PD-L1 and HER2 Expression in Gastroesophageal Cancer: a Matched Case Control Study.
Adult
Aged
Aged, 80 and over
B7-H1 Antigen
/ genetics
Biomarkers, Tumor
/ genetics
Case-Control Studies
Combined Modality Therapy
Esophageal Neoplasms
/ genetics
Female
Follow-Up Studies
Gene Expression Regulation, Neoplastic
Humans
Male
Middle Aged
Prognosis
Receptor, ErbB-2
/ genetics
Retrospective Studies
Stomach Neoplasms
/ genetics
Survival Rate
CPS
Esophageal tumor
Gastric tumor
Gastroesophageal junction tumor
Gastroesophageal tumor
HER2
Immunotherapy
PD-L1
TPS
Journal
Pathology oncology research : POR
ISSN: 1532-2807
Titre abrégé: Pathol Oncol Res
Pays: Switzerland
ID NLM: 9706087
Informations de publication
Date de publication:
Oct 2020
Oct 2020
Historique:
received:
05
10
2019
accepted:
23
04
2020
pubmed:
7
5
2020
medline:
13
7
2021
entrez:
7
5
2020
Statut:
ppublish
Résumé
Immunotherapy with check-point inhibitors serves as a promising treatment strategy in patients with upper gastrointestinal (GI) tumors. Human epidermal growth factor receptor 2 (HER2) is the only identified therapeutic target in upper GI tumors, whose potential interaction with programmed death-ligand 1 (PD-L1) is unknown. The aim of this study was the investigation of PD-L1 and HER2 in upper GI tumors. We retrospectively identified patients with HER2 positive gastroesophageal cancers and matched them with a HER2 negative group. We investigated the tumor specimens for HER2 status and PD-L1 expression, with the following assessments being performed: i) staining of tumor cells in terms of tumor proportion score (TPS), ii) staining for tumor-associated immune cells (TAIs), iii) interface pattern and iv) combined positive score (CPS). Both HER2 positive and negative group consisted of 59 patients. Expression of PD-L1 in TAIs and interface pattern were associated with a favorable outcome (p = 0.02, HR = 0.8; p = 0.04, HR = 0.39; respectively) in patients with localized disease, whereas TPS was associated with an unfavorable outcome in patients with advanced tumor (p = 0.02, HR = 1.4). These effects were HER2 independent. PD-L1 expression in its different assessment is equally observed in HER2 positive and negative patients. Future studies will show whether dual inhibition of HER2 and PD-L1 improves survival of this selected patient population.
Identifiants
pubmed: 32372174
doi: 10.1007/s12253-020-00814-2
pii: 10.1007/s12253-020-00814-2
pmc: PMC7471145
doi:
Substances chimiques
B7-H1 Antigen
0
Biomarkers, Tumor
0
CD274 protein, human
0
ERBB2 protein, human
EC 2.7.10.1
Receptor, ErbB-2
EC 2.7.10.1
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
2225-2235Subventions
Organisme : Medizinische Universität Wien
ID : n.a.
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