Value, Evidence, & Outcomes - Oncology, Eli Lilly & Company, Indianapolis, IN 46285, USA.
Global Statistical Sciences, Eli Lilly & Company, Sydney, NSW, Australia.
Immunotherapy. 2023 Mar;15(4):293-309. doi: 10.2217/imt-2022-0252. Epub 2023 Feb 7.
This systematic literature review and network meta-analysis evaluated the efficacy and safety of sintilimab + pemetrexed + platinum versus US FDA-approved/National Comprehensive Cancer Network-recommended immune checkpoint inhibitor (ICI) combination therapies for untreated advanced/metastatic non-squamous non-small-cell lung cancer without / aberrations. Bayesian network meta-analysis was the base-case analysis and included assessment of fixed and random effects, and independent and simultaneous models, adjusting for baseline risk (placebo response). Chemotherapy was the common comparator. Sintilimab + pemetrexed + platinum was associated with significantly longer progression-free survival than atezolizumab + platinum + nab-paclitaxel (hazard ratio [HR]: 0.57; 95% credible interval [CrI]: 0.40-0.82) and nivolumab + ipilimumab + pemetrexed + platinum (HR: 0.66; 95% CrI: 0.48-0.92). Sintilimab + pemetrexed + platinum and pembrolizumab + pemetrexed + platinum showed comparable progression-free survival (HR: 0.96; 95% CrI: 0.71-1.30). There was no significant difference in overall survival (HR range: 0.61-0.81) or overall response rates (odds ratio [OR] range: 0.29-0.75) between sintilimab + pemetrexed + platinum and the other ICI combinations. The incidence of high-grade adverse events was higher with sintilimab + pemetrexed + platinum than with nivolumab + ipilimumab (OR: 0.46; 95% CrI: 0.33-0.64) or without chemotherapy (OR: 0.25; 95% CrI: 0.19-0.34), with no significant difference between sintilimab + pemetrexed + platinum and the other ICI combinations. Sintilimab + pemetrexed + platinum showed comparable efficacy and safety versus US standard-of-care first-line ICI combinations for advanced/metastatic non-squamous non-small-cell lung cancer.
本系统评价和网络荟萃分析评估了信迪利单抗联合培美曲塞和铂类与美国食品药品监督管理局(FDA)批准/国家综合癌症网络推荐的未经治疗的晚期/转移性非鳞状非小细胞肺癌的免疫检查点抑制剂(ICI)联合治疗方案的疗效和安全性,且无 / 异常。贝叶斯网络荟萃分析是基本分析,包括固定和随机效应评估,以及独立和同时模型,调整基线风险(安慰剂反应)。化疗是常见的比较组。信迪利单抗联合培美曲塞和铂类与阿特珠单抗联合铂类和 nab-紫杉醇(风险比[HR]:0.57;95%可信区间[CrI]:0.40-0.82)和纳武利尤单抗联合伊匹单抗联合培美曲塞和铂类(HR:0.66;95% CrI:0.48-0.92)相比,无进展生存期显著延长。信迪利单抗联合培美曲塞和铂类与帕博利珠单抗联合培美曲塞和铂类的无进展生存期相似(HR:0.96;95% CrI:0.71-1.30)。总生存期(HR 范围:0.61-0.81)或总缓解率(比值比[OR]范围:0.29-0.75)在信迪利单抗联合培美曲塞和铂类与其他 ICI 联合治疗方案之间无显著差异。信迪利单抗联合培美曲塞和铂类与纳武利尤单抗联合伊匹单抗(OR:0.46;95% CrI:0.33-0.64)或无化疗(OR:0.25;95% CrI:0.19-0.34)相比,高级别不良事件发生率更高,但与其他 ICI 联合治疗方案相比无显著差异。信迪利单抗联合培美曲塞和铂类与美国标准护理一线 ICI 联合治疗方案在晚期/转移性非鳞状非小细胞肺癌中的疗效和安全性相当。