Kinase Fusions in Spitz Melanocytic Tumors: The Past, the Present, and the Future

Author:

Daruish Maged1ORCID,Ambrogio Francesca2,Colagrande Anna3,Marzullo Andrea3,Alaggio Rita4,Trilli Irma5,Ingravallo Giuseppe3ORCID,Cazzato Gerardo3ORCID

Affiliation:

1. Dorset County Hospital NHS Foundation Trust, Dorchester DT1 2JY, UK

2. Section of Dermatology and Venereology, Department of Precision and Regenerative Medicine and Ionian Area (DiMePRe-J), University of Bari “Aldo Moro”, 70124 Bari, Italy

3. Section of Molecular Pathology, Department of Precision and Regenerative Medicine and Ionian Area (DiMePRe-J), University of Bari “Aldo Moro”, 70124 Bari, Italy

4. Pathology Unit, Department of Laboratories, Bambino Gesù Children’s Hospital, IRCCS, 00165 Rome, Italy

5. Department of Interdisciplinary Medicine, University of Bari “Aldo Moro”, 70124 Bari, Italy

Abstract

In recent years, particular interest has developed in molecular biology applied to the field of dermatopathology, with a focus on nevi of the Spitz spectrum. From 2014 onwards, an increasing number of papers have been published to classify, stratify, and correctly frame molecular alterations, including kinase fusions. In this paper, we try to synthesize the knowledge gained in this area so far. In December 2023, we searched Medline and Scopus for case reports and case series, narrative and systematic reviews, meta-analyses, observational studies—either longitudinal or historical, case series, and case reports published in English in the last 15 years using the keywords spitzoid neoplasms, kinase fusions, ALK, ROS1, NTRK (1-2-3), MET, RET, MAP3K8, and RAF1. ALK-rearranged Spitz tumors and ROS-1-rearranged tumors are among the most studied and characterized entities in the literature, in an attempt (although not always successful) to correlate histopathological features with the probable molecular driver alteration. NTRK-, RET-, and MET-rearranged Spitz tumors present another studied and characterized entity, with several rearrangements described but as of yet incomplete information about their prognostic significance. Furthermore, although rarer, rearrangements of serine–threonine kinases such as BRAF, RAF1, and MAP3K8 have also been described, but more cases with more detailed information about possible histopathological alterations, mechanisms of etiopathogenesis, and also prognosis are needed. The knowledge of molecular drivers is of great interest in the field of melanocytic diagnostics, and it is important to consider that in addition to immunohistochemistry, molecular techniques such as FISH, PCR, and/or NGS are essential to confirm and classify the different patterns of mutation. Future studies with large case series and molecular sequencing techniques are needed to allow for a more complete and comprehensive understanding of the role of fusion kinases in the spitzoid tumor family.

Publisher

MDPI AG

Reference78 articles.

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2. Spitz melanocytic tumours—A review;Yeh;Histopathology,2022

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4. WHO Classification of Tumours Editorial Board (2023). Skin Tumours, International Agency for Research on Cancer. [5th ed.]. Available online: https://tumourclassification.iarc.who.int/chapters/64.

5. A review of kinase fusions in melanocytic tumors;Shalin;Lab. Investig.,2017

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