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新辅助化疗后胸腔镜根治性切除术治疗非小细胞肺癌患者(ⅢA期)

Thoracoscopic radical resection in the treatment of NSCLC patients (stage IIIA) after neoadjuvant chemotherapy.

作者信息

Zhao Liang, Zhang Lingling, Gong Fang, Xu Jie

机构信息

Department of Oncology, Binzhou People's Hospital, Binzhou 256610, China.

出版信息

J BUON. 2021 Mar-Apr;26(2):313-319.

PMID:34076974
Abstract

PURPOSE

We aimed to investigate the efficacy and safety of thoracoscopic radical resection of lung cancer in the treatment of patients with stage IIIA non-small cell lung cancer (NSCLC) after neoadjuvant chemotherapy.

METHODS

A total of 132 NSCLC patients (stage IIIA) were collected. Among them, 66 received preoperative neoadjuvant chemotherapy and thoracoscopic radical resection of lung cancer (NACT group), and 66 underwent thoracoscopic radical resection of lung cancer directly (control group). Next, the downstaging of the tumor was analyzed after neoadjuvant chemotherapy, and the R0 resection rate, surgical conditions, postoperative complications, and changes in the levels of serum tumor markers were compared between the two groups of patients.

RESULTS

The response rate of neoadjuvant chemotherapy was 51.5% (34/66), and the overall downstaging rate was 53.0% (35/66) after neoadjuvant chemotherapy, with 34 cases of T downstaging and 35 cases of N downstaging. The operative time was clearly shorter in the NACT group than that in control group. The R0 resection rate in the NACT group was prominently higher than that in the the control group. The follow-up results uncovered that the 3-year overall survival (OS) and 3-year progression-free survival (PFS) rates were 50.0% and 21.2% in the NACT group, and 36.4% and 6.1% in the control group, respectively. Based on the results of log-rank test, the OS and PFS of patients in the NACT group were markedly better than those in the control group.

CONCLUSIONS

Neoadjuvant chemotherapy benefits patients with NSCLC (stage IIIA), and it is capable of effectively leading to pathological down-staging, elevating the R0 resection rate, significantly improving the survival of patients and considerably repressing the progression of the disease.

摘要

目的

我们旨在研究新辅助化疗后胸腔镜下肺癌根治术治疗ⅢA期非小细胞肺癌(NSCLC)患者的疗效和安全性。

方法

共收集132例ⅢA期NSCLC患者。其中,66例接受术前新辅助化疗及胸腔镜下肺癌根治术(新辅助化疗组),66例直接接受胸腔镜下肺癌根治术(对照组)。接下来,分析新辅助化疗后肿瘤降期情况,并比较两组患者的R0切除率、手术情况、术后并发症及血清肿瘤标志物水平变化。

结果

新辅助化疗有效率为51.5%(34/66),新辅助化疗后总体降期率为53.0%(35/66),其中T降期34例,N降期35例。新辅助化疗组手术时间明显短于对照组。新辅助化疗组R0切除率显著高于对照组。随访结果显示,新辅助化疗组3年总生存率(OS)和3年无进展生存率(PFS)分别为50.0%和21.2%,对照组分别为36.4%和6.1%。基于对数秩检验结果,新辅助化疗组患者的OS和PFS明显优于对照组。

结论

新辅助化疗对NSCLC(ⅢA期)患者有益,能够有效导致病理降期,提高R0切除率,显著改善患者生存率并大幅抑制疾病进展。

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