- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT00440973
Safety Study of Specific Tumor Target Drug Plus Immune System Therapy in Patients With Kidney Cancer
Phase II Study of Interleukin- 2 and Bevacizumab in Patients With Progressive Metastatic Renal Cell Carcinoma
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
Detaillierte Beschreibung
The standard first-line treatment for patients with metastatic RCC is IL-2 at higher doses, but associated with higher frequency of toxicities. IL-2 given at lower doses have demonstrated similar results than higher doses but it requires further study. RCC is highly vascular and expresses high levels of VEGF. Bevacizumab is a monoclonal antibody directed against the Vascular Endothelial Growth Factor (VEGF) responsible for angiogenesis.
The study is designed to evaluate a response defined as time to progression, safety and toxicity in patients with metastatic renal cell carcinoma. Tissue correlation to evaluate the impact of vascular VEGF on clinical outcome will be retrospectively performed
Studientyp
Einschreibung (Tatsächlich)
Phase
- Phase 2
Kontakte und Standorte
Studienorte
-
-
Texas
-
Houston, Texas, Vereinigte Staaten, 77030
- Baylor College of Medicine - Methodist Hospital
-
-
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Beschreibung
Inclusion Criteria:
- Pathological proof of clear cell carcinoma (or mixed tumors ≥ 75% clear cell component)
- Evidence of measurable metastatic disease, no progression diseases or the patient's condition will not need radiotherapy in the next 4 weeks.
- Previous definitive radiotherapy to 1 metastatic site is acceptable
- At least 4 weeks have elapsed since radiation therapy
- Patients must be free of serious co-morbidity and have a life expectancy of ≥24 weeks
- Patients should have adequate physiologic reserves as evidence of adequate performance status, blood parameters, hepatic and kidney function, no evidence of active cardiac diseases and showing an acceptable function and adequate coagulation profile.
Exclusion Criteria:
- History of central nervous System metastases
- Known HIV positive
- Recent history of brain's vascular disease within 6 months; patients requiring regular antianginal therapy (coronary disease) or insufficient circulation in lower extremities are not eligible
- Active autoimmune disease
- Patients who have had steroid therapy in the past three weeks
- Patients taking concurrent anticancer drugs
- Biphosphonates (Zometa) are not allowed, unless started 4 weeks prior to participation in the study
- Female patients pregnant or breast-feeding
- The patient has an unstable medical condition, such as uncontrolled Diabetes mellitus or Hypertension; active infections requiring systemic antibiotics, antivirals, or antifungal; clinical evidence of cardiac or pulmonary dysfunction including, uncontrolled arrhythmias, unstable coagulation disorders; or recent myocardial infarction (within 6 months)
- Any condition including abnormal laboratory results, that in the opinion of the investigator places the patient at an unacceptable risk if he/she participate in the study
- Prior malignancy (within the last 3 years), except for adequately treated basal cell or squamous cell skin cancer, in situ cervical cancer or other cancer for which the patient has been - free for at least 3 years
- Uncontrolled Blood pressure > 150/100
- Major surgical procedure, open biopsy, or significant traumatic injury within 28 days prior to Day 0, anticipation of need for major surgical procedure during the course of the study
- Minor surgery 7 days before day 0
- Serious, non healing wound, ulcer, or bone fracture; and,inability to accomplish the treatment
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: N / A
- Interventionsmodell: Einzelgruppenzuweisung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Sonstiges: treatment arm
PI relocated, currently data is no longer available
|
monoclonal antibody with anti-angiogenesis properties used as chemotherapy
Andere Namen:
immunotherapy - cytokine signaling molecule used as an immune system regulator to trigger T & B lymphocyte proliferation
Andere Namen:
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
time to progression
Zeitfenster: During study (currently data no longer available)
|
currently data no longer available
|
During study (currently data no longer available)
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Collect data on tumor responses produced by interleukin-2 and Bevacizumab
Zeitfenster: During study (currently data no longer available)
|
currently data no longer available
|
During study (currently data no longer available)
|
|
Evaluate safety and toxicity of the combination of interleukin-2 and Bevacizumab for patients with progressive metastatic renal cell carcinoma.
Zeitfenster: During study (currently data no longer available)
|
currently data no longer available
|
During study (currently data no longer available)
|
Mitarbeiter und Ermittler
Mitarbeiter
Ermittler
- Hauptermittler: Robert J. Amato, D.O., Baylor College of Medicine - Methodist Hospital
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn
Primärer Abschluss (Tatsächlich)
Studienabschluss (Tatsächlich)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Schätzen)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Schätzen)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
- Neubildungen nach histologischem Typ
- Neubildungen
- Urologische Neubildungen
- Urogenitale Neoplasmen
- Neubildungen nach Standort
- Nierenerkrankungen
- Urologische Erkrankungen
- Adenokarzinom
- Neubildungen, Drüsen und Epithelien
- Nierentumoren
- Karzinom, Nierenzelle
- Karzinom
- Physiologische Wirkungen von Arzneimitteln
- Agenten des peripheren Nervensystems
- Analgetika
- Agenten des sensorischen Systems
- Analgetika, nicht narkotisch
- Antineoplastische Mittel
- Antineoplastische Mittel, immunologische
- Angiogenese-Inhibitoren
- Angiogenese-modulierende Mittel
- Wuchsstoffe
- Wachstumshemmer
- Bevacizumab
- Interleukin-2
Andere Studien-ID-Nummern
- PAC IRB #03-0194-05
- 16117 (Andere Kennung: Principal Investigator)
Plan für individuelle Teilnehmerdaten (IPD)
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