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ICOSLG Is Associated with Anti-PD-1 and Concomitant Antihistamine Treatment Response in Advanced Melanoma.

Authors :
Mallardo, Domenico
Fordellone, Mario
Ottaviano, Margaret
Marano, Giuseppina
Vitale, Maria Grazia
Mallardo, Mario
Capasso, Mariagrazia
De Cristofaro, Teresa
Capone, Mariaelena
Meinardi, Teresa
Paone, Miriam
Sabatelli, Patrizia
De Filippi, Rosaria
Cesano, Alessandra
Cavalcanti, Ernesta
Caracò, Corrado
Warren, Sarah
Budillon, Alfredo
Simeone, Ester
Ascierto, Paolo Antonio
Source :
International Journal of Molecular Sciences; Nov2024, Vol. 25 Issue 22, p12439, 12p
Publication Year :
2024

Abstract

We previously demonstrated that patients with metastatic unresectable stage IIIb–IV melanoma receiving cetirizine (a second-generation H1 antagonist antihistamine) premedication with immunotherapy had better outcomes than those not receiving cetirizine. In this retrospective study, we searched for a gene signature potentially predictive of the response to the addition of cetirizine to checkpoint inhibition (nivolumab or pembrolizumab with or without previous ipilimumab). Transcriptomic analysis showed that inducible T cell costimulator ligand (ICOSLG) expression directly correlated with the disease control rate (DCR) when detected with a loading value > 0.3. A multivariable logistic regression model showed a positive association between the DCR and ICOSLG expression for progression-free survival and overall survival. ICOSLG expression was associated with CD64, a specific marker of M1 macrophages, at baseline in the patient samples who received cetirizine concomitantly with checkpoint inhibitors, but this association was not present in subjects who had not received cetirizine. In conclusion, our results show that the clinical advantage of concomitant treatment with cetirizine during checkpoint inhibition in patients with malignant melanoma is associated with high ICOSLG expression, which could predict the response to immune checkpoint inhibitor blockade. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
16616596
Volume :
25
Issue :
22
Database :
Complementary Index
Journal :
International Journal of Molecular Sciences
Publication Type :
Academic Journal
Accession number :
181170798
Full Text :
https://doi.org/10.3390/ijms252212439