Vascular Malformations Clinical Trial
Official title:
Electrosclerotherapy as a Novel Treatment Option for Capillary Malformations: A Pilot Study
Capillary malformations (port-wine stains) consist of abnormally developed capillary blood
vessels in the skin. To date, laser therapy is the only widely accepted treatment modality
for capillary malformations, but this therapy has a suboptimal effect in approximately
50-60% of patients.
Intralesional bleomycin injections (sclerotherapy) are a common effective treatment option
for vascular malformations with blood vessels with larger diameters. However, bleomycin
cannot be injected adequately in the small sized vessels of capillary malformations. The use
of an electric field over the tissue (electroporation) may solve this problem: it increases
cell membrane permeability and therefore promotes localized delivery of drugs, within
(endothelial) cells.
Electroporation in combination with bleomycin sclerotherapy ('electrosclerotherapy') may
therefore offer new therapeutic options for capillary malformations. This proof of principle
study aims to explore the effectiveness, safety and feasibility of this potential treatment
option in a within-patient-controlled pilot study.
Capillary malformations are congenital abnormalities of the capillaries in the skin. These
abnormally developed blood vessels cause a red color of the skin (also known as 'port-wine
stain'),often in combination with a cobble-stone like aspect of the skin. Currently, the
only widely accepted treatment option is laser therapy, in which the abnormal blood vessels
are targeted with photocoagulation. However, in approximately 50-60% of patients, treatment
outcome of laser therapy is suboptimal. Furthermore, re-darkening of the capillary
malformation often occurs after laser therapy. Hence, there is a need for an alternative
treatment option - especially for treatment-resistant and recurrent capillary malformations.
Intralesional bleomycin injections (sclerotherapy) are a common treatment option for
vascular malformations of blood vessels and lymphatic vessels with a larger diameter (venous
and lymphatic malformations). According to the literature, this treatment is effective in
approximately 80-90% of patients. Unfortunately, the diameter of capillary blood vessels is
too small, and therefore adequate localized injections of bleomycin are not possible in
capillary malformations.
'Electroporation' is a physical phenomenon that causes an alteration of the structure of
cell membranes through the exposure of cells to a short but intense electric field; this
modification of the cell membrane increases its permeability. After electroporation,
molecules that normally do not cross the cell membrane, either by diffusion or by active
transport, can reach the intracellular environment. Therefore, electroporation is an ideal
method for localized drug delivery, in particular for localized bleomycin delivery.
The combination of electroporation and bleomycin is already used in a variety of skin
lesions, such as squamous cell carcinoma, with a surprisingly high rate of complete
remission. Especially in vascular tumors, such as Kaposi sarcoma, there is an extremely high
percentage of complete remission (90%), since the combination of bleomycin and
electroporation causes a 'vascular lock' and intravascular thrombosis of tumor
vascularization, leading to tumor regression.
This phenomenon (intravascular thrombosis and lesion regression) is exactly the intended
effect of capillary malformation treatment.
The investigators therefore hypothesize that intralesional bleomycin injections combined
with electroporation (electrosclerotherapy) can be an alternative treatment option for
capillary malformations. This proof of principle study aims to explore the feasibility of
this potential treatment option in a small patient sample.
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