IDT: Improving Diagnosis and Treatment of Metastatic Advanced Prostate Cancer

Sponsor
Royal Marsden NHS Foundation Trust (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT04984395
Collaborator
(none)
50
1
34
1.5

Study Details

Study Description

Brief Summary

The aim of this study is to provide clinical evidence to determine if Whole Body Magnetic Resonance Imaging (WBMRI) with a novel technique called diffusion-weighted imaging (DWI) can improve current treatment for APC patients, allowing for early identification of disease progression or treatment response, hence facilitating clinical decision-making and leading to improvement in patient care. The IDT study includes two retrospective analyses and a single centre prospective observational study for APC patients.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Post-treatment CT-guided bone marrow biopsy

Detailed Description

Metastatic Advanced Prostate Cancer occurs when cancer spreads from the prostate to other parts of the body (bones, lymph nodes or other organs), with bones being the commonest site of spread in prostate cancer. These cancer growths are called metastases. APC metastases are diverse (heterogeneous) in their growth pattern, such that not all metastases will respond to the same treatment.

Study Design

Study Type:
Observational
Anticipated Enrollment :
50 participants
Observational Model:
Other
Time Perspective:
Prospective
Official Title:
Improving Diagnosis and Treatment of Metastatic Advanced Prostate Cancer Through Better Imaging With Whole-Body Magnetic Resonance Imaging With Diffusion Weighted Imaging
Anticipated Study Start Date :
Jul 30, 2021
Anticipated Primary Completion Date :
May 31, 2024
Anticipated Study Completion Date :
May 31, 2024

Outcome Measures

Primary Outcome Measures

  1. Retrospective analysis: WBMRI parameters [Month 1-26]

    Prognostic association of derived pre-treatment WBMRI parameters, total disease volume (tDV) and apparent diffusion coefficient (ADC) for prediction of overall survival.

  2. Retrospective analysis: Diagnostic performance of MET-RADS-P [Month 1-26]

    Accuracy of MET-RADS-P to assess response to systemic treatment.

  3. Single centre prospective observational imaging study [Month 6-38]

    Pairwise correlations of percentage of ADC change with: Tumour regression grading according to the international system of Salzer-Kuntschnik Changes in biopsy tumour content and tumour/necrosis ratio Fat fraction percentage with bone marrow adipose tissue/fibrosis reported by histopathology analysis.

Secondary Outcome Measures

  1. Retrospective analysis: WBMRI parameters [Month 1-26]

    Prognostic association of baseline tDV and ADC for prediction of radiographic Progression Free Survival (rPFS) using Prostate Cancer Working Group 3 criteria (PCWG3) and Skeletal Related Events (SREs).

  2. Retrospective analysis: Diagnostic performance of MET-RADS-P [Month 1-26]

    Inter-observer agreement - determine prognostic association of MET-RADS-P response for prediction of overall survival.

  3. Single centre prospective observational imaging study [Month 6-38]

    Fraction of bone biopsies with sufficient tumour yield for genomic sequencing.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
No
Inclusion Criteria:

Retrospective study A Baseline WBMRI scans in metastatic APC patients acquired up to 8 weeks prior to the initiation of a new line of therapy.

Retrospective study B Paired WBMRI scans in metastatic APC patients at baseline within 8 weeks prior to treatment and at 12 ± 3 weeks after systemic treatment

Prospective study C Written informed consent. Age ≥18 years. Advanced prostate cancer patients with indication for systemic anti-cancer therapy to be enrolled in a clinical study.

Participants must have a baseline WBMRI and CT-guided bone marrow biopsy.

Exclusion Criteria:

Prospective Study C Patient is claustrophobic. Contraindications to MRI examination (e.g., cardiac pacemakers, cochlear implants).

Contacts and Locations

Locations

Site City State Country Postal Code
1 The Royal Marsden NHS Foundation Trust Sutton Surrey United Kingdom SM2 5PT

Sponsors and Collaborators

  • Royal Marsden NHS Foundation Trust

Investigators

  • Principal Investigator: Nina Tunariu, The Royal Marsden NHS FT

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Royal Marsden NHS Foundation Trust
ClinicalTrials.gov Identifier:
NCT04984395
Other Study ID Numbers:
  • CCR5459
First Posted:
Jul 30, 2021
Last Update Posted:
Jul 30, 2021
Last Verified:
May 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 30, 2021