- ICH GCP
- US-Register für klinische Studien
- Klinische Studie 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
Studienübersicht
Status
Intervention / Behandlung
Detaillierte Beschreibung
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.
Studientyp
Einschreibung (Tatsächlich)
Phase
- Phase 1
Kontakte und Standorte
Studienorte
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Illinois
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Chicago, Illinois, Vereinigte Staaten, 60611
- Robert H. Lurie Comprehensive Cancer Center, Northwestern University
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Maryland
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Baltimore, Maryland, Vereinigte Staaten, 21201
- University of Maryland Greenebaum Cancer Center
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North Carolina
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Chapel Hill, North Carolina, Vereinigte Staaten, 27599
- University of North Carolina
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Tennessee
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Nashville, Tennessee, Vereinigte Staaten, 37232
- Vanderbilt-Ingram Cancer Center, Vanderbilt University
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Virginia
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Richmond, Virginia, Vereinigte Staaten, 23298
- Virginia Commonwealth University/Massey Cancer Center
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Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Beschreibung
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
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: N / A
- Interventionsmodell: Einzelgruppenzuweisung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
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Experimental: 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.
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Starting dose: 1.3 mg/sq m
Andere Namen:
Starting dose: 8 mg/sq m
Andere Namen:
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Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Maximum tolerated dose
Zeitfenster: 2 years
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Dose at which no more than 1 dose-limiting toxicity is observed in as many as 6 patients
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2 years
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Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Pharmacodynamic responses
Zeitfenster: 2 years
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To explore candidate pharmacodynamic markers for use in subsequent phase II trials.
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2 years
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Mitarbeiter und Ermittler
Sponsor
Mitarbeiter
Ermittler
- Hauptermittler: Thomas C. Shea, MD, UNC Lineberger Comprehensive Cancer Center
- Studienstuhl: Steven Grant, MD, Virginia Commonwealth University
- Hauptermittler: Sho Ma, MD, PhD, Northwestern University & Robert H Lurie Comprehensive Cancer Center
- Hauptermittler: Amy Kimball, MD, PhD, University of Maryland Greenebaum Cancer Center
- Hauptermittler: Nishitha Reddy, MBBS, Vanderbilt-Ingram Cancer Center, Vanderbilt University
Publikationen und hilfreiche Links
Nützliche Links
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Tatsächlich)
Primärer Abschluss (Tatsächlich)
Studienabschluss (Tatsächlich)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Schätzen)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
- Chronische lymphatische Leukämie im Stadium I
- nicht zusammenhängendes kleines lymphozytisches Lymphom im Stadium II
- rezidivierendes kleines lymphozytisches Lymphom
- kleines lymphozytisches Lymphom im Stadium I
- Kleines lymphozytisches Lymphom im Stadium III
- kleines lymphozytisches Lymphom im Stadium IV
- angrenzendes kleines lymphozytisches Lymphom im Stadium II
- Extranodales Marginalzonen-B-Zell-Lymphom des Schleimhaut-assoziierten lymphatischen Gewebes
- Nodales Marginalzonen-B-Zell-Lymphom
- refraktäre chronische lymphatische Leukämie
- Chronische lymphatische Leukämie im Stadium II
- Chronische lymphatische Leukämie im Stadium III
- Chronische lymphatische Leukämie im Stadium IV
- angioimmunoblastisches T-Zell-Lymphom
- anaplastisches großzelliges Lymphom
- extranodales NK/T-Zell-Lymphom vom nasalen Typ bei Erwachsenen
- peripheres T-Zell-Lymphom
- hepatosplenisches T-Zell-Lymphom
Zusätzliche relevante MeSH-Bedingungen
- Erkrankungen des Immunsystems
- Neubildungen nach histologischem Typ
- Neubildungen
- Lymphoproliferative Erkrankungen
- Lymphatische Erkrankungen
- Immunproliferative Erkrankungen
- Lymphom, Non-Hodgkin
- Leukämie, B-Zell
- Lymphom
- Leukämie
- Leukämie, lymphozytär, chronisch, B-Zell
- Leukämie, lymphatisch
- Lymphom, T-Zell
- Antineoplastische Mittel
- Antibiotika, antineoplastische
- Bortezomib
- Romidepsin
Andere Studien-ID-Nummern
- MCC-12215 (Andere Kennung: VCU Massey Cancer Center)
- P30CA016059 (US NIH Stipendium/Vertrag)
- R21CA137823 (US NIH Stipendium/Vertrag)
- CDR0000652509 (Registrierungskennung: PDQ)
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