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British Journal of Dermatology· 2026Q1· Review

Precision Medicine for Somatic Mutation-Driven Vascular Anomalies

Yi Ji, Jiangyuan Zhou, Yuru Lan, Yi Ji

Short summary

Somatic mutations activating PI3K/AKT/mTOR and RAS/MAPK pathways drive vascular anomalies, enabling precision medicine approaches with targeted therapies like mTOR, PI3Kα, and MEK inhibitors showing significant clinical efficacy.

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Key points

  • Somatic mutations in PI3K/AKT/mTOR and RAS/MAPK pathways are the primary drivers of vascular anomalies.
  • Genotype-phenotype correlations link specific mutations (e.g., PIK3CA, KRAS) to distinct vascular anomaly types.
  • Targeted therapies (mTOR, PI3Kα, MEK inhibitors) demonstrate significant clinical efficacy against pathway-specific anomalies.
  • Therapeutic resistance and drug dependency remain key challenges in current treatment paradigms.

AI-generated from the title and abstract; the full text is not read.

Abstract

Abstract Vascular anomalies, including proliferative vascular tumours and structural malformations, are largely driven by postzygotic somatic mutations that constitutively activate key signalling pathways, mainly the PI3K/AKT/mTOR and RAS/MAPK pathways. This molecular understanding has shifted clinical management from empiric interventions towards precision medicine. In this review, the interactions between somatic mosaicism, germline predispositions (e.g., PTEN hamartoma tumour syndrome), and microenvironmental risk factors in the context of lesional progression are described. We synthesized data on genotype‒phenotype correlations—such as PIK3CA mutations in lymphatic and venous malformations, KRAS/MAP2K1 mutations in arteriovenous malformations, and cerebral cavernous malformation (CCM) complex dysfunctions in cerebral cavernous anomalies—while fundamentally differentiating the mechanistic dependencies of true malformations from those of proliferative tumours. Targeted therapies, including mTOR, PI3Kα, and MEK inhibitors, have exhibited significant clinical efficacy in the treatment of pathway-specific anomalies. Despite these advances, therapeutic resistance and drug dependency persist. Future directions include the development of integrated diagnostic frameworks combining tissue biopsies with longitudinal cell-free DNA (cfDNA) monitoring, optimizing dual-pathway combination strategies, and advancing cellular models to reshape the management of vascular anomalies.

The authors' abstract, as published at the source. British Journal of Dermatology, 2026 · DOI ↗

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Field: Neurology (Medicine)

NeurologyMedicine