Yamanaka Yuta, Ota Takayo, Masuoka Yutaka, Takeyasu Yuki, Nakamura Satoaki, Terashima Masaaki, Yoshioka Hiroshige, Fukuoka Masahiro, Kurata Takayasu
Department of Thoracic Oncology, Kansai Medical University Hospital, 2-5-1 Shinmachi, Hirakatashi 573-1010, Osaka, Japan.
Medical Oncology, Izumi City General Medical Center, 4-5-1 Wakechou, Izumishi 594-0073, Osaka, Japan.
Cancers (Basel). 2024 Sep 11;16(18):3127. doi: 10.3390/cancers16183127.
Despite advancements in diagnosing and treating non-small cell lung cancer (NSCLC), the prognosis remains poor. Immune checkpoint inhibitors have shown promise in enhancing survival rates. Therefore, this study aimed to investigate the safety of nivolumab administration with concurrent chemoradiation therapy (CCRT) in patients with unresectable locally advanced NSCLC. Twelve patients with unresectable locally advanced NSCLC at Kansai Medical University Hospital and Izumi City General Medical Center were enrolled from May 2018 to September 2020. They received nivolumab (360 mg) tri-weekly twice, weekly carboplatin (AUC 2 min × mg/mL) and paclitaxel (40 mg/m) for 6 weeks, and thoracic radiotherapy (60 Gy/30 fractions), followed by maintenance nivolumab therapy (360 mg, tri-weekly) for 6 months. The primary endpoint was incidence of dose-limiting toxicities (DLTs), and the secondary endpoints included safety, response rate, progression-free survival (PFS), overall survival (OS), 2-year survival rate, and treatment completion rate. Three patients completed the protocol. Nine discontinued due directly to interstitial pneumonia (three) and pneumonia (one). Ten patients (83.3%) experienced a grade 3 or higher event, of which three (25%) experienced a grade 4 or higher event, and of these, one (8.3%) experienced a grade 5 event. Three patients experienced DLTs. Concurrent nivolumab with CCRT was tolerated in unresectable locally advanced NSCLC, which offers potential treatment benefits.
尽管在非小细胞肺癌(NSCLC)的诊断和治疗方面取得了进展,但其预后仍然很差。免疫检查点抑制剂在提高生存率方面显示出了前景。因此,本研究旨在调查纳武单抗联合同步放化疗(CCRT)治疗不可切除的局部晚期NSCLC患者的安全性。2018年5月至2020年9月,关西医科大学医院和和泉市综合医疗中心招募了12例不可切除的局部晚期NSCLC患者。他们接受纳武单抗(360mg),每三周给药两次,每周给予卡铂(AUC 2 min×mg/mL)和紫杉醇(40mg/m),持续6周,并进行胸部放疗(60Gy/30次分割),随后进行纳武单抗维持治疗(360mg,每三周一次),持续6个月。主要终点是剂量限制性毒性(DLT)的发生率,次要终点包括安全性、缓解率、无进展生存期(PFS)、总生存期(OS)、2年生存率和治疗完成率。3例患者完成了方案。9例患者因间质性肺炎(3例)和肺炎(1例)直接停药。10例患者(83.3%)发生3级或更高等级的事件,其中3例(25%)发生4级或更高等级的事件,其中1例(8.3%)发生5级事件。3例患者出现DLT。不可切除的局部晚期NSCLC患者对纳武单抗联合CCRT耐受性良好,这提供了潜在的治疗益处。