Huangfu Rui, Hou Kun, Zhao Jie, Wu Shikui, Ping Yaodong
School of Pharmacy, Inner Mongolia Medical University, Hohhot, China.
Department of Pharmacy, Peking University Cancer Hospital Inner Mongolia Hospital, Hohhot, China.
Front Immunol. 2025 Apr 1;16:1547978. doi: 10.3389/fimmu.2025.1547978. eCollection 2025.
Immune treatment beyond progression (ITBP) has emerged as a novel therapeutic strategy in oncology. This systematic review and meta-analysis aim to evaluate the efficacy and safety of ITBP in patients with lung cancer, while also identifying characteristics of populations that may benefit most from this treatment approach.
This study adheres to the PRISMA guidelines. We searched PubMed, Embase, and the Cochrane Library for relevant literature on immunotherapy for lung cancer, using self-constructed databases up until February 1, 2024. The study includes real-world data from patients with lung cancer undergoing ITBP, categorized into two groups: non-ITBP (NTBP) and ITBP. Two authors independently conducted literature screening, quality assessment, and data extraction. The primary efficacy indicators include overall survival (OS), progression-free survival (PFS), objective response rate (ORR), and disease control rate (DCR). The safety indicator assessed was the incidence of immune-related adverse events (irAEs).
We included 9 studies with a total of 5,141 patients with lung cancer, comprising 2,051 patients in the ITBP group and 3,090 in the NTBP group. Patients receiving ITBP showed significantly better outcomes than those receiving NTBP, including superior OS and PFS following treatment beyond progression (OS: hazard ratio (HR) 0.72, 95% confidence interval (CI) 0.68-0.77, P < 0.05; PFS: HR 0.63, 95% CI 0.51-0.78, P < 0.05). Additionally, the ITBP group demonstrated higher ORR and DCR (ORR: odds ratio (OR) 0.48, 95% CI 0.31-0.75, P < 0.05; DCR: OR 0.37, 95% CI 0.24-0.57, P < 0.05). No significant difference in the incidence of irAEs was found between the two groups (OR 1.24, 95% CI 0.83-1.85, P > 0.05). Subgroup analysis revealed that factors such as age, gender, lung cancer subtype, and smoking history significantly influenced OS outcomes in the ITBP group.
Our findings suggest that ITBP is an effective treatment strategy for patients with lung cancer. Further research should focus on identifying specific patient populations that benefit from ITBP and exploring the potential efficacy of combining ITBP with other therapeutic regimens.
https://www.crd.york.ac.uk/prospero/, identifier CRD42024513475.
进展后免疫治疗(ITBP)已成为肿瘤学中的一种新型治疗策略。本系统评价和荟萃分析旨在评估ITBP在肺癌患者中的疗效和安全性,同时确定可能最受益于这种治疗方法的人群特征。
本研究遵循PRISMA指南。我们在PubMed、Embase和Cochrane图书馆中搜索了截至2024年2月1日的关于肺癌免疫治疗的相关文献,并使用自建数据库。该研究纳入了接受ITBP的肺癌患者的真实世界数据,分为两组:非ITBP(NTBP)组和ITBP组。两位作者独立进行文献筛选、质量评估和数据提取。主要疗效指标包括总生存期(OS)、无进展生存期(PFS)、客观缓解率(ORR)和疾病控制率(DCR)。评估的安全指标是免疫相关不良事件(irAE)的发生率。
我们纳入了9项研究,共5141例肺癌患者,其中ITBP组2051例,NTBP组3090例。接受ITBP的患者比接受NTBP的患者表现出显著更好的结果,包括进展后治疗后的OS和PFS更优(OS:风险比(HR)0.72,95%置信区间(CI)0.68 - 0.77,P < 0.05;PFS:HR 0.63,95% CI 0.51 - 0.78,P < 0.05)。此外,ITBP组显示出更高的ORR和DCR(ORR:优势比(OR)0.48,95% CI 0.31 - 0.75,P < 0.05;DCR:OR 0.37,95% CI 0.24 - 0.57,P < 0.05)。两组之间irAE的发生率没有显著差异(OR 1.24,95% CI 0.83 - 1.85,P > 0.05)。亚组分析显示,年龄、性别、肺癌亚型和吸烟史等因素对ITBP组的OS结果有显著影响。
我们的研究结果表明,ITBP是肺癌患者的一种有效治疗策略。进一步的研究应集中在确定从ITBP中受益的特定患者群体,并探索将ITBP与其他治疗方案联合使用的潜在疗效。