PRL-SRL-IHHE: Sirolimus in the Treatment for Infantile Hepatic Hemangioendothelioma(IEEH)

Sponsor
Shanghai Children's Medical Center (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT04406870
Collaborator
(none)
36
1
1
60
0.6

Study Details

Study Description

Brief Summary

Infantile hepatic hemangioendothelioma (IHHE) is an infantile hemangioma involving the liver.Since 2008, propranolol has been used for the treatment of hemangioma, and some researchers have also started to report the use of propranolol for the treatment of infantile hepatic hemangioma in children. Sirolimus can be used in patients with vascular malformations such as hemangiomas. IHHE is also an infantile hemangioma involving the liver,thus sirolimus may paly the role in treatment of IHHE.The clinical trial explores the efficacy of sequential treatment of sirolimus to refractory IHHE patients resistant with propranolol, to improve the therapeutic effect, reduce the side effects of traditional treatment methods (hormones, interferon), and reduce the number of operations and interventions and to provide a clinical basis for the application of the new therapeutics model of IHHE of "propranolol + sequential sirolimus treatment".

Condition or Disease Intervention/Treatment Phase
Phase 4

Detailed Description

According to the World Health Organization(WHO) classification of digestive system tumors in the fourth edition in 2010, infantile hepatic hemangioendothelioma (IHHE) is an infantile hemangioma involving the liver. It is a benign tumor, which can be subgrouped into focal, multifocal, and diffusing in children, as well as combining vascular malformations of the skin, brain, digestive tract and other organs.Since 2008, propranolol has been used for the treatment of hemangioma, and some researchers have also started to report the use of propranolol for the treatment of infantile hepatic hemangioma in children.And more and more clinicians unanimously recommend propranolol as first-line medication for the treatment of IHHE.However, there are few solutions to propranolol-resistant IHHE. Sirolimus is a serine/threonine kinase which plays a pivotal role in cell mortality, angiogenesis and cell growth. Sirolimus can be used in patients with vascular malformations such as hemangiomas. Children with vascular malformations received 0.1mg/kg of sirolimus orally every day and maintained the blood concentration at 8-15ng/ml. The lesions gradually disappear with time going on. Therefore, sirolimus can be used as a second-line medicine for refractory hemangioma and vascular malformation.Interestingly, the investigator's previous study which is retrospective analysis of 30 patients has indicated the effective rate of propranolol alone in treating infantile hepatic endothelial tumor (IHHE) was 57.7%, while that of sequential treatment combined with sirolimus was 84.6%.So, this clinical trial is going to explore the efficacy of sequential treatment of sirolimus to refractory IHHE patients resistant with propranolol,to improve the therapeutic effect,furtherly, reduce the side effects of traditional treatment methods (hormones, interferon), as well as the number of operations and interventions and to provide a clinical guide for the novel therapeutics model of propranolol combined with sirolimus for sequential treatment of infantile hepatic hemangioendothelioma.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
36 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Intervention Model Description:
Recruiting patients with IHHE who have no response to propranolol after 3 months. Then propranolol combined with sirolimus will be given.Recruiting patients with IHHE who have no response to propranolol after 3 months. Then propranolol combined with sirolimus will be given.
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Sirolimus in the Treatment for Propranolol-resistant Infantile Hepatic Hemangioendothelioma
Anticipated Study Start Date :
Jul 1, 2020
Anticipated Primary Completion Date :
Jun 30, 2024
Anticipated Study Completion Date :
Jun 30, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention

patients with propranolol-resistant IHHE are given propranolol combined with sirolimus

Drug: Sirolimus Oral Product
Patients with IHHE wil be treated with propranolol (1 mg / kg , twice a day, after meals), and then evaluation will be performed after 3 months (changes of the tumor size measured by ultrasound examination, and changes of tumor volume measured by abdominal enhancement CT).It will be admitted into the group once the tumor volume shrinks <30%.Then propanolol combined with sirolimus will be given. Propranolol will be given at 1mg/kg,twice a day and sirolimus will be given at 0.8mg/m²(body surface area), twice a day. Recording and doing assessment of tumor size, adverse effects as well as complicated symptoms.
Other Names:
  • TORISEL
  • rapamycin
  • Drug: propranolol
    Patients with IHHE wil be treated with propranolol (1 mg / kg , twice a day, after meals), and then evaluation will be performed after 3 months (changes of the tumor size measured by ultrasound examination, and changes of tumor volume measured by abdominal enhancement CT).It will be admitted into the group once the tumor volume shrinks <30%.Then propanolol combined with sirolimus will be given. Propranolol will be given at 1mg/kg,twice a day and sirolimus will be given at 0.8mg/m²(body surface area), twice a day. Recording and doing assessment of tumor size, adverse effects as well as complicated symptoms.
    Other Names:
  • xin de an (chinese name means making me comfortable)
  • Outcome Measures

    Primary Outcome Measures

    1. Change of tumor size [1 month]

      measuring the tumor size by ultrasound

    Secondary Outcome Measures

    1. Change of PIVKA-II [1 month]

      Using PIVKA-II assay kit (ARCHITECT I2000SR REFURB, Abbott, America).

    2. Change of alpha-1 fetoprotein (AFP) [1 month]

      Using the AFP assay kit (ARCHITECT AFP, Abbott, America).

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    1 Month to 36 Months
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Confirmed as IHHE

    • Age between 1 month and 36 months

    • Receiving propranolol for 3 months but the tumor size shrinks <30%

    • With written informed consent

    Exclusion Criteria:
    • Confirmed as hepatoblastoma

    • Have accepted surgical resection

    • Clinical data missing

    • Patients with Kasabach-Merritt phenomenon

    • Receiving propranolol for 3 months and the tumor size shrinks >30%

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Shanghai Children's Medical Center Shanghai Jiaotong University School of Medicine Shanghai Shanghai China 200127

    Sponsors and Collaborators

    • Shanghai Children's Medical Center

    Investigators

    • Study Chair: Song Gu, Doctor, Shanghai Children's Medical Center

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Shanghai Children's Medical Center
    ClinicalTrials.gov Identifier:
    NCT04406870
    Other Study ID Numbers:
    • PRL-SRL-IHHE
    First Posted:
    May 29, 2020
    Last Update Posted:
    May 29, 2020
    Last Verified:
    May 1, 2020
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Product Manufactured in and Exported from the U.S.:
    No
    Keywords provided by Shanghai Children's Medical Center
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of May 29, 2020