An observational study in Carcinoma, Renal Cell, sponsored by Assistance Publique - Hôpitaux de Paris. Completed at 1 site in France. Open to participants aged 18 Years to 85 Years. Per ClinicalTrials.gov, last updated 2015-10-06.
Sponsored by Assistance Publique - Hôpitaux de Paris · Observational
The goal is to study the impact of functional MRI and CT evaluation of changes in tumor vessels induced by anti-angiogenic treatment in patients with metastatic RCC.
The hypothesis is that good responders and poor responders will have different responses induced by anti-angiogenic treatment, and that the detection of theses changes by functional imaging can improve the therapeutic management.
Functional CT and MRI will be performed in 200 patients before the beginning of antiangiogenic treatment, 7 days after and every 6 week until tumor progression (as defined by the RECIST criteria). Perfusion and diffusion parameters will be measured using a dedicated software.
The aim is to evaluate the capacity of functional CT and functional MRI to measure reliable biomarkers capable of evaluating the efficacy of anti-angiogenic treatment.
Patient and methods
Patients will be followed until tumor progression (as defined by RECIST) or during 2 years following inclusion if there is no progression.
Progression is defined following the RECIST criteria.
MRI examination will have two parts: the first one will be a diffusion weighted sequence focused on the same functional target as the one imaged on CT, and the second one will be a dynamic acquisition using a T1 weighted gradient echo sequence with less than 4 s sampling time during 5min following the bolus injection of contrast agent.
Diffusion coefficient maps will be obtained using linear regression. The microvascular parametric maps yielding as tissue blood flow, tissue blood volume, mean transit time, permeability surface area product and tissue interstitial volume will be calculated for both the CT and MRI dynamic series using a proprietary software by means of compartmental modeling with an arterial input function (AIF).
Mean parameters will be recorded for different regions of interest (ROI) in the tumors (whole tumor, periphery, center).
Morphological CT images will be analyzed following the RECIST criteria.
-Statistical analysis The functional parameters will be analyzed for inter-observer reproducibility. The correlation between parameters obtained using functional CT and functional MRI will tested.
Patients will be classified as good responders and poor responders according to RECIST follow-up.
The correlation between each baseline functional parameter and the RECIST response will be tested to evaluate the usefulness of the baseline parameters as predictors of response.
The correlation between each parameter's changes under treatment as compared to the baseline value will be tested to evaluate the efficacy of each parameter to detect the response to the anti-angiogenic drug. The precocity of the detection of the response using the parameter variations will be also tested.
Finally, the economical impact of the use of the microvascular parameters as biomarkers of treatment efficacy will be tested.
6,741 studies on the registry are indexed under Carcinoma; 1,161 are open to participants now.
This study's enrollment of 107 is below the median of 149 across 1,175 observational studies indexed under Carcinoma.
Browse Carcinoma studies →Assistance Publique - Hôpitaux de Paris is the lead sponsor of 3,505 studies on the registry; 1,006 are open to participants now.
Counted across the registry records on this site, refreshed daily.
oncologic hospital visit
Exclusion Criteria:
RECIST criteria evolution
time-to-progression with anti-angiogenic traitment evaluated by RECIST criteria
Time frame: at day 7 and after every 6 at 16 weeks during 2 years
Validation of the technical and acquisition measurement models
Validation of the technical and acquisition measurement models of tumor perfusion MRI and CT, and diffusion MRI, study of reproducibility
Time frame: at day 7 and after every 6 at 16 weeks during 2 years
Assessment of potential drug costs
Assessment of potential drug costs avoided by use of innovative prognostic criteria for adapting treatment
Time frame: at the end
This study is completed, as verified in Feb 2009. You cannot join it, but the record below documents what was studied.
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Assistance Publique - Hôpitaux de Paris