Current Trends in Mucosal Melanomas: An Overview

Author:

Santeufemia Davide Adriano1ORCID,Palmieri Giuseppe2ORCID,Miolo Gianmaria3ORCID,Colombino Maria4,Doro Maria Grazia4ORCID,Frogheri Laura4,Paliogiannis Panagiotis5ORCID,Capobianco Giampiero6ORCID,Madonia Massimo7,Cossu Antonio5ORCID,Lo Re Giovanni8,Corona Giuseppe9ORCID

Affiliation:

1. Oncology Unit, Alghero General Hospital, 07041 Alghero, Italy

2. Immuno-Oncology & Targeted Cancer Biotherapies, Unit of Cancer Genetics, University of SassariIRGB-CNR, 07100 Sassari, Italy

3. Preventive Medical Oncology, CRO Aviano, National Cancer Institute, IRCCS, 33081 Aviano, Italy

4. Institute of Genetic and Biomedical Research (IRGB), National Research Council (CNR), 07100 Sassari, Italy

5. Department of Medical, Surgical and Experimental Sciences, University of Sassari, 07100 Sassari, Italy

6. Department of Clinical and Experimental Medicine, Gynecologic and Obstetric Clinic, University of Sassari, 07100 Sassari, Italy

7. Department of Clinical and Experimental Medicine, Urologic Clinic, University of Sassari, 07100 Sassari, Italy

8. Immuno-Related Tumor Medical Oncology, CRO Aviano, National Cancer Institute, IRCCS, 33081 Aviano, Italy

9. Immunopathology and Cancer Biomarkers, CRO Aviano, National Cancer Institute, IRCCS, 33081 Aviano, Italy

Abstract

Primary mucosal melanomas (MMs) are uncommon tumors originating from melanocytes located in the mucous membranes at various anatomic sites within the body. MM significantly differs from cutaneous melanoma (CM) regarding epidemiology, genetic profile, clinical presentation, and response to therapies. Despite these differences, that have important implications for both disease diagnosis and prognosis, MMs are usually treated in the same way as CM but exhibit a lower response rate to immunotherapy leading to a poorer survival rate. Furthermore, a high inter-patient variability can be observed in relation to therapeutic response. Recently, novel “omics” techniques have evidenced that MM lesions have different genomic, molecular, and metabolic landscapes as compared with CM lesions, thus explaining the heterogeneity of the response. Such specific molecular aspects might be useful to identify new biomarkers aimed at improving the diagnosis and selection of MM patients who could benefit from immunotherapy or targeted therapy. In this review, we have focused on relevant molecular and clinical advancements for the different MM subtypes in order to describe the updated knowledge relating to main diagnostic, clinical, and therapeutic implications as well as to provide hints on likely future directions.

Funder

Italian Ministry of Health—Ricerca Corrente

Publisher

MDPI AG

Subject

Cancer Research,Oncology

Reference122 articles.

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