 5 年总生存率(OS)。采用多变量 Cox 回归校正肿瘤大小和 VPI 状态,确定接受辅助化疗与 OS 之间的关系。
共确定了 61454 名 NSCLC 患者,其临床肿瘤大小<4cm,并根据大小、VPI 和辅助化疗进行分组。无 VPI 的联合肿瘤大小 5 年 OS 高于有 VPI 的患者(66.2%比 59.5%,P<0.001)。无论肿瘤大小如何,有 VPI 的肿瘤大小(0 至≤1、1 至≤2、2 至≤3 和 3 至≤4cm)的 OS 均较低(均 P≤0.010)。当所有肿瘤大小合并时,接受 VPI 并接受辅助化疗的患者 5 年 OS 较未接受辅助化疗的患者有所提高(65.5%比 58.8%,P<0.001)。当按肿瘤大小分组时,只有直径 3 至≤4cm 的 VPI 肿瘤患者接受辅助化疗后 5 年 OS 有统计学意义的增加(68.8%比 49.9%,P<0.001)。在 OS 的多变量 Cox 回归中,辅助化疗与肿瘤大小为 3 至≤4cm 的患者的 5 年 OS 显著延长相关(风险比=0.62,95%置信区间 0.46-0.83,P=0.001)。
VPI 仍然是临床淋巴结阴性、T2a 或更低的 NSCLC 患者的预后不良因素。指南建议考虑对高危 T2aN0、切缘阴性的患者(包括 VPI 患者)进行化疗。基于分析,由于观察到 5 年 OS 优势,应专门考虑对 VPI 直径 3 至≤4cm 的患者进行辅助化疗。