Mapping MAGE-A4 expression in solid cancers for targeted therapies

Melanoma-associated antigen A4 (MAGE-A4) is a promising target for anticancer therapy. However, limited contemporary data are available on the details of MAGE-A4 protein expression in different cancer types. In this study, the protein expression of MAGE-A4 is comprehensively studied in patients with unresectable and/or metastatic solid cancers to identify indications of the highest unmet medical need for anti-MAGE-A4 therapy. FFPE tumor sections from 200 patients, predominantly HLA-A*02:01 positive (<i>n</i> = 193), were examined using immunohistochemistry (IHC) to detect MAGE-A4 expression. The patient cohort comprised various cancer types to pinpoint differences in the prevalence and intensity of MAGE-A4 positivity. MAGE-A4 expression was observed in 35% (69 patients) of the overall cohort. Certain cancer types exhibited notably higher frequencies of MAGE-A4 positivity. Specifically, adenoid cystic carcinoma demonstrated the highest prevalence at 82%, followed by liposarcoma at 67%. Ovarian serous/high-grade carcinoma showed a 64% positivity rate, identical to that observed in squamous non-small cell lung cancer (NSCLC). Head and neck squamous cell carcinoma (HNSCC) presented a 60% prevalence, while esophageal cancer had a 54% prevalence of MAGE-A4 expression. These data highlight the variability of MAGE-A4 expression across different cancer types and underscore its relevance as a potential target of novel precision medicines. The significant presence of MAGE-A4 in specific cancers suggests potential for stratified therapeutic approaches and warrants further investigation into its role in oncogenesis and treatment response.

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Publication Details

Journal
Frontiers in Oncology
Published
2025-03-13
DOI
https://doi.org/10.3389/fonc.2025.1484182
Primary Topic
Immunotherapy and Immune Responses
Type
article
Field-Weighted Citation Impact
0.00

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article

Mapping MAGE-A4 expression in solid cancers for targeted therapies

Oliver Edgar Bechter, Ivan Dimitrov, Leena Gandhi, Christian Heichinger et al.
Frontiers in Oncology
Immunotherapy and Immune Responses
article

Mapping MAGE-A4 expression in solid cancers for targeted therapies

Oliver Edgar Bechter, Ivan Dimitrov, Leena Gandhi, Christian Heichinger, Nino Keshelava, Florian Heil, Emiliano Calvo, Andreas Roller, Elena Garralda, Iben Spanggaard, Juanita Suzanne Lopez, Rachel Galot, Jayesh Desai, Sylvie Rottey, Natascha Rieder, Iris Martinez Quetglas, Christin Habigt
article en

Abstract

Melanoma-associated antigen A4 (MAGE-A4) is a promising target for anticancer therapy. However, limited contemporary data are available on the details of MAGE-A4 protein expression in different cancer types. In this study, the protein expression of MAGE-A4 is comprehensively studied in patients with unresectable and/or metastatic solid cancers to identify indications of the highest unmet medical need for anti-MAGE-A4 therapy. FFPE tumor sections from 200 patients, predominantly HLA-A*02:01 positive (<i>n</i> = 193), were examined using immunohistochemistry (IHC) to detect MAGE-A4 expression. The patient cohort comprised various cancer types to pinpoint differences in the prevalence and intensity of MAGE-A4 positivity. MAGE-A4 expression was observed in 35% (69 patients) of the overall cohort. Certain cancer types exhibited notably higher frequencies of MAGE-A4 positivity. Specifically, adenoid cystic carcinoma demonstrated the highest prevalence at 82%, followed by liposarcoma at 67%. Ovarian serous/high-grade carcinoma showed a 64% positivity rate, identical to that observed in squamous non-small cell lung cancer (NSCLC). Head and neck squamous cell carcinoma (HNSCC) presented a 60% prevalence, while esophageal cancer had a 54% prevalence of MAGE-A4 expression. These data highlight the variability of MAGE-A4 expression across different cancer types and underscore its relevance as a potential target of novel precision medicines. The significant presence of MAGE-A4 in specific cancers suggests potential for stratified therapeutic approaches and warrants further investigation into its role in oncogenesis and treatment response.

Frontiers in OncologyVol. 15
Roche (Switzerland) (CH), Cliniques Universitaires Saint-Luc (BE), Institute of Cancer Research (GB), Peter MacCallum Cancer Centre (AU), Ghent University Hospital (BE), Copenhagen University Hospital (DK), Rigshospitalet (DK), Roche Pharma AG (Germany) (DE), Dana-Farber Cancer Institute (US), Royal Marsden Hospital (GB), Vall d'Hebron Hospital Universitari (ES), UCLouvain (BE), KU Leuven (BE)
F. Hoffmann-La Roche
Good health and well-being
Openalex Percentile: Top 95%
Immunotherapy and Immune Responses
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