15P Verteporfin might potentiate the effects of anti-PD-1 therapy in melanoma-bearing mice model

escaping indels (AUC of 0.67 in GEL and 0.62 in HMF, vs 0.56 and 0.54 for TMB).Additional genomic features under investigation will be presented at the meeting.While initial responders had higher immune infiltrate, AR and DR tumours had comparable TME compositions.By deconvolving cell type contributions to gene expression, we found that bulk IFNg pathway expression was driven by tumour cells and was lower in DR while T cell IFNg was higher in DR patients.Conclusions: Distinct genomic and phenotypic features predict initial and durable responses to first line ICI in melanoma, suggesting separate biomarkers might be needed to accurately stratify groups.

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Publication Details

Journal
Immuno-Oncology Technology
Published
2024-12-01
DOI
https://doi.org/10.1016/j.iotech.2024.100898
Primary Topic
Histone Deacetylase Inhibitors Research
Type
article
Field-Weighted Citation Impact
0.00

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article

15P Verteporfin might potentiate the effects of anti-PD-1 therapy in melanoma-bearing mice model

Zoltán Hegedüs, János Tibor Fekete, András Lánczky, Balázs Győrffy et al.
Immuno-Oncology Technology
Histone Deacetylase Inhibitors Research
article

15P Verteporfin might potentiate the effects of anti-PD-1 therapy in melanoma-bearing mice model

Zoltán Hegedüs, János Tibor Fekete, András Lánczky, Balázs Győrffy, Andrea Kovács, Nabil Sayour, L Szabó, Zoltán Varga, Szonja Kovacs, Ágnes Paál, Tamás Kovács, Péter Ferdinandy
article en

Abstract

escaping indels (AUC of 0.67 in GEL and 0.62 in HMF, vs 0.56 and 0.54 for TMB).Additional genomic features under investigation will be presented at the meeting.While initial responders had higher immune infiltrate, AR and DR tumours had comparable TME compositions.By deconvolving cell type contributions to gene expression, we found that bulk IFNg pathway expression was driven by tumour cells and was lower in DR while T cell IFNg was higher in DR patients.Conclusions: Distinct genomic and phenotypic features predict initial and durable responses to first line ICI in melanoma, suggesting separate biomarkers might be needed to accurately stratify groups.

Immuno-Oncology TechnologyVol. 24
Semmelweis University (HU), HUN-REN Research Centre for Natural Sciences (HU)
Amgen, Francis Crick Institute, Gordon and Rose McAlpine Foundation for Neuroscience Research, Cancer Research UK, National Institute for Health and Care Research, Rosetrees Trust
Zero hunger
Openalex Percentile: Top 80%
Histone Deacetylase Inhibitors Research
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15P Verteporfin might potentiate the effects of anti-PD-1 therapy in melanoma-bearing mice model — Zoltán Hegedüs, János Tibor Fekete, et al. · Immuno-Oncology Technology (2024) | TGRS Research Map | TGRS