Leukemia, Myeloid, Chronic-Phase
Conditions
Brief summary
This project is a Phase II clinical trial that aims at evaluating efficacy and tolerance of the combination of pioglitazone (Actos®) and imatinib mesylate (STI571, CGP57148, Gleevec®) in patients with Chronic Myelogenous Leukemia (CML) in stable major molecular response (i.e. a BCRABL/ABL ratio assessed by RTQ-PCR equal to or lower than 0.1% according to the European Leukemia Net recommendations) after at least 2 years of therapy with imatinib. Imatinib mesylate (Gleevec®) is the gold standard for the treatment of CML in chronic phase (O Brian et al. 2003, Druker et al. 2006). Despite a high efficacy of the drug, CML is not eradicated by imatinib alone in almost any of the patients. Treatment discontinuation in patients treated by imatinib and in complete molecular remission for more than 2 years yield molecular relapses within 6 months in half of the patients,indicating the persistence of CML progenitor cells. STAT5 expression is required for CML stem cell engraftment and expansion in mouse models. STAT5 is the target of the dysregulated activity of BCR-ABL in CML. Recently, Stephane Prost et al. demonstrated that PPAR-γ is a negative regulator of STAT5A and STAT5B gene expression. Data obtained suggest that PPAR-γ agonists may have potential therapeutic value in reversing myeloproliferative disorders. On the basis of our preclinical studies, we went ahead and administered pioglitazone to one patient who suffered from both diabetes type II and CML with residual disease after continuous treatment with Gleevec. The amount of BCR-ABL transcript detected by QPCR decreased dramatically during the first 3 months of combined (Gleevec + ACTOS) therapy to become undetectable thereafter until 9 months post-treatment, the latest time point assessed. This striking anecdotal result now forms the rationale for filing this formal Phase II clinical trial application.
Interventions
DRUGAdd-on therapy
Pioglitazone therapy
Sponsors
Versailles Hospital
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Patient aged 18y or more 2. Signed informed consent 3. Patient with Philadelphia chromosome positive chronic phase CML and M BCR-ABL transcript positivity 4. Treatment with imatinib for more than 2 years 5. No dose modification of imatinib within the last 3 months 6. Complete cytogenetic response on the last cytogenetic analysis within the last 12 months 7. Major molecular remission without complete molecular remission 8. ECOG grade 0 to 2 9. SGOT et SGPT ≤ 2.5 N 10. Bilirubin in serum ≤ 1.5 N 11. Women of childbearing potential (WOCBP) must be using an adequate method of contraception
Exclusion criteria
1. Participation in another clinical trial with any investigative drug within 30 days prior to study enrollment 2. Prior history of hematopoietic stem cell transplantation (autologous or allogenic) 3. Patient requiring anti-diabetic medication 4. Cardiovascular disease: * Stage I to IV congestive heart failure (CHF) as determined by the New York Heart Association (NYHA) classification system for heart failure * Myocardial infarction within the previous 6 months * Symptomatic cardiac arrhythmia requiring treatment 5. Grade III or IV fluid retention 6. Known osteoporosis with therapy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The rate of patients achieving a complete molecular response (Sensitivity 10-5 or Bcr Abl/Abl ratio < 0.001 %) 24 weeks after the initiation of pioglitazone, confirmed on by a second determination 2 months later. | 26 weeks |
Secondary
| Measure | Time frame |
|---|---|
| Adverse events | 5 years |
| Duration of the complete molecular response | 5 years |
| The rate of patients achieving a complete molecular response (Sensitivity 10-5 or Bcr-Abl/Abl ratio < 0.001 %) | 14 months |
| Survival | 5 years |
| Progression free survival | 5 years |
Countries
France
Contacts
PRINCIPAL_INVESTIGATORRousselot Philippe, MD
CH Versailles
Outcome results
None listed