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Atezolizumab Monotherapy or Plus Chemotherapy in First-Line Treatment for Advanced Non-Small Cell Lung Cancer Patients: A Meta-Analysis
被引:3
|作者:
Li, Dan-Ni
[1
,2
,3
]
Lu, Wen-Qing
[1
,2
,3
]
Yang, Bo-Wen
[1
,2
,3
]
Zhang, Ling-Yun
[1
,2
,3
]
Jin, Bo
[1
,2
,3
]
Wang, Shuo
[1
,2
,3
]
Che, Xiao-Fang
[1
,2
,3
]
Li, Ce
[1
,2
,3
]
Liu, Yun-Peng
[1
,2
,3
]
Qu, Xiu-Juan
[1
,2
,3
]
机构:
[1] China Med Univ, Dept Med Oncol, Hosp 1, Shenyang, Peoples R China
[2] China Med Univ, Key Lab Anticanc Drugs & Biotherapy Liaoning Prov, Hosp 1, Shenyang, Peoples R China
[3] Liaoning Prov Clin Res Ctr Canc, Shenyang, Peoples R China
来源:
基金:
中国国家自然科学基金;
关键词:
non-small cell lung cancer (NSCLC);
programmed cell death-ligand 1 (PD-L1);
atezolizumab;
chemotherapy;
first-line;
PEMBROLIZUMAB;
D O I:
10.3389/fimmu.2021.666909
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Background Atezolizumab plus chemotherapy has been recommended as a first-line treatment option for patients with advanced non-small cell lung carcinoma (NSCLC) irrespective of programmed cell death-ligand 1 (PD-L1) expression. Currently, little is known about the efficacy and treatment-related adverse effects (TRAEs) of subtracting chemotherapy from the combination for patients with high PD-L1 expression. Thus, we performed an indirect comparison between atezolizumab plus chemotherapy and atezolizumab alone. Methods A total of five eligible randomized controlled trials (RCTs) were identified from PubMed, EMBASE, and Cochrane Central controlled trial registries, using keywords including atezolizumab, PD-1, PD-L1, NSCLC, and RCT. The clinical outcomes of objective response rate (ORR), progression-free survival (PFS), OS, and TRAEs were extracted and evaluated. Using indirect analysis, the efficacy and TRAEs were compared between arm A (atezolizumab plus chemotherapy) and arm C (atezolizumab), linked by arm B (chemotherapy). Results Direct comparison revealed that both atezolizumab plus chemotherapy (HR 0.65, P = 0.003) and atezolizumab alone (HR 0.59, P = 0.010) significantly improved OS compared with chemotherapy. More importantly, the indirect comparison showed that atezolizumab plus chemotherapy was not superior to atezolizumab regarding OS (RR 1.10, P =0.695) and ORR (RR 1.11, P = 0.645). However, patients who received atezolizumab combined with chemotherapy experienced more >= grade 3 TRAEs (RR 4.23, P<0.001) and TRAEs leading to drug discontinuation (RR 3.60, P<0.001) than those treated with atezolizumab monotherapy. Conclusions Atezolizumab monotherapy might be a better treatment option for patients with advanced NSCLC and high PD-L1 expression than atezolizumab plus chemotherapy.
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