Hand-foot Syndrome Clinical Trial
Official title:
Half‐Side Controlled Analysis of the Effect of Topical Brimonidine Tartrate on the Frequency and Severity of Hand‐Foot Syndrome (HFS) in Cancer Patients Receiving Antineoplastic Agents (BRIMOCAN)
Comparative analysis of the severity of Hand-Foot-Syndrome (HFS) of palms treated with brimonidine tartrate gel or with standard care Urea 10% containing lotion in cancer patients receiving antineoplastic therapy to show a preventive effect of cutaneous brimonidine treatment on severity of HFS symptoms.
Hand-foot syndrome (HFS) is an adverse event frequently associated with the use of classical
chemotherapeutic agents such as capecitabine or pegylated liposomal doxorubicin, as well as
targeted cancer drugs such as sorafenib or other tyrosine-kinase inhibitors. If the toxicity
progresses edematous swelling, blistering and desquamation can lead to ulcerations of the
palms and soles. Additionally, patients may be affected by nail-toxicities, such as
discoloration, ridging, pitting up to complete onycholysis and pain. Today, cooling of hands
and feet during infusion chemotherapy as well as preventive treatment with topical
formulations containing urea 10% (e.g. Excipial U10 Lipolotion®) is considered as standard of
care. Yet, these strategies are limited by intricateness, patient inconvenience and low
efficacy. Hence, at this point the satisfactory treatment of HFS remains an unmet medical
need, as until now, no effective therapy is available to prevent or reduce HFS symptoms
during the cycle of chemotherapeutic treatment.
Recently, brimonidine 3 mg/g gel (Mirvaso®) has been approved as a topical treatment of
facial erythema of rosacea in adult patients. Brimonidine is an effective agonist of
α2-adrenoreceptors thereby, in analogy to skin cooling, leading to peripheral
vasoconstriction.
Against this background, the following hypothesis was developed:
The topical application brimonidine 3 mg/g gel (Mirvaso®) may prevent or reduce the severity
of HFS in cancer patients that receive respective antineoplastic agents.
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