TY - JOUR
T1 - TREM2-Expressing Multinucleated Giant Macrophages Are a Biomarker of Good Prognosis in Head and Neck Squamous Cell Carcinoma
AU - Gessain, Grégoire
AU - Anzali, Ahmed Amine
AU - Lerousseau, Marvin
AU - Mulder, Kevin
AU - Bied, Mathilde
AU - Auperin, Anne
AU - Stockholm, Daniel
AU - Signolle, Nicolas
AU - Sassi, Farah
AU - Marques Da Costa, Maria Eugenia
AU - Marchais, Antonin
AU - Sayadi, Alexandre
AU - Weidner, Daniela
AU - Uderhardt, Stefan
AU - Blampey, Quentin
AU - Nakkireddy, Sumanth Reddy
AU - Broutin, Sophie
AU - Dutertre, Charles Antoine
AU - Busson, Pierre
AU - Walter, Thomas
AU - Marhic, Alix
AU - Moya-Plana, Antoine
AU - Guerlain, Johanne
AU - Breuskin, Ingrid
AU - Casiraghi, Odile
AU - Gorphe, Philippe
AU - Classe, Marion
AU - Scoazec, Jean Yves
AU - Blériot, Camille
AU - Ginhoux, Florent
N1 - Publisher Copyright:
© 2024 The Authors; Published by the American Association for Cancer Research.
PY - 2024/12/1
Y1 - 2024/12/1
N2 - Patients with head and neck squamous cell carcinomas (HNSCC) often have poor outcomes due to suboptimal risk management and treatment strategies; yet integrating novel prognostic biomarkers into clinical practice is challenging. Here, we report the presence of multinucleated giant cells (MGC)—a type of macrophages—in tumors from patients with HNSCC, which are associated with a favorable prognosis in treatment-naive and preoperative chemotherapy–treated patients. Importantly, MGC density increased in tumors following preoperative therapy, suggesting a role of these cells in the antitumoral response. To enable clinical translation of MGC density as a prognostic marker, we developed a deep-learning model to automate its quantifi-cation on routinely stained pathological whole slide images. Finally, we used spatial transcriptomic and proteomic approaches to describe the MGC-related tumor microenvironment and observed an increase in central memory CD4 T cells. We defined an MGC-specific signature resembling to TREM2-expressing mononuclear tumor-associated macrophages, which colocalized in keratin tumor niches. Significance: Novel individual biomarkers are needed to guide therapeutic decisions for patients with head and neck cancer. We report for the first time, granulomas of TREM2-expressing multinucleated giant macrophages in keratin-rich tumor niches, as a biomarker of favorable prognosis and developed a deep-learning model to automate its quantification on routinely stained pathological slides.
AB - Patients with head and neck squamous cell carcinomas (HNSCC) often have poor outcomes due to suboptimal risk management and treatment strategies; yet integrating novel prognostic biomarkers into clinical practice is challenging. Here, we report the presence of multinucleated giant cells (MGC)—a type of macrophages—in tumors from patients with HNSCC, which are associated with a favorable prognosis in treatment-naive and preoperative chemotherapy–treated patients. Importantly, MGC density increased in tumors following preoperative therapy, suggesting a role of these cells in the antitumoral response. To enable clinical translation of MGC density as a prognostic marker, we developed a deep-learning model to automate its quantifi-cation on routinely stained pathological whole slide images. Finally, we used spatial transcriptomic and proteomic approaches to describe the MGC-related tumor microenvironment and observed an increase in central memory CD4 T cells. We defined an MGC-specific signature resembling to TREM2-expressing mononuclear tumor-associated macrophages, which colocalized in keratin tumor niches. Significance: Novel individual biomarkers are needed to guide therapeutic decisions for patients with head and neck cancer. We report for the first time, granulomas of TREM2-expressing multinucleated giant macrophages in keratin-rich tumor niches, as a biomarker of favorable prognosis and developed a deep-learning model to automate its quantification on routinely stained pathological slides.
UR - http://www.scopus.com/inward/record.url?scp=85210584881&partnerID=8YFLogxK
U2 - 10.1158/2159-8290.CD-24-0018
DO - 10.1158/2159-8290.CD-24-0018
M3 - Article
C2 - 39270324
AN - SCOPUS:85210584881
SN - 2159-8274
VL - 14
SP - 2352
EP - 2366
JO - Cancer Discovery
JF - Cancer Discovery
IS - 12
ER -