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Effect of PD-L1 Expression for the PD-1/L1 Inhibitors on Non-small Cell Lung Cancer: A Meta-analysis Based on Randomised Controlled Trials.
- Source :
-
Clinical Oncology . Oct2023, Vol. 35 Issue 10, p640-651. 12p. - Publication Year :
- 2023
-
Abstract
- As PD-L1 expression has been proposed as one of the cancer biomarkers for non-small cell lung cancer (NSCLC), the predictive value of tumour proportional score (TPS) in the effect of immunotherapy [programmed death protein-1/ligand 1 (PD-1/L1) inhibitors] for NSCLC is worth exploring further. Here, we aimed to summarise the outcomes of current NSCLC randomised controlled trials (RCTs) and explore the predictive value of TPS in clinical immunotherapy, including immune checkpoint inhibitors (ICIs) with or without chemotherapy. RCTs published by PubMed, Medline, Embase and Scopus before February 2023 comparing immunotherapy (PD-1/L1 with or without other therapy) versus a control group in advanced or metastatic NSCLC were included to assess the prognosis according to the patients' TPS with 1% and 50% as the thresholds. The primary endpoints were overall survival and progression-free survival. In total, 28 RCTs containing 17 266 participants with advanced or metastatic NSCLC were included in this meta-analysis. Statistical results showed that compared with TPS <1%, ≥1% or within 1–49%, patients with TPS ≥50% benefited more significantly from the immunotherapy. A subgroup analysis showed that when TPS was <1%, ≥1% or within 1–49%, ICIs + chemotherapy had better efficacy than ICIs alone; PD-1 (such as pembrolizumab) inhibitors had better efficacy than PD-L1 inhibitors (such as atezolizumab). The efficacy of immunotherapy (PD-1/L1 inhibitors) for advanced or metastatic NSCLC is influenced by TPS. • For patients with advanced NSCLC, the efficacy of immunotherapy is related to TPS. • For patients with TPS>50%, immunotherapy has ideal efficacy. • For patients with high PD-L1 expression, immunotherapy can be recommended first. [ABSTRACT FROM AUTHOR]
- Subjects :
- *LUNG cancer
*ONLINE information services
*DRUG efficacy
*PROGRAMMED death-ligand 1
*PREDICTIVE tests
*META-analysis
*IMMUNE checkpoint inhibitors
*MEDICAL information storage & retrieval systems
*SYSTEMATIC reviews
*GENE expression
*TREATMENT effectiveness
*DESCRIPTIVE statistics
*TUMOR markers
*MEDLINE
*PROGRESSION-free survival
*OVERALL survival
Subjects
Details
- Language :
- English
- ISSN :
- 09366555
- Volume :
- 35
- Issue :
- 10
- Database :
- Academic Search Index
- Journal :
- Clinical Oncology
- Publication Type :
- Academic Journal
- Accession number :
- 171393648
- Full Text :
- https://doi.org/10.1016/j.clon.2023.07.012