JOURNAL ONKOLOGIE – STUDIE
Contrast-Enhanced Ultrasound Imaging in Diagnosing Liver Cancer in Patients With Cirrhosis
Rekrutierend
NCT-Nummer:
NCT03318380
Studienbeginn:
Januar 2018
Letztes Update:
08.12.2020
Wirkstoff:
-
Indikation (Clinical Trials):
Fibrosis, Liver Cirrhosis
Geschlecht:
Alle
Altersgruppe:
Erwachsene (18+)
Phase:
-
Sponsor:
Sidney Kimmel Cancer Center at Thomas Jefferson University
Collaborator:
National Cancer Institute (NCI), GE Healthcare, Bracco Diagnostics, Inc,
Studienleiter
Principal Investigator
Sidney Kimmel Cancer Center at Thomas Jefferson University
Kontakt
Kontakt:
Phone: 215-503-0587
E-Mail: Andrej.Lyshchik@jefferson.edu» Kontaktdaten anzeigen
Studienlocations (3 von 11)
University of California San Diego
92093 San Diego
United StatesRekrutierend» Google-Maps
Ansprechpartner:
Yuko Kono, MD
E-Mail: ykono@ucsd.edu» Ansprechpartner anzeigenSidney Kimmel Cancer Center at Thomas Jefferson University
19107 Philadelphia
United StatesRekrutierend» Google-Maps
Ansprechpartner:
Andrej Lyshchik, MD, PhD
E-Mail: Andrej.Lyshchik@jefferson.edu» Ansprechpartner anzeigenAlbert Einstein Medical Center
19141 Philadelphia
United StatesRekrutierend» Google-Maps
Ansprechpartner:
Shuchi Rodgers, MD
Phone: 215-456-3439
E-Mail: rodgersS@einstein.edu» Ansprechpartner anzeigen
92093 San Diego
United StatesRekrutierend» Google-Maps
Ansprechpartner:
Yuko Kono, MD
E-Mail: ykono@ucsd.edu» Ansprechpartner anzeigenSidney Kimmel Cancer Center at Thomas Jefferson University
19107 Philadelphia
United StatesRekrutierend» Google-Maps
Ansprechpartner:
Andrej Lyshchik, MD, PhD
E-Mail: Andrej.Lyshchik@jefferson.edu» Ansprechpartner anzeigenAlbert Einstein Medical Center
19141 Philadelphia
United StatesRekrutierend» Google-Maps
Ansprechpartner:
Shuchi Rodgers, MD
Phone: 215-456-3439
E-Mail: rodgersS@einstein.edu» Ansprechpartner anzeigen
Vanderbilt University
37240 Nashville
United StatesRekrutierend» Google-Maps
Ansprechpartner:
Geoffrey Wile, MD
E-Mail: geoffrey.wile@vanderbilt.edu» Ansprechpartner anzeigenUniversity of Texas Southwestern Medical Center
75390 Dallas
United StatesRekrutierend» Google-Maps
Ansprechpartner:
David Fetzer, MD
E-Mail: David.Fetzer@UTSouthwestern.edu» Ansprechpartner anzeigenSwedish Medical Center
98104 Seattle
United StatesAbgebrochen» Google-MapsUniversity of Calgary
T2N 2T9 Calgary
CanadaRekrutierend» Google-Maps
Ansprechpartner:
Stephanie Wilson, MD
E-Mail: stephanie.wilson@ahs.ca» Ansprechpartner anzeigenUniversity of Paris
Paris
FranceNoch nicht rekrutierend» Google-Maps
Ansprechpartner:
Valerie Vilgrain
E-Mail: valerie.vilgrain@aphp.fr» Ansprechpartner anzeigenUniversity of Bologna
40138 Bologna
ItalyRekrutierend» Google-Maps
Ansprechpartner:
Fabio Piscaglia, MD
E-Mail: fabio.piscaglia@unibo.it» Ansprechpartner anzeigenUniversity of Bern
Bern
SwitzerlandRekrutierend» Google-Maps
Ansprechpartner:
Annalisa Berzigotti
E-Mail: Annalisa.Berzigotti@insel.ch» Ansprechpartner anzeigenKing's College Hospital
London
United KingdomRekrutierend» Google-Maps
Ansprechpartner:
Paul Sidhu, MD
E-Mail: paulsidhu@nhs.net» Ansprechpartner anzeigen
Alle anzeigen 37240 Nashville
United StatesRekrutierend» Google-Maps
Ansprechpartner:
Geoffrey Wile, MD
E-Mail: geoffrey.wile@vanderbilt.edu» Ansprechpartner anzeigenUniversity of Texas Southwestern Medical Center
75390 Dallas
United StatesRekrutierend» Google-Maps
Ansprechpartner:
David Fetzer, MD
E-Mail: David.Fetzer@UTSouthwestern.edu» Ansprechpartner anzeigenSwedish Medical Center
98104 Seattle
United StatesAbgebrochen» Google-MapsUniversity of Calgary
T2N 2T9 Calgary
CanadaRekrutierend» Google-Maps
Ansprechpartner:
Stephanie Wilson, MD
E-Mail: stephanie.wilson@ahs.ca» Ansprechpartner anzeigenUniversity of Paris
Paris
FranceNoch nicht rekrutierend» Google-Maps
Ansprechpartner:
Valerie Vilgrain
E-Mail: valerie.vilgrain@aphp.fr» Ansprechpartner anzeigenUniversity of Bologna
40138 Bologna
ItalyRekrutierend» Google-Maps
Ansprechpartner:
Fabio Piscaglia, MD
E-Mail: fabio.piscaglia@unibo.it» Ansprechpartner anzeigenUniversity of Bern
Bern
SwitzerlandRekrutierend» Google-Maps
Ansprechpartner:
Annalisa Berzigotti
E-Mail: Annalisa.Berzigotti@insel.ch» Ansprechpartner anzeigenKing's College Hospital
London
United KingdomRekrutierend» Google-Maps
Ansprechpartner:
Paul Sidhu, MD
E-Mail: paulsidhu@nhs.net» Ansprechpartner anzeigen
Studien-Informationen
Detailed Description:PRIMARY OBJECTIVES:
I. To evaluate the sensitivity, specificity, positive and negative predictive values of
contrast-enhanced ultrasound (CEUS) for diagnosis of hepatocellular carcinoma (HCC) in
patients at risk for HCC in a multicenter setting.
SECONDARY OBJECTIVES:
I. To validate CEUS Liver Imaging Reporting and Data System (LI-RADS) and determine the
prevalence of HCC in each CEUS LI-RADS category.
II. To evaluate inter-reader reliability of CEUS for HCC diagnosis. III. To evaluate
covariates that might limit diagnostic performance of CEUS for HCC diagnosis.
Ein-/Ausschlusskriterien
Inclusion Criteria:- Capable of making informed decisions regarding his/her treatment
- Have known cirrhosis or other risk factors for HCC, based on American Association for
the Study of Liver Diseases (AASLD) and European Association for the Study of the
Liver (EASL) guidelines (applicable in each site jurisdictions)
- Patients with untreated focal liver observations on liver ultrasound or multiphase
contrast-enhanced CT or MRI performed as part of clinical standard of care within 4
weeks before patient enrollment.
OR
• Patients with untreated focal liver observations scheduled for follow-up multiphase
contrast-enhanced CT or MRI, biopsy or surgical excision as part of clinical standard of
care. CEUS should be performed within 4 weeks before or after follow-up imaging or within 4
weeks before biopsy or surgical excision.
Exclusion Criteria:
- Patients who are pregnant or lactating
- Patients with focal liver observations less than 5 mm or greater than 5 cm in size
- Patients with contraindications to CEUS
- Patients with contraindications to both CT and MRI
- Patients who are medically unstable, terminally ill, or whose clinical course is
unpredictable
- Liver nodule previously treated with trans-arterial or thermal ablation
- Patients who have received an investigational drug in the 30 days before CEUS, or will
receive one within 72 hour after their CEUS exam
Studien-Rationale
Primary outcome:1. Sensitivity of contrast-enhanced ultrasound evaluation (CEUS) for diagnosis of Hepatocellular cancer using a 95% confidence interval 95% confidence interval for HCC diagnosis using CEUS LR-5 classification (Time Frame - Up to 12 months):
A value of 67% for sensitivity is expected based on recent meta-analysis studies of CEUS for focal liver mass characterization.
2. Specificity of contrast-enhanced ultrasound evaluation (CEUS) for diagnosis of Hepatocellular cancer using a 95% confidence interval (Time Frame - Up to 12 months):
A value of 91% for specificity is expected based on recent meta-analysis studies of CEUS for focal liver mass characterization.
3. Positive Predictive Value of contrast-enhanced ultrasound evaluation (CEUS) for diagnosis of Hepatocellular cancer using a 95% confidence interval (Time Frame - Up to 12 months):
A value of 93% for Positive Predicative Value is expected based on recent meta-analysis studies of CEUS for focal liver mass characterization.
4. Negative Predictive Value of contrast-enhanced ultrasound evaluation (CEUS) for diagnosis of Hepatocellular cancer using a 95% confidence interval (Time Frame - Up to 12 months):
A value of 60% for Negative predictive value is expected based on recent meta-analysis studies of CEUS for focal liver mass characterization.
Geprüfte Regime
- Dynamic Contrast-Enhanced Ultrasound Imaging:
Undergo CEUS
Quelle: ClinicalTrials.gov