Sun Hongfu, Li Minghao, Huang Wei, Zhang Jian, Wei Shihong, Yang Yongjing, Wang Zhongtang, Ye Shucheng, Gong Heyi, Zhang Yaowen, Li Jie, Song Haixia, Wang Lifang, Chen Xiangming, Lin Haiqun, Ding Gaofeng, Li Hongwei, Zheng Anping, Ma Xuezhen, Chen ShaoShui, Liu Liping, Zhang Kaixian, Fu Chengrui, Liu Wenzhi, Wang Jing, Zhang Xiaqin, Liu Tingting, Han Dan, Zhao Qian, Wu Peipei, Yuan Qianqian, Tian LiJun, Zhang Ping, Wu Xueqin, Chen Fei, Zhang Zicheng, Li Baosheng
Department of Radiation Oncology, Shandong Cancer Hospital and Institute, Shandong First Medical University, Shandong Academy of Medical Sciences, Jinan, China.
Department of Radiotherapy, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.
J Clin Oncol. 2025 Feb;43(4):412-421. doi: 10.1200/JCO.23.02075. Epub 2024 Oct 7.
This multicenter, randomized, phase III clinical trial (Northern Radiation Oncology Group of China-002) focused on patients with oligo-organ metastatic non-small cell lung cancer (NSCLC) who have epidermal growth factor receptor () mutations. We aimed to investigate whether first-line concurrent thoracic radiotherapy (TRT) and EGFR-tyrosine kinase inhibitors (TKIs), compared with TKIs alone, could achieve better survival.
The patients in the TKI plus TRT group received 60 Gy to primary lung tumor and positive regional lymph nodes. Radiotherapy for metastases to other sites was determined by clinicians. The primary end point was the progression-free survival (PFS). Secondary end points included overall survival (OS) and treatment-related adverse events (TRAEs). The first and second interim analyses were performed in March 2021 and March 2022.
Between April 14, 2016, and February 25, 2022, a total of 118 patients were enrolled. Compared with the TKI alone group, the TKI plus TRT group achieved significantly better PFS (hazard ratio [HR], 0.57; = .004) and OS (HR, 0.62; = .029). The median PFS was 10.6 months in the TKI alone group and 17.1 months in the TKI plus TRT group. The median OS was 26.2 months and 34.4 months in the TKI alone group and TKI plus TRT group, respectively. The TKI plus TRT group showed better local control but was associated with a higher incidence of severe TRAEs (11.9% 5.1%).
For patients with -mutated oligo-organ metastatic NSCLC treated with first-line EGFR-TKIs, concurrent TRT improves the PFS and OS, and TRAEs are acceptable and tolerable.
这项多中心、随机、III期临床试验(中国北方放射肿瘤学组-002)聚焦于患有寡器官转移的非小细胞肺癌(NSCLC)且具有表皮生长因子受体()突变的患者。我们旨在研究一线同步胸部放疗(TRT)联合表皮生长因子受体酪氨酸激酶抑制剂(TKIs)与单纯使用TKIs相比,是否能获得更好的生存效果。
TKIs联合TRT组的患者接受60 Gy的剂量照射原发性肺肿瘤和阳性区域淋巴结。对转移至其他部位的放疗由临床医生决定。主要终点是无进展生存期(PFS)。次要终点包括总生存期(OS)和治疗相关不良事件(TRAEs)。首次和第二次中期分析分别在2021年3月和2022年3月进行。
在2016年4月14日至2022年2月25日期间,共纳入118例患者。与单纯TKIs组相比,TKIs联合TRT组的PFS(风险比[HR],0.57; = 0.004)和OS(HR,0.62; = 0.029)显著更好。单纯TKIs组的中位PFS为10.6个月,TKIs联合TRT组为17.1个月。单纯TKIs组和TKIs联合TRT组的中位OS分别为26.2个月和34.4个月。TKIs联合TRT组显示出更好的局部控制,但严重TRAEs的发生率更高(11.9% 对5.1%)。
对于一线接受表皮生长因子受体酪氨酸激酶抑制剂治疗的具有突变的寡器官转移非小细胞肺癌患者,同步TRT可改善PFS和OS,且TRAEs是可接受和耐受的。