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Alvocidib in Treating Patients With Metastatic or Unresectable Refractory Solid Tumors or Hematologic Malignancies

13. Dezember 2013 aktualisiert von: National Cancer Institute (NCI)

A Phase I Clinical, Pharmacokinetic and Pharmacodynamic Study of Flavopiridol in Patients With Refractory Solid Tumors and Hematologic Malignancies

This phase I trial is studying the side effects and best dose of alvocidib in treating patients with metastatic or unresectable refractory solid tumors or hematologic malignancies. Drugs used in chemotherapy, such as alvocidib, work in different ways to stop cancer cells from dividing so they stop growing or die.

Studienübersicht

Detaillierte Beschreibung

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.

Studientyp

Interventionell

Einschreibung (Tatsächlich)

100

Phase

  • Phase 1

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienorte

    • Massachusetts
      • Boston, Massachusetts, Vereinigte Staaten, 02115
        • Dana-Farber Cancer Institute

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

18 Jahre und älter (Erwachsene, Älterer Erwachsener)

Akzeptiert gesunde Freiwillige

Nein

Studienberechtigte Geschlechter

Alle

Beschreibung

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

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: N / A
  • Interventionsmodell: Einzelgruppenzuweisung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: 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.

Gegeben IV
Andere Namen:
  • FLAVO
  • Flavopiridol
  • HMR1275
  • L-868275
Korrelative Studien
Andere Namen:
  • pharmakologische Studien
Korrelative Studien
Andere Namen:
  • 18FDG
  • FDG
Correlative studies
Andere Namen:
  • 18F-FLT
  • 3'-Desoxy-3'-[18F]fluorthymidin
  • Fluorthymidin F-18
Korrelative Studien
Andere Namen:
  • HAUSTIER
  • FDG-PET
  • PET-Scan
  • Tomographie, Emission berechnet

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Zeitfenster
Dosislimitierende Toxizität (DLT)
Zeitfenster: 28 Tage
28 Tage
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
Zeitfenster: 28 days
28 days

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Pharmacokinetic parameters, including maximum concentration (Cmax), half-life, area under the curve (AUC), clearance, and volume of distribution
Zeitfenster: 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.
24 hours, 48 hours, 72 hours, and 8 weeks
Potency of alvocidib in plasma based on change in proliferation of stimulated peripheral blood mononuclear cells (PBMCs)
Zeitfenster: Baseline to up to 72 hours of day 1 course 1
Baseline to up to 72 hours of day 1 course 1
Change in tumor metabolism and proliferation assessed by fludeoxyglucose F 18 (FDG) and fluorine F 18 fluorothymidine (FLT) positron emission tomography (PET)
Zeitfenster: Baseline to up to day 19 of course 2
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.
Baseline to up to day 19 of course 2

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Ermittler

  • Hauptermittler: Geoffrey Shapiro, Dana-Farber Cancer Institute

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn

1. August 2003

Primärer Abschluss (Tatsächlich)

1. Juni 2006

Studienabschluss

7. Dezember 2022

Studienanmeldedaten

Zuerst eingereicht

3. Oktober 2003

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

6. Oktober 2003

Zuerst gepostet (Schätzen)

7. Oktober 2003

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Schätzen)

16. Dezember 2013

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

13. Dezember 2013

Zuletzt verifiziert

1. Dezember 2013

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Andere Studien-ID-Nummern

  • NCI-2009-00039 (Registrierungskennung: CTRP (Clinical Trial Reporting Program))
  • 03-082 (Dana-Farber Cancer Institute)
  • P 6052
  • CDR0000331689
  • 6052 (CTEP)
  • U01CA062490 (US NIH Stipendium/Vertrag)

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

Produkt, das in den USA hergestellt und aus den USA exportiert wird

Nein

Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .

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