Propranolol therapy in infantile hemangioma: it is not just about the beta

JC Lee, O Modiri, RW England… - Plastic and …, 2021 - journals.lww.com
JC Lee, O Modiri, RW England, CJ Shawber, JK Wu
Plastic and Reconstructive Surgery, 2021journals.lww.com
Background: Propranolol, a nonselective β-adrenergic receptor antagonist, is approved by
the US Food and Drug Administration to treat problematic infantile hemangiomas, but a
subset of patients experience treatment complications. Parents wary of long-term use and
side effects consult plastic surgeons on surgical options or as a second opinion.
Understanding the mechanism (s) of action of propranolol will allow plastic surgeons to
better inform parents. Methods: A systemic literature search was performed to query …
Abstract
Background:
Propranolol, a nonselective β-adrenergic receptor antagonist, is approved by the US Food and Drug Administration to treat problematic infantile hemangiomas, but a subset of patients experience treatment complications. Parents wary of long-term use and side effects consult plastic surgeons on surgical options or as a second opinion. Understanding the mechanism (s) of action of propranolol will allow plastic surgeons to better inform parents.
Methods:
A systemic literature search was performed to query published translational and basic science studies on propranolol effects on infantile hemangiomas and cells derived from these lesions.
Results:
In experimental studies, propranolol was antiproliferative and cytotoxic against hemangioma endothelial and stem cells and affected infantile hemangioma perivascular cell contractility. Propranolol inhibited migration, network formation, vascular endothelial growth factor A production, and vascular endothelial growth factor receptor 2 activation and down-regulated PI3K/AKT and mitogen-activated protein kinase signaling in hemangioma endothelial cells, but it increased ERK1/2 activity in hemangioma stem cells. At effective clinical doses, measured propranolol plasma concentration is 100 times higher than necessary for complete β-adrenergic receptor blockade, yet was 10 to 100 times less than required to induce hemangioma stem cell death.
Conclusions:
Propranolol targets multiple cell types in infantile hemangiomas by means of β-adrenergic receptor–dependent and–independent mechanisms. Plasma concentration played a significant role. At clinically relevant doses, incomplete infantile hemangioma suppression may explain the rebound phenomenon and worsening ulceration, and propranolol off target effects may lead to commonly reported adverse effects, such as sleep and gastrointestinal disturbances. Propranolol limitations and complications underscore the importance of surgical treatment options in cases of rebound and severe adverse effects. Surgical intervention remains an important treatment choice when parents are hesitant to use propranolol.
Lippincott Williams & Wilkins