38P Biomarkers predictive of response to immune checkpoint inhibitor therapy in patients with metastatic melanoma

Results: The patients included: melanoma (n14), NSCLC (n10), endometrial cancer (n4), breast cancer (n3), GI cancer (n 1), head/neck cancer (n1), RCC (n1) and urothelial cancer (n1), treated with ICI alone (n21) or with chemotherapy (n14).At 12 months of follow-up, 47.1% had experienced an irAE with 80.8% grade 1-2 and 19.2% grade 3-4.Neutrophil counts (P0.02) and the neutrophil/lymphocyte ratio (P0.05) were higher at baseline in patients experiencing an irAE.Furthermore increases in the percent of total CD4+ (P0.03),Th1 (P0.04), and Tfh1 (P0.01)cells, coupled with decreases in Th17 (P0.003) and Tfh17 (P0.03) cells in the blood at 8-11 weeks on treatment were significantly associated with an irAE.Conclusions: These results suggest that changes in the relative balance of neutrophils and specific CD4+ T cell subpopulations were linked with an irAE.Our ongoing studies will further investigate changes in cytokine and gene expression profiles to deepen our understanding of these associations.This study marks a first step toward identifying biomarkers that anticipate the onset of an irAE and consequently reduce the need for immunosuppressive treatment that could compromise the efficacy of ICIs.Clinical trial identification: NCT05429866.

Authors

Institutions

Publication Details

Journal
Immuno-Oncology Technology
Published
2024-12-01
DOI
https://doi.org/10.1016/j.iotech.2024.100920
Primary Topic
Cancer Immunotherapy and Biomarkers
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

38P Biomarkers predictive of response to immune checkpoint inhibitor therapy in patients with metastatic melanoma

Claudia Burz, Bob Engle
Immuno-Oncology Technology
Cancer Immunotherapy and Biomarkers
article

38P Biomarkers predictive of response to immune checkpoint inhibitor therapy in patients with metastatic melanoma

Claudia Burz, Bob Engle
article en

Abstract

Results: The patients included: melanoma (n14), NSCLC (n10), endometrial cancer (n4), breast cancer (n3), GI cancer (n 1), head/neck cancer (n1), RCC (n1) and urothelial cancer (n1), treated with ICI alone (n21) or with chemotherapy (n14).At 12 months of follow-up, 47.1% had experienced an irAE with 80.8% grade 1-2 and 19.2% grade 3-4.Neutrophil counts (P0.02) and the neutrophil/lymphocyte ratio (P0.05) were higher at baseline in patients experiencing an irAE.Furthermore increases in the percent of total CD4+ (P0.03),Th1 (P0.04), and Tfh1 (P0.01)cells, coupled with decreases in Th17 (P0.003) and Tfh17 (P0.03) cells in the blood at 8-11 weeks on treatment were significantly associated with an irAE.Conclusions: These results suggest that changes in the relative balance of neutrophils and specific CD4+ T cell subpopulations were linked with an irAE.Our ongoing studies will further investigate changes in cytokine and gene expression profiles to deepen our understanding of these associations.This study marks a first step toward identifying biomarkers that anticipate the onset of an irAE and consequently reduce the need for immunosuppressive treatment that could compromise the efficacy of ICIs.Clinical trial identification: NCT05429866.

Immuno-Oncology TechnologyVol. 24
Iuliu Hațieganu University of Medicine and Pharmacy (RO), Institute of Oncology Prof. Dr. Ion Chiricuta (RO)
Good health and well-being
Openalex Percentile: Top 60%
Cancer Immunotherapy and Biomarkers
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.