4.5 Article

Efficacy and safety of propranolol cream in infantile hemangioma: A prospective pilot study

Journal

JOURNAL OF PHARMACOLOGICAL SCIENCES
Volume 149, Issue 2, Pages 60-65

Publisher

JAPANESE PHARMACOLOGICAL SOC
DOI: 10.1016/j.jphs.2022.03.004

Keywords

Propranolol; Cream; Infantile hemangioma; Pilot study; Infants

Funding

  1. Japan Research Foundation for Clinical Pharmacology
  2. Japan Foundation for Pediatric Research

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This study evaluated the efficacy and safety of topical propranolol in infants with infantile hemangioma. The results showed that topical propranolol may be an effective and safe treatment option, particularly for small and superficial hemangiomas in cosmetically problematic areas.
Infantile hemangioma (IH) is a common tumor in infants that gradually resolves and is often untreated. However, for cosmetic reasons, parents often opt for treatment. Oral propranolol, the first-line therapy for IH, is sometimes associated with several side effects, including hypotension, bradycardia, and hypoglycemia. No clinical studies on topical propranolol have been conducted using standardized procedures. We evaluated the efficacy and safety of topical propranolol in patients with IH. This multicenter, prospective pilot study was conducted from June 2019 to October 2020 and involved eight Japanese infants aged 35-150 days with proliferating IH. Patients were treated with 5% propranolol cream twice daily. We examined the efficacy rate based on central evaluation (complete or near-complete healing of the target hemangioma) at weeks 24 and 12, respectively, compared to baseline values. The efficacy rate at week 24 was 68.8% (95% confidence interval: 44.1-85.9%). The surface area, maximum diameter, and color intensity of the target IH decreased over time. Adverse event and drug-related adverse event rates were 87.5% and 0%, respectively. Propranolol cream may be effective and safe in Japanese patients with IH and may be considered a first-choice treatment for small and superficial IHs in cosmetically problematic areas. ?? 2022 The Authors. Production and hosting by Elsevier B.V. on behalf of Japanese Pharmacological Society. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/ licenses/by-nc-nd/4.0/).

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