- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT01567930
Temsirolimus as Second-line Therapy in HCC
A Phase II Study of Temsirolimus as Second-line Therapy in Patients With Advanced, Unresectable Hepatocellular Carcinoma
Studienübersicht
Status
Intervention / Behandlung
Detaillierte Beschreibung
Currently, no standard therapy exists for patients who progress on sorafenib. mTOR signaling is often up-regulated in HCC promoting cell growth and survival. This process is inhibited by rapamycin, a specific inhibitor of mTOR. Temsirolimus, a rapamycin analog, may delay tumor progression by inhibiting mTOR in HCC.Intervention: Temsirolimus IV
Eligible patients will receive temsirolimus IV on days 1,8,15 every 21 days. Treatment will continue till disease progression or untolerable side effects
Studientyp
Einschreibung (Voraussichtlich)
Phase
- Phase 2
Kontakte und Standorte
Studienorte
-
-
Tennessee
-
Memphis, Tennessee, Vereinigte Staaten, 38120
- Rekrutierung
- Boston Baskin Cancer Foundation
-
-
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Beschreibung
Inclusion Criteria:
Patients must have advanced unresectable or metastatic hepatocellular carcinoma (HCC). Prior diagnosis of HCC could have been established histologically or based on one of the following criteria:
- Liver mass > 2cm: Characteristic enhancement on at least one imaging technique(triphasic CT scan, MRI, or contrast enhanced ultrasound) or AFP > 200 ng/ml.
- Liver mass between 1 and 2 cm: Characteristic enhancement on two imaging techniques.Diagnosis of HCC must have been confirmed by biopsy if non-characteristic enhancement on imaging.
- All patients must have received exactly one prior systemic therapy (cytotoxic chemotherapy or targeted therapies) and must not be eligible for further locoregional treatment modalities.
- All patients must have measurable disease per RECIST criteria.
- Patients with previous locoregional therapies, including but not limited to radio-frequency ablation, cryoablation, percutaneous ethanol injection, chemo-embolization, hepatic artery embolization, and hepatic artery infused FUDR, stereotactic radiotherapy are eligible provided they have documented progression of their disease or have measurable extrahepatic disease.
- Patients must have an ECOG performance status of 0 - 2 (see Appendix B).
- Patients must be greater than or equal to 18 years of age.
- Patients with Child-Pugh class A (score of 5-6) or class B (score of 7-9) are eligible.
Patients must have adequate organ function as defined by:
- AST, ALT and Alkaline phosphatase ≤ 5x upper limit of normal (ULN)
- Total Bilirubin < 2 mg/dl.
- Creatinine clearance ≥ 15ml/min & patients must not be dialysis dependent.
Patients must have adequate bone marrow function as defined by:
- Leukocytes ≥ 2000 / mm3 or absolute neutrophil count (ANC) ≥ 1000 / mm3
- Platelet count ≥ 75000 / mm3
- Pregnant and nursing women will be excluded from this study. All patients of reproductive potential must agree to use adequate birth control measures to be eligible for study enrollment.
- Prior palliative radiotherapy is permissible provided it has been completed at least 2 weeks prior to study entry and the patient has recovered from any radiation-related side effects.
- Patients must not be receiving any other investigational agents or other anti-cancer therapies. At least 28 days must have elapsed since completion of previous systemic therapy prior to study entry and the patient should have recovered from all toxicities related to prior therapy.
- Patients must not have a history of other malignancies that are active and require therapy (other than non-melanoma skin cancers).
Exclusion Criteria:
- Patients with prior treatment with any mTOR inhibitor are not eligible.
- Patients with a history of an uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris,cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements are not eligible.
- Patients taking cytochrome P450 enzyme-inducers or inhibitors are not eligible.
- Patients with a known history of HIV infection are not eligible.
- Patients with uncontrolled hyperlipidemia or hypercholesterolemia are not eligible (fasting serum cholesterol > 350 mg/dL or fasting serum triglycerides > 400 mg/dL).
- Patients with a known history or clinical evidence of CNS metastases are not eligible.
- Patients who, in the best judgment of the investigator, will not be able to comply with the requirements of the protocol are not eligible.
Patients with Child-Pugh class C liver disease are not eligible.
-
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: N / A
- Interventionsmodell: Einzelgruppenzuweisung
- Maskierung: Keine (Offenes Etikett)
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
|---|---|
|
Disease Progression
|
The primary outcome measure is to determine the proportion of patients who are progression free at 3 months.
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
|---|---|
|
Response rate
|
Response rate, clinical benefit rate (complete + partial response + stable disease > 12 weeks) and overall survival with temsirolimus
|
|
Safety and tolerability
|
Number and frequency of adverse events and serious adverse events will be monitored.
|
|
Biochemical response
|
Biochemical response (>50% decline in AFP levels from baseline) with temsirolimus
|
|
Pharmacokinetics
|
Pharmacokinetics will be assessed: AUC pre-dose, 1, 3, 24,48, 72 and 162 hours post dose.
|
|
Circulating tumor cells levels
|
Feasibility and utility of circulating tumor cells in this patient population
|
Mitarbeiter und Ermittler
Mitarbeiter
Ermittler
- Hauptermittler: Jasgit Sachdev, MD, University of Tennessee Cancer Institute
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn
Primärer Abschluss (Voraussichtlich)
Studienabschluss (Voraussichtlich)
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
- Erkrankungen des Verdauungssystems
- Neubildungen nach histologischem Typ
- Neubildungen
- Neubildungen nach Standort
- Adenokarzinom
- Neubildungen, Drüsen und Epithelien
- Neoplasmen des Verdauungssystems
- Leberkrankheiten
- Lebertumoren
- Karzinom
- Karzinom, hepatozellulär
- Physiologische Wirkungen von Arzneimitteln
- Antiinfektiva
- Antineoplastische Mittel
- Immunsuppressive Mittel
- Immunologische Faktoren
- Antibakterielle Mittel
- Antibiotika, antineoplastische
- Antimykotika
- Sirolimus
Andere Studien-ID-Nummern
- 3066K1-2247
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 .
Klinische Studien zur Temsirolimus
-
Sheba Medical CenterStanley Medical Research InstituteUnbekanntSchizophrenie | Schizoaffektiven StörungIsrael
-
St. Joseph's Healthcare HamiltonPfizer; McMaster UniversityAbgeschlossenNierenzellkarzinomKanada
-
Gustave Roussy, Cancer Campus, Grand ParisAbgeschlossenPatienten mit fortgeschrittenen oder metastasierten soliden TumorenFrankreich
-
Canadian Cancer Trials GroupPfizerAktiv, nicht rekrutierendFortgeschrittene seltene TumorenKanada
-
AVEO Pharmaceuticals, Inc.Abgeschlossen
-
Dana-Farber Cancer InstituteWyeth is now a wholly owned subsidiary of Pfizer; Millennium Pharmaceuticals...AbgeschlossenMultiples MyelomVereinigte Staaten
-
Nader SanaiBarrow Neurological Institute; Ivy Brain Tumor CenterBeendetGliom | Glioblastom | Hochgradiges Gliom | Gliom, bösartigVereinigte Staaten
-
Children's Hospital Medical Center, CincinnatiZurückgezogenLymphom, B-Zell | Leukämie, B-ZelleVereinigte Staaten
-
M.D. Anderson Cancer CenterAktiv, nicht rekrutierendFortgeschrittener KrebsVereinigte Staaten
-
Mathias Witzens-HarigCharite University, Berlin, Germany; Ludwig-Maximilians - University of Munich; Johann Wolfgang Goethe University Hospital und andere MitarbeiterUnbekanntDiffuses großzelliges B-Zell-LymphomDeutschland