- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT01265979
WB-DWI for Early Prediction of Therapy Response in Patients With Advanced Metastatic GIST Treated With Regorafenib
Whole Body Diffusion-weighted MRI (WB-DWI) for Early Prediction and Evaluation of Therapy Response in Patients With Advanced Metastatic Gastrointestinal Stromal Tumors (GIST) Treated With Regorafenib.
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Aim of the study
- To assess whole body diffusion-weighted magnetic resonance imaging (WB-DWI) for the assessment and early prediction of response of treatment with regorafenib or placebo in patients with advanced, metastatic gastro-intestinal stromal tumors (GIST)
- Evaluation of pretreatment apparent diffusion coefficient (ADC) and b1000 signal intensity (SI) of GIST visualized on the WB-DWI as predictor of time to progression, determined by progression-free survival (PFS)
- Evaluation of WB-DWI using changes of high b-value SI and ADC early during treatment (2weeks after start of therapy; allowed optimal window 10-14 days) as early predictor of time to progression or patient benefit according to RECIST (stable disease + partial response + complete response)
- Evaluation of WB-DWI for treatment follow-up 3 months after initiation of treatment. Confirmation of prior published pilot study (Dunet V et al, J Nucl Med 2010)
- Comparison of WB-DWI with conventional CT imaging for response assessment
Undersøgelsestype
Tilmelding (Faktiske)
Kontakter og lokationer
Studiesteder
-
-
-
Leuven, Belgien, 3000
- Radiology Department
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Barn
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Prøveudtagningsmetode
Studiebefolkning
Beskrivelse
Inclusion Criteria:
- patients with advanced, metastatic gastro-intestinal stromal tumors treated with regorafenib or placebo
Exclusion Criteria:
- in case of a known contraindication for MRI (eg. pacemaker), the patient will not be admitted to the study
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Tidsperspektiver: Fremadrettet
Kohorter og interventioner
Gruppe / kohorte |
Intervention / Behandling |
|---|---|
|
GIST treated with regorafenib/placebo
patients with advanced, metastatic gastro-intestinal stromal tumors treated with regorafenib or placebo
|
These studies will be performed on a 3 Tesla (T) MR system.
A major advantage of 3T compared to 1.5T is the improved signal to noise ratio that allows whole-body studies to be faster and without application of external antennas, which greatly improves patient comfort.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
WB-DWI as early predictor for regorafenib treatment response
Tidsramme: jan 2011-dec 2011
|
Primary aim of the study: To assess whole body diffusion-weighted magnetic resonance imaging (WB-DWI) for the assessment and early prediction of response of treatment with regorafenib or placebo in patients with advanced, metastatic gastro-intestinal stromal tumors (GIST) |
jan 2011-dec 2011
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Evaluation WB-DWI parameters in correlation with progression free survival (PFS)
Tidsramme: jan 2011-dec 2011
|
Evaluation of
of GIST visualized on the WB-DWI as predictor of progression free survival (PFS) |
jan 2011-dec 2011
|
Samarbejdspartnere og efterforskere
Efterforskere
- Ledende efterforsker: Vincent Vandecaveye, Prof.Dr., University Hospital Gasthuisberg, department of Radiology
Datoer for undersøgelser
Studer store datoer
Studiestart
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Skøn)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- S52989
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
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