Efficacy of Rapamycin in the Treatment of Cervico-facial Lymphatic Malformations (RAPAMALYMPH)
Primary Purpose
Lymphatic Malformation, Pediatric
Status
Recruiting
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
rapamycin
MRI
Rapamycin dosage
Sponsored by
About this trial
This is an interventional treatment trial for Lymphatic Malformation focused on measuring cervico-facial, rapamycin
Eligibility Criteria
Inclusion Criteria:
- Patient from 0 to 18 years of age, presenting with poly-cystic suprahyoid or mediastinal lymphatic.
- with chronic pain or functional respiratory or swallowing impairment with a CDS score < 8
- Curative treatment is not possible or associated with a high risk of morbidity ,mortality and functional and cosmetic impairment
- Karnofsky Score (> 10 years of age) or Lansky score (≤10 years of age) > 50%
Biology
- Neutrophils count≥1.0 x 109/L
- Platelets count ≥ 100 x 109/L
- Hemoglobin ≥ 8 g/dL
- Bilirubin ≤ 1,5 ULN
- Transaminases < 2,5 ULN
- Serum albumin ≥ 2 g/dL.
- LDL cholesterol <160 mg/dL
- Triglycerides < 150 mg/dL
- Negative test of pregnancy if relevant
- Social security affiliation
- At least 2 months after a previous procedure on the malformation
Exclusion Criteria:
- Non-respect of inclusion criteria
- Other immunosuppressive therapy or long-term general corticosteroid therapy without a 28-day washout period
- renal failure
- Liver failure
- Digestive disease leading to rapamycin malabsorption
- uncontrolled or severe infectious disease
- Patients requiring treatment interfering with CYP3A4 isoenzyme (rifampicin, rifabutin, carbamazepine, phenobarbital, phenytoin) or inhibiting CYP3A4 isoenzyme's activity (ketoconazole, voriconazole, itraconazole, telithromycin, clarithromycin, Diltiazem, Verapamil, nicardipine, clotrimazole, fluconazole , troleandomycin, bromocriptine, cimetidine, danazol, protease inhibitors) -patients requiring treatment by cisapride and metoclopramide
- Concomitant administration of mTOR inhibitor
- Peanuts or soya allergy
- Impossibility to receive informed consent
- Absence of social security affiliation
- refusal to sign consent
- Ongoing pregnancy or breastfeeding
- refusal to participate
Sites / Locations
- Hôpital Jeanne de Flandres, CHURecruiting
- Hu Robert Debre Aphp - ParisRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
SIROLIMUS
Arm Description
Outcomes
Primary Outcome Measures
Response rate to rapamycin
Volumetric assessment by MRI. A response is considered as positive if volume decrease is superior to 1/5th of the initial volume.
Secondary Outcome Measures
Kinetic of rapamycin response
MRI assessment of the volume
Efficacy of rapamycin on clinical symptoms
Clinical and fiberscopy evaluation by scoring
Pediatric Quality of Life Inventory (PedsQL 4) Scales
Assesses health-related quality of life among children with chronic and acute diseases
Biological response to rapamycin
biological effect of mTOR blockage by measuring pAKT, p70S6 kinase, pMEK, and VEGF C, VEGFR3
Rapamycin side effects
Side effect assessment using the NCI-CTC 3.0 scale
Full Information
NCT ID
NCT03243019
First Posted
August 1, 2017
Last Updated
August 16, 2022
Sponsor
University Hospital, Lille
Collaborators
Ministry of Health, France
1. Study Identification
Unique Protocol Identification Number
NCT03243019
Brief Title
Efficacy of Rapamycin in the Treatment of Cervico-facial Lymphatic Malformations
Acronym
RAPAMALYMPH
Official Title
Evaluation of the Efficacy of Rapamycin in the Treatment of Cervico-facial Lymphatic Malformations of Poor Prognosis
Study Type
Interventional
2. Study Status
Record Verification Date
August 2022
Overall Recruitment Status
Recruiting
Study Start Date
June 25, 2018 (Actual)
Primary Completion Date
February 2025 (Anticipated)
Study Completion Date
February 2025 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Lille
Collaborators
Ministry of Health, France
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
To evaluate the efficacy of Rapamycin in extended cervicofacial lymphatic malformations in pediatric patients. Rapamycin is administered oral for a 6 month period.
The success rate is determined by volume reduction superior to 1/5e of the initial volume measured by MRI, impact on QOL and reduction of bleeding in case of mucosal involvement.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lymphatic Malformation, Pediatric
Keywords
cervico-facial, rapamycin
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
28 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
SIROLIMUS
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
rapamycin
Intervention Description
oral administration
Intervention Type
Device
Intervention Name(s)
MRI
Intervention Description
cervicofacial MRI
Intervention Type
Biological
Intervention Name(s)
Rapamycin dosage
Intervention Description
Biological dosage of Rapamycin level
Primary Outcome Measure Information:
Title
Response rate to rapamycin
Description
Volumetric assessment by MRI. A response is considered as positive if volume decrease is superior to 1/5th of the initial volume.
Time Frame
At 3 months
Secondary Outcome Measure Information:
Title
Kinetic of rapamycin response
Description
MRI assessment of the volume
Time Frame
At 3, 6 and 12 months
Title
Efficacy of rapamycin on clinical symptoms
Description
Clinical and fiberscopy evaluation by scoring
Time Frame
At 3, 6 and 12 months
Title
Pediatric Quality of Life Inventory (PedsQL 4) Scales
Description
Assesses health-related quality of life among children with chronic and acute diseases
Time Frame
Baseline, at 3, 6 and 12 months
Title
Biological response to rapamycin
Description
biological effect of mTOR blockage by measuring pAKT, p70S6 kinase, pMEK, and VEGF C, VEGFR3
Time Frame
Baseline and at 6 months
Title
Rapamycin side effects
Description
Side effect assessment using the NCI-CTC 3.0 scale
Time Frame
Monthly during 1 years
10. Eligibility
Sex
All
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patient from 0 to 18 years of age, presenting with poly-cystic suprahyoid or mediastinal lymphatic.
with chronic pain or functional respiratory or swallowing impairment with a CDS score < 8
Curative treatment is not possible or associated with a high risk of morbidity ,mortality and functional and cosmetic impairment
Karnofsky Score (> 10 years of age) or Lansky score (≤10 years of age) > 50%
Biology
Neutrophils count≥1.0 x 109/L
Platelets count ≥ 100 x 109/L
Hemoglobin ≥ 8 g/dL
Bilirubin ≤ 1,5 ULN
Transaminases < 2,5 ULN
Serum albumin ≥ 2 g/dL.
LDL cholesterol <160 mg/dL
Triglycerides < 150 mg/dL
Negative test of pregnancy if relevant
Social security affiliation
At least 2 months after a previous procedure on the malformation
Exclusion Criteria:
Non-respect of inclusion criteria
Other immunosuppressive therapy or long-term general corticosteroid therapy without a 28-day washout period
renal failure
Liver failure
Digestive disease leading to rapamycin malabsorption
uncontrolled or severe infectious disease
Patients requiring treatment interfering with CYP3A4 isoenzyme (rifampicin, rifabutin, carbamazepine, phenobarbital, phenytoin) or inhibiting CYP3A4 isoenzyme's activity (ketoconazole, voriconazole, itraconazole, telithromycin, clarithromycin, Diltiazem, Verapamil, nicardipine, clotrimazole, fluconazole , troleandomycin, bromocriptine, cimetidine, danazol, protease inhibitors) -patients requiring treatment by cisapride and metoclopramide
Concomitant administration of mTOR inhibitor
Peanuts or soya allergy
Impossibility to receive informed consent
Absence of social security affiliation
refusal to sign consent
Ongoing pregnancy or breastfeeding
refusal to participate
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Pierre Fayoux, MD
Phone
3 20 44 50 67
Ext
+33
Email
pierre.fayoux@chru-lille.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Pierre Fayoux, MD
Organizational Affiliation
University Hospital, Lille
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hôpital Jeanne de Flandres, CHU
City
Lille
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
pierre Fayoux, MD
Facility Name
Hu Robert Debre Aphp - Paris
City
Paris
Country
France
Individual Site Status
Recruiting
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Efficacy of Rapamycin in the Treatment of Cervico-facial Lymphatic Malformations
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