Sintilimab plus chemotherapy for first-line treatment of advanced or metastatic nonsquamous non-small-cell lung cancer: network meta-analysis

被引:6
作者
Molife, Cliff [1 ]
Brnabic, Alan [2 ]
Stefaniak, Victoria J. [3 ]
Belger, Mark A. [4 ]
Gruver, Kristi [5 ]
Chen, Jing, V [6 ]
Souri, Saman [6 ]
Blumenschein, George R. [7 ]
机构
[1] Eli Lilly & Co, Value Evidence & Outcomes Oncol, Indianapolis, IN 46285 USA
[2] Eli Lilly & Co, Global Stat Sci, Sydney, NSW, Australia
[3] Eli Lilly & Co, Med Affairs, Indianapolis, IN 46285 USA
[4] Eli Lilly & Co, Global Stat Sci, Windlesham, Surrey, England
[5] Eli Lilly & Co, Global Sci Commun, Indianapolis, IN 46285 USA
[6] Med Decis Modeling, Indianapolis, IN 46268 USA
[7] Univ Texas MD Anderson Canc Ctr, Dept Thorac & Head & Neck Med Oncol, Houston, TX 77030 USA
关键词
anti-PD-1; anti-PD-L1; immunotherapy; network meta-analysis; non-squamous non-small-cell lung cancer; sintilimab; CLINICAL-PRACTICE GUIDELINES; MAINTENANCE BEVACIZUMAB; OPEN-LABEL; PHASE-III; NSCLC; PEMBROLIZUMAB; PLATINUM; SAFETY; SURVIVAL; EFFICACY;
D O I
10.2217/imt-2022-0252
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Aim: 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 EGFR/ALK aberrations. Methods: 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. Results: 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. Conclusion: 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. Tweetable abstractNetwork meta-analysis of 11 trials shows comparable efficacy and safety between sintilimab plus chemotherapy and US FDA-approved immunotherapy combinations for untreated advanced/metastatic nonsquamous NSCLC. Plain language summarySintilimab is an immunotherapy drug that was successfully developed and tested in China to treat a kind of lung cancer that has spread, called advanced non-squamous non-small-cell lung cancer (NSCLC). The ORIENT-11 clinical study showed that adding sintilimab to two types of chemotherapy (pemetrexed and platinum) as the first treatment for people in China with advanced non-squamous NSCLC was safe and effective in reducing the risk of cancer spreading, growing or getting worse, compared with chemotherapy alone. Our study combined and analyzed the results from 11 clinical studies to look at how well sintilimab with chemotherapy may work compared with immunotherapy drugs approved in the USA. The results showed that sintilimab with chemotherapy is as effective and safe as immunotherapy drugs approved in the USA to treat people with advanced non-squamous NSCLC. These results may help doctors and payers when deciding how to treat people with this disease.
引用
收藏
页码:293 / 309
页数:17
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