- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT00049400
S0355 Ixabepilone in Treating Patients With Advanced Solid Tumors or Lymphomas and Liver Dysfunction
A Phase I Pharmacokinetic Study Of Epothilone B Analogue BMS-247550 (NSC 710428D) In Patients With Advanced Malignancies And Varying Levels Of Liver Dysfunction
RATIONALE: Drugs used in chemotherapy work in different ways to stop tumor cells from dividing so they stop growing or die.
PURPOSE: This phase I trial is studying the side effects and best dose of ixabepilone in treating patients with advanced solid tumors or lymphomas and liver dysfunction.
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
OBJECTIVES:
- Determine the levels of hepatic impairment at which dose modifications of ixabepilone are required in patients with advanced solid tumors or lymphomas and varying levels of liver dysfunction.
- Determine the effect of hepatic dysfunction on the plasma pharmacokinetics of this drug in these patients.
- Determine the toxic effects of this drug at varying levels of hepatic dysfunction in these patients.
OUTLINE: This is a dose-escalation, multicenter study. Patients are stratified according to liver function (normal vs mild dysfunction vs moderate dysfunction vs severe dysfunction).
Patients receive ixabepilone IV over 3 hours on day 1. Courses repeat every 3 weeks in the absence of disease progression or unacceptable toxicity.
Cohorts of 3-6 patients receive escalating doses of ixabepilone until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which at least 2 of 3 or 2 of 6 patients experience dose-limiting toxicity. Once the MTD is determined, at least 6 but no more than 12 patients are treated at the recommended phase II dose.
Patients are followed for 30 days.
PROJECTED ACCRUAL: A total of 12-84 patients (6-12 for stratum 1; 2-18 for stratum 2; 2-24 for stratum 3; and 2-30 for stratum 4) will be accrued for this study within 12 months.
Tipo di studio
Iscrizione (Effettivo)
Fase
- Fase 1
Contatti e Sedi
Luoghi di studio
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California
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Duarte, California, Stati Uniti, 91010-3000
- City of Hope Comprehensive Cancer Center
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Los Angeles, California, Stati Uniti, 90089-9181
- USC/Norris Comprehensive Cancer Center and Hospital
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Sacramento, California, Stati Uniti, 95817
- University of California Davis Cancer Center
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Illinois
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Maywood, Illinois, Stati Uniti, 60153
- Cardinal Bernardin Cancer Center at Loyola University Medical Center
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Kansas
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Kansas City, Kansas, Stati Uniti, 66160-7357
- Kansas Masonic Cancer Research Institute at the University of Kansas Medical Center
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Ohio
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Cleveland, Ohio, Stati Uniti, 44195
- Cleveland Clinic Taussig Cancer Center
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Cleveland, Ohio, Stati Uniti, 44106
- Case Comprehensive Cancer Center
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Independence, Ohio, Stati Uniti, 44131
- Community Oncology Group at Cleveland Clinic Cancer Center
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Wooster, Ohio, Stati Uniti, 44691
- Cleveland Clinic - Wooster
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Texas
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Fort Sam Houston, Texas, Stati Uniti, 78234
- Brooke Army Medical Center
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Lackland AFB, Texas, Stati Uniti, 78236
- Wilford Hall Medical Center
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San Antonio, Texas, Stati Uniti, 78229-3900
- University of Texas Health Science Center at San Antonio
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Washington
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Bellingham, Washington, Stati Uniti, 98225
- St. Joseph Hospital Community Cancer Center
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Bremerton, Washington, Stati Uniti, 98310
- Olympic Hematology and Oncology
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Mt. Vernon, Washington, Stati Uniti, 98273
- Skagit Valley Hospital Cancer Care Center
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Seattle, Washington, Stati Uniti, 98104
- Harborview Medical Center
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Seattle, Washington, Stati Uniti, 98104
- Fred Hutchinson Cancer Research Center
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Seattle, Washington, Stati Uniti, 98122-4307
- Swedish Cancer Institute at Swedish Medical Center - First Hill Campus
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Seattle, Washington, Stati Uniti, 98195-6043
- University Cancer Center at University of Washington Medical Center
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Seattle, Washington, Stati Uniti, 98104-1387
- Group Health Central Hospital
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Sedro-Wooley, Washington, Stati Uniti, 98284
- North Puget Oncology at United General Hospital
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Spokane, Washington, Stati Uniti, 99202
- Cancer Care Northwest - Spokane South
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Wenatchee, Washington, Stati Uniti, 98801-2028
- Wenatchee Valley Medical Center
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
DISEASE CHARACTERISTICS:
Histologically or cytologically confirmed solid tumor or lymphoma for which standard curative or palliative measures do not exist or are no longer effective
- Pathological confirmation of diagnosis not required in patients with liver mass, raised alpha-fetoprotein levels (at least 500 ng/mL), and positive serology for hepatitis consistent with a diagnosis of hepatocellular carcinoma
- Any solid tumor or lymphoma tumor type eligible
- Must have had thoracic and upper abdominal CT scan, including entire liver and adrenals, within 28 days before study entry
Patients with glioma or brain metastases must be on a stable dose of corticosteroids and be seizure-free for the past month
- Prior whole brain or gamma knife radiotherapy required for known brain metastases
- No unstable or untreated (non-irradiated) brain metastases
PATIENT CHARACTERISTICS:
Age
- 18 and over
Performance status
- Zubrod 0-2
Life expectancy
- Not specified
Hematopoietic
- Absolute neutrophil count at least 1,500/mm^3
- Platelet count at least 100,000/mm^3
- No active hemolysis
Hepatic
- See Disease Characteristics
- Patients with biliary obstruction for which a shunt has been placed are allowed if shunt is in place for at least 10 days and liver function is stable
- Abnormal liver function (bilirubin and SGOT) allowed regardless of cause (metastases or other causes)
- No evidence of biliary sepsis
Renal
- Creatinine no greater than 1.5 mg/dL
Cardiovascular
- No symptomatic congestive heart failure
- No unstable angina pectoris
- No cardiac arrhythmia
Other
- No concurrent uncontrolled illness
- No ongoing or active infection
- No uncontrolled diarrhea
- No peripheral neuropathy grade II or greater
- No psychiatric illness or social situation that would preclude study compliance
- HIV negative
- Not pregnant or nursing
- Negative pregnancy test
- Fertile patients must use effective barrier contraception
PRIOR CONCURRENT THERAPY:
Biologic therapy
- No concurrent immunotherapy for malignancy
Chemotherapy
- More than 2 weeks since prior chemotherapy (6 weeks for nitrosoureas or mitomycin)
- No other concurrent chemotherapy for malignancy
Endocrine therapy
- See Disease Characteristics
- No concurrent oral contraceptives
No concurrent hormone therapy for malignancy
- Concurrent luteinizing hormone-releasing hormone agonists allowed
Radiotherapy
- See Disease Characteristics
- More than 4 weeks since prior radiotherapy and recovered
- No concurrent radiotherapy for malignancy
Surgery
- More than 2 weeks since prior major surgery
Other
- Recovered from prior therapy
- No concurrent medications that are known to be inhibitors of CYP3A4
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: treatment
Single-arm, dose-escalation of BMS-247550
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BMS-247550 as a 3-hour infusion on Day 1 of a three-week cycle
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Lasso di tempo |
|---|---|
|
dose defining
Lasso di tempo: Treatment delays >2 weeks constitute a DLT
|
Treatment delays >2 weeks constitute a DLT
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Progression
Lasso di tempo: 30 days after going off study
|
20% increase in the sum of longest diameters of target measurable lesions over smallest sum observed (over baseline if no decrease during therapy) using the same techniques as baseline.
|
30 days after going off study
|
|
Symptomatic deterioration
Lasso di tempo: 30 days after going off study
|
Global deterioration of health status requiring discontinuation of treatment without objective evidence of progression.
|
30 days after going off study
|
Collaboratori e investigatori
Sponsor
Collaboratori
Investigatori
- Investigatore principale: Chris H. Takimoto, MD, PhD, Institute for Drug Development
Pubblicazioni e link utili
Pubblicazioni generali
- Takimoto CH, Liu PY, Lenz H, et al.: A phase I pharmacokinetic (PK) study of the epothilone B analogue, ixabepilone (BMS-247550) in patients (pts) with advanced malignancies and varying degrees of hepatic impairment. A SWOG Early Therapeutics Committee and NCI Organ Dysfunction Working Group Trial. [Abstract] J Clin Oncol 24 (Suppl 18): A-2004, 2006.
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
- tumore solido adulto non specificato, protocollo specifico
- Linfoma immunoblastico a grandi cellule dell'adulto in stadio IV
- linfoma diffuso a grandi cellule dell'adulto ricorrente
- linfoma immunoblastico a grandi cellule dell'adulto ricorrente
- linfoma di Burkitt ricorrente dell'adulto
- linfoma di Hodgkin ricorrente dell'adulto
- linfoma diffuso a piccole cellule recidivante dell'adulto
- linfoma diffuso a cellule miste ricorrente dell'adulto
- stadio IV adulto linfoma diffuso a piccole cellule clivate
- linfoma mantellare in stadio IV
- linfoma ricorrente della zona marginale
- piccolo linfoma linfocitico ricorrente
- piccolo linfoma linfocitico stadio IV
- linfoma della zona marginale in stadio IV
- linfoma a cellule B della zona marginale nodale
- linfoma splenico della zona marginale
- linfoma linfoblastico ricorrente dell'adulto
- linfoma mantellare ricorrente
- Linfoma cutaneo non-Hodgkin a cellule T in stadio IV
- linfoma non-Hodgkin cutaneo ricorrente a cellule T
- linfoma dell'intestino tenue
- Linfoma linfoblastico adulto stadio IV
- leucemia/linfoma a cellule T dell'adulto in stadio IV
- leucemia/linfoma a cellule T dell'adulto ricorrente
- linfoma intraoculare
- linfoma angioimmunoblastico a cellule T
- linfoma anaplastico a grandi cellule
- linfoma primitivo del sistema nervoso centrale
- recurrent grade 1, 2, or 3 follicular lymphoma
- stage IV adult diffuse large cell or mixed cell lymphoma
- stage IV adult Burkitt lymphoma or Hodgkin lymphoma
- stage IV grade 1, 2, or 3 follicular lymphoma
- extranodal marginal zone B-cell lymphoma of MALT
Termini MeSH pertinenti aggiuntivi
- Malattie dell'apparato digerente
- Malattie del sistema immunitario
- Neoplasie per tipo istologico
- Neoplasie
- Malattie linfoproliferative
- Malattie linfatiche
- Disturbi immunoproliferativi
- Neoplasie per sede
- Neoplasie gastrointestinali
- Neoplasie dell'apparato digerente
- Malattie gastrointestinali
- Malattie intestinali
- Malattie del fegato
- Linfoma
- Neoplasie intestinali
Altri numeri di identificazione dello studio
- S0355 (Altro identificatore: SWOG)
- U10CA032102 (Sovvenzione/contratto NIH degli Stati Uniti)
- P30CA016087 (Sovvenzione/contratto NIH degli Stati Uniti)
- U01CA076642 (Sovvenzione/contratto NIH degli Stati Uniti)
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 .