- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT00963274
Bortezomib and Romidepsin in Patients With Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
Phase I Study of Bortezomib and Romidepsin in Patients With Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma, Indolent B-Cell Lymphoma, Peripheral T-Cell Lymphoma or Cutaneous T-Cell Lymphoma
Studieoversigt
Status
Intervention / Behandling
Detaljeret beskrivelse
OBJECTIVES:
Primary
- Determine the maximum tolerated dose (MTD) for the combination of bortezomib and romidepsin administered weekly x 3 every (q) 4wk in patients with CLL/SLL, indolent B-cell lymphoma, PTCL or cutaneous T-cell lymphoma (CTCL).
Secondary
- Determine safety and tolerance and describe the toxicities of the combination.
- Demonstrate adequate methods for the assessment of pharmacodynamic responses of CLL cells to the combination with respect to effects on NF-kappa B (nuclear RelA and processing of p52 as a marker of p100 processing), expression of the NF-kappa B-dependent proteins XIAP and Bcl-xL, and Bim, and document pharmacodynamic responses observed in the course of this study * Document the pharmacodynamic responses associated with this regimen in these patients.
- Document the anticancer activity of this regimen in these patients.
OUTLINE: Patients receive bortezomib IV over 3-5 seconds and romidepsin IV over 4 hours on days 1, 8, and 15. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.
Blood samples from patients with chronic lymphocytic leukemia are collected at baseline and after day 1 of course 1 of study treatment for pharmacodynamic and correlative laboratory studies.
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Fase 1
Kontakter og lokationer
Studiesteder
-
-
Illinois
-
Chicago, Illinois, Forenede Stater, 60611
- Robert H. Lurie Comprehensive Cancer Center, Northwestern University
-
-
Maryland
-
Baltimore, Maryland, Forenede Stater, 21201
- University of Maryland Greenebaum Cancer Center
-
-
North Carolina
-
Chapel Hill, North Carolina, Forenede Stater, 27599
- University of North Carolina
-
-
Tennessee
-
Nashville, Tennessee, Forenede Stater, 37232
- Vanderbilt-Ingram Cancer Center, Vanderbilt University
-
-
Virginia
-
Richmond, Virginia, Forenede Stater, 23298
- Virginia Commonwealth University/Massey Cancer Center
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
DISEASE CHARACTERISTICS:
* Diagnosis of 1 of the following:
- CLL or SLL, relapsed or refractory
Indolent B-cell lymphoma, relapsed or refractory:
- Follicle center lymphoma, follicular or diffuse
- Marginal zone B-cell lymphoma (splenic, nodal, extranodal [this includes mucosa associated lymphoid tissue (MALT)])
- Lymphoplasmacytic lymphoma
PTCL, relapsed or refractory:
- Anaplastic large cell lymphoma, anaplastic lymphoma kinase (ALK)-positive
- Anaplastic large cell lymphoma, ALK-negative
- Angioimmunoblastic T-cell lymphoma
- Enteropathy-associated T-cell lymphoma
- Extranodal natural killer (NK)/T-cell lymphoma, nasal type
- Hepatosplenic T-cell lymphoma
- PTCL, not otherwise specified (NOS)
- Subcutaneous panniculitis-like T-cell lymphoma
CTCL:
* CTCL with subtypes of mycosis fungoides Stage IB or higher, Sézary syndrome, or primary cutaneous anaplastic large cell lymphoma who have failed a previous systemic treatment, as per the following:
- Stage IA plaque, IB, or IIA: At least 4 prior conventional and/or experimental regimens (topical or systemic, including psoralen-ultraviolet light [PUVA] and systemic corticosteroids)
- Stage IIB, III, or IV: At least 1 prior systemic regimen (systemic corticosteroids alone or PUVA alone do not count as systemic regimens for this purpose) NOTE: Repeated use of the same regimen is considered 1 regimen
Prior allogeneic stem cell transplant is allowed provided that all of the following conditions are met:
- >= 6 months have elapsed since allogeneic transplant
- No Graft vs. Host Disease (GVHD) is present
- Not currently on immunosuppressive therapy
- No prior or concurrent CNS malignancy
PATIENT CHARACTERISTICS:
- ECOG performance status 0-1
- ANC > 1,500/mm^3
- Platelet count > 75,000/mm^3
- Hemoglobin > 7.5 g/dL (transfusion allowed)
- Serum creatinine ≤ 1.2 mg/dL or actual or calculated creatinine clearance > 60 mL/min
- AST and ALT ≤ 2.5 times upper limit of normal (ULN)
- Bilirubin ≤ ULN
- Serum potassium ≥ 3.5 mEq/L (supplementation allowed)
- Serum magnesium ≥ 1.7 mEq/L (supplementation allowed)
- Not pregnant or nursing
- Negative pregnancy test
- Fertile patients must use effective non-hormonal contraception
- Willing and able to comply with protocol requirements
- No prior severe allergic reactions to bortezomib, boron, mannitol, or romidepsin
- No progressing toxicity secondary to bortezomib
- No grade 1 peripheral neuropathy with pain or ≥ grade 2 peripheral neuropathy by NCI-CTCAE criteria (v4.0) within the past 14 days
No condition related to ischemic heart disease, heart failure, or the risk of torsades de pointes or sudden cardiac death, including any of the following:
- History of sustained ventricular tachycardia, ventricular fibrillation, torsades de pointes, or resuscitated cardiac arrest unless currently addressed with an implantable cardiac defibrillator
- Baseline heart rate > 140 beats per minute
- Known congenital long QT syndrome
- QTc interval > 480 milliseconds
- Type II second-degree atrio-ventricular (AV) block, third-degree AV block, or ventricular rate < 50 beats per minute
Myocardial infarction within the past 6 months
- Patients who have had a myocardial infarction 6-12 months ago are eligible provided they are asymptomatic and have a negative cardiac risk assessment (i.e., treadmill stress test, nuclear medicine stress test, or stress echocardiogram)
Angina upon ordinary physical activity
- Angina only with strenuous, rapid, or prolonged exertion allowed
ECG with evidence of cardiac ischemia, as defined by the following:
- ST depression of ≥ 2 mm, measured from isoelectric line to ST segment
- T-wave inversion ≥ 4 mm, measured from isoelectric line to peak of T-wave
- NYHA class II-IV congestive heart failure
- Known left ventricular ejection fraction < 40% by MUGA scan or < 50% by echocardiogram or MRI
- Known hypertrophic cardiomegaly or restrictive cardiomyopathy
- No uncontrolled hypertension, defined as persistent blood pressure ≥ 160/95 mm Hg despite medical management
- No clinically significant active infection, including known HIV infection or hepatitis B or C
- No other malignancy within the past 3 years except completely resected basal cell carcinoma or squamous cell carcinoma of the skin, in situ malignancy, or curatively treated low-risk prostate cancer
- No concurrent medical condition that, in the investigator's opinion, would compromise study treatment or assessment of toxicity
PRIOR CONCURRENT THERAPY:
- See Disease Characteristics
- At least 3 weeks since prior chemotherapy, radiation therapy or investigational agents. If steroids for cancer control have been used, patients must be off theses agents for at least 1 week before starting treatment. (Maintenance therapy for non-malignant disease with prednisone or steroid equivalent dose less than 10 mg/day is permitted)
- Prior allogeneic stem cell transplantation allowed provided all of the following conditions are met:
- Greater than or equal to 6 months have elapsed since allogeneic transplant
- No Graft vs. Host Disease (GVHD) is present
- More than 4 weeks since prior bortezomib
- No concurrent oral hormonal contraceptives
- No concurrent potent or moderate CYP3A4 inhibitors
- No concurrent anti-arrhythmic agents
No concurrent treatment with any drugs that are generally accepted to having a risk of causing torsades de pointes (class 1 drugs)
- Class 2 or 3 drugs allowed at the discretion of the investigator
- No other concurrent systemic therapy for the malignancy
- Concurrent warfarin (coumadin) allowed
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: N/A
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: bortezomib + romidepsin
Bortezomib via a short intravenous infusion (3-5 seconds) followed by romidepsin via a 4 hour intravenous infusion weekly x 3 every 4 weeks.
In order to identify appropriate doses, different subjects will be treated with different drug doses and observed for the effects, especially the side effects associated with higher doses.
|
Starting dose: 1.3 mg/sq m
Andre navne:
Starting dose: 8 mg/sq m
Andre navne:
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Maximum tolerated dose
Tidsramme: 2 years
|
Dose at which no more than 1 dose-limiting toxicity is observed in as many as 6 patients
|
2 years
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Pharmacodynamic responses
Tidsramme: 2 years
|
To explore candidate pharmacodynamic markers for use in subsequent phase II trials.
|
2 years
|
Samarbejdspartnere og efterforskere
Sponsor
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Thomas C. Shea, MD, UNC Lineberger Comprehensive Cancer Center
- Studiestol: Steven Grant, MD, Virginia Commonwealth University
- Ledende efterforsker: Sho Ma, MD, PhD, Northwestern University & Robert H Lurie Comprehensive Cancer Center
- Ledende efterforsker: Amy Kimball, MD, PhD, University of Maryland Greenebaum Cancer Center
- Ledende efterforsker: Nishitha Reddy, MBBS, Vanderbilt-Ingram Cancer Center, Vanderbilt University
Publikationer og nyttige links
Hjælpsomme links
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Skøn)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
- stadium I kronisk lymfatisk leukæmi
- ikke-sammenhængende trin II lille lymfocytisk lymfom
- tilbagevendende lille lymfocytisk lymfom
- stadium I lille lymfatisk lymfom
- stadium III lille lymfatisk lymfom
- stadium IV lille lymfocytisk lymfom
- sammenhængende fase II lille lymfocytisk lymfom
- ekstranodal marginal zone B-celle lymfom af slimhinde-associeret lymfoid væv
- nodal marginal zone B-celle lymfom
- refraktær kronisk lymfatisk leukæmi
- stadium II kronisk lymfatisk leukæmi
- stadium III kronisk lymfatisk leukæmi
- stadium IV kronisk lymfatisk leukæmi
- angioimmunoblastisk T-celle lymfom
- anaplastisk storcellet lymfom
- voksen nasal type ekstranodal NK/T-celle lymfom
- perifert T-celle lymfom
- hepatosplenisk T-celle lymfom
Yderligere relevante MeSH-vilkår
- Sygdomme i immunsystemet
- Neoplasmer efter histologisk type
- Neoplasmer
- Lymfoproliferative lidelser
- Lymfesygdomme
- Immunproliferative lidelser
- Lymfom, Non-Hodgkin
- Leukæmi, B-celle
- Lymfom
- Leukæmi
- Leukæmi, lymfatisk, kronisk, B-celle
- Leukæmi, lymfoid
- Lymfom, T-celle
- Antineoplastiske midler
- Antibiotika, antineoplastisk
- Bortezomib
- Romidepsin
Andre undersøgelses-id-numre
- MCC-12215 (Anden identifikator: VCU Massey Cancer Center)
- P30CA016059 (U.S. NIH-bevilling/kontrakt)
- R21CA137823 (U.S. NIH-bevilling/kontrakt)
- CDR0000652509 (Registry Identifier: PDQ)
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .