Optimized CBT for Pts With High-risk Hematologic Malignancies Who Have Relapsed After First ASCT
Summary
The goal of this clinical research study is to learn if intermediate-intensity conditioning therapy followed by a cord blood transplant can help to control high-risk hematological malignancies in patients who need a second allogeneic stem cell transplantation.
Detailed description
Primary Objective: To evaluate 1-year overall survival (OS) following CBT with intermediate dose intensity conditioning for patients in need of a second allogeneic stem cell transplantation. Secondary Objectives: Speed and success of neutrophil and platelet engraftment. Incidences of graft failure. • Incidence of day 100 grade II-IV and III-IV aGVHD and day 180 grades II-IV and III-IV aGVHD. Incidence of 1-year, 2-year, and 3-year cGVHD. Incidence of TRM (100 days, 6 months, 1 and 2 years). The probabilities of relapse, OS, PFS, and GRFS at 1 year, 2, and 3 years as listed in the secondary endpoints in section 2.2. Correlative laboratory studies investigating graft versus leukemia biology.
Arms & interventions
- DrugDrugs Cyclophosphamide
Given as standard of care treatment through IV infusion
- DrugFludarabine
Given as standard of care treatment through IV infusion
- DrugThiotepa
Given as standard of care treatment through IV infusion
- DrugTacrolimus
Given as standard of care treatment through IV infusion
- DrugMycophenolate mofetil
Given as standard of care treatment through IV infusion
Outcome measures
Primary
Safety and Adverse Events (AEs)
Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 5.0
Time frame: Through study completion; an average of 1 year.
Eligibility criteria
Study locations (1)
The University of Texas M. D. Anderson Cancer Center
Houston, Texas, 77030