Zhang Jianfei, Liu Min, Li Dongyang, Luo Jiali, Wang Min
Department of Oncology, The First People's Hospital of Jingdezhen, No. 317, Zhonghua North Road, Zhushan District, Jingdezhen City, 333000, China.
Department of Nursing, The First People's Hospital of Jingdezhen, Jingdezhen City, 333000, China.
World J Surg Oncol. 2025 Jul 10;23(1):273. doi: 10.1186/s12957-025-03934-8.
The combination of PD-1/PD-L1 inhibitors with chemotherapy (PC) has shown promise in treating advanced NSCLC. However, its added benefit over chemotherapy alone in Chinese patients remains unclear. We performed an updated synthesis of phase 3 randomized controlled trails (RCTs) to assess both therapeutic effectiveness and associated safety of PC therapy in this population.
We systematically searched six different databases for relevant publications. Only phase 3 RCTs enrolling Chinese individuals with advanced NSCLC, contrasting PC and standalone chemotherapy, were eligible. The main outcomes were overall survival (OS) and progression-free survival (PFS). Tumor responses and adverse effects (AEs) were assessed as secondary indicators.
Eleven phase 3 trials including 3712 Chinese participants were analyzed. The PC group showed significant better OS (Hazard ratio [HR]: 0.65 [0.60, 0.72], P < 0.00001), and PFS (HR: 0.49 [0.46, 0.53], P < 0.00001). Better survival rate at 6 to 60 months was observed in those given PC. Presence of brain metastases and receiving pembrolizumab were associated with improved outcomes in the PC subgroup. Regarding tumor responses, PC led to longer duration of response (HR: 0.43 [0.36, 0.50], P < 0.00001), and a higher objective response rate (risk ratio [RR]: 1.60 [1.49, 1.72], P < 0.00001). However, PC group exhibited more AEs and immune-related AEs (irAEs) in all severity levels.
PIC may offer superior clinical benefits over chemotherapy alone in Chinese patients with advanced NSCLC, though with irAEs that warrants careful monitoring.
PD-1/PD-L1抑制剂与化疗(PC)联合应用在治疗晚期非小细胞肺癌(NSCLC)方面已显示出前景。然而,在中国患者中,其相对于单纯化疗的额外益处仍不明确。我们对3期随机对照试验(RCT)进行了更新的综合分析,以评估PC疗法在该人群中的治疗效果和相关安全性。
我们系统地检索了六个不同的数据库以查找相关出版物。只有纳入中国晚期NSCLC患者、对比PC与单纯化疗的3期RCT符合条件。主要结局为总生存期(OS)和无进展生存期(PFS)。肿瘤反应和不良反应(AE)被评估为次要指标。
分析了11项3期试验,包括3712名中国参与者。PC组显示出显著更好的OS(风险比[HR]:0.65[0.60,0.72],P<0.00001)和PFS(HR:0.49[0.46,0.53],P<0.00001)。接受PC治疗的患者在6至60个月时的生存率更高。脑转移的存在和接受帕博利珠单抗与PC亚组中更好的结局相关。关于肿瘤反应,PC导致更长的反应持续时间(HR:0.43[0.36,0.50],P<0.00001)和更高的客观缓解率(风险比[RR]:1.60[1.49,1.72],P<0.00001)。然而,PC组在所有严重程度水平上均表现出更多的AE和免疫相关AE(irAE)。
在晚期NSCLC中国患者中,PC可能比单纯化疗提供更好的临床益处,尽管存在需要仔细监测的irAE。