Overview

This trial is active, not recruiting.

Conditions myelodysplastic syndrome, acute myeloid leukemia
Treatment decitabine
Phase phase 1
Sponsor Seoul St. Mary's Hospital
Collaborator Janssen, LP
Start date January 2011
End date September 2014
Trial size 19 participants
Trial identifier NCT01277484, DEC-KOR-9007

Summary

Brief Scientific Rationale:

Decitabine has been shown to be effective for treatment of MDS and associated with very limited extramedullary toxicity at the lower doses. Furthermore, the hypomethylating effects of decitabine require an extended period of therapy and are likely to be more beneficial in the setting of a minimal residual disease after transplantation. The drug might exert a cytoreductive effect on the MDS clone, but ex vivo expansion strategy using decitabine and HDAC inhibitor provides a potential to expand the number of hematopoietic stem cells. There are lots of evidence which showed the the drug have immunostimulatory effects and can be used to enhance graft-versus leukemia effects. And also, some investigator suggested that decitabine could induce FOXP3 expression, promoting the conversion of naïve T cells to Tregs which are known to suppress GVHD while maintaining GVL effect in allo-SCT setting. As such, decitabine is an ideal agent to be investigated in the post-transplant setting.

The investigators hypothesized that post-transplant maintenance therapy with decitabine may reduce relapse rate, which may maximize the beneficial effects from reduced TRM of ATG-containing FB4 or FB2 conditioning regimen in higher-risk MDS or AML evolving from MDS patients.

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Endpoint classification safety study
Intervention model single group assignment
Masking open label
Primary purpose treatment
Arm
(Experimental)
For the patients who achieve remission after allogeneic BMT and meet the enrollment criteria, decitabine will be given at a dose of 5mg/kg/day ~ 15mg/kg/day iv over 1 hour for 5 consecutive days starting 42-90 days after transplantation. The drug will be repeated every 4 weeks for up to 12 cycles.
decitabine Dacogen
1. Dose finding study (cycle 1-cycle4) Indicated dose for 5 consecutive days every 28 days Cohort 1: 5mg/m2 of decitabine Cohort 2 and 3:Dose escalation up to 15mg/m2 using a mechanism-based pharmacokinetic / pharmacodynamic model

Primary Outcomes

Measure
Dose and schedule finding of post-BMT Decitabine Treatment
time frame: For up to 2 years after the start of Decitabine

Secondary Outcomes

Measure
Transplant outcomes of Decitabine maintenance treatment following transplantation
time frame: For up to 2 years after the start of Decitabine

Eligibility Criteria

Male or female participants from 18 years up to 65 years old.

Inclusion Criteria for allogeneic transplantation:: - Patients with a diagnosis of MDS (IPSS intermediate-2 or higher) before allogeneic transplantation - HLA-compatible unrelated (HLA-A, -B, -C and -DRB1 matched or with 2 allele mismatch) - Performance status < ECOG 2 - Acceptable organ function defined as:Serum creatinine < 1.5 times the institutional ULN,Serum bilirubin < 1.5 times the institutional ULN,AST, ALT and alkaline phosphatase < 3 times the institutional ULN. Inclusion Criteria for decitabine maintenance therapy: - 6 to 10 weeks after alloHSCT - patients who are confirmed complete remission(CR) within 2 weeks for treatment start(CR:less than 5% blasts in an aspirate bone marrow sample or no leukemic blasts in the peripheral blood, no cytogenetic aberrations) - Performance status < ECOG 2 - Acceptable organ function defined as:Serum creatinine < 1.5 times the institutional ULN,Serum bilirubin < 1.5 times the institutional ULN,AST, ALT and alkaline phosphatase < 3 times the institutional ULN. - Platelet count ≥ 30,000/μL without platelet transfusion for 7 days and ANC ≥ 1,000/μL without colony stimulating factor support at the time of enrollment - Written informed consent form Exclusion Criteria: - HIV positive - Active uncontrolled infection - Pregnancy or breastfeeding - patients who have residual disease after allo SCT or primary graft failure - Uncontrolled grade 3- 4 acute GVHD - patients who are known or suspected hypersensitivity to decitabine - patient who are not suitable for the trial in accordance with principal investigator's decision

Additional Information

Official title Single Arm, Open Label, Phase I Study for Dose and Schedule Finding of Decitabine in Patients With Higher-risk MDS and MDS/AML Receiving Allogeneic Stem Cell Transplantation
Principal investigator Yoo-Jin Kim, MD, PhD
Description 1. Transplant course - BMT from an HLA-matched sibling or a suitably matched (up to 2-allele mismatched) family or unrelated donor will be performed according to the policies of the institute. - A preparative regimen will be started 6 days before the day of stem cell infusion 1. Myeloablative-intensity conditioning regimen: FB4+ATG 2. Reduced-intensity conditioning regimen; FB2+ATG 3. Graft-versus-host disease prophylaxis - Sibling transplant: Cyclosporine and short-course Methotrexate - Unrelated transplant: Tacrolimus and short-course Methotrexate - The dose of calcineurin inhibitors (cyclosporine and tacrolimus) will be gradually tapered from day 60 (for all sibling transplants) or day 90 (for all unrelated transplants) and discontinued within 2 or 3 months after SCT in the absence of graft-versus-host disease. 2. Decitabine maintenance course - For the patients who finish the above transplant procedure and meet the enrollment criteria, decitabine will be given at a dose of 5mg/m2/day ~ 15mg/m2/day iv over 1 hour for 5 consecutive days. The drug will be repeated every 4 weeks for up to 12 cycles. - Dose escalation strategy between cohorts and between cycles in the same cohort patients will be based upon the quantitatively measured hematological toxicity (e.g., ANC or platelet count at nadir). In other words, a mechanism-based pharmacokinetic / pharmacodynamic model developed using sparsely sampled patients' PK data and toxicity response will be used to titrate next cycle doses for the patients and initial doses for new cohort patients. In other words, a mechanism-based pharmacokinetic / pharmacodynamic model developed using sparsely sampled patients' PK data and toxicity response will be used to titrate next cycle doses for the patients and initial doses for new cohort patients.
Trial information was received from ClinicalTrials.gov and was last updated in November 2015.
Information provided to ClinicalTrials.gov by Seoul St. Mary's Hospital.