Zhang Baishen, Bao Hejing, Li Zhanquan, Chen Jing, Yu Hui, Li Meichen, Cai Muyan, Chen Likun
Sun Yat-Sen University Cancer Center, State Key Laboratory of Oncology in South China, Guangdong Provincial Clinical Research Center for Cancer, Guangzhou, PR China.
Department of Oncology, Panyu Central Hospital, Guangzhou, PR China.
Lung Cancer. 2025 Jan;199:108021. doi: 10.1016/j.lungcan.2024.108021. Epub 2024 Nov 8.
Small cell lung cancer (SCLC) is a highly malignant tumor with an extremely poor prognosis. In the currentera of immunotherapy, the role of immune checkpoint inhibitors (ICIs) in the second-line treatment of patients with extensive-stage SCLC (ES-SCLC) who have progressed to initial chemoimmunotherapy remains unclear.
A multicenter retrospective study were conducted, involving patients with ES-SCLC who received second-line (2L) therapy after progression to first-line chemoimmunotherapy. Patients were divided into 2L-ICIs group and 2L-non-ICIs group according to whether ICIs were added to the 2L treatment. The efficacy and adverse events of the two groups were analyzed and compared.
A total of 103 patients were included in this study, with 53 in the 2L-ICIs group and 50 in the 2L-non-ICIs group. The 2L-ICIs group demonstrated a longer median progression-free survival (PFS) compared to the 2L-non-ICIs group (4.4 months vs 3.9 months, HR = 0.45, p = 0.001). Similarly, median overall survival was also prolonged in the 2L-ICIs group (10.0 months vs 6.9 months, HR = 0.56, p = 0.015). Cox regression analysis revealed that the addition of ICIs to 2L treatment was an independent prognostic factor for both PFS and OS in ES-SCLC patients. Subgroup analysis indicated that patients with a first-line PFS of ≥6 months could potentially benefit more from 2L ICIs. Furthermore, the occurrence of adverse events in the two groups exhibited a similar pattern.
For ES-SCLC patients who have progressed to first-line chemoimmunotherapy, adding ICIs to second-line treatment may be considered as an option with limited benefit but manageable adverse effects.
小细胞肺癌(SCLC)是一种高度恶性的肿瘤,预后极差。在当前免疫治疗时代,免疫检查点抑制剂(ICIs)在一线化疗免疫治疗进展后的广泛期小细胞肺癌(ES-SCLC)患者二线治疗中的作用仍不明确。
进行了一项多中心回顾性研究,纳入一线化疗免疫治疗进展后接受二线(2L)治疗的ES-SCLC患者。根据2L治疗中是否添加ICIs,将患者分为2L-ICIs组和2L-非ICIs组。分析并比较两组的疗效和不良事件。
本研究共纳入103例患者,2L-ICIs组53例,2L-非ICIs组50例。与2L-非ICIs组相比,2L-ICIs组的中位无进展生存期(PFS)更长(4.4个月对3.9个月,HR = 0.45,p = 0.001)。同样,2L-ICIs组的中位总生存期也延长了(10.0个月对6.9个月,HR = 0.56,p = 0.015)。Cox回归分析显示,2L治疗中添加ICIs是ES-SCLC患者PFS和OS的独立预后因素。亚组分析表明,一线PFS≥6个月的患者可能从2L ICIs中获益更多。此外,两组不良事件的发生情况呈现相似模式。
对于一线化疗免疫治疗进展的ES-SCLC患者,二线治疗中添加ICIs可作为一种选择,其益处有限但不良反应可控。