- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT00070239
Alvocidib in Treating Patients With Metastatic or Unresectable Refractory Solid Tumors or Hematologic Malignancies
A Phase I Clinical, Pharmacokinetic and Pharmacodynamic Study of Flavopiridol in Patients With Refractory Solid Tumors and Hematologic Malignancies
Aperçu de l'étude
Statut
Les conditions
Description détaillée
PRIMARY OBJECTIVE:
I. Determine the maximum tolerated dose of flavopiridol in patients with metastatic or unresectable refractory solid tumors or hematologic malignancies. (Accrual for patients with hematologic malignancies temporarily closed as of 11/30/04)
SECONDARY OBJECTIVES:
I. Determine the safety profile and toxic effects of this drug in these patients.
II. Determine the pharmacokinetics of this drug in these patients. III. Determine, by pharmacodynamic assays, the ability of this drug to inhibit cyclin-dependent kinase activity in tumor tissue, normal proliferating tissues, circulating tumor cells, and in plasma in these patients.
IV. Determine, preliminarily, the antitumor activity of this drug in these patients.
OUTLINE: This is a 2-part, dose-escalation, multicenter study.
PART 1 (closed to accrual as of 8/2005): Patients receive alvocidib IV over 1 hour on days 1, 8, and 15.
Cohorts of 3-6 patients receive escalating doses of alvocidib until the maximum tolerated dose (MTD)* is determined.
PART 2: Patients receive alvocidib IV over 1 hour at or below the MTD determined in part 1 and then receive a maintenance dose of alvocidib IV over 1-6 hours on days 1, 8, and 15. Cohorts of 3-6 patients receive escalating durations of the maintenance dose of alvocidib until the MTD* is determined. An additional cohort of 10-20 patients receives alvocidib over 1 hour on days 1 and 15 at the MTD.
NOTE: *The MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose-limiting toxicity.
In both parts, courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.
Patients are followed at 1 month and then every 2 months thereafter.
Type d'étude
Inscription (Réel)
Phase
- La phase 1
Contacts et emplacements
Lieux d'étude
-
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Massachusetts
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Boston, Massachusetts, États-Unis, 02115
- Dana-Farber Cancer Institute
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-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
Inclusion Criteria:
Histologically confirmed malignancy, including the following types:
- Hematologic malignancy, including any of the following: (Accrual for patients with hematologic malignancies temporarily closed as of 11/30/04)
- Mantle cell lymphoma
- Morphologically confirmed disease
- CD20 and CD5 positive
- Any other refractory lymphoma
- Chronic lymphocytic leukemia
Rai stage III or IV and meeting at least 1 of the following criteria for active disease:
- Weight loss > 10% in the last 6 months
- Fatigue
- Fever or night sweats with no evidence of infection
- Progressive anemia or thrombocytopenia
- Progressive lymphocytosis with a lymphocyte doubling time of < 6 months
- Marked hypogammaglobulinemia or paraproteinemia
- Progressive splenomegaly and/or lymphadenopathy
- Multiple myeloma
- Disease confirmed by bone marrow aspirate and/or biopsy
- Relapsed or refractory disease after the most recent treatment regimen
- Quantifiable monoclonal immunoglobulin in serum and/or urine
Solid tumor, including but not limited to any of the following:
- Breast cancer
- Histologically or cytologically confirmed stage IV invasive disease
- HER-2 positivity not required for study enrollment
- Tumor overexpressing HER-2 should be confirmed by immunohistochemistry OR fluorescence in situ hybridization
- Small cell lung cancer
- Extensive stage or limited stage disease in relapse
- Extrapulmonary small cell carcinoma allowed
- Squamous cell carcinoma of the head and neck
- Metastatic, recurrent, or refractory disease
- Renal cell carcinoma
- Mesothelioma
- Pleural or peritoneal disease of epithelial, sarcomatoid, or mixed subtype
- Melanoma
- Kaposi's sarcoma
- Metastatic or unresectable disease for which standard therapy does not exist or is no longer effective
- Measurable or nonmeasurable disease (solid tumor patients)
- Measurable disease defined as at least 1 unidimensionally measurable lesion ≥ 20 mm by conventional techniques or 10 mm by spiral CT scan
Nonmeasurable disease includes any of the following:
- All other lesions, including lesions < 20 mm by conventional techniques or 10 mm by spiral CT scan
- Bone lesions
- Cytologically positive pleural or peritoneal disease
- Elevated tumor marker (e.g., CEA, CA 125, CA 19-9, or other tumor marker)
- Multinodular or confluent nonmeasurable pulmonary, hepatic, adrenal, intra-abdominal, or skin metastases
- Previously treated with at least 1 chemotherapy regimen*
- Prior therapy may have included combined modality treatment (e.g., full-dose chemotherapy and radiotherapy with radiosensitizing chemotherapy)
- Prior therapy with flavopiridol allowed provided the patient was enrolled in a flavopiridol clinical trial employing a different schedule NOTE: *Except in cases where chemotherapy is not known to be effective (e.g., renal cell carcinoma, chondrosarcoma, or gastrointestinal stromal tumor)
- No active CNS metastases
History of CNS metastases allowed provided all of the following criteria are met:
- Previously treated and stable and asymptomatic for at least 4 weeks since the completion of treatment
- Image documentation required
- Off steroids or on a stable dose of steroids for at least 1 week
Hormone receptor status:
- Not specified
Age
- 18 and over
Sex
- Male or female
Menopausal status
- Not specified
Performance status
- ECOG 0-1 OR
- Karnofsky 70-100%
Life expectancy
- More than 12 weeks
Hematopoietic
- Absolute neutrophil count > 1,000/mm^3*
- Platelet count > 75,000/mm^3 (50,000 for hematologic malignancies)* (Accrual for patients with hematologic malignancies temporarily closed as of 11/30/04) NOTE: *Unless abnormality is caused by tumor burden and not cumulative prior chemotherapy
Hepatic
- Bilirubin normal
- AST/ALT ≤ 2.5 times upper limit of normal (ULN) (5 times ULN if liver metastases are present)
Renal
- Creatinine ≤ 2.0 mg/dL OR
- Creatinine clearance ≥ 60 mL/min
Cardiovascular
- No myocardial infarction within the past 6 months
- No unstable angina within the past 6 months
- No transient ischemic attack or cerebrovascular accident within the past 6 months
- No history of arterial vascular events
- No new cardiac arrhythmias likely to be related to cardiac ischemia within the past 6 months
- No symptomatic congestive heart failure
Pulmonary
- No history of pulmonary embolism within the past 6 months
Gastrointestinal
- No chronic diarrheal disease within the past 6 months
- No severe malnutrition
- No intractable emesis
Other
- Not pregnant or nursing
- Negative pregnancy test
- Fertile patients must use effective hormonal or barrier contraception
- No ongoing or active infection
- No other concurrent uncontrolled illness
- No psychiatric illness or social situation that would preclude study compliance
- At least 3 weeks since prior chemotherapy (6 weeks for nitrosoureas or mitomycin)
- At least 3 weeks since prior radiotherapy No prior radiotherapy to 50% or more of bone marrow
- Recovered from all prior therapy No other concurrent investigational agents No concurrent combination antiretroviral therapy for HIV-positive patients
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: N / A
- Modèle interventionnel: Affectation à un seul groupe
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: Treatment
PART 1 (closed to accrual as of 8/2005): Patients receive alvocidib IV over 1 hour on days 1, 8, and 15. Cohorts of 3-6 patients receive escalating doses of alvocidib until the MTD* is determined. PART 2: Patients receive alvocidib IV over 1 hour at or below the MTD determined in part 1 and then receive a maintenance dose of alvocidib IV over 1-6 hours on days 1, 8, and 15. Cohorts of 3-6 patients receive escalating durations of the maintenance dose of alvocidib until the MTD* is determined. An additional cohort of 10-20 patients receives alvocidib over 1 hour on days 1 and 15 at the MTD. NOTE: *The MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose-limiting toxicity. In both parts, courses repeat every 28 days in the absence of disease progression or unacceptable toxicity. |
Étant donné IV
Autres noms:
Études corrélatives
Autres noms:
Études corrélatives
Autres noms:
Correlative studies
Autres noms:
Études corrélatives
Autres noms:
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Délai |
|---|---|
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Toxicité dose-limitante (DLT)
Délai: 28 jours
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28 jours
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MTD (or recommended phase II dose), defined as one dose level below that which produces two instances of DLT during the first 28-day course and the level at which no more than one of six patients experiences DLT during course 1
Délai: 28 days
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28 days
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Pharmacokinetic parameters, including maximum concentration (Cmax), half-life, area under the curve (AUC), clearance, and volume of distribution
Délai: 24 hours, 48 hours, 72 hours, and 8 weeks
|
Determined by nonlinear regression analysis of geometric mean plasma profile.
Cmax in patients w/stable disease or response at 8 weeks compared to those who progressed using Mann-Whitney test.
Wilcoxon signed-rank test to compare concentration and metabolic ratios directly following infusion and 24, 48, 72 hrs later.
Concentration and metabolic ratios compared in patients w/ and w/o toxicities of diarrhea, neutropenia, and asthenia using Mann- Whitney test.
Fisher's exact test to assess association of flavopiridol systemic metabolism (low vs. high metabolic ratio) w/development of toxicity.
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24 hours, 48 hours, 72 hours, and 8 weeks
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Potency of alvocidib in plasma based on change in proliferation of stimulated peripheral blood mononuclear cells (PBMCs)
Délai: Baseline to up to 72 hours of day 1 course 1
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Baseline to up to 72 hours of day 1 course 1
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Change in tumor metabolism and proliferation assessed by fludeoxyglucose F 18 (FDG) and fluorine F 18 fluorothymidine (FLT) positron emission tomography (PET)
Délai: Baseline to up to day 19 of course 2
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Each type of pre- and post-treatment scans may be analyzed as paired data.
The FDG and FLT data will be correlated to explore the relationship between tumor metabolism and tumor proliferation, for example, using Pearson or Spearman correlation coefficient.
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Baseline to up to day 19 of course 2
|
Collaborateurs et enquêteurs
Parrainer
Les enquêteurs
- Chercheur principal: Geoffrey Shapiro, Dana-Farber Cancer Institute
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude
Achèvement primaire (Réel)
Achèvement de l'étude
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Estimation)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Estimation)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
- Tumeurs
- Tumeurs par site
- Maladies hématologiques
- Tumeurs hématologiques
- Effets physiologiques des médicaments
- Mécanismes moléculaires de l'action pharmacologique
- Inhibiteurs d'enzymes
- Agents antinéoplasiques
- Substances de croissance
- Inhibiteurs de croissance
- Radiopharmaceutiques
- Inhibiteurs de protéine kinase
- Fluorodésoxyglucose F18
- Alvocidib
Autres numéros d'identification d'étude
- NCI-2009-00039 (Identificateur de registre: CTRP (Clinical Trial Reporting Program))
- 03-082 (Dana-Farber Cancer Institute)
- P 6052
- CDR0000331689
- 6052 (CTEP)
- U01CA062490 (Subvention/contrat des NIH des États-Unis)
Informations sur les médicaments et les dispositifs, documents d'étude
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produit fabriqué et exporté des États-Unis.
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