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Spots Global Cancer Trial Database for Metastatic Colorectal Cancer: Treatment Response With Dynamic Contrast MRI

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We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Metastatic Colorectal Cancer: Treatment Response With Dynamic Contrast MRI

Official Title: Angle Interleaved Projection Reconstruction With K-Space Weighted Image Reconstruction for Dynamic Contrast MRI of Cancer Therapy Response

Study ID: NCT00820456

Interventions

DCE-MRI

Study Description

Brief Summary: The objectives for this study include: * Testing a unique way of imaging people with colorectal cancer and other cancers that has spread to the liver using magnetic resonance imaging (MRI); * Seeing if the MRI process can be used across multiple imaging platforms; * Determining whether the results of the imaging can be reproduced; * Reviewing how MRI results relate to cancer response to combination therapy and to clinical endpoints.

Detailed Description: This study will investigate the use of projection reconstruction dynamic contrast-enhanced MRI (DCE-MRI) as a surrogate marker of tumor vascularity in patients treated with the antiangiogenic agent bevacizumab. DCE-MRI is gaining popularity as a method to assess the functional response of tumors to agents targeting the vascular endothelial growth factor (VGEF) pathways. DCE-MRI measurements have been proposed as a non-invasive measure of both tumor biologic activity and (in the case of antivascular therapy) early response to treatment. A number of phase I and II studies demonstrate the ability for DCE-MRI to detect perfusion changes associated with tumor biologic response to vascularly targeted agents. It has been suggested that pre-treatment DCE-MRI might identify tumors with high intrinsic perfusion and that these tumors will be more likely to respond to antivascular-based therapies. However, the current use of DCE-MRI in clinical settings is challenging. Trade-offs between spatial coverage, time, and spatial resolution make this technique difficult to implement in human studies and may limit its reliability. The use of projection reconstruction-based acquisition can mitigate the need for these trade-offs and can simultaneously provide high temporal and spatial resolution data for DCE-MRI analysis.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Penn State University Hershey Medical Center, Hershey, Pennsylvania, United States

Fox Chase Cancer Center, Philadelphia, Pennsylvania, United States

Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, United States

Thomas Jefferson University Hospital, Philadelphia, Pennsylvania, United States

University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, United States

Contact Details

Name: Mark Rosen, MD, PhD

Affiliation: University of Pennsylvania

Role: PRINCIPAL_INVESTIGATOR

Name: Larry Dougherty, PhD

Affiliation: University of Pennsylvania

Role: STUDY_CHAIR

Name: Donald Mitchell, MD

Affiliation: Thomas Jefferson University

Role: STUDY_CHAIR

Name: Peter J O'Dwyer, MD

Affiliation: University of Pennsylvania

Role: STUDY_CHAIR

Name: Michael D Feldman, MD, PhD

Affiliation: University of Pennsylvania

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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