Carcinoma, Renal CellREMISCANNCT00842790
Impact of Predicting Anti-angiogenic Response in mRCC Using Functional Imaging
An observational study of Carcinoma, Renal Cell, run by Assistance Publique - Hôpitaux de Paris at 1 site in France.
Trial summary
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… Read more about this study
- Who is it for?
- Ages 18 to 85 years
- Conditions the study is for
- Carcinoma, Renal Cell
- How many people
- 107 participants
- Where
- 1 siteFrance
- Study dates
- Sep 2008to Jul 2014
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 85 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: oncologic hospital visit
Who may be able to join
- with metastatic RCC
- without previous recent antiangiogenic treatment
Who cannot join
- severe renal insufficiency
- allergy to contrast agents
- pregnancy
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Medical and Economical Impact of Predicting the Response to Anti-angiogenic Treatment in Metastatic Renal Cell Carcinoma Using Functional CT and MRI
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.
Read the detailed description
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 200 patients with metastatic RCC will be enrolled in the study. Patients will be recruited by an oncologist and the images will be acquired by a radiologist.
Patients will be followed until tumor progression (as defined by RECIST) or during 2 years following inclusion if there is no progression.
- Imaging data acquisition Morphological and functional imaging will be obtained before the beginning of the anti-angiogenic treatment, at 7±2 days and every 6 weeks until tumor progression.
Progression is defined following the RECIST criteria.
- CT examination will be have two parts: the first one will be a dynamic acquisition during 3 min (using low kV)focused on a "functional target lesion" during bolus injection of a contrast agent for functional analysis, and the second one will be a morphologic acquisition over the chest, the abdomen and the pelvis for RECIST evaluation.
- 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.
- Imaging data analysis The examinations will be anonymized and transferred to a workstation for processing. Images will be processed by two independent readers.
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.
- Conditions
- Carcinoma, Renal Cell
- Keywords
- Carcinoma, Renal Cell [C04.557.470.200.025.390], Angiogenesis Inhibitors [D27.505.954.248.025], Tomography Scanners, X-Ray Computed [E07.913], Magnetic Resonance Imaging [E01.370.350.825.500], Diffusion Magnetic Resonance Imaging [E01.370.350.825.500.150], Perfusion [E05.680]
- Medical subject headings
- Carcinoma, Renal Cell, Carcinoma
What is being measured
The primary outcome is the main question the study is designed to answer.
RECIST criteria evolution
time-to-progression with anti-angiogenic traitment evaluated by RECIST criteria
Measured: at day 7 and after every 6 at 16 weeks during 2 years
Secondary outcomes (2)
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
Measured: 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
Measured: at the end
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted12 Feb 2009 (estimated)
- Study startSep 2008
- Primary completionJul 2014
- Study completionJul 2014
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Carcinoma, Renal CellStudies of the same condition, open and under way.
- More trials run by Assistance Publique - Hôpitaux de ParisThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 107 participants (actual)
Sponsor and investigators
- Lead sponsor
- Assistance Publique - Hôpitaux de Paris
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Stephane OUDARD, PhD, Principal investigator, Assistance Publique - Hôpitaux de ParisCharles-André Cuenod, PhD, Study director, Assistance Publique - Hôpitaux de Paris
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00842790
- Sponsor's protocol ID
- P060407
- Acronym
- REMISCAN
- Status last verified
- Feb 2009
- First submitted
- 11 Feb 2009
- Last updated
- 6 Oct 2015
- Results posted
- No
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 6 Oct 2015. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Medical and Economical Impact of Predicting the Response to Anti-angiogenic Treatment in Metastatic Renal Cell Carcinoma Using Functional CT and MRI
- ClinicalTrials.gov ID
- NCT00842790
- Acronym / sponsor ID
- REMISCAN / P060407
- Conditions
- Carcinoma, Renal Cell
- Keywords
- Carcinoma, Renal Cell [C04.557.470.200.025.390], Angiogenesis Inhibitors [D27.505.954.248.025], Tomography Scanners, X-Ray Computed [E07.913], Magnetic Resonance Imaging [E01.370.350.825.500], Diffusion Magnetic Resonance Imaging [E01.370.350.825.500.150], Perfusion [E05.680]
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 107 participants (actual)
- Lead sponsor
- Assistance Publique - Hôpitaux de ParisUniversity, hospital or other
- Study start
- Sep 2008
- Primary completion
- Jul 2014 (actual)
- Study completion
- Jul 2014 (actual)
- First posted
- 12 Feb 2009 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Detailed description
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 200 patients with metastatic RCC will be enrolled in the study. Patients will be recruited by an oncologist and the images will be acquired by a radiologist.
Patients will be followed until tumor progression (as defined by RECIST) or during 2 years following inclusion if there is no progression.
- Imaging data acquisition Morphological and functional imaging will be obtained before the beginning of the anti-angiogenic treatment, at 7±2 days and every 6 weeks until tumor progression.
Progression is defined following the RECIST criteria.
- CT examination will be have two parts: the first one will be a dynamic acquisition during 3 min (using low kV)focused on a "functional target lesion" during bolus injection of a contrast agent for functional analysis, and the second one will be a morphologic acquisition over the chest, the abdomen and the pelvis for RECIST evaluation.
- 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.
- Imaging data analysis The examinations will be anonymized and transferred to a workstation for processing. Images will be processed by two independent readers.
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.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
Who may qualify
- Ages
- 18 to 85 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- oncologic hospital visit
Key inclusion criteria (2 listed)
- with metastatic RCC
- without previous recent antiangiogenic treatment
Key exclusion criteria (3 listed)
- severe renal insufficiency
- allergy to contrast agents
- pregnancy
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
RECIST criteria evolution
Time frame: at day 7 and after every 6 at 16 weeks during 2 years
time-to-progression with anti-angiogenic traitment evaluated by RECIST criteria
2 secondary outcomes
Validation of the technical and acquisition measurement models
Time frame: at day 7 and after every 6 at 16 weeks during 2 years
Assessment of potential drug costs
Time frame: at the end
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 6 Oct 2015.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Stephane OUDARD, PhD principal investigator
Assistance Publique - Hôpitaux de Paris
Charles-André Cuenod, PhD study director
Assistance Publique - Hôpitaux de Paris
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Carcinoma, Renal Cell, run by Assistance Publique - Hôpitaux de Paris at 1 site in France.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 6 Oct 2015. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
RECIST criteria evolution (time frame: at day 7 and after every 6 at 16 weeks during 2 years). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Oct 2015.