Overview
This randomized controlled trial aims to compare guided discontinuation with maintenance treatment of sirolimus in pediatric patients with KHE.
Description
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.
Eligibility
Inclusion Criteria:
- Participant diagnosed with KHE with or without KMP
- Participant age 0-12 years
- Participant with detailed medical records of the disease at the time of screening
- Participant with at least two years of remission of KHE and no previous toxicity or adverse events
- Participant with normal liver and kidney function
- Participant with signed and dated informed consent from the guardian(s)
Exclusion Criteria:
- Participant with other hematological diseases
- Participant with other solid tumor
- Participant with general disease such as hypertension, diabetes, adrenal insufficiency, neurological diseases, liver and kidney dysfunction, and cardiopulmonary insufficiency.
- Participant with infectious diseases
- Unwilling participant