Du Jincheng, Wang Xinyu, Fan Liwen, Shan Xinyuan, Li Muyao, Liu Linlin
Department of Radiotherapy, China-Japan Union Hospital of Jilin University, Changchun, 130000, China.
Jilin Provincial Key Laboratory of Early Screening and Health Management for Cancer, Changchun, 130000, China.
Heliyon. 2023 Mar 23;9(4):e14794. doi: 10.1016/j.heliyon.2023.e14794. eCollection 2023 Apr.
In recent years, the introduction of immune checkpoint inhibitors (ICIs) has revolutionized the treatment of extensive-stage small cell lung carcinoma (ES-SCLC), but the optimal combination of ICI and standard chemotherapy strategy is yet to be established. The aim of this network meta-analysis (NMA) was to identify which first-line combination strategy is optimal for patients with ES-SCLC.
PubMed, Embase, Cochrane Library, and the proceedings of international conferences, including American Society of Clinical Oncology and European Society for Medical Oncology meetings, were searched for randomized controlled trials (RCTs) published through October 31, 2022. The collected primary outcomes were overall survival (OS), progression-free survival (PFS), and grade 3-5 treatment-related adverse events (TRAEs).
Our NMA study included six phase 3 and three phase 2 RCTs including 4037 patients and 10 first-line regimens. Regarding effectiveness, the addition of programmed cell death 1 (PD-1) or programmed cell death ligand 1 (PD-L1) inhibitors to standard chemotherapy provided greater efficacy than chemotherapy alone. However, cytotoxic T lymphocyte-associated antigen-4 inhibitors were not associated with satisfactory prognoses. Serplulimab plus carboplatin-etoposide (vs. standard chemotherapy, hazard ratio [HR] = 0.63; 95% CI = 0.49-0.82) and nivolumab plus platinum-etoposide (HR = 0.65; 95% confidence interval [CI] = 0.46-0.91) displayed the greatest benefit regarding OS. In terms of PFS, serplulimab plus carboplatin-etoposide yielded the best benefit of all treatments (HR = 0.48; 95% CI = 0.39-0.6). The combination of ICIs and chemotherapy caused more toxicity in general, but durvalumab plus platinum-etoposide (odds ratio [OR] = 0.98; 95% CI = 0.68-1.4), atezolizumab plus carboplatin-etoposide (OR = 1.04; 95% CI = 0.68-1.6), and adebrelimab plus platinum-etoposide (OR = 1.02; 95% CI = 0.52-2) displayed similar safety as standard chemotherapy. Subgroup analysis by race illustrated that serplulimab plus carboplatin-etoposide was associated with the best OS in Asian patients. And in non-Asian patients, the combination of PD-1/PD-L1 inhibitors and chemotherapy (pembrolizumab plus platinum-etoposide, durvalumab plus platinum-etoposide, and durvalumab and tremelimumab plus platinum-etoposide) displayed superiority to standard chemotherapy.
The results of our NMA study suggested that serplulimab plus carboplatin-etoposide and nivolumab plus platinum-etoposide are associated with the best OS as first-line treatments for patients with ES-SCLC. Serplulimab plus carboplatin-etoposide was associated with the best PFS. In Asian patients, serplulimab plus carboplatin-etoposide had the best OS.
This study is registered with PROSPERO, number CRD42022345850.
近年来,免疫检查点抑制剂(ICI)的引入彻底改变了广泛期小细胞肺癌(ES-SCLC)的治疗方式,但ICI与标准化疗策略的最佳组合尚未确立。本网络荟萃分析(NMA)的目的是确定哪种一线联合策略对ES-SCLC患者最为理想。
检索了PubMed、Embase、Cochrane图书馆以及国际会议论文集,包括美国临床肿瘤学会和欧洲医学肿瘤学会会议,以查找截至2022年10月31日发表的随机对照试验(RCT)。收集的主要结局指标为总生存期(OS)、无进展生存期(PFS)以及3-5级治疗相关不良事件(TRAEs)。
我们的NMA研究纳入了6项3期和3项2期RCT,共4037例患者以及10种一线治疗方案。在疗效方面,在标准化疗基础上加用程序性细胞死亡蛋白1(PD-1)或程序性细胞死亡配体1(PD-L1)抑制剂比单纯化疗疗效更佳。然而,细胞毒性T淋巴细胞相关抗原4抑制剂并未带来令人满意的预后。斯鲁利单抗联合卡铂-依托泊苷(与标准化疗相比,风险比[HR]=0.63;95%置信区间[CI]=0.49-0.82)以及纳武利尤单抗联合铂类-依托泊苷(HR=0.65;95%置信区间[CI]=0.46-0.91)在OS方面显示出最大获益。在PFS方面,斯鲁利单抗联合卡铂-依托泊苷在所有治疗中获益最佳(HR=0.48;95%CI=0.39-0.6)。ICI与化疗联合总体上导致更多毒性,但度伐利尤单抗联合铂类-依托泊苷(优势比[OR]=0.98;95%CI=0.68-1.4)、阿替利珠单抗联合卡铂-依托泊苷(OR=1.04;95%CI=0.68-1.6)以及阿得贝利单抗联合铂类-依托泊苷(OR=1.02;95%CI=0.52-2)显示出与标准化疗相似的安全性。按种族进行的亚组分析表明,斯鲁利单抗联合卡铂-依托泊苷在亚洲患者中OS最佳。在非亚洲患者中,PD-1/PD-L1抑制剂与化疗联合(帕博利珠单抗联合铂类-依托泊苷、度伐利尤单抗联合铂类-依托泊苷以及度伐利尤单抗和曲美木单抗联合铂类-依托泊苷)优于标准化疗。
我们的NMA研究结果表明,斯鲁利单抗联合卡铂-依托泊苷以及纳武利尤单抗联合铂类-依托泊苷作为ES-SCLC患者的一线治疗与最佳OS相关。斯鲁利单抗联合卡铂-依托泊苷与最佳PFS相关。在亚洲患者中,斯鲁利单抗联合卡铂-依托泊苷OS最佳。
本研究已在PROSPERO注册,注册号为CRD42022345850。