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Updated: Jan 15, 2026

A Patient-Derived Xenograft Model for Venous Malformation
Published on: June 15, 2020
Treating venous malformations with nanomedicines
Weimin Tang1,2, Daniel S Kohane1,3, Kathleen Cullion1,2
1Laboratory for Biomaterials and Drug Delivery, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
Abstract:
Venous malformations (VMs) are congenital vascular anomalies that cause pain, bleeding, and functional impairment, yet current first-line therapies such as sclerotherapy and surgical resection are limited by complications and high recurrence rates. Nanomedicine provides a promising alternative by exploiting the enhanced permeation and retention (EPR)-like effect to achieve selective accumulation of nanoparticles (NPs) within VMs. Preclinical studies support the use of NPs not only for improved drug delivery but also for non-pharmacologic based treatment, such as photothermal therapy. Furthermore, active targeting strategies involving surface-functionalized NPs offer the potential for enhanced specificity and treatment efficacy. Despite these advances, clinical translation faces challenges such as heterogeneity in EPR efficiency, depth-limited delivery, and pediatric safety concerns. Continued efforts to create more effective, pediatric-specific drug delivery systems are essential for developing safer, more efficient, and minimally invasive nanomedicine therapy for patients with VMs.
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