- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT01687400
Genomic Predictors of Decitabine Response in Patients With Acute Myeloid Leukemia or Myelodysplastic Syndromes
Genomic Predictors of Decitabine Response in AML/MDS
Studieöversikt
Status
Betingelser
Intervention / Behandling
Studietyp
Inskrivning (Faktisk)
Fas
- Fas 2
Kontakter och platser
Studieorter
-
-
Missouri
-
Saint Louis, Missouri, Förenta staterna, 63110
- Washington University School of Medicine
-
-
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
Tar emot friska volontärer
Kön som är behöriga för studier
Beskrivning
Inclusion Criteria:
All of the following:
- Patient must have non-M3 AML or MDS
An adverse risk karyotype defined by:
- Complex karyotype by cytogenetics, or
- Deletion of all or part of chromosome 5, 7, 12, or 17 defined by FISH or cytogenetics, or
- Somatic TP53 mutation
All of the following:
- Patient must have an ECOG performance status ≤ 2.
- Patient must have >10% disease burden measured by cytomorphology, flow cytometry, or cytogenetics.
- Patient must have peripheral white blood cell count < 50,000/mcl.
Patient must have adequate organ function, defined as:
- Total bilirubin < 1.5 x ULN
- AST/ALT < 2.5 x ULN
- Serum creatinine < 2.0 x ULN
- Patient must have undergone ≤ 2 cycles of prior hypomethylating agent (decitabine or azacitidine).
- Patient must be enrolled in HRPO# 201011766 ("Tissue Acquisition for Analysis of Genetic Progression Factors in Hematologic Diseases").
- Patient must be > 18 years of age.
- Patient must be able to understand and willing to sign an IRB-approved written informed consent document.
Exclusion Criteria:
- Patient must not be pregnant or nursing
- Patient must not have acute promyelocytic leukemia or t(15;17) observed by FISH.
- Patient must not have known central nervous system (CNS) leukemia
- Patient must not have a history of positive human immunodeficiency virus (HIV) serology
- Patient must not have a history of positive hepatitis C serology
- Patient must not have undergone prior allogeneic stem cell transplant
- Patient must not have any uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, ongoing or active graft-versus-host disease (GVHD), congestive heart failure of New York Heart Association (NYHA) class 3 or 4, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situation that would limit compliance with study requirements
- Patient must not have had radiation therapy within 14 days of enrollment
- Patient must not have received any chemotherapy within 21 days of enrollment and any acute treatment-related toxicities must have returned to baseline. Patients may be receiving hydrea at time of enrollment.
Studieplan
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: N/A
- Interventionsmodell: Enskild gruppuppgift
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Experimentell: Decitabine
Patients receive decitabine IV over 1 hour on days 1-10 of a 28-day cycle.
Treatment continues for 2 cycles.
Patients then receive decitabine IV over 1 hour on days 1-10, 1-5, or 1-3 (depending on response).
Treatment continues in the absence of disease progression or unacceptable toxicity.
|
Andra namn:
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Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Correlation of Patient Specific Mutations With Overall Response Rate
Tidsram: 4 months (4 treatment cycles)
|
-Best response after 4 treatment cycles as assessed according to International Working Group (IWG) criteria; bone marrow for gene sequencing will be collected at baseline; mutations will be correlated with overall response rate --Complete remission (CR), Complete remission with incomplete hematologic recovery (CRi), Marrow complete remission (mCR), Partial remission (PR), Stable disease (SD), Progressive disease (PD) |
4 months (4 treatment cycles)
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Compare Outcomes of a 10-day Decitabine Per Cycle Regimen to a 5-day Regimen (Historical Controls)
Tidsram: 4 months (4 treatment cycles)
|
The overall response rate (CR/CRi/mCR/PR) and complete response rate (CR/CRi/mCR) will be compared with historical controls.
Response assessed according to IWG criteria.
|
4 months (4 treatment cycles)
|
|
Rate of Mutation Clearance During Treatment
Tidsram: Up to Day 56
|
Samples collected at baseline and after 10, 28 and 56 days of therapy; the rate of mutation clearance was measured as mean VAF change per day of treatment and was estimated using linear mixed model for repeated measurement data .
|
Up to Day 56
|
|
Peripheral Blood Decitabine Plasma Levels
Tidsram: Day 4
|
|
Day 4
|
|
Change in Bone Marrow Methylcytosine
Tidsram: Baseline and Day 10
|
-Change of total bone marrow deoxyribonucleic acid (DNA) methylcytosine from baseline to Day 10
|
Baseline and Day 10
|
Samarbetspartners och utredare
Utredare
- Huvudutredare: Welch John, M.D., Ph.D., Washington University School of Medicine
Publikationer och användbara länkar
Studieavstämningsdatum
Studera stora datum
Studiestart (Faktisk)
Primärt slutförande (Faktisk)
Avslutad studie (Faktisk)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Uppskatta)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
- Patologiska processer
- Neoplasmer efter histologisk typ
- Neoplasmer
- Sjukdom
- Benmärgssjukdomar
- Hematologiska sjukdomar
- Precancerösa tillstånd
- Syndrom
- Myelodysplastiska syndrom
- Leukemi
- Leukemi, myeloid
- Leukemi, Myeloid, Akut
- Preleukemi
- Molekylära mekanismer för farmakologisk verkan
- Enzyminhibitorer
- Antimetaboliter, antineoplastiska
- Antimetaboliter
- Antineoplastiska medel
- Decitabin
Andra studie-ID-nummer
- 201210102
Plan för individuella deltagardata (IPD)
Planerar du att dela individuella deltagardata (IPD)?
Läkemedels- och apparatinformation, studiedokument
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