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UnknownNCT01255319

Cyclophosphamide, Fludarabine and Antithymocyte Globulin Conditioning in Myelodysplastic Syndrome (MDS)

Conditioning With Cyclophosphamide, Fludarabine and Antithymocyte Globulin for Allogeneic Hematopoietic Cell Transplantation in Lower Risk Myelodysplastic Syndrome

Status
Unknown
Phase
Study type
Observational
Enrollment
15 (estimated)
Sponsor
Cooperative Study Group A for Hematology · Network
Sex
All
Age
15 Years
Healthy volunteers
Not accepted

Summary

To evaluate the feasibility and efficacy of the conditioning regimen with cyclophosphamide, fludarabine and antithymocyte globulin (CyFluATG) for allogeneic hematopoietic cell transplantation (HCT) in patients with lower risk myelodysplastic syndrome (MDS).

Detailed description

Conditioning therapy * Cytoxan 50 mg/kg/d on d-3 to -2 * Fludarabine 30 mg/m2 on d-6 to -2 * Antithymocyte globulin (ATG; Thymoglobulin®) 1.5 mg/kg/d (for HLA-matched sibling donor HCT) or 3.0 mg/kg/d (for other alternative donor HCT) * Methylpd 2 mg/kg/d on d-4 to -1 Mobilization and harvest * G-CSF 10 mcg/kg/d s.c. on d-3 to 0 * Harvest of PBMCs on d 0 to +1 Donor G PBMC infusion * Infuse G-PBMCs on d 0 to d+1. GVHD prophylaxis * Cyclosporine 1.5 mg/kg i.v. q 12 hrs beginning on d-1 and changed to oral dosing (with twice the i.v. dose) when oral intake is possible. Tapered beginning between d+30 and d+60. * Methotrexate 15 mg/m2 i.v. on d+2, and 10 mg/m2 i.v. on d+4 and d+7 Preemptive dose-escalating DLIs * Begin at d+120 or at least 2 wks after IST discontinuation. * Failure to achieve full donor chimerism No evidence of GVHD * CD3+ cell dose increment q 4 wks -+ cell dose: HLA-matched donor HCT (1 x 107/kg, 5 x 107/kg, 1 x 108/kg), HLA-matched unrelated donor HCT (1 x 106/kg, 5 x 106/kg, 1 x 107/kg), HLA-matched familial donor HCT (1 x 105/kg, 5 x 105/kg, 1 x 106/kg)

Conditions

Timeline

Start date
2010-11-01
Primary completion
2012-11-01
Completion
2014-11-01
First posted
2010-12-07
Last updated
2010-12-07

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT01255319. Inclusion in this directory is not an endorsement.