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NCT Number: NCT03243019

Efficacy of Rapamycin in the Treatment of Cervico-facial Lymphatic Malformations

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.

Recruiting

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Key information

Age range

Up to 18 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Hôpital Jeanne de Flandres, CHU, Lille, France

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Rapamycin

Drug

oral administration

MRI

Device

cervicofacial MRI

Rapamycin dosage

Biological

Biological dosage of Rapamycin level

Primary outcomes

  1. Response rate to rapamycin

    Time frame: At 3 months

    Volumetric assessment by MRI. A response is considered as positive if volume decrease is superior to 1/5th of the initial volume.

Secondary outcomes

  1. Kinetic of rapamycin response

    Time frame: At 3, 6 and 12 months

    MRI assessment of the volume

  2. Efficacy of rapamycin on clinical symptoms

    Time frame: At 3, 6 and 12 months

    Clinical and fiberscopy evaluation by scoring

  3. Pediatric Quality of Life Inventory (PedsQL 4) Scales

    Time frame: Baseline, at 3, 6 and 12 months

    Assesses health-related quality of life among children with chronic and acute diseases

  4. Biological response to rapamycin

    Time frame: Baseline and at 6 months

    biological effect of mTOR blockage by measuring pAKT, p70S6 kinase, pMEK, and VEGF C, VEGFR3

  5. Rapamycin side effects

    Time frame: Monthly during 1 years

    Side effect assessment using the NCI-CTC 3.0 scale

Study contacts

Contact information is provided by the study sponsor or research team.

Pierre Fayoux, MD

CONTACT

[email protected]

3 20 44 50 67 ext. +33

Sponsors and collaborators

Lead sponsor

University Hospital, Lille

Other

Collaborators

  • Ministry of Health, France

Registry information

Official study title

Evaluation of the Efficacy of Rapamycin in the Treatment of Cervico-facial Lymphatic Malformations of Poor Prognosis

Acronym: RAPAMALYMPH

Important dates

Study start
2018
Primary completion
2027
Study completion
2027
First posted
Aug 8, 2017
Registry last updated
May 22, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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