Concordance, Correlation, and Clinical Impact of Standardized PD-L1 and TIL Scoring in SCCHN.

CPS PD-L1 TILs concordance prognosis spatiotemporal heterogeneity squamous cell carcinoma of head and neck

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
14 May 2022
Historique:
received: 13 04 2022
revised: 02 05 2022
accepted: 11 05 2022
entrez: 28 5 2022
pubmed: 29 5 2022
medline: 29 5 2022
Statut: epublish

Résumé

The clinical significance of tumor-infiltrating lymphocytes (TILs) and programmed cell death-ligand 1 (PD-L1) expression has been thoroughly researched in squamous cell carcinoma of the head and neck (SCCHN). To address the impact of intra- and intertumoral heterogeneity in these biomarkers, we explored the concordance of PD-L1 combined positive score (CPS) and stromal TILs in different paired tissue sample types, while evaluating their internal relationship and prognostic impact. A total of 165 tissue blocks from 80 SCCHN patients were reviewed for TILs and PD-L1 CPS. Concordance between paired tissue samples was evaluated, and their association with several clinicopathological variables, overall survival (OS), and disease-free survival (DFS) was determined. Biopsies and paired resection material were severely discordant in 39% and 34% of samples for CPS and TIL count, respectively, of which CPS was underscored in 27% of biopsies. In paired primary tumor-metastatic lesions, the disagreement was lower for CPS (19%) but not for TIL count (44%). PD-L1 CPS was correlated with prolonged OS when calculated from tissue acquirement, while extended OS and DFS were observed for high TIL density. Intertumoral and, especially, intratumoral heterogeneity were confounding factors when determining PD-L1 CPS and TIL count on paired tissue samples, indicating the increasing necessity of assessing both biomarkers on representative tissue material. Although TILs hold valuable prognostic information in SCCHN, the robustness of PD-L1 as a biomarker in SCCHN remains ambiguous.

Sections du résumé

BACKGROUND BACKGROUND
The clinical significance of tumor-infiltrating lymphocytes (TILs) and programmed cell death-ligand 1 (PD-L1) expression has been thoroughly researched in squamous cell carcinoma of the head and neck (SCCHN). To address the impact of intra- and intertumoral heterogeneity in these biomarkers, we explored the concordance of PD-L1 combined positive score (CPS) and stromal TILs in different paired tissue sample types, while evaluating their internal relationship and prognostic impact.
METHODS METHODS
A total of 165 tissue blocks from 80 SCCHN patients were reviewed for TILs and PD-L1 CPS. Concordance between paired tissue samples was evaluated, and their association with several clinicopathological variables, overall survival (OS), and disease-free survival (DFS) was determined.
RESULTS RESULTS
Biopsies and paired resection material were severely discordant in 39% and 34% of samples for CPS and TIL count, respectively, of which CPS was underscored in 27% of biopsies. In paired primary tumor-metastatic lesions, the disagreement was lower for CPS (19%) but not for TIL count (44%). PD-L1 CPS was correlated with prolonged OS when calculated from tissue acquirement, while extended OS and DFS were observed for high TIL density.
CONCLUSION CONCLUSIONS
Intertumoral and, especially, intratumoral heterogeneity were confounding factors when determining PD-L1 CPS and TIL count on paired tissue samples, indicating the increasing necessity of assessing both biomarkers on representative tissue material. Although TILs hold valuable prognostic information in SCCHN, the robustness of PD-L1 as a biomarker in SCCHN remains ambiguous.

Identifiants

pubmed: 35626035
pii: cancers14102431
doi: 10.3390/cancers14102431
pmc: PMC9139955
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : MSD Belgium BV/SRL
ID : KW/2091/ONC/029/009

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Auteurs

Stijn Jeroen De Keukeleire (SJ)

Department of Medical Oncology, University Hospital Ghent, 9000 Ghent, Belgium.
Department of Internal Medicine, University Hospital Brussels, 1090 Jette, Belgium.

Tijl Vermassen (T)

Department of Medical Oncology, University Hospital Ghent, 9000 Ghent, Belgium.
Drug Research Unit Ghent, Ghent University Hospital, 9000 Ghent, Belgium.
Cancer Research Institute Ghent (CRIG), 9000 Ghent, Belgium.

Philippe Deron (P)

Department of Head and Neck Surgery, Ghent University Hospital, 9000 Ghent, Belgium.

Wouter Huvenne (W)

Drug Research Unit Ghent, Ghent University Hospital, 9000 Ghent, Belgium.
Department of Head and Neck Surgery, Ghent University Hospital, 9000 Ghent, Belgium.

Fréderic Duprez (F)

Department of Radiation Oncology, Ghent University Hospital, 9000 Ghent, Belgium.

David Creytens (D)

Cancer Research Institute Ghent (CRIG), 9000 Ghent, Belgium.
Department of Pathology, Ghent University Hospital, 9000 Ghent, Belgium.

Jo Van Dorpe (J)

Department of Pathology, Ghent University Hospital, 9000 Ghent, Belgium.

Liesbeth Ferdinande (L)

Department of Pathology, Ghent University Hospital, 9000 Ghent, Belgium.

Sylvie Rottey (S)

Department of Medical Oncology, University Hospital Ghent, 9000 Ghent, Belgium.
Drug Research Unit Ghent, Ghent University Hospital, 9000 Ghent, Belgium.
Cancer Research Institute Ghent (CRIG), 9000 Ghent, Belgium.

Classifications MeSH