Division of Respiratory Medicine, Mito Medical Center, University of Tsukuba, Mito, Japan.
Division of Respiratory Medicine, Faculty of Clinical Medicine, University of Tsukuba, Tsukuba, Japan.
In Vivo. 2023 Sep-Oct;37(5):2203-2209. doi: 10.21873/invivo.13320.
BACKGROUND/AIM: Atezolizumab is a monoclonal antibody that targets programmed death-ligand 1 (PD-L1) expressed on cancer cells derived from various organs and antigen-presenting cells and is currently commonly used in combination with chemotherapy. We conducted a study to clarify the current status of response to atezolizumab monotherapy in clinical practice and clarify the factors that contribute to long-term response and survival.
We conducted a retrospective review of patients with advanced non-small cell lung cancer (NSCLC) treated with atezolizumab monotherapy from April 2018 to March 2023 at 11 Hospitals.
The 147 patients evaluated had a progression-free survival (PFS) of 3.0 months and an overall survival of 7.0 months. Immune-related adverse events of any grade were observed in 13 patients (8.8%), grade 3 or higher in nine patients (6.1%), and grade 5 with pulmonary toxicity in one patient (0.7%). Favorable factors related to PFS were 'types of NSCLC other than adenocarcinoma'. Favorable factors for overall survival were 'performance status 0-1' and 'treatment lines up to 3'. There were 16 patients (10.9%) with PFS >1 year. No characteristic clinical findings were found in these 16 patients compared to the remaining 131 patients.
Efficacy and immune-related adverse events of NSCLC patients associated with atezolizumab monotherapy were comparable to those of previous clinical trial results. Knowledge of characteristics of patients who are most likely to benefit from atezolizumab monotherapy is a crucial step towards implementing appropriate prescribing.
背景/目的:阿替利珠单抗是一种单克隆抗体,靶向源自各种器官的癌细胞和抗原呈递细胞表达的程序性死亡配体 1(PD-L1),目前常用于与化疗联合使用。我们进行了一项研究,以阐明阿替利珠单抗单药治疗在临床实践中的当前反应情况,并阐明有助于长期反应和生存的因素。
我们对 2018 年 4 月至 2023 年 3 月在 11 家医院接受阿替利珠单抗单药治疗的晚期非小细胞肺癌(NSCLC)患者进行了回顾性研究。
评估的 147 例患者的无进展生存期(PFS)为 3.0 个月,总生存期为 7.0 个月。13 例患者(8.8%)发生任何等级的免疫相关不良事件,9 例患者(6.1%)发生 3 级或更高等级的免疫相关不良事件,1 例患者(0.7%)发生 5 级肺毒性。与 PFS 相关的有利因素是“非腺癌类型的 NSCLC”。与总生存期相关的有利因素是“体力状况 0-1”和“治疗线数达 3”。16 例患者(10.9%)的 PFS 超过 1 年。与其余 131 例患者相比,这些 16 例患者没有发现特征性的临床发现。
与阿替利珠单抗单药治疗相关的 NSCLC 患者的疗效和免疫相关不良事件与之前的临床试验结果相当。了解最有可能从阿替利珠单抗单药治疗中获益的患者的特征是实施适当处方的关键步骤。