Status:
COMPLETED
A Novel Sequential Treatment of Salvage and Reduced Intensity Conditioning (RIC) Chemotherapy for Allogeneic Stem-Cell Transplantation (SCT) for Primary Refractory and Relapsed Acute Myelogenous Leukemia (AML)
Lead Sponsor:
Weill Medical College of Cornell University
Collaborating Sponsors:
Jazz Pharmaceuticals
Conditions:
Acute Myelogenous Leukemia
Myelodysplastic Syndrome
Eligibility:
All Genders
18-70 years
Phase:
PHASE1
Brief Summary
This open-label Phase I study is designed to determine the maximum tolerated dose (MTD) for CPX-351 followed by a reduced intensity conditioning regimen and incorporates a dose-escalation schedule tha...
Eligibility Criteria
Inclusion
- Patients are included, if they fulfill at least one of the following criteria defining refractory or relapsed AML according to previously established criteria 1-3: (1) Primary induction failure (PIF) after ≥ 2 cycles of chemotherapy. (2) First relapse. (3) Relapse refractory to salvage chemotherapy (4) Second or subsequent relapse.
- Patients with MDS, either refractory anemia with excess blasts (RAEB) I or RAEB II
- Age between 18 and 70 years old.
- Patients must have a Karnofsky Performance Status \> 70.
- Each patient must be willing to participate as a research subject and must sign an informed consent form.
- If the patient has a history of a prior malignancy, they must be without any evidence of disease of that prior malignancy for at least 2 years before being eligible for transplant on this protocol. This excludes skin cancers that may have been excised within that 2 year period.
- Patients must have adequate physical function measured by:
- Cardiac: asymptomatic or if symptomatic then left ventricular ejection fraction (LVEF) at rest must be \> 50% and must improve with exercise.
- Hepatic: \< 3x upper limit of normal (ULN) alanine aminotransferase (ALT) and \< 1.5 total serum bilirubin, unless liver is involved with the disease or there is congenital benign hyperbilirubinemia.
- Renal: serum creatinine within normal range for age or if serum creatinine is outside the normal range, then creatinine clearance \> 60-ml/min.
- Pulmonary: asymptomatic or if symptomatic, diffusing capacity of carbon monoxide (DLCO) \> 45% of predicted (corrected for hemoglobin)
Exclusion
- Impaired renal function with a measured or calculated creatinine clearance of less than 60 ml/min.
- Impaired hepatic function defined as a bilirubin greater than 1.5 x upper limit of normal or alanine aminotransferase (ALT) or aspartate aminotransferase (AST) greater than 3 x normal.
- Serious active or uncontrolled infection (Infections are controlled when patients are afebrile and hemodynamically stable for 72 hours) or medical condition.
- Women who are pregnant or breast feeding. Women of childbearing age must use adequate contraception and have a negative pregnancy test.
- Impaired pulmonary function with a DLCO less than 45% predicted.
- Impaired cardiac function with an ejection fraction less than 50% of predicted by echocardiogram or multigated acquisition scan (MUGA).
- Prior daunorubicin therapy with a cumulative dose of more than 368 mg/m2 or equivalent. The anthracycline agents commonly used in treating myeloid malignancies are doxorubicin, idarubicin and mitoxantron.
- For example, a patient who receives 7 + 3 (daunorubicin 180 mg/m2) for induction and MEC regimen (mitoxantrone, etoposide, cytaragine; mitoxantrone 48 mg/m2) for salvage. The cumulative daunorubicin equivalent is 180 + (48x2) = 278 mg/m2.
- Other systemic anticancer therapy or ongoing toxicities from such therapy.
- Patients with a history of and/or current evidence of myocardial impairment (e.g. cardiomyopathy, ischemic heart disease, significant valvular dysfunction, hypertensive heart disease, congestive heart failure), resulting in heart failure by New York Heart Association Class III or IV staging.
- Patients with Wilson disease or other Copper-related disorders.
Key Trial Info
Start Date :
June 2 2009
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 27 2017
Estimated Enrollment :
47 Patients enrolled
Trial Details
Trial ID
NCT00875693
Start Date
June 2 2009
End Date
December 27 2017
Last Update
January 17 2018
Active Locations (1)
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1
Weill Cornell Medical College
New York, New York, United States, 10021