search
Back to results

Functional Imaging in the Assessment of mRCC Response to Sunitinib

Primary Purpose

Metastatic Renal Cell Carcinoma

Status
Withdrawn
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Magnetic Resonance Imaging (MRI)
Sponsored by
Imperial College Healthcare NHS Trust
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Metastatic Renal Cell Carcinoma focused on measuring Clear cell renal cell carcinoma, Stage IV renal cell carcinoma, Anti-angiogenic therapy, Response assessment, Magnetic resonance imaging

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with newly diagnosed (i.e. treatment naive) metastatic clear cell renal cell carcinoma judged by their treating physician to have the potential to derive benefit from anti-angiogenic therapy
  • Histopathologically confirmed clear cell renal cell carcinoma
  • Male or female aged 18 years or older

Exclusion Criteria:

  • Previous medical treatment for renal cancer
  • Cardiac pacemaker or other contra-indication to magnetic resonance imaging
  • Contra-indication to intravenous Gadolinium
  • Pregnancy or breastfeeding

Sites / Locations

  • Imperial College Healthcare NHS Trust

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Metastatic renal cell carcinoma

Arm Description

Patients with clear cell renal cell carcinoma treated with anti-angiogenic therapies

Outcomes

Primary Outcome Measures

To determine if functional MRI techniques are able to detect treatment-related changes in patients with metastatic renal cell carcinoma treated with sunitinib

Secondary Outcome Measures

Repeatability of Arterial Spin Label and Diffusion Weighted MRI parameters
Changes in imaging parameters with treatment
Correlation of imaging parameters with progression free survival
Correlation of imaging parameters with overall survival

Full Information

First Posted
September 30, 2013
Last Updated
November 20, 2015
Sponsor
Imperial College Healthcare NHS Trust
search

1. Study Identification

Unique Protocol Identification Number
NCT01977586
Brief Title
Functional Imaging in the Assessment of mRCC Response to Sunitinib
Official Title
Pilot Study to Evaluate the Feasibility of Functional MRI in Metastatic Renal Cell Carcinoma (mRCC) With Test--retest Repeatability and Early Response Assessment
Study Type
Interventional

2. Study Status

Record Verification Date
August 2015
Overall Recruitment Status
Withdrawn
Why Stopped
Difficulty in recruiting suitable patients at centre
Study Start Date
April 2014 (undefined)
Primary Completion Date
August 2015 (Actual)
Study Completion Date
August 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Imperial College Healthcare NHS Trust

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The aim of this study is to assess whether functional magnetic resonance imaging (MRI) techniques are able to detect which patients with metastatic renal cell carcinoma will derive benefit from treatment with anti-angiogenic drugs early in their treatment. Early response assessment would allow selection of the most appropriate treatment option for each individual patient.
Detailed Description
Renal cell carcinoma (RCC) is a highly vascularized tumour that is dependent on new vessel formation (angiogenesis) for growth and spread beyond the kidney (metastases). In recent years a new class of drugs have been developed which target the formation of this blood supply, stopping tumour growth and resulting in increased survival. These anti-angiogenic drugs such as Sunitinib, Pazopanib, Axitinib and Everolimus are now the standard of care in metastatic RCC (mRCC) in the United Kingdom. Currently we assess if cancers are responding to treatment by looking at changes in the size of the tumour and metastases using computed tomography. However, the positive effects of drugs such as sunitinib do not always show a change in size, particularly early in treatment. Therefore we need to develop alternative methods for assessing if patients are responding in order to optimise individual management plans and prevent unnecessary toxicity and cost. The aim of this study is to assess if three different functional magnetic resonance imaging (MRI) techniques are able to predict which patients will derive benefit from anti-angiogenic therapy early in their treatment. The study will recruit patients with mRCC who are going to be treated with anti-angiogenic drugs. These patients will have an MRI scan before they commence treatment and then a further scan after one treatment cycle (4 weeks) in addition to their normal clinical follow-up. The sequences being evaluated (arterial spin labeling, diffusion-weighted imaging and dynamic contrast imaging) look at the blood supply to the cancer and it is expected that there will be different changes in this blood supply in patients who are benefiting from treatment compared to those who are not responding. Early knowledge of response will help doctors choose the most appropriate treatment option for each individual patient. Consenting patients with treatment naïve metastatic clear cell RCC will be recruited to the study. Before commencing anti-angiogenic therapy, patients will undergo 3 Tesla MRI covering the primary tumour or largest metastatic deposit identified from their staging CT examination if prior nephrectomy has been performed. Following 4 weeks of therapy (one treatment cycle), patients will undergo repeat MR imaging using the same protocol.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Metastatic Renal Cell Carcinoma
Keywords
Clear cell renal cell carcinoma, Stage IV renal cell carcinoma, Anti-angiogenic therapy, Response assessment, Magnetic resonance imaging

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Metastatic renal cell carcinoma
Arm Type
Experimental
Arm Description
Patients with clear cell renal cell carcinoma treated with anti-angiogenic therapies
Intervention Type
Other
Intervention Name(s)
Magnetic Resonance Imaging (MRI)
Primary Outcome Measure Information:
Title
To determine if functional MRI techniques are able to detect treatment-related changes in patients with metastatic renal cell carcinoma treated with sunitinib
Time Frame
At baseline and following one treatment cycle (expected 4 weeks) with anti-angiogenic therapy
Secondary Outcome Measure Information:
Title
Repeatability of Arterial Spin Label and Diffusion Weighted MRI parameters
Time Frame
At baseline MRI scan
Title
Changes in imaging parameters with treatment
Time Frame
At baseline and following one treatment cycle (expected 4 weeks) with anti-angiogenic therapy
Title
Correlation of imaging parameters with progression free survival
Time Frame
Time from study enrolment to progression assessed by RECIST v1.1 on computed tomography performed after every three treatment cycles (up to 36 months)
Title
Correlation of imaging parameters with overall survival
Time Frame
Time from study enrolment to date of death from any cause (up to 36 months)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with newly diagnosed (i.e. treatment naive) metastatic clear cell renal cell carcinoma judged by their treating physician to have the potential to derive benefit from anti-angiogenic therapy Histopathologically confirmed clear cell renal cell carcinoma Male or female aged 18 years or older Exclusion Criteria: Previous medical treatment for renal cancer Cardiac pacemaker or other contra-indication to magnetic resonance imaging Contra-indication to intravenous Gadolinium Pregnancy or breastfeeding
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nishat Bharwani, MRCP FRCR
Organizational Affiliation
Imperial College Healthcare NHS Trust
Official's Role
Principal Investigator
Facility Information:
Facility Name
Imperial College Healthcare NHS Trust
City
London
Country
United Kingdom

12. IPD Sharing Statement

Learn more about this trial

Functional Imaging in the Assessment of mRCC Response to Sunitinib

We'll reach out to this number within 24 hrs