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

Maged Daruish1, Francesca Ambrogio2, Anna Colagrande3

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

PubMed

Insights

Molecular biology advances have clarified kinase fusions in spitzoid neoplasms. Further research is needed to fully understand their role in melanocytic diagnostics and prognosis.

Area of Science:

  • Dermatopathology
  • Molecular Biology
  • Oncology

Background:

  • Growing interest in molecular alterations, specifically kinase fusions, in spitzoid neoplasms.
  • Increased publication volume since 2014 on classifying and understanding these molecular changes.

Purpose of the Study:

  • Synthesize current knowledge on molecular drivers in spitzoid neoplasms.
  • Review literature on kinase fusions (ALK, ROS1, NTRK, MET, RET, MAP3K8, RAF1) in spitzoid tumors.
  • Identify knowledge gaps regarding prognostic significance and etiopathogenesis.

Main Methods:

  • Comprehensive literature search of Medline and Scopus (up to December 2023).
  • Inclusion of various study types (case reports, reviews, meta-analyses) published in English over the last 15 years.
  • Keywords included spitzoid neoplasms and specific kinase fusion genes.

Main Results:

  • ALK- and ROS1-rearranged Spitz tumors are well-studied, with efforts to correlate histology and molecular drivers.
  • NTRK-, RET-, and MET-rearranged tumors are characterized, but prognostic data is incomplete.
  • Rarer rearrangements (BRAF, RAF1, MAP3K8) require more detailed case information for understanding.

Conclusions:

  • Knowledge of molecular drivers is crucial for melanocytic diagnostics.
  • Immunohistochemistry, FISH, PCR, and NGS are essential for accurate classification.
  • Large-scale studies using molecular sequencing are needed for a comprehensive understanding of fusion kinases in spitzoid tumors.

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