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- Klinische proef NCT01078961
An Expanded Cohort Trial of Bortezomib and Sorafenib in Advanced Malignant Melanoma
7 juni 2016 bijgewerkt door: Ryan Sullivan, M.D., Massachusetts General Hospital
A Phase I Expanded Cohort Trial of Bortezomib and Sorafenib in Advanced Malignant Melanoma
This research study involves the use of two investigational drugs: sorafenib and bortezomib.
Sorafenib is designed to stop the growth of cells caused by changes associated with cancer.
Bortezomib is designed to stop cancer cells from getting rid of waste products.
This causes the cells to build up toxic levels of waste that leads to cell death.
In the laboratory, the combination of sorafenib and bortezomib has been shown to fight cancer cells better than either drug alone.
We are looking to determine if the combination of sorafenib and bortezomib is a safe treatment for patients with advanced melanoma.
The effectiveness of this combination will also be assessed.
Studie Overzicht
Toestand
Voltooid
Conditie
Interventie / Behandeling
Gedetailleerde beschrijving
- Since we are looking for the highest dose of the study drug that can be administered safely without severe or unmanageable side effects in participants that have melanoma, not everyone who participates will receive the same dose of the study drug. The dose participants will get will depend upon the number of participants who have been enrolled in the study before and how well they tolerated their doses.
- Each treatment cycle lasts 28 days. Participants will take sorafenib orally twice a day and will receive bortezomib as an out-patient intravenous injection on Days 1, 8 and 15 of every cycle.
- At the end of each treatment cycle, participants will be examined to determine whether their disease has worsened, improved or stayed the same, and to see if they are experiencing any side effects of treatment. The following tests will be done at these visits: physical examination, vital signs, blood tests and scans (repeated every 2 months).
- Once the maximum tolerated dose of sorafenib and bortezomib have been determined, an additional 12 participants will be enrolled in this study. This is called the expansion cohort of this study. Participants enrolled in this cohort will be required to undergo a biopsy of the tumor lesion before they start study treatment and an additional biopsy after you start study treatment.
Studietype
Ingrijpend
Inschrijving (Werkelijk)
11
Fase
- Fase 1
Contacten en locaties
In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.
Studie Locaties
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Massachusetts
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Boston, Massachusetts, Verenigde Staten, 02215
- Beth Israel Deaconess Medical Center
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Boston, Massachusetts, Verenigde Staten, 02115
- Dana-Farber Cancer Institute
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Boston, Massachusetts, Verenigde Staten, 02114
- Massachusetts General Hospital
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Deelname Criteria
Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
18 jaar en ouder (Volwassen, Oudere volwassene)
Accepteert gezonde vrijwilligers
Nee
Geslachten die in aanmerking komen voor studie
Allemaal
Beschrijving
Inclusion Criteria:
- Histological or cytological confirmation of malignant melanoma that is metastatic or unresectable
- Measurable disease, defined as at least one lesion that can be accurately measured in at least one dimension as 10mm or greater with spiral CT scan
- Patients may have received up to 4 prior treatments for their disease including immunotherapies such as high-dose interleukin 2 and antibodies directed against the human cytotoxic T-lymphocyte antigen 4
- 18 years of age or older
- Life expectancy of greater than three months
- ECOG Performance status of 0 or 1
- Adequate organ and marrow function as outlined in the protocol
- Women of childbearing potential must have a negative serum pregnancy test performed within 7 days prior to the start of treatment
- INT < 1.5 or a PT/PTT within normal limits. Patients receiving anti-coagulation treatment wih an agent such as warfarin or heparin may be allowed to participate. For patients on warfarin, the INR should be measured prior to initiation of sorafenib and monitored at least weekly, or as defined by the local standard of care, until INR is stable
- Women of child-bearing potential and men must agree to use adequate contraception prior to study entry and for the duration of study participation.
Exclusion Criteria:
- Chemotherapy or radiotherapy within 4 weeks (6 weeks for nitrosoureas or mitomycin C) prior to entering the study or those who have not recovered from adverse events dur to agents administered more than 4 weeks earlier
- Participants may not be receiving any other study agents
- Known, active CNS disease, including primary brain tumor, seizures not controlled with standard medical therapy, any unstable or untreated brain metastasis, or history of stroke within the past 12 months
- Prior therapy with bortezomib, sorafenib, or other proteasome inhibitor
- History of allergic reactions attributed to compounds of similar chemical or biologic composition to sorafenib and bortezomib
- Participants receiving any medications or substances that are inducers of CYP3A4
- Known cardiac disease including congestive heart failure > class II NHYA, unstable angina or new onset angina, myocardial infarction within the past 6 months, or electrocardiographic evidence of acute ischemic or active conduction system abnormalities. Prior to study entry, any ECG abnormality at screening has to be documented by the investigator as not medically relevant
- Cardiac ventricular arrhythmias requiring anti-arrhythmic therapy
- Uncontrolled intercurrent illness
- Pregnant women
- Individuals with a history of a different malignancy are ineligible except for the circumstances outlined in the protocol
- HIV-positive individuals on combination antiretroviral therapy
- Uncontrolled hypertension despite optimal medical management
- Thrombolic or embolic events
- Pulmonary hemorrhage/bleeding event CTCAE Grade 2 or greater within 4 weeks of first dose of study drug
- Any other hemorrhage/bleeding event CTCAE Grade 3 or greater within 4 weeks of first dose of study drug
- Serious non-healing wound, ulcer or bone fracture
- Evidence or history of bleeding diathesis or coagulopathy
- Major surgery, open biopsy or significant traumatic injury within 4 weeks of first study drug
- Any condition that impairs patient's ability to swallow whole pills
- Any malabsorption problem
- Known hypersensitivity to boron or mannitol
- Grade 2 or greater peripheral neuropathy within 14 days before enrollment
Studie plan
Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.
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: Dosis escalatie
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Given intravenously on days 1, 8 and 15 of each 28 day cycle
400mg taken orally twice a day
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Maximally tolerated dose
Tijdsspanne: 2 years
|
To determine the maximally tolerated dose of weekly bortezomib in combination with 400mg twice daily sorafenib.
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2 years
|
|
Document and summarize toxicities
Tijdsspanne: 2 years
|
To document and summarize the toxicities of weekly bortezomib in combination with 400mg twice daily sorafenib
|
2 years
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Anti-tumor activity
Tijdsspanne: 2 years
|
To document the anti-tumor activity of weekly bortezomib in combination with sorafenib by describing the six-month progression free survival, one-year progression-free survival, and objective response rate.
|
2 years
|
Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Sponsor
Medewerkers
Onderzoekers
- Hoofdonderzoeker: Ryan J. Sullivan, MD, Massachusetts General Hospital
Publicaties en nuttige links
De persoon die verantwoordelijk is voor het invoeren van informatie over het onderzoek stelt deze publicaties vrijwillig ter beschikking. Dit kan gaan over alles wat met het onderzoek te maken heeft.
Studie record data
Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.
Bestudeer belangrijke data
Studie start
1 september 2010
Primaire voltooiing (Werkelijk)
1 februari 2013
Studie voltooiing (Werkelijk)
1 juni 2016
Studieregistratiedata
Eerst ingediend
1 maart 2010
Eerst ingediend dat voldeed aan de QC-criteria
1 maart 2010
Eerst geplaatst (Schatting)
2 maart 2010
Updates van studierecords
Laatste update geplaatst (Schatting)
8 juni 2016
Laatste update ingediend die voldeed aan QC-criteria
7 juni 2016
Laatst geverifieerd
1 januari 2013
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
- Neoplasmata per histologisch type
- Neoplasmata
- Neuro-ectodermale tumoren
- Neoplasmata, kiemcellen en embryonaal
- Neoplasmata, zenuwweefsel
- Neuro-endocriene tumoren
- Nevi en melanomen
- Melanoma
- Moleculaire mechanismen van farmacologische werking
- Enzymremmers
- Antineoplastische middelen
- Proteïnekinaseremmers
- Sorafenib
- Bortezomib
Andere studie-ID-nummers
- 09-443
- X05297 (Andere identificatie: Millennium Pharmaceuticals)
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .