- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT00397488
Sunitinib in Treating Patients With Progressive Metastatic Transitional Cell Cancer of the Urothelium
Phase II Study of Sunitinib in Metastatic Transitional Cell Carcinoma of the Urothelium
RATIONALE: Sunitinib may stop the growth of tumor cells by blocking some of the enzymes needed for their growth and by blocking blood flow to the tumor.
PURPOSE: This phase II trial is studying how well sunitinib works in treating patients with progressive metastatic transitional cell cancer of the urothelium.
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
OBJECTIVES:
Primary
- Determine the response rate in patients with progressive metastatic transitional cell carcinoma of the urothelium treated with sunitinib malate.
- Determine the safety of this regimen in these patients.
Secondary
Determine the time to disease progression in patients treated with this regimen.
- To determine time to tumor progression (TTP) for sunitinib malate on a continuous dosing schedule for treatment of metastatic urothelial carcinoma.
- To estimate sunitinib and SU012662 trough plasma concentration (Ctrough) data for the continuous daily schedule and to determine potential association with efficacy and safety.
Tipo di studio
Iscrizione (Effettivo)
Fase
- Fase 2
Contatti e Sedi
Luoghi di studio
-
-
New York
-
New York, New York, Stati Uniti, 10021
- Memorial Sloan-Kettering Cancer Center
-
-
Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
DISEASE CHARACTERISTICS:
Histologically confirmed transitional cell carcinoma of the urothelium, including 1 of the following sites:
- Bladder
- Urethra
- Ureter
- Renal pelvis
Progressive metastatic disease
- Progressive disease defined as new or progressive lesions on cross-sectional imaging
- Progressed despite prior treatment with cytotoxic chemotherapy
- Measurable disease
Previously treated disease, as defined by the following:
- Received treatment with 1-4 cytotoxic agents
Prior therapy must have included ≥ 1 of the following:
- Cisplatin
- Carboplatin
- Paclitaxel
- Docetaxel
- Gemcitabine hydrochloride
- Prior cytotoxic agents in the perioperative or metastatic setting allowed and may have been administered sequentially (e.g., first-line treatment followed by second-line treatment at time of progression) or all as part of a single regimen
- No symptomatic CNS metastases
PATIENT CHARACTERISTICS:
- Karnofsky performance status 60-100%
- Absolute neutrophil count ≥ 1,000/mm³
- Platelet count ≥ 100,000/mm³
- Hemoglobin ≥ 8.0 g/dL
- Bilirubin ≤ 1.5 mg/dL (unless Gilbert's disease is present)
- AST and ALT ≤ 2.5 times upper limit of normal (ULN) (5 times ULN if liver function abnormalities are due to underlying malignancy)
- Creatinine ≤ 2.0 mg/dL
- Not pregnant or nursing
- Negative pregnancy test
- Fertile patients must use effective contraception
None of the following within the past 6 months:
- Myocardial infarction
- Severe or unstable angina
- Coronary or peripheral artery bypass graft
- Symptomatic congestive heart failure
- Cerebrovascular accident or transient ischemic attack
- Pulmonary embolism
- No ongoing cardiac dysrhythmias ≥ grade 2
- No prolonged QTc interval on baseline ECG
- No uncontrolled hypertension, defined as blood pressure > 150/100 mm Hg despite optimal medical therapy
- No preexisting thyroid abnormality (i.e., thyroid function tests that cannot be maintained in the normal range with medication)
- No known HIV- or AIDS-related illness or other active infection
PRIOR CONCURRENT THERAPY:
- See Disease Characteristics
- At least 4 weeks since prior radiotherapy or chemotherapy
- At least 4 weeks since prior major surgery
- No other concurrent investigational drugs
- No concurrent participation in another clinical trial (supportive care trials or non-treatment trials [e.g., quality of life] allowed)
- No concurrent therapeutic doses of warfarin (low-dose warfarin ≤ 2 mg once daily for thromboembolic prophylaxis allowed)
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: N / A
- Modello interventistico: Assegnazione di gruppo singolo
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Sperimentale: Sunitinib
This is a phase II trial of Sunitinib in patients with metastatic urothelial carcinoma.
Sunitinib will be administered at a dose of 50 mg orally once daily for four consecutive weeks followed by a two-week rest period for the initial population.
A second cohort of patients will be enrolled, who will receive 37.5 mg of sunitinib orally, on a continuous dosing schedule.
Intra-patient dose reduction may be required depending on the type and severity of individual toxicity encountered.
Re-staging imaging studies will be performed after every cycle of treatment during the first 4 cycles and subsequently after every other cycle.
Patients may continue on study as long as they are tolerating therapy and in the absence of disease progression.
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Overall Objective Response
Lasso di tempo: 2 years
|
Response rate as measured by RECIST criteria.
The best overall response is the best response recorded from the start of the treatment until disease progression/recurrence (taking as reference for PD the smallest measurements recorded since the treatment started).
In general, the patient's best response assignment will depend on the achievement of both measurement and confirmation criteria
|
2 years
|
Collaboratori e investigatori
Investigatori
- Investigatore principale: Dean F. Bajorin, MD, Memorial Sloan Kettering Cancer Center
Studiare le date dei record
Studia le date principali
Inizio studio
Completamento primario (Effettivo)
Completamento dello studio (Effettivo)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Stima)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Stima)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
- carcinoma vescicale ricorrente
- carcinoma della vescica in stadio IV
- carcinoma a cellule transizionali metastatico della pelvi renale e dell'uretere
- carcinoma a cellule transizionali ricorrenti della pelvi renale e dell'uretere
- carcinoma a cellule transizionali della vescica
- carcinoma uretrale ricorrente
- carcinoma uretrale associato a carcinoma invasivo della vescica
- carcinoma dell'uretra anteriore
- carcinoma dell'uretra posteriore
Termini MeSH pertinenti aggiuntivi
- Neoplasie per tipo istologico
- Neoplasie
- Neoplasie urologiche
- Neoplasie urogenitali
- Neoplasie per sede
- Malattie renali
- Malattie urologiche
- Carcinoma
- Neoplasie, ghiandolari ed epiteliali
- Malattie della vescica urinaria
- Malattie dell'uretere
- Malattie uretrali
- Neoplasie renali
- Neoplasie della vescica urinaria
- Carcinoma, cellula di transizione
- Neoplasie ureterali
- Neoplasie uretrali
- Effetti fisiologici delle droghe
- Meccanismi molecolari dell'azione farmacologica
- Inibitori enzimatici
- Agenti antineoplastici
- Inibitori dell'angiogenesi
- Agenti di modulazione dell'angiogenesi
- Sostanze per la crescita
- Inibitori della crescita
- Inibitori della chinasi proteica
- Sunitinib
Altri numeri di identificazione dello studio
- 06-081
- MSKCC-06081
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .