Takeda Yuichiro, Kusaba Yusaku, Tsukita Yoko, Uemura Yukari, Miyauchi Eisaku, Yamamoto Takaya, Mayahara Hiroshi, Hata Akito, Nakayama Hidetsugu, Tanaka Satoshi, Uchida Junji, Usui Kazuhiro, Toyoda Tatsuya, Tamiya Motohiro, Morimoto Masahiro, Oya Yuko, Kodaira Takeshi, Jingu Keiichi, Sugiura Hisatoshi
Department of Respiratory Medicine, National Center for Global Health and Medicine, 1-21-1 Toyama Shinjuku-ku, Tokyo 162-8655, Japan.
Department of Respiratory Medicine, Tohoku University Graduate School of Medicine, 1-1 Seiryo-machi, Aoba-Ku, Sendai 980-8574, Japan.
Clin Transl Radiat Oncol. 2022 Aug 23;37:57-63. doi: 10.1016/j.ctro.2022.08.010. eCollection 2022 Nov.
Intensity-modulated radiotherapy (IMRT) is currently used more commonly than 3-dimensional conformal radiation for definitive thoracic radiation. We examined the efficacy profiles of concurrent chemoradiotherapy (CCRT) with IMRT after durvalumab became clinically available.
We reviewed the clinical records of patients with stage III non-small cell lung cancer (NSCLC) treated with CCRT and IMRT at seven centers in Japan and investigated relapse and survival from May 2018 to December 2019. The primary endpoint of this report was progression-free survival (PFS).
Among 107 patients enrolled in the study, 87 were sequentially administered durvalumab. From CCRT commencement, patients were followed up for a median period of 29.7 months. The median PFS at the end of the CCRT was 20.7 months. Among the 87 patients, 58 experienced disease relapses, of whom 36 (62.1 %) had distant metastases. Multivariate Cox regression analysis revealed that a favorable response to CCRT, a radiation dose ≥ 62 Gy, and stage IIIA NSCLC were associated with prolonged PFS (all P = 0.04). Multivariate logistic regression by landmark analysis revealed that mortality risk factors were durvalumab treatment duration ≤ 11.7 months, a lower maximum grade of immune-related adverse events, FEV < 2805 mL, and radiation dose < 62 Gy (P = 0.01, 0.01, 0.03, and 0.04, respectively).
In patients with NSCLC receiving CCRT using IMRT, long PFS was associated with a better response to CCRT, stage IIIA NSCLC, and an increased radiation dose. The duration of durvalumab consolidation also played an essential role in the survival of patients receiving CCRT with IMRT. (250 words).
在度伐利尤单抗临床应用后,调强放疗(IMRT)目前在确定性胸部放疗中比三维适形放疗使用更为普遍。我们研究了同步放化疗(CCRT)联合IMRT的疗效情况。
我们回顾了日本七个中心接受CCRT和IMRT治疗的III期非小细胞肺癌(NSCLC)患者的临床记录,并调查了2018年5月至2019年12月期间的复发和生存情况。本报告的主要终点是无进展生存期(PFS)。
在纳入研究的107例患者中,87例序贯给予度伐利尤单抗。从CCRT开始,患者中位随访29.7个月。CCRT结束时的中位PFS为20.7个月。在这87例患者中,58例出现疾病复发,其中36例(62.1%)发生远处转移。多因素Cox回归分析显示,对CCRT反应良好、放射剂量≥62 Gy和IIIA期NSCLC与PFS延长相关(所有P = 0.04)。通过标志性分析进行的多因素逻辑回归显示,死亡风险因素为度伐利尤单抗治疗持续时间≤11.7个月、免疫相关不良事件的最高分级较低、第一秒用力呼气容积(FEV)<2805 mL和放射剂量<62 Gy(P分别为0.01、0.01、0.03和0.04)。
在接受IMRT联合CCRT治疗的NSCLC患者中,长PFS与对CCRT反应更好、IIIA期NSCLC和放射剂量增加相关。度伐利尤单抗巩固治疗的持续时间在接受IMRT联合CCRT治疗的患者生存中也起着重要作用。 (250字)