A Narrative Review of the State of the Art of CCR4-Based Therapies in Cutaneous T-Cell Lymphomas: Focus on Mogamulizumab and Future Treatments.

CCR4 CTCL chemokine cutaneous inflammatory lymphoma mediators oncology protein skin

Journal

Antibodies (Basel, Switzerland)
ISSN: 2073-4468
Titre abrégé: Antibodies (Basel)
Pays: Switzerland
ID NLM: 101587489

Informations de publication

Date de publication:
22 Apr 2024
Historique:
received: 05 02 2024
revised: 03 04 2024
accepted: 16 04 2024
medline: 28 5 2024
pubmed: 28 5 2024
entrez: 28 5 2024
Statut: epublish

Résumé

The CCR4 receptor is a pivotal target in cutaneous T-cell lymphoma (CTCL) therapy due to its role in impairing immune responses against malignant T-cells and expression profiles. Monoclonal antibodies like mogamulizumab effectively bind to CCR4, reducing tumour burden and enhancing patient outcomes by inhibiting the receptor's interaction with ligands, thereby hindering malignant T-cell migration and survival. Combining CCR4 antibodies with chemotherapy, radiation, and other drugs is being explored for synergistic effects. Additionally, small-molecular inhibitors, old pharmacological agents interacting with CCR4, and CAR-T therapies are under investigation. Challenges include drug resistance, off-target effects, and patient selection, addressed through ongoing trials refining protocols and identifying biomarkers. Despite advancements, real-life data for most of the emerging treatments are needed to temper expectations. In conclusion, CCR4-targeted therapies show promise for CTCL management, but challenges persist. Continued research aims to optimise treatments, enhance outcomes, and transform CTCL management. This review aims to elucidate the biological rationale and the several agents under various stages of development and clinical evaluation with the actual known data.

Identifiants

pubmed: 38804300
pii: antib13020032
doi: 10.3390/antib13020032
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Auteurs

Corrado Zengarini (C)

Department of Medical and Surgical Sciences (DIMEC), University of Bologna, 40138 Bologna, Italy.
Dermatology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40138 Bologna, Italy.

Alba Guglielmo (A)

Dermatology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40138 Bologna, Italy.
Institute of Dermatology, Azienda Sanitaria Universitaria Friuli Centrale (ASUFC), 33100 Udine, Italy.

Martina Mussi (M)

Department of Medical and Surgical Sciences (DIMEC), University of Bologna, 40138 Bologna, Italy.
Dermatology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40138 Bologna, Italy.

Giovanna Motta (G)

Department of Medical and Surgical Sciences (DIMEC), University of Bologna, 40138 Bologna, Italy.
Division of Haematopathology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40138 Bologna, Italy.

Claudio Agostinelli (C)

Department of Medical and Surgical Sciences (DIMEC), University of Bologna, 40138 Bologna, Italy.
Division of Haematopathology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40138 Bologna, Italy.

Elena Sabattini (E)

Department of Medical and Surgical Sciences (DIMEC), University of Bologna, 40138 Bologna, Italy.
Division of Haematopathology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40138 Bologna, Italy.

Bianca Maria Piraccini (BM)

Department of Medical and Surgical Sciences (DIMEC), University of Bologna, 40138 Bologna, Italy.
Dermatology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40138 Bologna, Italy.

Alessandro Pileri (A)

Department of Medical and Surgical Sciences (DIMEC), University of Bologna, 40138 Bologna, Italy.
Dermatology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40138 Bologna, Italy.

Classifications MeSH