Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2021 Dec 3;13(23):6090.
doi: 10.3390/cancers13236090.

Prognostic Role of PD-L1 Expression in Invasive Breast Cancer: A Systematic Review and Meta-Analysis

Affiliations
Review

Prognostic Role of PD-L1 Expression in Invasive Breast Cancer: A Systematic Review and Meta-Analysis

Magno Belém Cirqueira et al. Cancers (Basel). .

Abstract

Programmed death ligand 1 (PD-L1) has been investigated in various types of cancer; however, the role of PD-L1 expression in breast cancer remains controversial. We performed a systematic review and meta-analysis to assess the association of PD-L1 expression with clinicopathological variables, overall survival (OS), and disease-free survival (DFS) in invasive breast cancer. A total of 965 articles were included from CINAHL, Embase, PubMed, and Scopus databases. Of these, 22 studies encompassing 6468 cases of invasive breast cancer were included in the systematic review, and 15 articles were included in the meta-analysis. PD-L1 expression was associated with age ≥ 50 years, lymph node status-negative, progesterone receptor-negative, Ki67 ≥ 20%, and human epidermal growth factor receptor 2 (HER2)-negative. PD-L1 positivity was associated with worse OS (hazard ratio, HR, 2.39; 95% confidence interval, CI, 1.26-3.52; p =< 0.000); however, there was no significant improvement in DFS (HR 0.17; 95% CI -0.12-0.46; p =< 0.252). PD-L1 positivity was significantly associated with the clinicopathological characteristics of favorable and unfavorable prognoses. However, the final clinical outcome was associated with lower OS and had no significant association with DFS.

Keywords: PD-L1; breast cancer; immunohistochemistry; prognosis.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Flowchart of study selection.
Figure 2
Figure 2
Forest plot of the proportion (%) of PD-L1 expression in tumor cells, immune cells, and both tumor and immune cells.
Figure 3
Figure 3
Forest plots of hazard ratios (HRs) for the effect of PD-L1 upregulation on overall survival (OS).
Figure 4
Figure 4
Forest plots of hazard ratios (HRs) for the effect of PD-L1 upregulation on disease-free survival (DFS).
Figure 5
Figure 5
Quality plot graphically representing the risk of bias (RoB) analysis. The most relevant sources of bias were assessed in primary-level studies using the Quality in Prognosis Studies (QUIPS) tool.
Figure 6
Figure 6
Funnel plot for the studies included in the meta-analysis.

References

    1. Zhang Y., Tian J., Qu C., Tang Z., Wang Y., Li K., Yang Y., Liu S. Prognostic value of programmed cell death ligand-1 expression in breast cancer: A meta-analysis. Medicine. 2020;99:e23359. doi: 10.1097/MD.0000000000023359. - DOI - PMC - PubMed
    1. Mina L.A., Lim S., Bahadur S.W., Firoz A.T. Immunotherapy for the Treatment of Breast Cancer: Emerging New Data. Breast Cancer. 2019;11:321–328. doi: 10.2147/BCTT.S184710. - DOI - PMC - PubMed
    1. Zhang Y., Kang S., Shen J., He J., Jiang L., Wang W., Guo Z., Peng G., Chen G., He J., et al. Prognostic significance of programmed cell death 1 (PD-1) or PD-1 ligand 1 (PD-L1) Expression in epithelial-originated cancer: A meta-analysis. Medicine. 2015;94:e515. doi: 10.1097/MD.0000000000000515. - DOI - PMC - PubMed
    1. Mittendorf E.A., Zhang H., Barrios C.H., Saji S., Jung K.H., Hegg R., Koehler A., Sohn J., Iwata H., Telli M.L., et al. Neoadjuvant atezolizumab in combination with sequential nab-paclitaxel and anthracycline-based chemotherapy versus placebo and chemotherapy in patients with early-stage triple-negative breast cancer (IMpassion031): A randomised, double-blind, phase 3 trial. Lancet. 2020;396:1090–1100. doi: 10.1016/S0140-6736(20)31953-X. - DOI - PubMed
    1. Adams S., Loi S., Toppmeyer D., Cescon D.W., De Laurentiis M., Nanda R., Winer E.P., Mukai H., Tamura K., Armstrong A., et al. Pembrolizumab monotherapy for previously untreated, PD-L1-positive, metastatic triple-negative breast cancer: Cohort B of the phase II KEYNOTE-086 study. Ann. Oncol. 2019;30:405–411. doi: 10.1093/annonc/mdy518. - DOI - PubMed