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Comparative outcomes of first-line PD-1/PD-L1 inhibitors plus chemotherapy for advanced squamous non-small cell lung cancer: a systematic review and network meta-analysis of randomized clinical trials.

作者信息

Liu Zhefeng, Wang Zhikuan, Zhu Jun, Tao Haitao, Huang Ziwei, Han Lu, Patel Akshay J, Hu Yi

机构信息

Senior Department of Oncology, The Fifth Medical Center of PLA General Hospital, Beijing, China.

Department of Radiation Oncology, Jiangsu Cancer Hospital, Nanjing, China.

出版信息

Transl Lung Cancer Res. 2025 Feb 28;14(2):563-574. doi: 10.21037/tlcr-2025-83. Epub 2025 Feb 27.


DOI:10.21037/tlcr-2025-83
PMID:40114962
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11921199/
Abstract

BACKGROUND: Head-to-head comparisons between the available first-line regimens with programmed cell death-1/programmed death-ligand 1 (PD-1/PD-L1) inhibitors and chemotherapy for advanced squamous non-small cell lung cancer (NSCLC) are lacking. Therefore, we conducted a systematic review and network meta-analysis to identify the optimal first-line regimen with PD-1/PD-L1 inhibitors plus chemotherapy for advanced squamous NSCLC. METHODS: A systematic review and network meta-analysis of randomized clinical trials (RCTs) were performed. PubMed, Embase, Web of Science, and the ClinicalTrials.gov databases and major annual conferences were searched. RCTs that compared PD-1/PD-L1 inhibitors plus chemotherapy with chemotherapy alone in patients with advanced squamous NSCLC were eligible for inclusion. Risk of bias was assessed using the Cochrane Risk of Bias Tool (version 2.0), and a funnel plot was used to assess the publication bias. RESULTS: A total of nine RCTs comprising 3,210 patients were included. When combined with chemotherapy, PD-1 inhibitors were superior to PD-L1 inhibitors in terms of overall survival (OS) [PD-1: hazard ratio (HR) 0.70, 95% credible interval (CrI): 0.62 to 0.79; PD-L1: HR 0.82, 95% CrI: 0.71 to 0.94] and progression-free survival (PFS) (PD-1: HR 0.50, 95% CrI: 0.45 to 0.55; PD-L1: HR 0.63, 95% CrI: 0.55 to 0.72). Moreover, the PD-1 inhibitor camrelizumab was the most effective agent in combined therapy for prolonging OS (HR 0.56, 95% CrI: 0.44 to 0.71) and PFS (HR 0.32, 95% CrI: 0.25 to 0.42), followed by the PD-L1 inhibitor sugemalimab (OS: HR 0.61, 95% CrI: 0.43 to 0.86; PFS: HR 0.37, 95% CrI: 0.26 to 0.52). Moreover, the addition of camrelizumab or tislelizumab to chemotherapy was associated with the improved objective response rate (ORR) and a longer duration of response (DoR). Regarding safety, pembrolizumab and camrelizumab were associated with the lowest risk of developing grade 3-5 treatment-related adverse events (TRAEs). Most of the trials were at low risk for bias, and no obvious publication bias was observed in the outcomes. CONCLUSIONS: When combined with first-line chemotherapy, camrelizumab has the potential to be a preferred option in patients with advanced squamous NSCLC. This finding might serve as a guideline to aid in the selection of first-line immunotherapy plus chemotherapy strategies for advanced squamous NSCLC.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6756/11921199/71aaa59eb2a5/tlcr-14-02-563-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6756/11921199/f0b9b91666ef/tlcr-14-02-563-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6756/11921199/7ff9f3abd49f/tlcr-14-02-563-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6756/11921199/bd78d3fa7351/tlcr-14-02-563-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6756/11921199/2da4f2440b25/tlcr-14-02-563-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6756/11921199/71aaa59eb2a5/tlcr-14-02-563-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6756/11921199/f0b9b91666ef/tlcr-14-02-563-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6756/11921199/7ff9f3abd49f/tlcr-14-02-563-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6756/11921199/bd78d3fa7351/tlcr-14-02-563-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6756/11921199/2da4f2440b25/tlcr-14-02-563-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6756/11921199/71aaa59eb2a5/tlcr-14-02-563-f5.jpg

相似文献

[1]
Comparative outcomes of first-line PD-1/PD-L1 inhibitors plus chemotherapy for advanced squamous non-small cell lung cancer: a systematic review and network meta-analysis of randomized clinical trials.

Transl Lung Cancer Res. 2025-2-28

[2]
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[3]
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[4]
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[5]
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Cochrane Database Syst Rev. 2021-4-30

[6]
Efficacy and safety of immune checkpoint inhibitors for advanced non-small cell lung cancer with or without PD-L1 selection: A systematic review and network meta-analysis.

Chin Med J (Engl). 2023-9-20

[7]
Immune checkpoint inhibitors chemotherapy as second-line therapy for advanced oesophageal squamous cell carcinoma: a systematic review and economic evaluation.

Therap Adv Gastroenterol. 2024-2-28

[8]
Efficacy and safety of PD-1 inhibitors as second-line treatment for advanced squamous esophageal cancer: a systematic review and network meta-analysis with a focus on PD-L1 expression levels.

Front Immunol. 2025-1-23

[9]
Efficacy and safety evaluation of frontline immunotherapy combinations in advanced esophageal squamous cell carcinoma: a network meta-analysis highlighting the value of PD-L1 expression positivity scores.

Front Immunol. 2024

[10]
Identifying optimal PD-1/PD-L1 inhibitors in first-line treatment of patients with advanced squamous non-small cell lung cancer in China: Updated systematic review and network meta-analysis.

Front Pharmacol. 2022-9-29

本文引用的文献

[1]
Global Disparities of Cancer and Its Projected Burden in 2050.

JAMA Netw Open. 2024-11-4

[2]
Tislelizumab plus chemotherapy versus chemotherapy alone as first-line treatment for advanced squamous non-small-cell lung cancer: final analysis of the randomized, phase III RATIONALE-307 trial.

ESMO Open. 2024-10

[3]
Efficacy and safety of personalized optimal PD-(L)1 combinations in advanced NSCLC: a network meta-analysis.

J Natl Cancer Inst. 2024-10-1

[4]
First-line treatments for advanced non-squamous non-small cell lung cancer with immune checkpoint inhibitors plus chemotherapy: a systematic review, network meta-analysis, and cost-effectiveness analysis.

Ther Adv Med Oncol. 2024-5-30

[5]
Cemiplimab plus chemotherapy versus chemotherapy alone in non-small cell lung cancer with PD-L1 ≥ 1 %: A subgroup analysis from the EMPOWER-Lung 3 part 2 trial.

Lung Cancer. 2024-7

[6]
A Brief Report of Durvalumab With or Without Tremelimumab in Combination With Chemotherapy as First-Line Therapy for Metastatic Non-Small-Cell Lung Cancer: Outcomes by Tumor PD-L1 Expression in the Phase 3 POSEIDON Study.

Clin Lung Cancer. 2024-5

[7]
Expanding Broad Molecular Reflex Testing in Non-Small Cell Lung Cancer to Squamous Histology.

Cancers (Basel). 2024-2-23

[8]
The efficacy and safety of immune-checkpoint inhibitors plus chemotherapy versus chemotherapy for non-small cell lung cancer: An updated systematic review and meta-analysis.

PLoS One. 2024

[9]
Outcomes of Immunotherapy Versus Chemotherapy as First-Line Treatment in Advanced NSCLC: A Meta-Analysis of Randomized Clinical Trials.

J Thorac Oncol. 2023-9

[10]
Pembrolizumab Plus Chemotherapy in Squamous Non-Small-Cell Lung Cancer: 5-Year Update of the Phase III KEYNOTE-407 Study.

J Clin Oncol. 2023-4-10

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