A Phase 2 interventional study of Fludarabine and Dexamethasone in Stem Cell Transplantation, sponsored by M.D. Anderson Cancer Center. Withdrawn at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2023-09-21.
Sponsored by M.D. Anderson Cancer Center · Phase 2, Interventional, and Treatment
To assess the outcomes of NRM when administering pharmacologic pretransplant immunosuppression (PTIS) followed by pretransplant reduced toxicity conditioning (RTC) and an allogeneic stem cell transplant (allo-SCT) and post-transplant graft-versus-host disease prophylaxis based on post-transplant cyclophosphamide (PT-Cy) in patients with inherited blood disorders.
Objectives
Primary:
To estimate the 100-day non-relapse mortality (NRM) rate when administering pharmacologic pretransplant immunosuppression (PTIS) followed by pretransplant reduced toxicity conditioning (RTC) and an allogeneic stem cell transplant (allo-SCT) and post-transplant graft-versus-host disease prophylaxis based on post-transplant cyclophosphamide (PT-Cy) in patients with inherited blood disorders.
Secondary outcomes include the following:
i. Immune reconstitution ii. Infectious complications iii. Quality of life (QOL) at 3 months,100 days, and 1 year post-transplant iv. OS, EFS, and GRFS v. Incidence of aGVHD at day 100. vi. Rate of chronic GVHD within the first-year post transplantation. vii. Rate of Graft failure
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Adequate major organ system function as demonstrated by:
Exclusion Criteria:
Drug: Fludarabine · Drug: Dexamethasone · Drug: Cyclophosphamide · Drug: Bortezomib · Drug: Rituximab · Drug: Busulfan · Drug: Cyclophosphamide (Cy) · Drug: Tacrolimus (or cyclosporine)
Drug: Fludarabine · Drug: Cyclophosphamide · Drug: Busulfan · Drug: Cyclophosphamide (Cy) · Drug: Tacrolimus (or cyclosporine) · Drug: Mycophenolate mofetil (MMF) · Drug: Rabbit ATG
40 mg/m2/day i.v.- by vein
Also known as: Fludara™
25 mg/m2/day i.v.-by vein
100 mg/m2 IV-by vein
Also known as: Cytoxan™
Four doses of bortezomib at a dose of 1.3 mg/m2 -injection under the skin
Also known as: Velcade®
Four doses of rituximab at a dose of 375 mg/m2- by vein
Also known as: Rituxan®
110 mg/m2 i.v-by vein
Also known as: Busulfex™
by vein
Also known as: Cytoxan™
by vein
given by PO
by vein
To determine the 100-day non-relapse mortality (NRM) rate when administering pharmacologic pretransplant immunosuppression (PTIS) followed by pretransplant reduced toxicity conditioning (RTC
Time frame: through study completion, an average of 1 year
This study is withdrawn, as verified in Sep 2023. You cannot join it, but the record below documents what was studied.
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M.D. Anderson Cancer Center