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表皮生长因子受体基因突变对第 8 版 TNM 分期病理Ⅱ-ⅢA 期(可切除)原发性肺癌术后预后的影响。

Effect of epidermal growth factor receptor gene mutation on the prognosis of pathological stage II-IIIA (8th edition TNM classification) primary lung cancer after curative surgery.

机构信息

Department of Thoracic Surgery, Kanagawa Cancer Center, 2-3-2 Nakao, Asahi, Yokohama, Kanagawa 241-8515, Japan; Department of Surgery, Yokohama City University, 3-9 Fukuura, Kanazawa, Yokohama, Kanagawa 236-0004, Japan.

Department of Thoracic Surgery, Kanagawa Cancer Center, 2-3-2 Nakao, Asahi, Yokohama, Kanagawa 241-8515, Japan.

出版信息

Lung Cancer. 2021 Dec;162:128-134. doi: 10.1016/j.lungcan.2021.11.002. Epub 2021 Nov 8.

Abstract

OBJECTIVES

This retrospective study aimed to elucidate the effect of epidermal growth factor receptor (EGFR) gene mutations on the prognosis of patients with pathological stage II-IIIA primary lung cancer after curative surgery.

MATERIALS AND METHODS

We enrolled 539 patients with p-stage II-IIIA (8th edition tumor-node-metastasis [TNM] classification) lung cancer who underwent curative resection at Kanagawa Cancer Center between January 2010 and December 2020 and whose tumors were tested for EGFR mutations. Relapse-free survival (RFS) and overall survival (OS) of patients with EGFR-mutant lung cancer (Mt, n = 126) including EGFR exon 21 L858R point mutation and EGFR exon 19 deletion mutation and EGFR mutation-wild lung cancer (Wt, n = 413) were analyzed using Kaplan-Meier curves and compared using a log-rank test. Cox regression analysis was performed to evaluate the effects of EGFR gene mutations on RFS and OS at each stage.

RESULTS

There were 56/256 patients with p-stage II EGFR-Mt/Wt and 70/157 patients with p-stage IIIA EGFR-Mt/Wt. The 5-year RFS rate of patients with EGFR-Mt/Wt was 46.6%/52.0% (p = 0.787) for p-stage II and 17.4%/29.7% (p = 0.929) for p-stage IIIA. The 5-year OS rate was 92.0%/65.7% (p = 0.001) for p-stage II and 56.0%/39.3% (p = 0.016) for p-stage IIIA. EGFR-Mt was not an independent prognostic factor for OS of patients with p-stage IIIA lung cancer (hazard ratio [HR], 0.95; 95% confidence interval [CI], 0.51-1.76; p = 0.872); however, EGFR-Mt was an independent favorable prognostic factor for OS of patients with p-stage II lung cancer (HR, 0.59; 95% CI, 0.36-0.96; p = 0.034).

CONCLUSION

The OS of lung cancer patients with p-stage II or IIIA, classified according to the 8th edition TNM classification, was remarkably favorable. Incorporating EGFR mutations to the anatomical TNM classification may lead to a more accurate prognosis prediction.

摘要

目的

本回顾性研究旨在阐明表皮生长因子受体(EGFR)基因突变对接受根治性手术的病理性 II 期-IIIA 期原发性肺癌患者预后的影响。

材料与方法

我们纳入了 539 名在 2010 年 1 月至 2020 年 12 月期间于神奈川癌症中心接受根治性切除术且肿瘤检测 EGFR 基因突变的 p 期 II-IIIA 期(第 8 版肿瘤-淋巴结-转移 [TNM] 分类)肺癌患者。分析包括 EGFR 外显子 21 L858R 点突变和 EGFR 外显子 19 缺失突变在内的 EGFR 突变型肺癌(Mt,n=126)和 EGFR 野生型肺癌(Wt,n=413)患者的无复发生存期(RFS)和总生存期(OS),采用 Kaplan-Meier 曲线进行分析,并采用对数秩检验进行比较。采用 Cox 回归分析评估 EGFR 基因突变对各期 RFS 和 OS 的影响。

结果

p 期 II 期有 56/256 例患者为 EGFR-Mt/Wt,p 期 IIIA 期有 70/157 例患者为 EGFR-Mt/Wt。EGFR-Mt/Wt 患者的 5 年 RFS 率在 p 期 II 期为 46.6%/52.0%(p=0.787),在 p 期 IIIA 期为 17.4%/29.7%(p=0.929)。5 年 OS 率在 p 期 II 期为 92.0%/65.7%(p=0.001),在 p 期 IIIA 期为 56.0%/39.3%(p=0.016)。EGFR-Mt 不是 p 期 IIIA 期肺癌患者 OS 的独立预后因素(风险比 [HR],0.95;95%置信区间 [CI],0.51-1.76;p=0.872);然而,EGFR-Mt 是 p 期 II 期肺癌患者 OS 的独立有利预后因素(HR,0.59;95%CI,0.36-0.96;p=0.034)。

结论

根据第 8 版 TNM 分类,p 期 II 期或 IIIA 期肺癌患者的 OS 显著良好。将 EGFR 突变纳入解剖 TNM 分类可能会导致更准确的预后预测。

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