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表皮生长因子受体(EGFR)重排的腺癌与静脉血栓栓塞的高发生率相关。

The EGFR-rearranged adenocarcinoma is associated with a high rate of venous thromboembolism.

作者信息

Wang Jing, Hu Bin, Li Tong, Miao Jinbai, Zhang Wenqian, Chen Shuo, Sun Yixin, Cui Songping, Li Hui

机构信息

Department of Thoracic Surgery, Beijing Chaoyang Hospital, Capital Medical University, Beijing 100020, China.

出版信息

Ann Transl Med. 2019 Dec;7(23):724. doi: 10.21037/atm.2019.12.24.

Abstract

BACKGROUND

The purpose of this study was to investigate the incidence of venous thromboembolism (VTE) in epidermal growth factor receptor (EGFR) mutations patients with lung adenocarcinoma, to provide clinical basis for the perioperative prevention and treatment of VTE in patients with lung cancer.

METHODS

This study included patients with invasive lung adenocarcinoma confirmed by pathology from July 2016 to March 2018 after surgical pulmonectomy in Thoracic Surgery Department of Beijing Chaoyang Hospital. All enrolled patients were tested for relevant gene mutations. All patients were classified as adenocarcinoma subtypes by the 2011 International Association for the Study of Lung Cancer (IASLC), American Thoracic Society (ATS) and European Respiratory Society (ERS). Patients were divided into the VTE group and the control group according to whether VTE occurred postoperatively. Baseline data, gene test results, operative data and tumor pathology data between the two groups were compared.

RESULTS

According to the inclusion criteria, a total of 323 patients underwent lung cancer surgery were analyzed in this study, including 148 males and 175 females, aged from 25 to 82 years old. Postoperative VTE occurred in 33 patients, with an incidence of 10.2%. Compared the baseline data, there were significant differences in age and BMI between the two groups, but no significant differences in other indicators. Comparing the results of postoperative genetic tests, the cases of exon 18, 19, 20, 21, 30, 31 mutation, exon 18 and 20 mixed mutation and exon 20 and 21 mixed mutation were 5, 42, 6, 57, 1, 3, 1 and 1. The total EGFR mutation rate in the enrolled patients was 36.2% (117/323). Among them, the proportion of EGFR mutation in the VTE group was significantly higher than that in the non-VTE group (60.6% 33.4%, P=0.002). Exon mutations in specific regions and mixed region of EGFR were not statistically significant between them; there was no statistical difference in the concomitant and gene mutations between them. Comparing the pathological conditions, the proportion of acinar dominant lung adenocarcinoma in the VTE group was higher than that in the non-VTE group (57.6% . 30.7%, P=0.002); other histologic subtypes showed no statistical difference. The D-dimer difference before and 1 day after surgery, preoperative FEV1, surgical method, duration of surgery and blood loss were statistically significant differences between the two groups. The results of univariate analysis showed that there were significant differences between the VTE group and the control group in proportion of EGFR mutant lung adenocarcinoma, age, BMI, D-dimer difference before and 1 day after surgery, preoperative FEV1, surgical method, duration of surgery, blood loss and proportion of acinar dominant lung adenocarcinoma (P<0.05). However, VTE was not significantly correlated with gender, or gene mutation and other factors. Multi-factor logistics regression analysis shows that Patients with EGFR gene mutation infiltrating lung adenocarcinoma, acinar dominant lung adenocarcinoma, FEV1 and difference of D-dimer (d1-pre) are independent risk factors for postoperative lung cancer complicated with VTE.

CONCLUSIONS

The incidence of VTE was 10.2% in patients with invasive lung adenocarcinoma without prophylactic anticoagulant therapy. gene mutation is an independent risk factor for postoperative VTE in lung cancer, and the incidence of VTE in adenocarcinoma with alveolar predominance is the highest. Other independent risk factors included the difference of D-dimer (d1-pre) and preoperative FEV1.

摘要

背景

本研究旨在调查表皮生长因子受体(EGFR)基因突变的肺腺癌患者静脉血栓栓塞症(VTE)的发生率,为肺癌患者围手术期VTE的防治提供临床依据。

方法

本研究纳入2016年7月至2018年3月在北京朝阳医院胸外科行肺叶切除术后经病理确诊的浸润性肺腺癌患者。所有入组患者均进行相关基因突变检测。所有患者均按照2011年国际肺癌研究协会(IASLC)、美国胸科学会(ATS)和欧洲呼吸学会(ERS)的标准进行腺癌亚型分类。根据术后是否发生VTE将患者分为VTE组和对照组。比较两组患者的基线资料、基因检测结果、手术资料及肿瘤病理资料。

结果

根据纳入标准,本研究共分析323例行肺癌手术的患者,其中男性148例,女性175例,年龄25~82岁。术后发生VTE 33例,发生率为10.2%。比较基线资料,两组患者年龄和BMI差异有统计学意义,其他指标差异无统计学意义。比较术后基因检测结果,外显子18、19、20、21、30、31突变、外显子18和20混合突变及外显子20和21混合突变的病例数分别为5、42、6、57、1、3、1和1例。入组患者EGFR总突变率为36.2%(117/323)。其中,VTE组EGFR突变比例显著高于非VTE组(60.6%对33.4%,P = 0.002)。EGFR特定区域及混合区域的外显子突变在两组间差异无统计学意义;两组间伴随的KRAS和NRAS基因突变差异无统计学意义。比较病理情况,VTE组腺泡为主型肺腺癌比例高于非VTE组(57.6%对30.7%,P = 0.002);其他组织学亚型差异无统计学意义。两组患者术后1天与术前D-二聚体差值、术前FEV1、手术方式、手术时长及失血量差异有统计学意义(P<0.05)。单因素分析结果显示,VTE组与对照组在EGFR突变型肺腺癌比例、年龄、BMI、术后1天与术前D-二聚体差值、术前FEV1、手术方式手术时长、失血量及腺泡为主型肺腺癌比例方面差异有统计学意义(P<0.05)。然而,VTE与性别、KRAS或NRAS基因突变等因素无显著相关性。多因素Logistic回归分析显示,EGFR基因突变的浸润性肺腺癌患者、腺泡为主型肺腺癌、FEV1及D-二聚体差值(d1-pre)是肺癌术后并发VTE的独立危险因素。

结论

未行预防性抗凝治疗的浸润性肺腺癌患者VTE发生率为10.2%。EGFR基因突变是肺癌术后VTE的独立危险因素,腺泡为主型腺癌VTE发生率最高。其他独立危险因素包括D-二聚体差值(d1-pre)和术前FEV1。

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