Efficacy of immune checkpoint inhibitors in advanced non-small cell lung cancer patients with KRAS mutations: A network meta-analysis

被引:1
作者
Zhang, Lin [1 ]
Chen, Wei [2 ]
Wei, Hongtao [1 ]
Yu, Junxian [1 ]
机构
[1] Capital Med Univ, Beijing Friendship Hosp, Dept Pharm, Beijing, Peoples R China
[2] Emergency Gen Hosp Beijing, Dept Pharm, Beijing, Peoples R China
关键词
immune checkpoint inhibitors; KRAS mutation; network meta-analysis; non-small cell lung cancer; programmed cell death ligand-1; programmed cell death-1; OPEN-LABEL; DOCETAXEL; PEMBROLIZUMAB; ATEZOLIZUMAB; MULTICENTER;
D O I
10.1111/crj.13745
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Objective: Previous studies have shown that immune checkpoint inhibitors can improve the survival of patients with advanced non-small cell lung cancer with KRAS mutations; however, there is a lack of comparisons between treatment regimens associated with immune checkpoint inhibitors, and our study aims to compare several treatment parties to find a more effective treatment regimen. Method: A comprehensive literature search was conducted across multiple databases, namely PubMed, Web of Science, Embase, and Cochrane Library, to identify relevant studies. The screened studies were thoroughly examined, and data were collected to establish a Bayesian framework. The study focused on two primary endpoints: overall survival (OS) and progression-free survival (PFS). Data analysis and graphical plotting using R software and Revman (version 5.3). It is worth mentioning that the study protocol was registered with the International Prospective Registry for Systematic Reviews, ensuring transparency and adherence to predetermined protocols (CRD42022379595). Result: In total, our analysis included six RCTs involving 469 patients with KRAS mutations. Among these patients, 224 received chemotherapy, while 245 were treated with immune checkpoint inhibitors. Meta-analysis results showed that the addition of ICIs could significantly improve OS and PFS (0.69, 95% CI 0.55, 0.86; 0.57, 95% CI 0.42, 0.77). The results of the network meta-analysis showed that Pembrolizumab could improve OS (HR 0.42, 95% CI 0.22-0.80) and Pembrolizumab emerged as the most effective treatment option for enhancing OS in patients (SUCRA 65.03%). Additionally, pembrolizumab in combination with chemotherapy showed improvement in PFS (HR 0.47, 95% CI 0.29-0.76). Conclusion: Our analysis found that among advanced NSCLC patients with KRAS gene mutations, first-line treatment with pembrolizumab alone demonstrated greater efficacy. Similarly, second-line treatment with nivolumab alone was found to be more effective in this patient population. However, the sample size of this study was limited, Therefore, additional clinical data is necessary to validate this finding in subsequent research.
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页数:11
相关论文
共 34 条
[1]   Sotorasib: First Approval [J].
Blair, Hannah A. .
DRUGS, 2021, 81 (13) :1573-1579
[2]   Nivolumab versus Docetaxel in Advanced Nonsquamous Non-Small-Cell Lung Cancer [J].
Borghaei, H. ;
Paz-Ares, L. ;
Horn, L. ;
Spigel, D. R. ;
Steins, M. ;
Ready, N. E. ;
Chow, L. Q. ;
Vokes, E. E. ;
Felip, E. ;
Holgado, E. ;
Barlesi, F. ;
Kohlhaeufl, M. ;
Arrieta, O. ;
Burgio, M. A. ;
Fayette, J. ;
Lena, H. ;
Poddubskaya, E. ;
Gerber, D. E. ;
Gettinger, S. N. ;
Rudin, C. M. ;
Rizvi, N. ;
Crino, L. ;
Blumenschein, G. R. ;
Antonia, S. J. ;
Dorange, C. ;
Harbison, C. T. ;
Finckenstein, F. Graf ;
Brahmer, J. R. .
NEW ENGLAND JOURNAL OF MEDICINE, 2015, 373 (17) :1627-1639
[3]   Targeting the Tumor Microenvironment: An Unexplored Strategy for Mutant KRAS Tumors [J].
Carvalho, Patricia Dias ;
Machado, Ana Luisa ;
Martins, Flavia ;
Seruca, Raquel ;
Velho, Sergia .
CANCERS, 2019, 11 (12)
[4]   The Efficacy of Immune Checkpoint Inhibitors vs. Chemotherapy for KRAS-Mutant or EGFR-Mutant Non-Small-Cell Lung Cancers: A Meta-Analysis Based on Randomized Controlled Trials [J].
Chen, Wei ;
Li, Ling ;
Cheng, Sheng ;
Yu, Junxian .
DISEASE MARKERS, 2022, 2022
[5]   Characteristics and Outcomes of Patients With Metastatic KRAS-Mutant Lung Adenocarcinomas: The Lung Cancer Mutation Consortium Experience [J].
El Osta, Badi ;
Behera, Madhusmita ;
Kim, Sungjin ;
Berry, Lynne D. ;
Sica, Gabriel ;
Pillai, Rathi N. ;
Owonikoko, Taofeek K. ;
Kris, Mark G. ;
Johnson, Bruce E. ;
Kwiatkowski, David J. ;
Sholl, Lynette M. ;
Aisner, Dara L. ;
Bunn, Paul A. ;
Khuri, Fadlo R. ;
Ramalingam, Suresh S. .
JOURNAL OF THORACIC ONCOLOGY, 2019, 14 (05) :876-889
[6]   Effect of mutant variants of the KRAS gene on PD-L1 expression and on the immune microenvironment and association with clinical outcome in lung adenocarcinoma patients [J].
Falk, Alexander T. ;
Yazbeck, Nathalie ;
Guibert, Nicolas ;
Chamorey, Emmanuel ;
Paquet, Agnes ;
Ribeyre, Lydia ;
Bence, Coraline ;
Zahaf, Katia ;
Leroy, Sylvie ;
Marquette, Charles-Hugo ;
Cohen, Charlotte ;
Mograbi, Baharia ;
Mazieres, Julien ;
Hofman, Veronique ;
Brest, Patrick ;
Hofman, Paul ;
Ilie, Marius .
LUNG CANCER, 2018, 121 :70-75
[7]   Atezolizumab versus docetaxel for patients with previously treated non-small-cell lung cancer (POPLAR): a multicentre, open-label, phase 2 randomised controlled trial [J].
Fehrenbacher, Louis ;
Spira, Alexander ;
Ballinger, Marcus ;
Kowanetz, Marcin ;
Vansteenkiste, Johan ;
Mazieres, Julien ;
Park, Keunchil ;
Smith, David ;
Artal-Cortes, Angel ;
Lewanski, Conrad ;
Braiteh, Fadi ;
Waterkamp, Daniel ;
He, Pei ;
Zou, Wei ;
Chen, Daniel S. ;
Yi, Jing ;
Sandler, Alan ;
Rittmeyer, Achim .
LANCET, 2016, 387 (10030) :1837-1846
[8]  
Gadgeel S, 2019, ANN ONCOL, V30, P64
[9]  
Herbst RS., 2019, ANN ONCOL, V30, pxi63, DOI [10.1093/annonc/mdz453.001, DOI 10.1093/ANNONC/MDZ453.001]
[10]   Impact of PD-L1 expression, driver mutations and clinical characteristics on survival after anti-PD-1/PD-L1 immunotherapy versus chemotherapy in non-small-cell lung cancer: A meta-analysis of randomized trials [J].
Huang, Qingyuan ;
Zhang, Hua ;
Hai, Josephine ;
Socinski, Mark A. ;
Lim, Eric ;
Chen, Haiquan ;
Stebbing, Justin .
ONCOIMMUNOLOGY, 2018, 7 (12)