Numata Takeshi, Nakamura Ryota, Shiozawa Toshihiro, Watanabe Hiroko, Okauchi Shinichiro, Ogara Gen, Tamura Tomohiro, Kikuchi Norihiro, Miyazaki Kunihiko, Hayashi Shigen, Yamashita Takaaki, Kurishima Koichi, Inagaki Masaharu, Satoh Hiroaki, Kaburagi Takayuki, Endo Takeo, Hizawa Nobuyuki
Departments of Respiratory Medicine and Surgery, National Hospital Organization Mito Medical Center, Ibarakimachi, Japan.
Division of Respiratory Medicine, Faculty of Clinical Medicine, University of Tsukuba, Tsukuba, Japan.
Cancer Diagn Progn. 2025 Jan 3;5(1):105-114. doi: 10.21873/cdp.10418. eCollection 2025 Jan-Feb.
BACKGROUND/AIM: Atezolizumab, one of the anti-PD-L1 antibodies, targets PD-L1 expressed on cancer cells and antigen-presenting cells. This immune checkpoint inhibitor is now commonly used in combination with chemotherapy. The objectives of this study were to confirm the treatment outcomes of combined atezolizumab plus chemotherapy, and to identify prognostic factors, with a particular focus on the impact of the site of metastasis in real-world clinical practice.
A retrospective review of clinical information on non-small cell lung cancer patients who received combined atezolizumab plus chemotherapy from May 2018 to August 2024 at our 11 hospitals was conducted.
The 141 patients evaluated had a median progression-free survival of 8.0 months and a median overall survival of 19.0 months. Multivariate analyses showed that 'absence of liver metastases', 'absence of adrenal metastases', 'first-line combined atezolizumab plus chemotherapy', and 'good performance status' were associated with progression-free survival and overall survival. Immune-related adverse events were observed in 27.7% of patients, with grade 3 or higher in 9.9% of patients, and grade 5 in 2.1% of patients.
Efficacy and immune-related adverse events associated with the combination of atezolizumab and chemotherapy in non-small cell lung cancer patients were comparable to previous clinical trials. To ensure that appropriate patients receive the most effective treatment, it is important to identify detailed prognostic factors, including clinical information, such as the affected metastatic organs. Continued research and further accumulation of knowledge in this area are eagerly anticipated.
背景/目的:阿替利珠单抗是一种抗程序性死亡配体1(PD-L1)抗体,作用于癌细胞和抗原呈递细胞上表达的PD-L1。这种免疫检查点抑制剂目前常用于联合化疗。本研究的目的是确认阿替利珠单抗联合化疗的治疗效果,并确定预后因素,特别关注在真实世界临床实践中转移部位的影响。
对2018年5月至2024年8月在我们11家医院接受阿替利珠单抗联合化疗的非小细胞肺癌患者的临床信息进行回顾性分析。
141例评估患者的中位无进展生存期为8.0个月,中位总生存期为19.0个月。多因素分析显示,“无肝转移”、“无肾上腺转移”、“一线阿替利珠单抗联合化疗”和“良好的身体状况”与无进展生存期和总生存期相关。27.7%的患者发生免疫相关不良事件,9.9%的患者为3级或更高等级,2.1%的患者为5级。
阿替利珠单抗联合化疗在非小细胞肺癌患者中的疗效和免疫相关不良事件与既往临床试验相当。为确保合适的患者接受最有效的治疗,识别详细的预后因素很重要,包括临床信息,如受累的转移器官。热切期待该领域持续的研究和知识的进一步积累。