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基因状态对具有影像学纯实性表现的临床I期非小细胞肺癌患者生存结局的影响。

Impact of genetic status on the survival outcomes of patients with clinical stage I non-small cell lung cancer with a radiological pure-solid appearance.

作者信息

Sun Ke, Li Meiling, Shang Mingdong, Su Xiaolian, Zhao Jiabi, Wang Bin, Wu Chunyan, Zhang Lei, Yang Shan, Sun Xiwen

机构信息

Department of Radiology, Huashan Hospital, Fudan University, Shanghai, China; Department of Radiology, Shanghai Pulmonary Hospital, Tongji University School of Medicine, 507 Zheng Min Road, Shanghai 200433, China.

Department of Radiology, Shanghai General Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.

出版信息

Lung Cancer. 2022 Apr;166:63-69. doi: 10.1016/j.lungcan.2022.02.005. Epub 2022 Feb 16.

Abstract

PURPOSE

To investigate whether genetic status is associated with the prognosis of patients with clinical stage (c-stage) I non-small cell lung cancer (NSCLC) with radiological pure-solid manifestations.

MATERIALS AND METHODS

We included 340 patients with pure-solid c-stage I NSCLC and evaluated their clinicopathological and genetic information. Disease recurrence and death were also observed at the end of the 5-year follow-up period. A Cox proportional hazards model was performed to identify the effect of clinicopathological variables, including genetic status, on oncological outcomes. Recurrence-free survival (RFS) and overall survival (OS) were calculated by Kaplan-Meier curves and were compared using log-rank tests.

RESULTS

The gene-mutation rate of c-stage I NSCLC with a radiological pure-solid appearance was 55.9% (190/340), and the frequencies of EGFR, KRAS, ALK, ROS1 and fused genes were 69.5% (132/190), 16.8% (32/190), 8.9% (17/190), 1.6% (3/190) and 3.2% (6/190), respectively. The 5-year RFS and OS rates of eligible patients were 57.1% and 76.5%, respectively. A multivariable analysis revealed that genetic status was an independent significant prognostic factor associated with RFS (hazard ratio [HR] = 1.416, 95% confidence interval [CI]: 1.020-1.964, p = 0.038) but not with OS. RFS was lower in the genetic mutation group compared with the wild-type group (p = 0.027), with 5-year RFS rate (65.7 vs. 51.6%), but the difference in OS (mutated group vs. wild-type group: 78.0% vs. 75.3%) was not statistically significant (p = 0.602). Additionally, we found that pathological nodal involvement (HR = 2.455, 95% CI: 1.745-3.454, p < 0.001 for RFS; HR = 2.204, 95% CI: 1.409-3.447, p = 0.001 for OS) was also a valuable prognostic factor in patients with pure-solid c-stage I NSCLC.

CONCLUSION

Our study provides a comprehensive description of the mutational landscape of c-stage I NSCLC, and indicates that genetic status has an impact on disease recurrence in patients with c-stage I NSCLC with pure-solid appearance.

摘要

目的

探讨基因状态与具有放射学纯实性表现的临床I期(c期)非小细胞肺癌(NSCLC)患者预后之间的相关性。

材料与方法

我们纳入了340例纯实性c期I期NSCLC患者,并评估了他们的临床病理和基因信息。在5年随访期结束时还观察了疾病复发和死亡情况。采用Cox比例风险模型来确定包括基因状态在内的临床病理变量对肿瘤学结局的影响。通过Kaplan-Meier曲线计算无复发生存期(RFS)和总生存期(OS),并使用对数秩检验进行比较。

结果

具有放射学纯实性表现的c期I期NSCLC的基因突变率为55.9%(190/340),EGFR、KRAS、ALK、ROS1和融合基因的频率分别为69.5%(132/190)、16.8%(32/190)、8.9%(17/190)、1.6%(3/190)和3.2%(6/190)。符合条件患者的5年RFS率和OS率分别为57.1%和76.5%。多变量分析显示,基因状态是与RFS相关的独立显著预后因素(风险比[HR]=1.416,95%置信区间[CI]:1.020-1.964;p=0.038),但与OS无关。基因突变组的RFS低于野生型组(p=0.027),5年RFS率分别为65.7%和51.6%,但OS的差异(突变组与野生型组:78.0%对75.3%)无统计学意义(p=0.602)。此外,我们发现病理淋巴结受累(RFS的HR=2.455,95%CI:1.745-3.454,p<0.001;OS的HR=2.204,95%CI:1.409-3.447,p=0.001)也是纯实性c期I期NSCLC患者的一个有价值的预后因素。

结论

我们的研究全面描述了c期I期NSCLC的突变图谱,并表明基因状态对具有纯实性表现的c期I期NSCLC患者的疾病复发有影响。

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