Myeloma Clinical Trial
— MALIMAROfficial title:
Development of a Machine Learning Support for Reading Whole Body Diffusion Weighted Magnetic Resonance Imaging (WB-DW-MRI) in Myeloma for the Detection and Quantification of the Extent of Disease Before and After Treatment
Verified date | January 2022 |
Source | Royal Marsden NHS Foundation Trust |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Diffusion-weighted Whole Body Magnetic Resonance Imaging (WB-MRI) is a new technique that builds on existing Magnetic Resonance Imaging (MRI) technology. It uses the movement of water molecules in human tissue to define with great accuracy cancerous cells from normal cells. Using this technique the investigators can much more accurately define the spread and rate of cancer growth. This information is vital in the selection of patients' treatment pathways. WB-MRI images are obtained for the entire body in a single scan. Unlike other imaging techniques such as computed Tomography (CT) or Positron Emission Tomography (PET) PET/CT there is no radiation exposure. Despite the considerable advantages that this new technique brings, including "at a glance" assessment of the extent of disease status, WB-MRI requires a significant increase in the time required to interpret one scan. This is because one whole body scan typically comprises several thousand images. Machine learning (ML) is a computer technique in which computers can be 'trained' to rapidly pin-point sites of disease and thus aid the radiologist's expert interpretation. If, as the investigators believe, this technique will help the radiologist to interpret scans of patients with myeloma more accurately and quickly, it could be more widely adopted by the NHS and benefit patient care. The investigators will conduct a three-phase research plan in which ML software will be developed and tested with the aim of achieving more rapid and accurate interpretation of WB-MRI scans in myeloma patients.
Status | Active, not recruiting |
Enrollment | 50 |
Est. completion date | December 31, 2022 |
Est. primary completion date | August 31, 2022 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 40 Years to 100 Years |
Eligibility | Inclusion Criteria (healthy volunteers): - Able to provide written informed consent - No contra-indication to MRI - 40 years or above in age (age matched as far as possible to WB-MRI scan set) - No known significant illness - No known metallic implant Exclusion Criteria: - Not able to provide written informed consent - A contra-indication to MRI - <40 years or above in age (age matched as far as possible to WB-MRI scan set) - A known significant illness - A known metallic implant |
Country | Name | City | State |
---|---|---|---|
United Kingdom | Imperial College, London | London | |
United Kingdom | Institute of Cancer Research, London | London | |
United Kingdom | Department of Radiology, The Royal Marsden NHS Foundation Trust | Sutton | Surrey |
Lead Sponsor | Collaborator |
---|---|
Royal Marsden NHS Foundation Trust | Imperial College London, Institute of Cancer Research, United Kingdom |
United Kingdom,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Predicting Segmentation Performance of the Machine Learning Algorithm | Percentage Agreement | 20 months | |
Primary | Sensitivity of Machine Learning Algorithm to detect Myeloma | Sensitivity for the detection of active myeloma on WB-MRI with and without ML support versus the reference standard | 20 months | |
Secondary | Level of Agreement in Assessment of Disease Burden | Agreement between readers and reference standard in scoring overall disease burden with and without ML intervention | 5 months | |
Secondary | Level of Agreement to Classify Disease Spread | Agreement of machine learning algorithm with reference standard to classify disease spread assessed as percentage accuracy | 20 months | |
Secondary | Quantification of Improvements to Correctly Identify Disease by Site and Reading Time | Per site sensitivity to diagnose active disease | 20 months | |
Secondary | Difference in Reading Time with and without Machine Learning | Difference in reading time assessed in minutes | 20 months | |
Secondary | Specificity for Identification of Active Disease with and without Machine Learning | Per site specificity to diagnose active disease | 20 months | |
Secondary | Sensitivity to detect Active Disease in non-Experienced Readers with and without Machine Learning | Per site sensitivity to diagnose active disease | 20 months | |
Secondary | Agreement in Categorisation of Active Disease | Percentage agreement | 20 months | |
Secondary | Difference in Reading Time for scoring Disease Burden with and without Machine Learning | Difference in reading time assessed in minutes | 5 months | |
Secondary | Agreement in Categorisation of Disease Responders and non-Responders with Reference Standard | Percentage Agreement | 5 months | |
Secondary | Agreement in Categorisation of Disease Responders and non-Responders in non-Experienced Readers | Percentage Agreement | 5 months | |
Secondary | Agreement in Assessment of Disease Burden in non-Experienced Readers | Percentage Agreement | 5 months | |
Secondary | Difference in Costs of Radiology Reading Time with and without Machine Learning | Selected denominations | 20 months |
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