Detailseite
Projekt Druckansicht

HCC Immunologie: Die Korrelation der Immunprofile mit dem Therapieerfolg

Antragsteller Dr. Philipp Haber
Fachliche Zuordnung Allgemein- und Viszeralchirurgie
Gastroenterologie
Förderung Förderung von 2018 bis 2021
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 415099712
 
Erstellungsjahr 2021

Zusammenfassung der Projektergebnisse

The initial research plan focused on exploring the immune landscape of HCC and its implications for treatment with immune checkpoint inhibitors in HCC. We established a wellannotated clinical cohort of 240 patients with RNA-, Whole-exome- and TCR sequencing data as well as comprehensive immunophenotyping via single- and multiplex immunostaining. Integrative analysis refined our understanding of the immune-based molecular classes. We defined five distinct subclasses, three of those representing immunogenic tumors and accounting for ~35% of the population and two representing non-inflamed tumors that harbor distinct mechanisms of immune evasion. When we applied these findings to a cohort of patients treated with anti-PD1 we found inflamed tumors to be more likely to exhibit response to therapy. Overall responding patients were characterized by active inflammatory signaling as captured by an increase in IFNy signaling and an intact antigen-presentation machinery with strong expression of MHC class II molecules. We developed a gene expression signature capable of reliably identifying responding patients and validated it in four publically available datasets. Of note, none of the previously reported signatures of response that derive from other cancer types were able to consistently distinguish between responders and nonresponders. Intriguingly, we observed that treatment with tyrosine-kinase inhibitors, until recently standard of care in frontline treatment of advanced HCC, appeared to modulate response patterns to subsequent immunotherapy. These findings have implications for clinical practice: as the treatment landscape of HCC evolves, biomarker discovery is likely to hinge on the acquisition of fresh biological samples prior to the initiation of a given systemic treatment. Our findings support the implementation of serial biopsies in clinical practice for patients with advanced HCC.

Projektbezogene Publikationen (Auswahl)

 
 

Zusatzinformationen

Textvergrößerung und Kontrastanpassung