Assessment of Tolerance of Mobilizing Peripheral Hematopoietic Stem Cells by Plerixafor in Sickle Cell Patients (DrepaMob)

Sickle cell disease is a genetic disorder caused by a point mutation in the coding region of the gene of beta-globin with the consequence the production of an abnormal (betas-globin). This mutation is responsible for the polymerization of deoxygenated HbS chains. Polymers make red blood cells (RBC) rigid, and change their shapes and are responsible of structural lesions of the membrane, altering the rheological properties of the RBC and altering blood flow of microcirculation. The two ultimate consequences of all these changes are intravascular haemolysis and the occurrence of vaso-occlusive episodes. Allogeneic hematopoietic stem cells (HSC) transplantation is the only curative treatment for these patients, but only 25% of them have a HLA-genoidentical family donor. In the absence of a compatible donor, gene therapy with model autograft could be a valid alternative. However, gene therapy for the curative treatment of sickle cell disease requires an optimal number of genetically modified HSC to reinject the patient. In contrast to beta-thalassemia patients, the mobilization of HSC in peripheral blood by growth factors such as G-CSF in patients with sickle cell can trigger a vaso-occlusive crisis.

The onset of action of plerixafor is very fast. In pharmacodynamic studies in healthy volunteers, mobilization peak of CD34 + cells was observed between 6 and 9 hours after administration of plerixafor. One injection per day for 1 to 2 days should be sufficient to achieve an optimal collection (unlike the 5-6 days required for mobilization of HSC in G-CSF used as the only growth factor). The duration of exposure to risk is thereby theoretically reduced.

We propose an drug test - Phase I/II trial - monocenter- non-comparative - not randomized - uncontrolled - Open.

In this protocol, we propose to assess the safety and efficacy of peripheral HSC mobilization in three major sickle cell patients (SS or Sbeta thalassemia) (or five, if results of the first 3 patients are not reproducible) by a single injection of plerixafor after significant decrease of HbS rate. Adequate number of CD34 + cells collected will be a key point in the success of possible and subsequent autologous graft of genetically modified HSC; a dose> 3.106 cells / kg CD34 + is necessary. Mobilized and collected cells will be stored for a possible future gene therapy or as not handled backup graft.

These three patients will be included sequentially; new inclusion will take place only if no serious adverse events have occurred in patients being participated in the trial. Recruitment will take place during the consultation in Apheresis Therapeutic Unit / Department of Biotherapy at the Necker-Enfants Malades Hospital. Patients being recruited from the cohort of adults with sickle cell disease at the Hospital Necker-Enfants Malades, the principal investigator will have seen the patient in consultation in the weeks preceding the decision to propose him to take part in research. This consultation will constitute within the framework of this protocol, prior medical examination.

Before plerixafor injection, the patient will be subjected to one or more red cell exchange order to reduce the post-transfusion HbS rate to less than 30% and if possible around 15%. If the patient is under treatment with hydroxyurea, it will be stopped 3 months before collecting peripheral HSC and replaced by an exchange transfusion to the rhythm of once per month.

If the patient is not under treatment with hydroxyurea, he will have only 2 or 3 exchange transfusions during the month before collecting peripheral HSC.

Treatment with plerixafor will be administered in the Adult Intensive Care Unit of the Necker - Enfants malades Hospital. He/She will be under scope, will receive oxygen therapy and hyperhydration (physiological saline per day); his/her ionogram and phosphatemia will be monitored. The procedures of mobilization and collection by apheresis peripheral HSC will be performed by the haematologist doctor and a specialist nurse. The HSC's collection will be made in Apheresis Therapeutic Unit. A member of the LTCG team will retrieve samples in intensive care and will provide their transport to the laboratory for possible transformation. The patient will remain hospitalized after collection of peripheral HSC under the same conditions of treatment and monitoring (scope, oxygen, hyperhydration) until the number of White Blood Cells remain lower than 10x10^9 / L or new income at their count base. HSB's collection and related hospitalisation will be performed according to JACIE (Joint Accreditation Committee of ISCT-EBMT) program and subsequent Standard Operating Procedures in force both at Clinical Unit and Laboratory of Cell and Gene Therapy (LTCG) of the Department of Biotherapy.

The dispensation of treatment will be performed by the Internal Use Pharmacy (PUI) of the Necker-Enfants malades Hospital. Specific prescriptions of plerixafor from the study will be made available to the investigators.

A total of 15 visits for patients with hydroxyurea at screening, and 12 visits for patients without hydroxyurea (including final visit) are scheduled for this trial. The total study duration is 24 months, the duration of inclusion is 14 months.

The data required for the analysis of the study will be reported in a paper case report forms.