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Tumor-immune landscape patterns before and after chemoradiation in resectable esophageal adenocarcinomas.

Authors :
Soeratram TT
Creemers A
Meijer SL
de Boer OJ
Vos W
Hooijer GK
van Berge Henegouwen MI
Hulshof MC
Bergman JJ
Lei M
Bijlsma MF
Ylstra B
van Grieken NC
van Laarhoven HW
Source :
The Journal of pathology [J Pathol] 2022 Mar; Vol. 256 (3), pp. 282-296. Date of Electronic Publication: 2021 Dec 10.
Publication Year :
2022

Abstract

Immunotherapy is a new anti-cancer treatment option, showing promising results in clinical trials. To investigate potential immune biomarkers in esophageal adenocarcinoma (EAC), we explored immune landscape patterns in the tumor microenvironment before and after neoadjuvant chemoradiation (nCRT). Sections from matched pretreatment biopsies and post-nCRT resection specimens (n = 188) were stained for (1) programmed death-ligand 1 (PD-L1, CD274); (2) programmed cell death protein 1 (PD-1, CD279), forkhead box P3 (FOXP3), CD8, pan-cytokeratin multiplex; and (3) an MHC class I, II duplex. The densities of tumor-associated immune cells (TAICs) were calculated using digital image analyses and correlated to histopathological nCRT response [tumor regression grade (TRG)], survival, and post-nCRT immune patterns. PD-L1 positivity defined by a combined positive score of >1 was associated with a better response post-nCRT (TRG 1-3 versus 4, 5, p = 0.010). In addition, high combined mean densities of CD8 <superscript>+</superscript> , FOXP3 <superscript>+</superscript> , and PD-1 <superscript>+</superscript> TAICs in the tumor epithelium and stroma of biopsies were associated with a better response (TRG 1-3 versus 4, 5, p = 0.025 and p = 0.044, respectively). Heterogeneous TAIC density patterns were observed post-nCRT, with significantly higher CD8 <superscript>+</superscript> and PD-1 <superscript>+</superscript> TAIC mean densities compared with biopsies (both p = 0.000). Three immune landscape patterns were defined post-nCRT: 'inflamed', 'invasive margin', and 'desert', of which 'inflamed' was the most frequent (57%). Compared with matched biopsies, resection specimens with 'inflamed' tumors showed a significantly higher increase in CD8 <superscript>+</superscript> density compared with non-inflamed tumors post-nCRT (p = 0.000). In this cohort of EAC patients, higher TAIC densities in pretreatment biopsies were associated with response to nCRT. This warrants future research into the potential of the tumor-immune landscape for patient stratification and novel (immune) therapeutic strategies. © 2021 The Authors. The Journal of Pathology published by John Wiley & Sons, Ltd on behalf of The Pathological Society of Great Britain and Ireland.<br /> (© 2021 The Authors. The Journal of Pathology published by John Wiley & Sons, Ltd on behalf of The Pathological Society of Great Britain and Ireland.)

Details

Language :
English
ISSN :
1096-9896
Volume :
256
Issue :
3
Database :
MEDLINE
Journal :
The Journal of pathology
Publication Type :
Academic Journal
Accession number :
34743329
Full Text :
https://doi.org/10.1002/path.5832