Cancer Center, Union Hospital, Tongji Medical College, 12443Huazhong University of Science and Technology, Wuhan, China.
Technol Cancer Res Treat. 2021 Jan-Dec;20:1533033821997819. doi: 10.1177/1533033821997819.
It was controversial that whether LUAD patients with brain metastases (BMs) and EGFR sensitive mutations should be conducted using brain radiotherapy when treated with first-generation EGFR-TKI. Herein, a retrospective study was designed to compare the efficacy of first-generation EGFR-TKI combined with brain radiotherapy and EGFR-TKI alone as first-line treatment for these LUAD patients.
We retrospectively analyzed the status of patients with advanced LUAD carrying EGFR sensitive mutations who received first-generation EGFR-TKI treatment in our center. iPFS was the first time of intracranial progression or death from the diagnosis of BMs, PFS was the time of progression of any site or death from the diagnosis of BMs, and OS was the time of confirmed BMs to death or the last follow-up time. Differences in characteristics between groups were compared using the Chi-square test. The Kaplan-Meier method was used to calculate the iPFS, PFS, and OS. Univariate analysis, multivariate analysis, and subgroup analysis were conducted by Cox regression model.
There were 77 patients (77/134, 57.5%) in the TKI + RT group and 57 patients (57/134, 42.5%) in the TKI group. TKI + RT group had a significant higher intracranial ORR and DCR, and the combination therapy was independently significantly associated with a longer iPFS (18.9 10.5 months, = 0.0009), systematic PFS (12.5 8.4 months, = 0.0071) and OS (30.8 . 22.7 months, = 0.0183). Females, non-smokers, and younger patients benefited more from the combination therapy. Subgroup analysis demonstrated that the combination therapy could improve the iPFS in patients with more than 3 BMs ( = 0.005); however, it couldn't improve the OS for these patients.
Our study confirmed the effect of the combination of EGFR-TKI and brain radiotherapy as first-line treatment for LUAD patients with BMs and EGFR sensitive mutations.
对于伴有脑转移(BMs)和 EGFR 敏感突变的 LUAD 患者,在使用第一代 EGFR-TKI 治疗时是否应进行脑部放疗,这一问题存在争议。在此,我们设计了一项回顾性研究,旨在比较第一代 EGFR-TKI 联合脑部放疗与第一代 EGFR-TKI 单药作为这些 LUAD 患者一线治疗的疗效。
我们回顾性分析了在我院接受第一代 EGFR-TKI 治疗的晚期 LUAD 伴 EGFR 敏感突变患者的状况。颅内无进展生存期(iPFS)为从 BMs 诊断开始至颅内进展或死亡的首次时间,无进展生存期(PFS)为从 BMs 诊断开始至任何部位进展或死亡的时间,总生存期(OS)为从 BMs 确诊至死亡或最后一次随访的时间。使用卡方检验比较组间特征的差异。采用 Kaplan-Meier 法计算 iPFS、PFS 和 OS。采用 Cox 回归模型进行单因素分析、多因素分析和亚组分析。
在 TKI+RT 组(n=77)和 TKI 组(n=57)中,分别有 77 例(77/134,57.5%)和 57 例(57/134,42.5%)患者。TKI+RT 组颅内客观缓解率(ORR)和疾病控制率(DCR)显著更高,联合治疗与更长的 iPFS(18.9 10.5 个月, =0.0009)、系统 PFS(12.5 8.4 个月, =0.0071)和 OS(30.8 . 22.7 个月, =0.0183)独立相关。女性、不吸烟者和年轻患者从联合治疗中获益更多。亚组分析表明,联合治疗可改善脑转移灶数大于 3 个患者的 iPFS( =0.005),但不能改善这些患者的 OS。
我们的研究证实了 EGFR-TKI 联合脑部放疗作为伴有脑转移和 EGFR 敏感突变的 LUAD 患者一线治疗的效果。