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Early Assessment of Treatment Response Using Functional Diffusion Mapping

Early Assessment of Treatment Response Using Functional Diffusion Mapping

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02064283
Enrollment
20
Registered
2014-02-17
Start date
2007-05-31
Completion date
2012-10-31
Last updated
2014-12-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prostate Cancer

Brief summary

This study will evaluate the feasibility of identifying changes in diffusion MRI characteristics of bone that correlates with response to therapy in men with metastatic prostate cancer.

Detailed description

This study will evaluate a special type of MRI (magnetic resonance imaging) scan that measures the movement of water molecules through tissue called diffusion MRI. Researchers are using this new MRI technology to track the diffusion, or movement, of water through tumor tissue, and map these changes as a cancer patient undergoes treatment. Early research seems to indicate that tumor cells restrict the movement of water, so as tumor cells die, the movement of water changes within the tumor. These changes in the movement (diffusion) of water may help doctors determine earlier than traditional tests whether a patient's cancer is responding (getting better) to treatment. This study will evaluate the feasibility of identifying changes in diffusion MRI characteristics of bone that correlates with response to therapy in men with metastatic prostate cancer.

Interventions

PROCEDUREDiffusion MRI

Sponsors

University of Michigan Rogel Cancer Center
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Masking
NONE

Eligibility

Sex/Gender
MALE
Healthy volunteers
No

Inclusion criteria

* Diagnosis of prostate cancer. * Evidence of metastatic disease by bone scan. * Patients must be initiating systemic therapy for metastatic disease. * New D2 disease beginning therapy with androgen deprivation. * CRPC (Castration Resistant Prostate Cancer) beginning systemic non hormonal therapy. * Patients must be willing to provide the blood samples for the correlative markers. * Patients must be able to lie flat in an MRI (Magnetic Resonance Imaging) magnet for 30-60 minutes. * Life expectancy of 12 weeks or greater. * All patients must be informed of the investigational nature of this study and must sign an informed consent in accordance with institutional and federal guidelines.

Exclusion criteria

* Contraindication to MRI imaging. * Patients who require sedation with general anesthesia to undergo MRI imaging. * Weight greater than 275 pounds.

Design outcomes

Primary

MeasureTime frameDescription
Change in diffusion MRI measurementsBaseline, 2 weeks and 9-12 weeksIdentify changes in Diffusion Magnetic Resonance Imaging (MRI) measurements and correlate the changes with response to therapy.

Secondary

MeasureTime frameDescription
Change in units/L of CK18Asp306Baseline, 2 weeks and 9-12 weeksLevels of CK18Asp396 can be measured in serum using a commercially available ELISA (Enzyme-linked Immunosorbent Assay). Changes in serum CK18Asp396 (a marker of apoptosis) will be correlated with functional diffusion maps and treatment response.
Change in levels of bone turnover markersBaseline, 2 weeks and 9-12 weeksCorrelate the changes in biochemical markers of bone turnover, such as N-telopeptide and bone-specific alkaline phosphatase, with functional diffusion maps and treatment response.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026