Harada Hideyuki, Hata Akito, Konno Masahiro, Mamesaya Nobuaki, Nakamatsu Kiyoshi, Haratani Koji, Yamamoto Takaya, Saito Ryota, Mayahara Hiroshi, Kokubo Masaki, Sato Yuki, Imano Nobuki, Masuda Takeshi, Fukuda Haruyuki, Sado Toshikatsu, Yoshimura Kenichi, Nishimura Yasumasa, Nakagawa Kazuhiko, Okamoto Isamu, Yamamoto Nobuyuki
Radiation and Proton Therapy Center, Shizuoka Cancer Center, Nagaizumi, Japan.
Division of Thoracic Oncology, Kobe Minimally Invasive Cancer Center, Kobe, Japan.
JTO Clin Res Rep. 2025 Mar 20;6(6):100828. doi: 10.1016/j.jtocrr.2025.100828. eCollection 2025 Jun.
Chemoradiotherapy (CRT) followed by durvalumab is the standard of care for unresectable locally advanced NSCLC. Limited prospective data have been reported on intensity-modulated radiotherapy (IMRT)-adapted CRT in the immunotherapy era.
In this multicenter prospective observational study, patients underwent IMRT-adapted CRT (platinum-doublet chemotherapy plus 60 Gy IMRT in 30 fractions under a prespecified radiation protocol), followed by consolidative durvalumab. The primary outcome was the durvalumab introduction rate within 42 days post-CRT.
Thirty-two patients with unresectable locally advanced NSCLC were enrolled between November 2019 and February 2021. Among the 28 evaluable cases, durvalumab was introduced in 24 (85.7%, 90% confidence interval: 70.2%-95.0%) of 28 patients after CRT, achieving the primary end point. All 29 patients who received IMRT completed the scheduled 60 Gy radiotherapy dose. One year of durvalumab treatment was completed in 12 of 24 patients (50%). In the 24 patients who were durvalumab-introduced, the median progression-free survival and overall survival were 20.9 (95% confidence interval: 6.9-not evaluable) months and not reached, respectively. Two-year progression-free survival and overall survival rates were 44% and 73%, respectively. Among the 29 patients in the safety analysis set, there were no treatment-related deaths or grade 4 nonhematological adverse events. Pneumonitis grade 1 was observed in 13 patients (45%), grade 2 in seven (24%), and grade 3 in one (3%).
High durvalumab introduction rate was reported after the completion of IMRT-adapted CRT under a prespecified radiation protocol. Its efficacy has been suggested, with favorable safety profiles, including a low incidence of severe pneumonitis.
University Hospital Medical Information Network database ID: UMIN000038366.
化疗放疗(CRT)后使用度伐利尤单抗是不可切除的局部晚期非小细胞肺癌(NSCLC)的标准治疗方案。在免疫治疗时代,关于调强放疗(IMRT)适应性CRT的前瞻性数据有限。
在这项多中心前瞻性观察研究中,患者接受IMRT适应性CRT(铂类双联化疗加60 Gy IMRT,分30次,遵循预先指定的放疗方案),随后进行巩固性度伐利尤单抗治疗。主要结局是CRT后42天内度伐利尤单抗的引入率。
2019年11月至2021年2月期间,纳入了32例不可切除的局部晚期NSCLC患者。在28例可评估病例中,CRT后28例患者中有24例(85.7%,90%置信区间:70.2%-95.0%)引入了度伐利尤单抗,达到了主要终点。所有29例接受IMRT的患者均完成了预定的60 Gy放疗剂量。24例患者中有12例(50%)完成了一年的度伐利尤单抗治疗。在引入度伐利尤单抗的24例患者中,中位无进展生存期和总生存期分别为20.9(95%置信区间:6.9-不可评估)个月和未达到。两年无进展生存率和总生存率分别为44%和73%。在安全性分析集中的29例患者中,没有与治疗相关的死亡或4级非血液学不良事件。13例患者(45%)观察到1级肺炎,7例(24%)为2级,1例(3%)为3级。
在预先指定的放疗方案下,IMRT适应性CRT完成后报告了高度伐利尤单抗引入率。已表明其疗效,安全性良好,包括严重肺炎的发生率较低。
大学医院医学信息网络数据库ID:UMIN000038366。