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Guided Discontinuation Versus Maintenance Treatment of Sirolimus in Pediatric Patients With Kaposiform Hemangioendothelioma: a Randomized Controlled Trial
This randomized controlled trial aims to compare guided discontinuation with maintenance treatment of sirolimus in pediatric patients with KHE.
Kaposiform Hemangioendothelioma (KHE) is a rare vascular tumor that occurs in infants and children. KHE is characterized by sheets of spindle cells with an infiltrative pattern in the dermis, subcutaneous fat, and muscle. It is locally aggressive and can cause Kasabach-Merritt phenomenon, a serious life-threatening coagulopathy characterized by profound thrombocytopenia and hypofibrinogenemia. Sirolimus, one of the mTOR inhibitors, has become a new and very effective treatment, which is especially reliable for KHE with KMP and has acceptable side effects. However, there is yet no strong evidence on the best practice of treatment length of sirolimus. This randomized controlled trial aims to compare guided discontinuation with maintenance treatment in pediatric patients with KHE in order to provide a basis for the optimal treatment duration of sirolimus, as well as the clinical characteristics of pediatric patients who can safely reduce the dose till withdrawal.
Age
0 - 12 years
Sex
ALL
Healthy Volunteers
No
Children's Hospital of Fudan University
Shanghai, Shanghai Municipality, China
Start Date
July 1, 2020
Primary Completion Date
February 1, 2023
Completion Date
July 1, 2023
Last Updated
September 26, 2023
30
ACTUAL participants
Sirolimus
DRUG
Lead Sponsor
Children's Hospital of Fudan University
NCT04056962
NCT04077515
Data Source & Attribution
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View ClinicalTrials.gov Terms and ConditionsNCT04409691