[SMARCA4突变对晚期EGFR突变型肺腺癌患者预后的影响]。

X Liang, Y Q Jiang, X Y Liu, J L Xu, J Li, R H Guo
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引用次数: 0

摘要

目的:探讨SMARCA4基因突变对表皮生长因子受体(EGFR)突变晚期肺腺癌患者预后的影响。方法:在纪念斯隆-凯特琳癌症中心(MSK) MetTropism研究中,960例晚期egfr突变肺腺癌患者被筛选并纳入MSK队列,其中男性313例,女性647例,中位[M(Q1, Q3)]年龄为64(56,72)岁。回顾性分析2018年1月至2022年12月南京医科大学第一附属医院肿瘤科接受EGFR酪氨酸激酶抑制剂(TKIs)治疗的178例晚期EGFR突变肺腺癌患者的资料。其中男性69例,女性109例,中位年龄63(54,69)岁。对南京医科大学第一附属医院的患者进行随访至2023年12月31日,整个队列中位随访时间为26.6个月(95%CI: 24.6 ~ 28.6),其中29例患者失访。采用Kaplan-Meier法绘制生存曲线,采用log-rank检验比较SMARCA4基因改变与预后的关系。结果:960例晚期egfr突变肺腺癌MSK队列患者中,SMARCA4基因变异率为4.2%(40/960)。无SMARCA4基因改变患者的中位总生存期(OS)为41.5个月(95%CI: 35.6 ~ 47.3)个月,优于SMARCA4基因改变患者的中位总生存期(OS)[15.6个月(95%CI: 7.9 ~ 23.4)个月],PHR (95%CI)为1.97(1.35 ~ 2.88)。在南京医科大学第一附属医院178例晚期egfr突变肺腺癌患者中,SMARCA4基因变异率为4.5%(8/178)。无SMARCA4基因改变患者的中位无进展生存期(PFS)为16.1 (95%CI: 12.2-20.0)个月,优于SMARCA4基因改变患者的中位PFS [6.0 (95%CI: 1.3-10.7)个月,PCI: 28.1-72.1)个月],也优于SMARCA4基因改变患者的中位OS [17.6 (95%CI: 15.4-19.8)个月,P=0.001]。结论:SMARCA4突变是影响晚期egfr突变型肺腺癌患者预后不良的重要因素。
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[Effect of SMARCA4 mutations on the outcomes of patients with advanced EGFR mutant lung adenocarcinoma].

Objective: To investigate the impact of SMARCA4 mutations on the outcomes of patients with advanced lung adenocarcinoma with epidermal growth factor receptor (EGFR) mutations. Methods: In the Memorial Sloan Kettering Cancer Center (MSK) MetTropism study, 960 patients with advanced EGFR-mutated lung adenocarcinoma were screened and included in the MSK cohort, composing of 313 males and 647 females, with a median [M(Q1, Q3)] age of 64 (56, 72) years. A retrospective analysis was conducted on the data of 178 patients with advanced EGFR-mutated lung adenocarcinoma who received EGFR tyrosine kinase inhibitors (TKIs) treatment in the Department of Oncology, the First Affiliated Hospital of Nanjing Medical University, from January 2018 to December 2022. Among these patients, 69 were males and 109 were females, with a median age of 63 (54, 69) years. The follow-up of patients from the First Affiliated Hospital of Nanjing Medical University was conducted up to December 31, 2023, with a median follow-up time of 26.6 (95%CI: 24.6-28.6) months for the entire cohort, and 29 patients were lost to follow-up. Survival curves were plotted using the Kaplan-Meier method, and the log-rank test was used to compare the relationship between SMARCA4 gene alternations and prognosis. Results: In the 960 patients of the MSK cohort with advanced EGFR-mutated lung adenocarcinoma, the SMARCA4 gene alternations rate was 4.2% (40/960). The median overall survival (OS) for patients without SMARCA4 gene alternations was 41.5 (95%CI: 35.6-47.3) months, which was superior to that of patients with SMARCA4 gene alternations [15.6 (95%CI: 7.9-23.4) months, P<0.001]. Patients with SMARCA4 gene alternations had a higher risk of mortality, with an HR (95%CI) of 1.97 (1.35 to 2.88). Among the 178 patients with advanced EGFR-mutated lung adenocarcinoma from the First Affiliated Hospital of Nanjing Medical University, the SMARCA4 gene alternations rate was 4.5% (8/178). The median progression-free survival (PFS) for patients without SMARCA4 gene alternations was 16.1 (95%CI: 12.2-20.0) months, which was superior to the median PFS of patients with SMARCA4 gene alternations [6.0 (95%CI: 1.3-10.7) months, P<0.001]. The median OS for patients without SMARCA4 gene alternations was 50.1 (95%CI: 28.1-72.1) months, which was also superior to the median OS of patients with SMARCA4 gene alternations [17.6 (95%CI: 15.4-19.8) months, P=0.001]. Conclusion: SMARCA4 alternation is an important factor associated with poor prognosis in patients with advanced EGFR-mutant lung adenocarcinoma.

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Zhonghua yi xue za zhi
Zhonghua yi xue za zhi Medicine-Medicine (all)
CiteScore
0.80
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400
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