Challenges and the Evolving Landscape of Assessing Blood-Based PD-L1 Expression as a Biomarker for Anti-PD-(L)1 Immunotherapy

While promising, PD-L1 expression on tumor tissues as assessed by immunohistochemistry has been shown to be an imperfect biomarker that only applies to a limited number of cancers, whereas many patients with PD-L1-negative tumors still respond to anti-PD-(L)1 immunotherapy. Recent studies using pati...

Full description

Bibliographic Details
Main Authors: Tao Wang, Desirée Denman, Silvia M. Bacot, Gerald M. Feldman
Format: Article
Language:English
Published: MDPI AG 2022-05-01
Series:Biomedicines
Subjects:
Online Access:https://www.mdpi.com/2227-9059/10/5/1181
_version_ 1797501293018742784
author Tao Wang
Desirée Denman
Silvia M. Bacot
Gerald M. Feldman
author_facet Tao Wang
Desirée Denman
Silvia M. Bacot
Gerald M. Feldman
author_sort Tao Wang
collection DOAJ
description While promising, PD-L1 expression on tumor tissues as assessed by immunohistochemistry has been shown to be an imperfect biomarker that only applies to a limited number of cancers, whereas many patients with PD-L1-negative tumors still respond to anti-PD-(L)1 immunotherapy. Recent studies using patient blood samples to assess immunotherapeutic responsiveness suggests a promising approach to the identification of novel and/or improved biomarkers for anti-PD-(L)1 immunotherapy. In this review, we discuss the advances in our evolving understanding of the regulation and function of PD-L1 expression, which is the foundation for developing blood-based PD-L1 as a biomarker for anti-PD-(L)1 immunotherapy. We further discuss current knowledge and clinical study results for biomarker identification using PD-L1 expression on tumor and immune cells, exosomes, and soluble forms of PD-L1 in the peripheral blood. Finally, we discuss key challenges for the successful development of the potential use of blood-based PD-L1 as a biomarker for anti-PD-(L)1 immunotherapy.
first_indexed 2024-03-10T03:16:18Z
format Article
id doaj.art-2d0d5a5f01224811a7d1dcd2da90d438
institution Directory Open Access Journal
issn 2227-9059
language English
last_indexed 2024-03-10T03:16:18Z
publishDate 2022-05-01
publisher MDPI AG
record_format Article
series Biomedicines
spelling doaj.art-2d0d5a5f01224811a7d1dcd2da90d4382023-11-23T10:12:14ZengMDPI AGBiomedicines2227-90592022-05-01105118110.3390/biomedicines10051181Challenges and the Evolving Landscape of Assessing Blood-Based PD-L1 Expression as a Biomarker for Anti-PD-(L)1 ImmunotherapyTao Wang0Desirée Denman1Silvia M. Bacot2Gerald M. Feldman3Office of Biotechnology Products, Office of Pharmaceutical Quality, Center for Drug Evaluation and Research, Food and Drug Administration, Silver Spring, MD 20993, USAOffice of Biotechnology Products, Office of Pharmaceutical Quality, Center for Drug Evaluation and Research, Food and Drug Administration, Silver Spring, MD 20993, USAOffice of Biotechnology Products, Office of Pharmaceutical Quality, Center for Drug Evaluation and Research, Food and Drug Administration, Silver Spring, MD 20993, USAOffice of Biotechnology Products, Office of Pharmaceutical Quality, Center for Drug Evaluation and Research, Food and Drug Administration, Silver Spring, MD 20993, USAWhile promising, PD-L1 expression on tumor tissues as assessed by immunohistochemistry has been shown to be an imperfect biomarker that only applies to a limited number of cancers, whereas many patients with PD-L1-negative tumors still respond to anti-PD-(L)1 immunotherapy. Recent studies using patient blood samples to assess immunotherapeutic responsiveness suggests a promising approach to the identification of novel and/or improved biomarkers for anti-PD-(L)1 immunotherapy. In this review, we discuss the advances in our evolving understanding of the regulation and function of PD-L1 expression, which is the foundation for developing blood-based PD-L1 as a biomarker for anti-PD-(L)1 immunotherapy. We further discuss current knowledge and clinical study results for biomarker identification using PD-L1 expression on tumor and immune cells, exosomes, and soluble forms of PD-L1 in the peripheral blood. Finally, we discuss key challenges for the successful development of the potential use of blood-based PD-L1 as a biomarker for anti-PD-(L)1 immunotherapy.https://www.mdpi.com/2227-9059/10/5/1181immune checkpoint inhibitoranti-PD-(L)1 immunotherapyliquid biopsybiomarkerPD-1PD-L1
spellingShingle Tao Wang
Desirée Denman
Silvia M. Bacot
Gerald M. Feldman
Challenges and the Evolving Landscape of Assessing Blood-Based PD-L1 Expression as a Biomarker for Anti-PD-(L)1 Immunotherapy
Biomedicines
immune checkpoint inhibitor
anti-PD-(L)1 immunotherapy
liquid biopsy
biomarker
PD-1
PD-L1
title Challenges and the Evolving Landscape of Assessing Blood-Based PD-L1 Expression as a Biomarker for Anti-PD-(L)1 Immunotherapy
title_full Challenges and the Evolving Landscape of Assessing Blood-Based PD-L1 Expression as a Biomarker for Anti-PD-(L)1 Immunotherapy
title_fullStr Challenges and the Evolving Landscape of Assessing Blood-Based PD-L1 Expression as a Biomarker for Anti-PD-(L)1 Immunotherapy
title_full_unstemmed Challenges and the Evolving Landscape of Assessing Blood-Based PD-L1 Expression as a Biomarker for Anti-PD-(L)1 Immunotherapy
title_short Challenges and the Evolving Landscape of Assessing Blood-Based PD-L1 Expression as a Biomarker for Anti-PD-(L)1 Immunotherapy
title_sort challenges and the evolving landscape of assessing blood based pd l1 expression as a biomarker for anti pd l 1 immunotherapy
topic immune checkpoint inhibitor
anti-PD-(L)1 immunotherapy
liquid biopsy
biomarker
PD-1
PD-L1
url https://www.mdpi.com/2227-9059/10/5/1181
work_keys_str_mv AT taowang challengesandtheevolvinglandscapeofassessingbloodbasedpdl1expressionasabiomarkerforantipdl1immunotherapy
AT desireedenman challengesandtheevolvinglandscapeofassessingbloodbasedpdl1expressionasabiomarkerforantipdl1immunotherapy
AT silviambacot challengesandtheevolvinglandscapeofassessingbloodbasedpdl1expressionasabiomarkerforantipdl1immunotherapy
AT geraldmfeldman challengesandtheevolvinglandscapeofassessingbloodbasedpdl1expressionasabiomarkerforantipdl1immunotherapy