Prevalence and prognostic role of PD-L1 in patients with gynecological cancers: A systematic review and meta-analysis

Our study aims to evaluate programmed cell death ligand-1 (PD-L1) expression and its prognostic significance in cervical cancer (CC), endometrial cancer (EC) and ovarian cancer (OC). Several electronic databases were searched. Fixed effects models or random effects models were employed to calculate...

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Published inCritical reviews in oncology/hematology Vol. 189; p. 104084
Main Authors Fu, Hanlin, Fu, Zhihui, Mao, Meng, Si, Lulu, Bai, Jing, Wang, Qian, Guo, Ruixia
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.09.2023
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Abstract Our study aims to evaluate programmed cell death ligand-1 (PD-L1) expression and its prognostic significance in cervical cancer (CC), endometrial cancer (EC) and ovarian cancer (OC). Several electronic databases were searched. Fixed effects models or random effects models were employed to calculate the pooled prevalence of PD-L1 positivity and pooled hazard ratios (HRs) as appropriate. Heterogeneity and publication bias were also assessed. The pooled prevalence of PD-L1 positivity was 58.1%, 33.8% and 37.5% for CC, EC and OC patients, respectively. There were significant differences in the pooled estimates after stratification by PD-L1-positive assessment criteria and antibody clones. PD-L1 positivity was associated with worse OS in CC and EC patients and poorer progression-free survival (PFS) in CC patients. The prevalence of PD-L1-positive expression was considerably high in CC and modestly high in EC and OC patients. PD-L1 expression has the potential to be a prognostic biomarker for predicting the clinical outcomes of patients with CC and EC but not OC. [Display omitted] •The prevalence of PD-L1-positive expression was 58.1% in CC patients, 33.8% in EC patients and 37.5% in OC patients.•The prevalence of PD-L1 positivity in the three GCs is subject to PD-L1-positive assessment criteria and antibody clones.•PD-L1 positivity was associated with worse OS in CC and EC patients and poorer PFS in CC patients.•The study provides a better understanding of the application of PD-L1-based immunotherapy for GCs.
AbstractList Our study aims to evaluate programmed cell death ligand-1 (PD-L1) expression and its prognostic significance in cervical cancer (CC), endometrial cancer (EC) and ovarian cancer (OC).OBJECTIVEOur study aims to evaluate programmed cell death ligand-1 (PD-L1) expression and its prognostic significance in cervical cancer (CC), endometrial cancer (EC) and ovarian cancer (OC).Several electronic databases were searched. Fixed effects models or random effects models were employed to calculate the pooled prevalence of PD-L1 positivity and pooled hazard ratios (HRs) as appropriate. Heterogeneity and publication bias were also assessed.METHODSSeveral electronic databases were searched. Fixed effects models or random effects models were employed to calculate the pooled prevalence of PD-L1 positivity and pooled hazard ratios (HRs) as appropriate. Heterogeneity and publication bias were also assessed.The pooled prevalence of PD-L1 positivity was 58.1%, 33.8% and 37.5% for CC, EC and OC patients, respectively. There were significant differences in the pooled estimates after stratification by PD-L1-positive assessment criteria and antibody clones. PD-L1 positivity was associated with worse OS in CC and EC patients and poorer progression-free survival (PFS) in CC patients.RESULTSThe pooled prevalence of PD-L1 positivity was 58.1%, 33.8% and 37.5% for CC, EC and OC patients, respectively. There were significant differences in the pooled estimates after stratification by PD-L1-positive assessment criteria and antibody clones. PD-L1 positivity was associated with worse OS in CC and EC patients and poorer progression-free survival (PFS) in CC patients.The prevalence of PD-L1-positive expression was considerably high in CC and modestly high in EC and OC patients. PD-L1 expression has the potential to be a prognostic biomarker for predicting the clinical outcomes of patients with CC and EC but not OC.CONCLUSIONSThe prevalence of PD-L1-positive expression was considerably high in CC and modestly high in EC and OC patients. PD-L1 expression has the potential to be a prognostic biomarker for predicting the clinical outcomes of patients with CC and EC but not OC.
Our study aims to evaluate programmed cell death ligand-1 (PD-L1) expression and its prognostic significance in cervical cancer (CC), endometrial cancer (EC) and ovarian cancer (OC). Several electronic databases were searched. Fixed effects models or random effects models were employed to calculate the pooled prevalence of PD-L1 positivity and pooled hazard ratios (HRs) as appropriate. Heterogeneity and publication bias were also assessed. The pooled prevalence of PD-L1 positivity was 58.1%, 33.8% and 37.5% for CC, EC and OC patients, respectively. There were significant differences in the pooled estimates after stratification by PD-L1-positive assessment criteria and antibody clones. PD-L1 positivity was associated with worse OS in CC and EC patients and poorer progression-free survival (PFS) in CC patients. The prevalence of PD-L1-positive expression was considerably high in CC and modestly high in EC and OC patients. PD-L1 expression has the potential to be a prognostic biomarker for predicting the clinical outcomes of patients with CC and EC but not OC.
Our study aims to evaluate programmed cell death ligand-1 (PD-L1) expression and its prognostic significance in cervical cancer (CC), endometrial cancer (EC) and ovarian cancer (OC). Several electronic databases were searched. Fixed effects models or random effects models were employed to calculate the pooled prevalence of PD-L1 positivity and pooled hazard ratios (HRs) as appropriate. Heterogeneity and publication bias were also assessed. The pooled prevalence of PD-L1 positivity was 58.1%, 33.8% and 37.5% for CC, EC and OC patients, respectively. There were significant differences in the pooled estimates after stratification by PD-L1-positive assessment criteria and antibody clones. PD-L1 positivity was associated with worse OS in CC and EC patients and poorer progression-free survival (PFS) in CC patients. The prevalence of PD-L1-positive expression was considerably high in CC and modestly high in EC and OC patients. PD-L1 expression has the potential to be a prognostic biomarker for predicting the clinical outcomes of patients with CC and EC but not OC. [Display omitted] •The prevalence of PD-L1-positive expression was 58.1% in CC patients, 33.8% in EC patients and 37.5% in OC patients.•The prevalence of PD-L1 positivity in the three GCs is subject to PD-L1-positive assessment criteria and antibody clones.•PD-L1 positivity was associated with worse OS in CC and EC patients and poorer PFS in CC patients.•The study provides a better understanding of the application of PD-L1-based immunotherapy for GCs.
ArticleNumber 104084
Author Si, Lulu
Fu, Hanlin
Fu, Zhihui
Bai, Jing
Mao, Meng
Wang, Qian
Guo, Ruixia
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Keywords Systematic review
Programmed cell death ligand-1
Prevalence
Prognosis
Gynecological cancers
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Snippet Our study aims to evaluate programmed cell death ligand-1 (PD-L1) expression and its prognostic significance in cervical cancer (CC), endometrial cancer (EC)...
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SubjectTerms B7-H1 Antigen - genetics
B7-H1 Antigen - metabolism
Endometrial Neoplasms
Female
Gynecological cancers
Humans
Ovarian Neoplasms
Prevalence
Prognosis
Programmed cell death ligand-1
Proportional Hazards Models
Systematic review
Uterine Cervical Neoplasms
Title Prevalence and prognostic role of PD-L1 in patients with gynecological cancers: A systematic review and meta-analysis
URI https://www.clinicalkey.com/#!/content/1-s2.0-S1040842823001725
https://www.ncbi.nlm.nih.gov/pubmed/37536446
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