Real-world treatment patterns and clinical outcomes in EGFR-mutant locally advanced lung adenocarcinoma: A multi-center cohort study

IF 7.6 Q1 ONCOLOGY
Nan Bi , Kunpeng Xu , Hong Ge , Ming Chen , Mingyan E , Li Zhang , Jianzhong Cao , Xu Zhang , Xiao Ding , Bing Xia , Lujun Zhao , Lijie Han , Jiancheng Li , Chen Hu , Luhua Wang
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引用次数: 0

Abstract

Objective

To investigate the optimal management of patients with epidermal growth factor receptor gene (EGFR) mutant locally advanced non-small cell lung cancer (LA-NSCLC).

Methods

Patients with unresectable stage III lung adenocarcinoma (LAC) harboring EGFR mutations from 2012 to 2018 were analyzed retrospectively, and were categorized into three groups according to the primary treatment: chemoradiotherpy (CRT) (group 1), combined radiation therapy (RT) and EGFR-tyrosine kinase inhibitors (TKI) with/without chemotherapy (group 2), and EGFR-TKI alone until tumor progression (group 3). Inverse probability of multiple treatment weighting (IPTW) of propensity score was used to compare overall survival (OS) and progression free survival (PFS) between treatments and account for confounding.

Results

A total of 104, 105, and 231 patients were categorized into groups 1, 2, and 3, respectively. After IPTW adjustment, the median PFS for each group was 12.4, 26.2, and 16.2 months (log-rank P < 0.001), and the median OS was 51.0, 67.4 and 49.3 months (log-rank P = 0.084), respectively. Compared with those in group 1, patients in group 2 had significantly improved PFS [adjusted hazard ratio HR (aHR), 0.40; 95% confidence interval (CI): 0.29, 0.54; P < 0.001] and OS (aHR, 0.61; 95% CI: 0.38, 0.98; P = 0.039). Patients in group 3 had prolonged PFS (aHR, 0.66; 95% CI: 0.50, 0.87; P = 0.003), but not OS (aHR, 0.90; 95% CI: 0.62, 1.32; P = 0.595). Doubly robust IPTW analysis and multivariable Cox regression analysis yielded similar findings.

Conclusions

EGFR-TKIs after chemoradiation or combined with radiation alone correlated with the longest PFS and OS (versus CRT or TKIs alone) in patients with EGFR-mutant unresectable LA-NSCLC. Well-designed prospective trials were warranted.

EGFR突变局部晚期肺腺癌的真实治疗模式和临床结果:一项多中心队列研究
目的探讨表皮生长因子受体基因(EGFR)突变的局部晚期非小细胞肺癌(LA-NSCLC)患者的最佳治疗方法。方法回顾性分析2012 - 2018年发生EGFR突变的不能切除的III期肺腺癌(LAC)患者,根据主要治疗方法分为3组:放化疗(CRT)(第1组),联合放疗(RT)和egfr -酪氨酸激酶抑制剂(TKI)联合化疗(第2组),以及单独使用EGFR-TKI直到肿瘤进展(第3组)。倾向评分多重治疗加权逆概率(IPTW)用于比较治疗之间的总生存期(OS)和无进展生存期(PFS),并考虑混杂因素。结果1组104例,2组105例,3组231例。经IPTW调整后,各组的中位PFS分别为12.4、26.2和16.2个月(log-rank P <0.001),中位OS分别为51.0、67.4和49.3个月(log-rank P = 0.084)。与1组比较,2组患者PFS明显改善[校正风险比HR (aHR), 0.40;95%置信区间(CI): 0.29, 0.54;P & lt;0.001]和OS (aHR, 0.61;95% ci: 0.38, 0.98;p = 0.039)。3组患者PFS延长(aHR, 0.66;95% ci: 0.50, 0.87;P = 0.003),但OS无统计学意义(aHR, 0.90;95% ci: 0.62, 1.32;p = 0.595)。双稳健IPTW分析和多变量Cox回归分析得出了类似的结果。结论在egfr突变不可切除的LA-NSCLC患者中,放化疗后的segfr -TKIs或单独放疗与最长的PFS和OS相关(与单独CRT或TKIs相比)。精心设计的前瞻性试验是必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
14.20
自引率
0.00%
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审稿时长
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