脑放疗联合表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKI)对发生脑转移的EGFR突变型非小细胞肺癌患者的疗效。
Efficacy of brain radiotherapy plus EGFR-TKI for EGFR-mutated non-small cell lung cancer patients who develop brain metastasis.
作者信息
Wang Wenxian, Song Zhengbo, Zhang Yiping
机构信息
Department of Chemotherapy, Zhejiang Cancer Hospital, Hangzhou, China.
Key Laboratory Diagnosis and Treatment Technology on Thoracic Oncology, Zhejiang province; Hangzhou, China.
出版信息
Arch Med Sci. 2018 Oct;14(6):1298-1307. doi: 10.5114/aoms.2018.78939. Epub 2018 Oct 23.
INTRODUCTION
To analyze the appropriate treatment methods or timing to use epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) and brain radiation treatment (RT) for symptomatic and asymptomatic brain metastases (BM) in patients with EGFR mutation non-small cell lung cancer (NSCLC).
MATERIAL AND METHODS
We retrospectively studied patients diagnosed with EGFR gene mutated NSCLC who developed brain metastasis between June 2006 and December 2015 at Zhejiang Cancer Hospital. Treatment data were assessed in 181 patients with 49 symptomatic BM and 132 asymptomatic BM retrospectively.
RESULTS
In 49 symptomatic BM patients, the median OS of the stereotactic radiosurgery (SRS)-treated group was longer than in the whole brain radiotherapy (WBRT) group (37.7 vs. 21.1 months) ( = 0.194). In the group of 132 asymptomatic brain metastasis patients, the median overall survival (mOS) was longer in upfront brain radiotherapy compared with the upfront TKI group (24.9 vs. 17.4 months) ( = 0.035). In further analysis regarding the timing of using radiotherapy, out of all 74 patients, 33 underwent concurrent TKI and brain radiation, 13 received TKI after first-line RT treatment and 28 patients received radiotherapy after TKI failure. The intracranial progression free survival (iPFS) of the three groups was 11.1 months, 11.3 months and 8.1 months ( = 0.032), respectively. The mOS of the three groups was 21.9 months, 26.2 months and 17.1 months, respectively ( = 0.085).
CONCLUSIONS
Our research indicated that delayed brain RT may result in inferior iPFS in EGFR mutated NSCLC patients with asymptomatic brain metastases, but no OS benefit was obtained. In addition, our study revealed that patients treated with SRS had a significantly longer OS for symptomatic BM. Future prospective study of the optimal management strategy with WBRT or SRS and TKI for this patient cohort is urgently needed.
引言
分析表皮生长因子受体(EGFR)酪氨酸激酶抑制剂(TKIs)及脑放射治疗(RT)用于治疗表皮生长因子受体突变的非小细胞肺癌(NSCLC)患者有症状和无症状脑转移(BM)的合适治疗方法或时机。
材料与方法
我们回顾性研究了2006年6月至2015年12月在浙江省肿瘤医院被诊断为EGFR基因突变的NSCLC且发生脑转移的患者。对181例患者的治疗数据进行回顾性评估,其中49例有症状脑转移患者,132例无症状脑转移患者。
结果
在49例有症状脑转移患者中,立体定向放射外科(SRS)治疗组的中位总生存期长于全脑放疗(WBRT)组(37.7个月对21.1个月)(P = 0.194)。在132例无症状脑转移患者组中, upfront脑放疗组的中位总生存期长于 upfront TKI组(24.9个月对17.4个月)(P = 0.035)。在关于放疗时机的进一步分析中,在所有74例患者中,33例接受了TKI与脑放疗同步治疗,13例在一线放疗治疗后接受TKI,28例在TKI治疗失败后接受放疗。三组的颅内无进展生存期(iPFS)分别为11.1个月、11.3个月和8.1个月(P = 0.032)。三组的中位总生存期分别为21.9个月、26.2个月和17.1个月(P = 0.085)。
结论
我们的研究表明,延迟脑放疗可能导致EGFR突变的NSCLC无症状脑转移患者的iPFS较差,但未获得总生存期益处。此外,我们的研究显示,接受SRS治疗的有症状脑转移患者的总生存期显著更长。迫切需要对该患者群体采用WBRT或SRS及TKI的最佳管理策略进行未来前瞻性研究。