- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT00022048
Bevacizumab in Treating Patients With Myelodysplastic Syndrome
Safety and Efficacy Trial of Bevacizumab: Anti-VEGF Humanized Monoclonal Antibody (NSC 704865) Therapy for Myelodysplastic Syndrome (MDS)
RATIONALE: Monoclonal antibodies, such as bevacizumab, can block cancer growth in different ways. Some block the ability of cancer cells to grow and spread. Others find cancer cells and help kill them or deliver cancer-killing substances to them.
PURPOSE: This phase I/II trial is to see if bevacizumab works in treating patients who have myelodysplastic syndrome.
Studieoversikt
Status
Intervensjon / Behandling
Detaljert beskrivelse
OBJECTIVES:
- Determine the hematologic responses, including changes in hemoglobin levels, neutrophil counts, platelet counts, and percentage of bone marrow blasts, in patients with myelodysplastic syndrome treated with bevacizumab.
- Determine the toxic effects of this regimen in these patients.
- Determine the tolerance in patients treated with this regimen.
- Determine bone marrow cytogenetic responses in patients treated with this regimen.
- Determine bone marrow microvessel density in patients treated with this regimen.
OUTLINE: This is a multicenter study. Patients are stratified according to International Prognostic Scoring System risk status (low (low or intermediate-1) vs high (intermediate-2 or high)).
Patients receive bevacizumab IV over 30-90 minutes. Treatment repeats every 2 weeks for 4-6 months in the absence of disease progression or unacceptable toxicity.
Patients are followed at weeks 1, 3, 5, 7, and 9.
PROJECTED ACCRUAL: A total of 16-25 patients will be accrued for this study within 2 years.
Studietype
Fase
- Fase 2
- Fase 1
Kontakter og plasseringer
Studiesteder
-
-
Arizona
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Tucson, Arizona, Forente stater, 85724
- Arizona Cancer Center at University of Arizona Health Sciences Center
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California
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Stanford, California, Forente stater, 94305-5750
- Stanford Cancer Center at Stanford University Medical Center
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Texas
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Houston, Texas, Forente stater, 77030-4009
- University of Texas - MD Anderson Cancer Center
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-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
DISEASE CHARACTERISTICS:
Histologically confirmed myelodysplastic syndrome (MDS)
- Refractory anemia (RA)
- RA with excess blasts (RAEB)
- RAEB in transformation
- RA with ringed sideroblasts
- Non-proliferative chronic myelomonocytic leukemia (WBC less than 12,000/mm^3)
At least 1 of the following cytopenias:
- Untransfused hemoglobin no greater than 10.0 g/dL and/or red cell transfusion dependent
- Absolute neutrophil count no greater than 1,800/mm^3 (neutropenia)
- Platelet count no greater than 100,000/mm^3 (thrombocytopenia)
- No secondary MDS
- No known brain metastases
PATIENT CHARACTERISTICS:
Age:
- 18 and over
Performance status:
- ECOG 0-2
- Karnofsky 60-100%
Life expectancy:
- More than 4 months
Hematopoietic:
- See Disease Characteristics
- Platelet count at least 20,000/mm^3
- No hemorrhagic illness within the past 3 weeks
- No hemolysis
- No iron deficiency
- No active blood loss
Hepatic:
- AST and ALT no greater than 2.5 times upper limit of normal (ULN)
- Bilirubin no greater than 2.0 mg/dL
- INR less than 2.0
- PTT less than 1.5 times ULN
Renal:
- Creatinine no greater than 2.0 mg/dL
- No renal dysfunction requiring dialysis within the past 6 months
- No nephrotic syndrome within the past 6 months
Cardiovascular:
- No myocardial infraction within the past 6 months
- No severe or unstable angina within the past 6 months
- No severe peripheral vascular disease (ischemic rest pain, non-healing wound or ulcer, or tissue loss) within the past 6 months
- No uncontrolled hypertension within the past 6 months
- No transient ischemic attack within the past 6 months
- No cerebrovascular accident within the past 6 months
- No deep venous or arterial thrombosis
- No coronary artery disease
- No symptomatic congestive heart failure (New York Heart Association class II-IV heart disease)
- No cardiac arrhythmia
- No vascular illness within the past 3 weeks
Pulmonary:
- No pulmonary embolism
Other:
- Not pregnant or nursing
- Negative pregnancy test
- Fertile patients must use effective contraception
No other active malignancy except localized squamous cell or basal cell skin cancer
- Prior cured malignancy allowed
- No trauma within the past 3 weeks
- No significant inflammatory disease within the past 3 weeks
- No serious non-healing wound, ulcer, or bone fracture
- No hypersensitivity to Chinese hamster ovary cell products or other recombinant human or humanized antibodies
- No other active severe disease
- No infection
- No psychiatric illness or social situation that would preclude study compliance
- HIV negative
PRIOR CONCURRENT THERAPY:
Biologic therapy:
- No prior allogeneic bone marrow transplantation
- At least 30 days since prior biologic response modifiers
- At least 30 days since prior hematopoietic growth factors
- At least 30 days since prior thalidomide
- No concurrent thalidomide
- No other concurrent biologic response modifiers
- No concurrent hematopoietic growth factors (including epoetin alfa)
- Concurrent filgrastim (G-CSF) for febrile neutropenia allowed
- Concurrent transfusions allowed
Chemotherapy:
- At least 30 days since prior chemotherapy
- No concurrent chemotherapy
Endocrine therapy:
- No concurrent corticosteroid therapy (more than 10 mg/day of prednisone or equivalent steroid dose) except for pre-medication for transfusions
Radiotherapy:
- At least 30 days since prior radiotherapy
- No concurrent radiotherapy
Surgery:
- At least 3 weeks since prior surgery (including biopsy of visceral organ)
Other:
- At least 10 days since prior anticoagulants
- No concurrent cytotoxic agents
- No other concurrent investigational agents
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
Samarbeidspartnere og etterforskere
Sponsor
Samarbeidspartnere
Etterforskere
- Studiestol: Peter L. Greenberg, MD, Stanford University
Studierekorddatoer
Studer hoveddatoer
Studiestart
Studiet fullført (Faktiske)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Anslag)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Anslag)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
- refraktær anemi
- refraktær anemi med ringmerkede sideroblaster
- refraktær anemi med overflødig blaster
- refraktær anemi med overskytende blaster i transformasjon
- kronisk myelomonocytisk leukemi
- de novo myelodysplastiske syndromer
- tidligere behandlede myelodysplastiske syndromer
- myelodysplastisk/myeloproliferativ neoplasma, ikke klassifiserbar
- atypisk kronisk myeloid leukemi, BCR-ABL1 negativ
Ytterligere relevante MeSH-vilkår
- Patologiske prosesser
- Neoplasmer etter histologisk type
- Neoplasmer
- Sykdom
- Benmargssykdommer
- Hematologiske sykdommer
- Forstadier til kreft
- Syndrom
- Myelodysplastiske syndromer
- Leukemi
- Preleukemi
- Myeloproliferative lidelser
- Myelodysplastiske-myeloproliferative sykdommer
- Fysiologiske effekter av legemidler
- Antineoplastiske midler
- Antineoplastiske midler, immunologiske
- Angiogenese-hemmere
- Angiogenesemodulerende midler
- Vekststoffer
- Veksthemmere
- Bevacizumab
Andre studie-ID-numre
- SUMC-MDA-ID-01152
- CDR0000068778 (Registeridentifikator: PDQ (Physician Data Query))
- MDA-ID-01152
- NCI-2771
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