Sirolimus Effect on Hypertrophic Syndromes Related Gene PIK3CA

Centre Hospitalier Universitaire Dijon16 enrolled

Overview

It was found that people who have an excessive growth in one or more parts of their body and normal growth in other parts, may have a change in genes responsible for controlling cell growth. This genetic discovery identified a possible treatment for this overgrowth, called Sirolimus. This is a pilot study, which help the investigators prepare a larger international study, which will aim to determine whether a treatment based Sirolimus is able to stop the excessive growth of one or more parties of their body in people who carry a genetic change in the PIK3CA gene (phosphatidylinosilol-3-kinase encoded by the gene PIK3CA).

The duration of participation is 15 months: * Visit screening: blood test, pre-clinical evaluation, urine collection and chest X-ray. * First 6 months: participants will have their overgrowth monitored. This step includes 2 visits taking place at the University Hospital of Dijon: complete clinical evaluation, MRI of the body part by the overgrowth and Dual-energy X-ray absorptiometry (DXA). * Next 6 months: participants will take Sirolimus. This step includes 2 visits (4 and 13 weeks after the start of treatment at local hospital): blood test, urine collection and clinical evaluation. and 1 end of study visit after 6 months of treatment taking place at the University Hospital of Dijon: blood test, complete clinical evaluation, urine collection, MRI and DXA. Participants will have several blood and urine tests between visits (1 and 2 weeks after the start of treatment at a local laboratory).

Study Type

INTERVENTIONAL

Allocation

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Eligibility

Sex: ALLMin age: 3 YearsMax age: 65 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Post-zygotic PIK3CA mutation * Age: 3-65 years * Measurable overgrowth, in current progression or with clinical history of overgrowth progression * Patient clinically stable * Presence of a disability, social or cosmetic impairment requiring treatment from the patient perspective, * Written informed consent form signed and dated by the subject or by the patient's legal representative Exclusion Criteria: * Pregnancy or lactation * Women and men of reproductive age without any effective method of contraception (during treatment and up to 12 weeks after sirolimus discontinuation) * Hypersensitivity to the active substance (sirolimus) or to any of the excipients * Impossibility to obtain written informed consent form signed by the subject or the patient's legal representative, or vulnerable adults * Treatment with Sirolimus in the last 4 weeks before the trial * Personal history of malignancy or current investigations for suspected malignancy * Active skin infection requiring antibiotics or antiviral treatments * HIV or hepatitis B or C infection * Past history of Mycobacterium tuberculosis infection * Active pneumopathy * Uncontrolled infection * Chronic liver disease (ASAT or Alanine amino transférase (ALAT)\> 3 times upper normal limit) * Stage 3 (or more) chronic renal insufficiency (eGFR\< 60mls/min) * Neutropenia with neutrophiles \< 1.0 x10\^9/L * Uncontrolled dyslipidemia * Inability to attend study visits

Locations (11)

CHU d'Angers

Angers, France

CHU de Bordeaux - GH Pellegrin

Bordeaux, France

CHU de DIJON

Dijon, France

Hôpital Jeanne de Flandre

Lille, France

CHRU de Montpellier - Hôpital Saint-Eloi

Montpellier, France

Hopitaux de Brabois Chu Nancy

Nancy, France

Hôpital mère-enfant de Nantes

Nantes, France

CHU Paris - Necker

Paris, France

HCL Lyon - CH Lyon Sud

Pierre-Bénite, France

Pôle Cardiovasculaire et Métabolique - Hôpital Larrey

Toulouse, France

...and 1 more locations

Outcomes

Primary Outcomes

Measure of the relative percentage of the excess tissue volume evolution at the affected site by volumetric MRI.

Time frame: Change from baseline at 6 and 12 months

Secondary Outcomes

Measure sites of overgrowth by DXA, MRI and circumferential measurements

Time frame: Change from baseline at 6 and 12 months

To determine optimal sirolimus dosing algorithms by plasma assay

Time frame: 12 months

Number of hospitalisation and surgery

Time frame: 12 months

quality of life measured by a questionnaire in the pre- and post-treatment periods

The WHO-QOL-BREF questionnaire will be used for adults. For children, PedsQL™ questionnaire for children and parents report for children questionnaires will be used

Time frame: At 6 and 12 months