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- Klinische proef NCT01164709
Nelfinavir Mesylate and Bortezomib in Treating Patients With Relapsed or Progressive Advanced Hematologic Cancer
Phase I Trial of Nelfinavir and Bortezomib in Advanced Hematologic Malignancies
RATIONALE: Nelfinavir mesylate and bortezomib may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Bortezomib may also stop the growth of hematologic cancer by blocking blood flow to the cancer. Giving nelfinavir mesylate together with bortezomib may kill more cancer cells.
PURPOSE: This phase I trial is studying the side effects and best dose of nelfinavir mesylate when given together with bortezomib in treating patients with relapsed or progressive advanced hematologic cancer.
Studie Overzicht
Toestand
Conditie
Interventie / Behandeling
Gedetailleerde beschrijving
OBJECTIVES:
- To assess the safety of nelfinavir mesylate in combination with bortezomib in patients with relapsed or progressive, advanced hematologic malignancies.
- To establish the phase II recommended dose of nelfinavir mesylate in these patients.
OUTLINE: This is a multicenter, dose-escalation study of nelfinavir mesylate.
Patients receive oral nelfinavir mesylate twice daily on days 1-21 and bortezomib IV on days 8, 11, 15, and 18 in course 1. Course 1 has a duration of 28 days. Beginning in course 2, patients receive oral nelfinavir mesylate twice daily on days 1-14 and bortezomib IV on days 1, 4, 8, and 11. Treatment repeats every 21 days for 2 courses. Patients with responding disease may continue to receive nelfinavir mesylate and bortezomib for up to 4 additional courses.
After completion of study treatment, patients are followed for 30 days.
Studietype
Inschrijving (Werkelijk)
Fase
- Fase 1
Contacten en locaties
Studie Locaties
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-
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Bern, Zwitserland, CH-3010
- Inselspital Bern
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Chur, Zwitserland, CH-7000
- Kantonsspital Graubuenden
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Lausanne, Zwitserland, CH-1011
- Centre Hospitalier Universitaire Vaudois
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St. Gallen, Zwitserland, CH-9007
- Kantonsspital - St. Gallen
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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:
Diagnosed with advanced hematologic malignancies meeting the following criteria:
Multiple myeloma
- Received ≥ 2 lines of prior chemotherapy (induction chemotherapy followed by high-dose chemotherapy and autologous stem cell transplant with or without maintenance therapy is considered one line of therapy)
- Acute myeloid leukemia
- Acute lymphoblastic leukemia
- Diffuse large B-cell lymphoma
- Hodgkin lymphoma
- Mantle cell lymphoma
Mature T- and NK-cell neoplasms restricted to the following WHO-defined entities:
- T-cell prolymphocytic leukemia
- T-cell large granular lymphocytic leukemia
- Aggressive NK-cell leukemia
- Adult T-cell leukemia/lymphoma
- Extranodal NK/T-cell lymphoma (nasal type)
- Mycosis fungoides
- Sézary syndrome
- Primary CD30-positive T-cell lymphoproliferative disorders
- Primary cutaneous anaplastic large cell lymphoma
- Primary cutaneous gamma-delta T-cell lymphoma
- Peripheral T-cell lymphoma (not otherwise specified)
- Angioimmunoblastic T-cell lymphoma
- Anaplastic large cell lymphoma (ALK-positive/ALK-negative)
- Grade 3B follicular lymphoma
- Relapsed following or progressed during standard therapy
Meeting the following criteria:
- Standard intensive therapy is not feasible
- Current disease state for which there is no standard effective therapy
- Refused standard therapy where no curative option exists
Measurable disease, defined as the following:
- Myeloma: measurable serum monoclonal protein > 1 g/dL for IgG, or > 0.5 g/dL for IgA, IgM or IgD, or difference between involved and uninvolved free light chain levels in serum > 100 mg/L
- Lymphoma: must have ≥ 1 lesion measurable by CT (longest diameter ≥ 15 mm)
- Acute leukemia: ≥ 20% blasts in bone marrow or in peripheral blood (≥ 200/mL blasts in peripheral blood)
- No HIV-associated lymphoma
PATIENT CHARACTERISTICS:
- WHO performance status 0-2
- Absolute neutrophil count ≥ 1,500/mm³
- Platelet count ≥ 75,000/mm³ (if bone marrow impairment, ≥ 20,000/mm^3)
- Hemoglobin > 80 g/L (if considered to be caused by the underlying hematologic malignancy or bone marrow impairment, > 80 g/L after transfusion)
- Bilirubin ≤ 1.5 times upper limit of normal (ULN) (if suspected hemolysis, direct bilirubin ≤ 1.5 times ULN)
- ALT ≤ 2.5 times ULN
- Calculated creatinine clearance > 30 mL/min
- Not pregnant or nursing
- Negative pregnancy test
- Fertile patients must use effective contraception during and for 12 months after completion of study treatment
- Willing and capable to comply with an oral regimen
- Capable of understanding information given by the investigator on the trial
- Able to adhere and remain in geographic proximity to allow proper staging, treatment, and followup
- No other non-hematologic malignancy within the past 5 years, except adequately treated cervical carcinoma in situ or localized nonmelanoma skin cancer
- No known chronic hepatitis B or C infection or known HIV infection
No serious underlying medical condition (at the judgment of the investigator) which would impair the ability of the patient to participate in the trial, including any of the following:
- Active autoimmune disease
- Uncontrolled diabetes
- Ongoing or active infection
- Symptomatic congestive heart failure
- Unstable angina pectoris
- Cardiac arrhythmia
- Psychiatric disorder
- No myocardial infarction within the past 6 months
- No polyneuropathy > grade 1 significantly interfering with activities of daily living or painful polyneuropathy
- No known hypersensitivity to trial drugs or hypersensitivity to any other component of the trial drugs
PRIOR CONCURRENT THERAPY:
- See Disease Characteristics
- No more than 4 prior lines of chemotherapeutic regimens (induction chemotherapy followed by high-dose chemotherapy and autologous stem cell transplant with or without maintenance therapy is considered one line of therapy)
- More than 30 days since prior treatment in a clinical trial
More than 30 days since prior and no concurrent chemotherapy or biologic agents
- For patients with acute leukemia, hydroxyurea may be given up to 48 hours before first administration of the trial treatment, and low dose cytarabine (up to 20 mg/m^2) and mitoxantrone up to 20 mg up to 14 days before first dosing
- At least 1 week since prior and no concurrent CYP3A4 modulators
- No concurrent other experimental drugs
- No concurrent radiotherapy
- No concurrent antineoplastic therapy with chemotherapeutic or biologic agents
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: NVT
- Interventioneel model: Opdracht voor een enkele groep
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Experimenteel: bortezomib + nelfinavir
escalation 3 by 3 cohorts
|
Bortezomib i.v., day 8, 11, 15, 18; 1.3 mg/m2
Andere namen:
p.o., days 1 to 21; dose level: (625), 1250, 1875, or 2500 mg, 2x/d
Andere namen:
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
|---|---|
|
Dose limiting toxicity
Tijdsspanne: during first cycle
|
during first cycle
|
Secundaire uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
|---|---|
|
Objective response
Tijdsspanne: during treatment
|
during treatment
|
|
Adverse events according to NCI CTCAE v.4.0
Tijdsspanne: during treatment + 30 days
|
during treatment + 30 days
|
Medewerkers en onderzoekers
Onderzoekers
- Studie stoel: Christoph Driessen, MD, Cantonal Hospital of St. Gallen
- Hoofdonderzoeker: Dagmar Hess, MD, Cantonal Hospital of St. Gallen
- Hoofdonderzoeker: Roger von Moos, MD, Kantonsspital Graubuenden
- Hoofdonderzoeker: Thomas Pabst, MD, University Hospital Inselspital, Berne
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 (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
- stadium III volwassen diffuus grootcellig lymfoom
- stadium IV graad 3 folliculair lymfoom
- stadium IV volwassen diffuus grootcellig lymfoom
- recidiverend graad 3 folliculair lymfoom
- recidiverend diffuus grootcellig lymfoom bij volwassenen
- volwassen acute myeloïde leukemie met 11q23 (MLL) afwijkingen
- volwassen acute myeloïde leukemie met inv(16)(p13;q22)
- volwassen acute myeloïde leukemie met t(15;17)(q22;q12)
- volwassen acute myeloïde leukemie met t(16;16)(p13;q22)
- volwassen acute myeloïde leukemie met t(8;21)(q22;q22)
- secundaire acute myeloïde leukemie
- recidiverende volwassen acute myeloïde leukemie
- recidiverend volwassen Hodgkin-lymfoom
- stadium III graad 3 folliculair lymfoom
- stadium III mantelcellymfoom
- stadium IV mantelcellymfoom
- terugkerend mantelcellymfoom
- stadium III volwassen Hodgkin-lymfoom
- stadium IV volwassen Hodgkin-lymfoom
- stadium III cutaan T-cel non-Hodgkin-lymfoom
- stadium IV cutaan T-cel non-Hodgkin-lymfoom
- recidiverend cutaan T-cel non-Hodgkin-lymfoom
- stadium III volwassen T-cel leukemie/lymfoom
- stadium IV volwassen T-cel leukemie/lymfoom
- recidiverende volwassen T-cel leukemie/lymfoom
- angioimmunoblastisch T-cellymfoom
- anaplastisch grootcellig lymfoom
- stadium III mycosis fungoides/Sezary-syndroom
- stadium IV mycosis fungoides/Sezary-syndroom
- recidiverende mycosis fungoides/Sezary-syndroom
- extranodaal NK/T-cellymfoom van het volwassen neustype
- refractair multipel myeloom
- recidiverende volwassen acute lymfatische leukemie
- prolymfocytische leukemie
- perifeer T-cellymfoom
- T-cel grote granulaire lymfocytenleukemie
- aggressive NK-cell leukemia
Aanvullende relevante MeSH-voorwaarden
- Hart-en vaatziekten
- Vaatziekten
- Ziekten van het immuunsysteem
- Neoplasmata per histologisch type
- Lymfoproliferatieve aandoeningen
- Lymfatische ziekten
- Immunoproliferatieve aandoeningen
- Hematologische ziekten
- Hemorragische aandoeningen
- Hemostatische aandoeningen
- Paraproteïnemieën
- Bloed eiwit stoornissen
- Neoplasmata
- Lymfoom
- Multipel myeloom
- Neoplasmata, plasmacel
- Leukemie
- Plasmacytoom
- Moleculaire mechanismen van farmacologische werking
- Anti-infectieuze middelen
- Antivirale middelen
- Enzymremmers
- Anti-hiv-middelen
- Antiretrovirale middelen
- Antineoplastische middelen
- Proteaseremmers
- HIV-proteaseremmers
- Virale proteaseremmers
- Bortezomib
- Nelfinavir
Andere studie-ID-nummers
- SAKK 65/08
- SWS-SAKK-65/08
- EU-21051
- SWS-SAKK-JC26866138LYM1005
- CDR0000681442 (Register-ID: CDR0000681442)
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