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.
Authors
- Oliver Edgar Bechter (ORCID: https://orcid.org/0000-0003-0667-3284)
- Ivan Dimitrov (ORCID: https://orcid.org/0000-0003-2686-6884)
- Leena Gandhi (ORCID: https://orcid.org/0000-0002-2398-9179)
- Christian Heichinger
- Nino Keshelava (ORCID: https://orcid.org/0009-0001-0978-3393)
- Florian Heil (ORCID: https://orcid.org/0000-0002-2056-0270)
- Emiliano Calvo (ORCID: https://orcid.org/0000-0003-4921-829X)
- Andreas Roller (ORCID: https://orcid.org/0000-0001-6335-0962)
- Elena Garralda (ORCID: https://orcid.org/0000-0002-4412-7842)
- Iben Spanggaard (ORCID: https://orcid.org/0000-0001-5925-2630)
- Juanita Suzanne Lopez (ORCID: https://orcid.org/0000-0001-8321-4212)
- Rachel Galot (ORCID: https://orcid.org/0000-0002-0596-4752)
- Jayesh Desai (ORCID: https://orcid.org/0000-0003-4246-9344)
- Sylvie Rottey
- Natascha Rieder (ORCID: https://orcid.org/0000-0002-2921-2280)
- Iris Martinez Quetglas (ORCID: https://orcid.org/0009-0009-9558-1517)
- Christin Habigt (ORCID: https://orcid.org/0009-0008-5806-7650)
Institutions
- 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)
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
Funders
- F. Hoffmann-La Roche