Acute Myelogenous Leukemia AML, Myelodysplastic Syndrome MDS
Conditions
Keywords
acute myelogenous leukemia (AML), myelodysplastic syndrome (MDS)
Brief summary
Phase II trial combining azacitidine with valproic acid as maintenance therapy post allogeneic stem cell transplantation in patients with high-risk MDS/AML. We hypothesize that adding valproic acid to azacitidine will improve outcomes via both direct anti-tumor and immunologically mediated antitumor response with alloreactive donor lymphocytes, having an additive effect and extending 1 year survival in patient with high-risk AML/MDS after hematopoietic stem cell transplant. Based on aforementioned data from the US Department of Health and Human Services, standard 1 year survival for AML after stem cell transplant is near 40%. We hypothesize that valproic acid and azacitidine will prolong survival, with a 1 year survival goal of 60%. In addition to assessing for 1 year survival, we will have secondary objectives of assessing progression-free survival, relapse, and toxicity. The primary toxicity endpoint from this will be cytopenias and infections.
Detailed description
To assess the combination of valproic acid and azacitidine in preventing relapse in patients with high-risk Acute Myeloid Leukemia (AML) and myelodysplastic syndrome (MDS) after allogeneic stem cell transplant. The primary objective of this study will be determining the 1 year overall survival from combining valproic acid (VPA) with 5-azacytidine (5-aza). To assess the effect that adding valproic acid to azacitidine will have in patient with high-risk Acute Myeloid Leukemia (AML) and myelodysplastic syndrome (MDS) after allogeneic stem cell transplant on the following endpoints
Interventions
DRUGVidaza and Valproic Acid
Days 1-5: 5-Azacytidine 40 mg/m\^2 daily Days 1-5: +Valproic acid 15 mg/kg daily Days 6-28: Valproic acid 15 mg/kg daily \*treatments will be repeated on the same days of each cycle for up to 4 total cycles. Each cycle will consist of 28 days.
Sponsors
Patrick Stiff
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
2 Years to 89 Years
Healthy volunteers
No
Inclusion criteria
1. All allograft patients \> 2 years of age. 2. Patients will have one of the following malignancies: a. Patients with refractory or relapsed: acute myelogenous leukemia (AML) (including inv16, t(8;21) or t(15;17)) or high risk myelodysplastic syndrome (MDS) (defined as bone marrow blasts \> or = 5%) are eligible. Patients may be in remission at the time of entry. 3. Patients with adequate organ function and performance status criteria measured by: 1. Karnofsky score greater than or equal to 70% or Performance status of \< or = 2 by the Eastern Cooperative Oncology Group (ECOG) scale 2. Adequate liver function (bilirubin of \< 2mg/dL, serum glutamate pyruvate transaminase \< 3 \* ULN) and renal function (creatinine \< 2mg/dL) 4. Signed informed consent indicating that patients are aware of the investigational nature of this study in accordance with the regulations of Loyola University Medical Center 5. Patients must have undergone allogeneic stem cell transplant within 40-60 days before starting treatment and be self-sufficient in caloric intake along with no active graft vs. host disease
Exclusion criteria
1. Nursing and pregnant females are excluded. 2. Active and uncontrolled infections will cause patients to be excluded. 3. Patients already receiving valproic acid or receiving other anticonvulsants will be excluded. 4. Low risk AML in complete remission 1, will not be candidates for this study. 5. Patients with an absolute neutrophil count less than 1500 will be excluded 6. Patients with platelets less than 50,000 will be excluded 7. Children less than 2 years of age will be excluded due to increased hepatotoxicity from valproic acid in this age group
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Survival | 1 year | Number of participants that survive post transplant for 1 year. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Disease Relapse | Day 0 to the day of first recurrance | The time to relapse is from Day 0 to the day of first hematologic, cytogenetic, or radiological evidence of recurrent disease. |
Countries
United States
Contacts
Primary ContactMary Lee, BSN
Backup ContactCeil Petrowsky, MSN
Outcome results
None listed