Extracorporeal Photopheresis Using Theraflex ECP™ for Patients With Refractory Chronic Graft Versus Host Disease (cGVHD)

Inclusion Criteria

• •Patients must have chronic GVHD (cGVHD) occurring after any type of HSC transplantation : with any type of donor (HLA-identical siblings or HLA-matched or mismatched family or unrelated donor); with any type of conditioning (full-intensity, reduced-intensity, nonmyeloablative, no conditioning); with any type of HSC (bone marrow, PBSC, cord blood) or after donor lymphocyte infusion.
• •Patients must have cGVHD primarily affecting at least one of the following organs: skin; oral mucosal; eye; liver; lung; joints; fascia. Gastro-intetinal (GI) cGVHD alone is not a sufficient inclusion criterion.
• •Patients must have cGVHD that has already been treated with first-line systemic therapy for at least 1 month at effective doses. First-line systemic therapy must have included at least prednisolone 1 mg/kg/day or equivalent. In case of formal contraindication to steroid therapy, first-line systemic therapy must have included therapeutic doses of at least one of the following drugs: tacrolimus or ciclosporine (if patient not treated with a calcineurin inhibitor at onset of cGVHD), sirolimus, everolimus, mycophenolate mofetyl.
• •Patients must require further salvage therapy for cGVHD because of either refractoriness or contraindication/intolerance to current therapy.
• •Need for salvage therapy is defined by any of the following criteria :
• •the development of 1 or more new sites of disease while being treated for chronic GVHD
• •progression of existing sites of disease while receiving treatment for chronic GVHD
• •failure to improve despite at least 1 month of standard treatment for chronic GVHD,
• •relapse/progression of cGVHD while tapering current treatment for cGVHD.
• •* Patients may have received any number of previous lines of treatment for cGVHD.
• •* Concomitant treatment with other immunosuppressors is allowed if they were started and maintained at constant dosage for at least one month before the start of ECP. Shorter delay can be accepted for patients with highly progressive GVHD requiring salvage therapy.
• •* Signed informed consent.
• •* Any age.
• •* Weight \> 15 Kg (because of leukapheresis). Weight \<15 Kg is acceptable if a suitable method of leukapheresis has been developed and approved at site.