- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT00349206
Sorafenib and Temsirolimus in Treating Patients With Metastatic, Recurrent, or Unresectable Melanoma
Phase 1 Study of the Combination of BAY 43-9006 (Sorafenib) and CCI-779 (Temsirolimus) in Patients With Metastatic Melanoma
Studieoversigt
Status
Intervention / Behandling
Detaljeret beskrivelse
PRIMARY OBJECTIVES:
I. To determine the maximum tolerated dose of temsirolimus when administered with sorafenib in patients with metastatic, recurrent, or unresectable melanoma.
II. To determine the safety and toxicity of this regimen in these patients.
SECONDARY OBJECTIVES:
I. To Determine the population pharmacokinetics of this regimen in these patients.
II. To correlate tumor and blood biomarkers with clinical outcome in patients treated with this regimen.
OUTLINE: This is a multicenter, phase I, dose-escalation study followed by a phase II, open-label study (2005-0215).
Patients receive temsirolimus IV over 30 minutes on days 1, 8, 15, and 22 and oral sorafenib once or twice daily on days 1-28. Treatment course repeats every 28 days for up to 6 courses in the absence of disease progression or unacceptable toxicity.
After completion of study treatment, patients are followed every 3-6 months.
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Fase 1
Kontakter og lokationer
Studiesteder
-
-
Texas
-
Houston, Texas, Forenede Stater, 77030
- M D Anderson Cancer Center
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Criteria:
- Histologically or cytologically confirmed melanoma, meeting 1 of the following criteria: recurrent or unresectable stage III disease, stage IV disease, non-choroidal origin.
- Tumor must be accessible to biopsy unless appropriate tumor sample collection has occurred within the past 3 months and patient agrees to provide these samples for this study.
- ECOG performance status 0-1.
- Bilirubin normal
- Creatinine normal or creatinine clearance ≥ 60 mL/min
- Not pregnant or nursing
- Negative pregnancy test
- Fertile patients must use effective contraception during and for 30 days after completion of study treatment.
- No history of allergic reactions attributed to compounds of similar chemical or biological composition to sorafenib or temsirolimus.
- No uncontrolled hypertension, defined as systolic blood pressure > 140 mm Hg on 2 separate days < 1 week prior to study entry OR diastolic pressure > 90 mm Hg on 2 separate days < 1 week prior to study entry.
- No evidence of bleeding diathesis or coagulopathy.
- No condition that would impair the ability to swallow pills (e.g., gastrointestinal tract disease resulting in an inability to take oral medication; requirement for IV alimentation; or active peptic ulcer disease).
- No uncontrolled illness including, but not limited to, any of the following: ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia or psychiatric illness or social situations that would limit study compliance.
- No traumatic injury within the past 3 weeks.
- No more than 1 prior systemic chemotherapy regimen for metastatic melanoma (Phase II).
- No prior sorafenib, temsirolimus, or any other agents targeting raf, vascular endothelial growth factor (VEGF)/VEGF receptor, or mTOR (Phase II).
- No prior surgical procedures affecting absorption.
- At least 3 weeks since prior major surgery.
- At least 4 weeks since prior chemotherapy (6 weeks for nitrosoureas or mitomycin C) for melanoma and recovered.
- At least 4 weeks since prior radiotherapy and recovered.
- Prior biologic or immunotherapeutic regimens allowed.
- Prior regional chemotherapy regimens (e.g., isolated limb perfusion) allowed but only 1 prior regional chemotherapy regimen allowed if all target lesions are within the prior regional treatment field.
- No concurrent enzyme-inducing antiepileptic drugs including, but not limited to, any of the following: phenytoin, carbamazepine, phenobarbital, rifampin or Hypericum perforatum (St. John's wort).
- No concurrent prophylactic hematopoietic colony-stimulating factors.
- No other concurrent investigational agents.
- No other concurrent anticancer agents or therapies for this cancer.
- No concurrent full-dose anticoagulation (i.e., warfarin, IV heparin, or low-molecular weight heparin).
- No concurrent grapefruit or grapefruit juice.
- No concurrent combination antiretroviral therapy for HIV-positive patients.
- Concurrent prophylactic anticoagulation therapy (e.g., low-dose warfarin) allowed provided PT INR < 1.1 times ULN.
- Unidimensionally measurable disease >= 20 mm by conventional techniques or >= 10 mm by spiral CT scan (longest diameter to be recorded) and margins of visible cutaneous metastatic lesions should be clearly defined and measured in at least one dimension as >= 10 mm.
- No known brain metastases unless the following criteria are met: no radiographical evidence of recurrences in the brain >= 3 months after complete resection of the brain metastases, asymptomatic brain metastases stable for >= 3 months since whole-brain radiation therapy and/or stereotactic radiosurgery and must not require steroid for brain metastases.
- WBC >= 3,000/mm³
- Absolute neutrophil count >= 1,500/mm³
- Platelet count >= 100,000/mm³
- Serum cholesterol =< 350 mg/dL
- Triglycerides =< 400 mg/dL
- AST/ALT =< 2.5 times upper limit of normal.
- No peripheral neuropathy > grade 2.
- At least 5 years since prior chemotherapy for other types of cancer.
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: Arm 1
Patients receive temsirolimus IV over 30 minutes on days 1, 8,15, and 22 and oral sorafenib once or twice daily on days 1-28.
|
Gives oralt
Andre navne:
Givet IV
Andre navne:
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Maximum tolerated dose of CCI-779 in combination with BAY43-9006 (Phase I) determined by DLT assessed by NCI Common Terminology Criteria for Adverse Events (CTCAE) version 4.0 (Phase I)
Tidsramme: 28 days
|
28 days
|
|
Objective response rate (complete response and partial response) CCI-779 in combination with BAY43-9006 (Phase II)
Tidsramme: Up to 5 years
|
Up to 5 years
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Progressionsfri overlevelse
Tidsramme: Varigheden af tiden fra behandlingsstart til datoen for første tegn på progression eller datoen for sidste opfølgning for patienter, der ikke udvikler sig, vurderet op til 5 år
|
Kaplan-Meier livstabelmetoder og Cox proportional hazards regressionsmodellering vil blive brugt til at analysere progressionsfri overlevelse og samlet overlevelse.
|
Varigheden af tiden fra behandlingsstart til datoen for første tegn på progression eller datoen for sidste opfølgning for patienter, der ikke udvikler sig, vurderet op til 5 år
|
|
Samlet overlevelse
Tidsramme: 5 år
|
Kaplan-Meier livstabelmetoder og Cox proportional hazards regressionsmodellering vil blive brugt til at analysere progressionsfri overlevelse og samlet overlevelse.
|
5 år
|
|
Ikke-kompartmentelle farmakokinetiske parametre for BAY43-9006 og CCI-779 estimeret ved hjælp af en valideret kommerciel software
Tidsramme: Uge 1 og 3
|
Maksimal koncentration (Cmax) og tid til Cmax (tmax) vil være de observerede værdier.
Areal under plasmakoncentration-tid-kurven fra nul til sidste observerbare tid (AUClast).
|
Uge 1 og 3
|
Samarbejdspartnere og efterforskere
Sponsor
Efterforskere
- Ledende efterforsker: Kevin Kim, M.D. Anderson Cancer Center
Datoer for undersøgelser
Studer store datoer
Studiestart
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 (Skøn)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
- Neoplasmer efter histologisk type
- Neoplasmer
- Neuroektodermale tumorer
- Neoplasmer, kimceller og embryonale
- Neoplasmer, nervevæv
- Neuroendokrine tumorer
- Nevi og melanomer
- Melanom
- Lægemidlers fysiologiske virkninger
- Molekylære mekanismer for farmakologisk virkning
- Anti-infektionsmidler
- Enzymhæmmere
- Antineoplastiske midler
- Immunsuppressive midler
- Immunologiske faktorer
- Antibakterielle midler
- Proteinkinasehæmmere
- Antibiotika, antineoplastisk
- Antifungale midler
- Sorafenib
- Sirolimus
Andre undersøgelses-id-numre
- NCI-2009-00131 (Registry Identifier: CTRP (Clinical Trial Reporting Program))
- P30CA016672 (U.S. NIH-bevilling/kontrakt)
- N01CM62202 (U.S. NIH-bevilling/kontrakt)
- CDR0000480157
- 2005-0215 (Anden identifikator: M D Anderson Cancer Center)
- 7149 (Anden identifikator: CTEP)
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 .