医学
内科学
化疗
肿瘤科
临床试验
肺癌
不利影响
临床研究阶段
临床终点
免疫疗法
完全响应
肺
随机对照试验
外科
癌症
进行性疾病
总体生存率
临床疗效
安全概况
代理终结点
疾病
呼吸道疾病
治疗效果
无进展生存期
性能状态
作者
Li Wang,Chuangzhou Rao,Q Wang,Kuofang Huang,Li Liu,Jin Zhao,Yan Wu,Jianing Chen,J P Qian,Haijiao Lu,Shifei Pan,Liangqin Nie,Haoran Tang,Hang Dong,Shi-Dong Jia,Yichao Zang,Tianqing Chu,Chunxia Su
标识
DOI:10.1038/s41467-026-74241-3
摘要
Although immunotherapy is approved for patients with high PD-L1 expression, optimal therapeutic strategies for PD-L1-negative populations remain undefined. This study (ChiCTR2300071681) assessed the efficacy and safety of cadonilimab (PD-1/CTLA-4 bispecific antibody) plus chemotherapy in patients with PD-L1-negative advanced non-small-cell lung cancer (NSCLC). The primary endpoint, 12-month progression-free survival (PFS) rate, is 42.1% (95% CI, 29.6%–60.0%), which has reached the prespecified threshold. Secondary endpoints include a median overall survival of not reached, a median PFS of 9.7 months, an objective response rate of 66.0%, a disease control rate of 100.0%, and a median duration of response of 9.5 months. Grade ≥3 treatment-related adverse events occur in 26 (52.0%) patients. cfDNA methylation-based molecular response predicts the actual clinical response approximately 5 cycles earlier than conventional radiographic evaluation. Baseline differentially methylated fragments scores show a significant correlation with PFS, with low-risk patients demonstrating a longer median PFS compared to high-risk patients (11.4 months versus 6.9 months). Overall, first-line cadonilimab plus chemotherapy shows an encouraging efficacy with a manageable safety profile for challenging-to-treat PD-L1-negative advanced NSCLC, warranting further evaluation in controlled studies. Therapeutic options for PD-L1–negative non–small-cell lung cancer (NSCLC) remain limited despite advances in immunotherapy. This study reports the efficacy and safety outcomes of a phase II trial evaluating cadonilimab plus chemotherapy in patients with PD-L1– negative advanced NSCLC.
科研通智能强力驱动
Strongly Powered by AbleSci AI