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- Klinische proef NCT00258271
Cladribine, Cytarabine, and Imatinib Mesylate in Treating Patients With Refractory or Relapsed Acute Myeloid Leukemia or Blastic Phase Chronic Myelogenous Leukemia
A Phase I Study of CLAG Regimen in Combination With Imatinib Mesylate (Gleevec) in Refractory or Relapsed Leukemias
RATIONALE: Drugs used in chemotherapy, such as cladribine and cytarabine, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Imatinib mesylate may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Giving cladribine and cytarabine together with imatinib mesylate may kill more cancer cells.
PURPOSE: This phase I trial is studying the side effects and best dose of imatinib mesylate when given together with cladribine and cytarabine in treating patients with refractory or relapsed acute myeloid leukemia or blastic phase chronic myelogenous leukemia.
Studie Overzicht
Toestand
Conditie
Interventie / Behandeling
Gedetailleerde beschrijving
OBJECTIVES:
- Determine the safety and feasibility of cladribine, cytarabine, and imatinib mesylate in patients with refractory or relapsed acute myeloid leukemia or blastic phase chronic myelogenous leukemia.
- Determine the maximum tolerated dose of imatinib mesylate in patients treated with this regimen.
- Correlate the expression of c-kit and the presence of c-kit mutations with clinical response in patients treated with this regimen.
- Correlate the in vitro inhibitory effects of imatinib mesylate and cytarabine on the proliferation and survival of leukemic cells with clinical response in patients treated with this regimen.
OUTLINE: This is a dose-escalation study of imatinib mesylate.
Patients receive oral imatinib mesylate once daily on days 1-15 and cladribine IV over 2 hours and cytarabine IV over 4 hours on days 3-7. Patients also receive filgrastim (G-CSF) subcutaneously on days 2-7. Treatment repeats every 15 days for 2 courses in the absence of disease progression or unacceptable toxicity.
Cohorts of 3-6 patients receive escalating doses of imatinib mesylate until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose-limiting toxicity.
After completion of study treatment, patients are followed periodically for up to 1 year.
PROJECTED ACCRUAL: A total of 12-18 patients will be accrued for this study.
Studietype
Inschrijving (Verwacht)
Fase
- Fase 1
Contacten en locaties
Studie Locaties
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New York
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Rochester, New York, Verenigde Staten, 14642
- James P. Wilmot Cancer Center at University of Rochester Medical Center
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-
Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
Accepteert gezonde vrijwilligers
Geslachten die in aanmerking komen voor studie
Beschrijving
DISEASE CHARACTERISTICS:
Diagnosis of acute myeloid leukemia (AML) or blastic phase chronic myelogenous leukemia (CML)
Refractory AML defined as any of the following:
- Failure to achieve complete response (CR) after 2 courses of induction chemotherapy
- Persistent bone marrow blasts > 40% after 1 course of induction chemotherapy
- Relapse of disease within 3 months since CR
Relapsed AML defined as the following:
- Any evidence of disease recurrence after CR (early relapse occurs within 3-12 months and late relapse occurs > 12 months later)
- No acute promyelocytic leukemia (AML-M3 FAB subgroup)
PATIENT CHARACTERISTICS:
Performance status
- ECOG 0-2
Life expectancy
- Not specified
Hematopoietic
- Not specified
Hepatic
- Bilirubin ≤ 2.0 mg/dL
- AST ≤ 2.5 times upper limit of normal
- No known chronic liver disease (e.g., chronic active hepatitis or cirrhosis)
Renal
- Creatinine < 2.5 mg/dL (if 2.0-2.5 mg/dL, glomerular filtration rate must be measured and dose of cytarabine adjusted if necessary)
Cardiovascular
- No New York Heart Association grade III-IV heart disease
- No congestive heart failure
- No myocardial infarction within the past 6 months
- Ejection fraction ≥ 30%
Other
- Not pregnant or nursing
- Negative pregnancy test
- Fertile patients must use effective barrier contraception during and for 3 months after completion of study treatment
- No uncontrolled systemic active infection
- No known HIV infection
- No history of allergic reaction attributed to compounds of similar chemical or biological composition to study drugs
- No history of other curatively treated malignancy except nonmelanoma skin cancer
PRIOR CONCURRENT THERAPY:
Biologic therapy
- No other concurrent biologic agents
Chemotherapy
- See Disease Characteristics
- No other concurrent chemotherapy
Endocrine therapy
- No concurrent birth control pills
Other
- More than 1 week since any prior investigational agent
- No other concurrent investigational agents or therapies
- No other concurrent anticancer agents
No concurrent therapeutic anticoagulation with warfarin
- Low molecular weight heparin or heparin allowed for therapeutic anticoagulation
- Mini-dose warfarin (e.g., 1 mg per day) allowed for prophylaxis of central venous catheter thrombosis
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
Medewerkers en onderzoekers
Sponsor
Onderzoekers
- Hoofdonderzoeker: Camille Abboud, MD, James P. Wilmot Cancer Center
Publicaties en nuttige links
Studie record data
Bestudeer belangrijke data
Studie start
Primaire voltooiing (Werkelijk)
Studie voltooiing (Werkelijk)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Schatting)
Updates van studierecords
Laatste update geplaatst (Schatting)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
- recidiverende volwassen acute myeloïde leukemie
- volwassen acute megakaryoblastische leukemie (M7)
- volwassen acute monoblastische leukemie (M5a)
- volwassen acute monocytische leukemie (M5b)
- volwassen acute myeloblastische leukemie met rijping (M2)
- volwassen acute myeloblastische leukemie zonder rijping (M1)
- volwassen acute myelomonocytische leukemie (M4)
- volwassen acute basofiele leukemie
- volwassen acute eosinofiele leukemie
- volwassen erytroleukemie (M6a)
- pure erytroïde leukemie bij volwassenen (M6b)
- blastische fase chronische myeloïde leukemie
- recidiverende chronische myeloïde leukemie
Aanvullende relevante MeSH-voorwaarden
- Pathologische processen
- Neoplasmata per histologisch type
- Neoplasmata
- Beenmergziekten
- Hematologische ziekten
- Myeloproliferatieve aandoeningen
- Neoplastische processen
- Celtransformatie, neoplastisch
- Kankerverwekkendheid
- Leukemie, myeloïde
- Leukemie
- Leukemie, Myelogeen, Chronisch, BCR-ABL Positief
- Ontploffingscrisis
- Fysiologische effecten van medicijnen
- Moleculaire mechanismen van farmacologische werking
- Anti-infectieuze middelen
- Antivirale middelen
- Enzymremmers
- Antimetabolieten, antineoplastische
- Antimetabolieten
- Antineoplastische middelen
- Immunosuppressieve middelen
- Immunologische factoren
- Proteïnekinaseremmers
- Cytarabine
- Imatinib-mesylaat
- Cladribine
Andere studie-ID-nummers
- CDR0000448638
- URCC-U26403
- URCC-RSRB-10427
- NOVARTIS-CSTI571AUS161
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
product vervaardigd in en geëxporteerd uit de V.S.
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