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Machine Learning in Myeloma Response (MALIMAR)

Primary Purpose

Myeloma

Status
Active
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Machine Learning (ML)
Sponsored by
Royal Marsden NHS Foundation Trust
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Myeloma focused on measuring Whole Body Diffusion Weighted, Magnetic Resonance Imaging, Machine Learning, Reading Time, Convolutional Neural Network, Algorithm, Diagnostic performance

Eligibility Criteria

40 Years - 100 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

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

Sites / Locations

  • Department of Radiology, The Royal Marsden NHS Foundation Trust
  • Institute of Cancer Research, London
  • Imperial College, London

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Other

Other

Other

Arm Label

Phase 1 - Mixed Scan Data Training Set

Phase 2 - Mixed Scan Data Validation Set

Phase 3 - Disease Burden Paired Data Set

Arm Description

Machine learning (ML): A mixed data set of 200 WB-MRI scans comprising scans obtained from 40 healthy volunteers (scanned for the purposes of the study), 40 previously acquired inactive myeloma WB-MRI scans and 120 previously acquired active myeloma WB-MRI scans, in which machine learning and convolutional neural networks will be trained to recognise healthy marrow, treated inactive previous myeloma and active myeloma. An algorithm will be developed for testing in phase 2.

Machine Learning (ML): A mixed data set of 353 WB-MRI scans as that comprising 50 healthy volunteers (scanned for the purposes of the study), and previously acquired scans from 303 myeloma patients, 100 of whom have inactive disease and 203 of whom have active myeloma. The scans will be read by radiologists in random order either with or without the support of for the detection of active myeloma. The diagnostic performance of the radiology reads with or without the machine learning support will be measured against an expert panel reference standard.

Machine Learning (ML): Approximately 200 paired WB-MRI scans from 100 patients (scanned at baseline with active disease and then post treatment) will be used to develop a machine learning tool to quantify the burden of disease. The machine learning algorithm will then be tested on a further additional set of 60 patients who previously had two WB-MRI scans comprising paired baseline (with active disease) and post treatment scans. The agreement of radiology readers to evaluate the burden of disease will be measured against the reference standard (expert panel) with and without machine learning support.

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

Level of Agreement in Assessment of Disease Burden
Agreement between readers and reference standard in scoring overall disease burden with and without ML intervention
Level of Agreement to Classify Disease Spread
Agreement of machine learning algorithm with reference standard to classify disease spread assessed as percentage accuracy
Quantification of Improvements to Correctly Identify Disease by Site and Reading Time
Per site sensitivity to diagnose active disease
Difference in Reading Time with and without Machine Learning
Difference in reading time assessed in minutes
Specificity for Identification of Active Disease with and without Machine Learning
Per site specificity to diagnose active disease
Sensitivity to detect Active Disease in non-Experienced Readers with and without Machine Learning
Per site sensitivity to diagnose active disease
Agreement in Categorisation of Active Disease
Percentage agreement
Difference in Reading Time for scoring Disease Burden with and without Machine Learning
Difference in reading time assessed in minutes
Agreement in Categorisation of Disease Responders and non-Responders with Reference Standard
Percentage Agreement
Agreement in Categorisation of Disease Responders and non-Responders in non-Experienced Readers
Percentage Agreement
Agreement in Assessment of Disease Burden in non-Experienced Readers
Percentage Agreement
Difference in Costs of Radiology Reading Time with and without Machine Learning
Selected denominations

Full Information

First Posted
May 1, 2018
Last Updated
January 7, 2022
Sponsor
Royal Marsden NHS Foundation Trust
Collaborators
Institute of Cancer Research, United Kingdom, Imperial College London
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1. Study Identification

Unique Protocol Identification Number
NCT03574454
Brief Title
Machine Learning in Myeloma Response
Acronym
MALIMAR
Official 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
Study Type
Interventional

2. Study Status

Record Verification Date
January 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
July 4, 2018 (Actual)
Primary Completion Date
August 31, 2022 (Anticipated)
Study Completion Date
December 31, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Royal Marsden NHS Foundation Trust
Collaborators
Institute of Cancer Research, United Kingdom, Imperial College London

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.
Detailed Description
Rationale: Diffusion-weighted whole body magnetic resonance imaging (WB-MRI) is a technique that depicts myeloma deposits in the bone marrow. WB-MRI covers the entire body during the course of a single scan and can be used to detect sites of disease without using ionising radiation. Although WB-MRI allows for "at a glance" assessment of disease burden, it requires significant expertise to accurately identify and quantify active myeloma. The technique is time-consuming to report due to the great number of images. A further challenge is recognising whether a patient has residual disease after treatment. Machine learning (ML) is a computer technique that can be trained to automatically detect disease sites in order to support the radiologist's interpretation. The investigators believe this technique will help the radiologist to interpret the scan more accurately and quickly. Machine learning algorithms have been successfully developed to recognise some other cancer types. The investigators believe that it may be successful in patients with myeloma, in whom The National Institute for Health and Care Excellence (NICE) recommend whole body MRI. This could allow the technique to be more widely used in the National Health Service (NHS). In the MALIMAR study the investigators will develop and test ML methods that have the potential to increase accuracy and reduce reading time of WB-MRI scans in myeloma patients. The investigators propose to develop ML tools to detect and quantify active disease before and after treatment based on WB-MRI. Research will be carried out at the Royal Marsden Hospital (RMH) NHS Foundation Trust, Institute of Cancer Research (ICR) London and Imperial College London. The investigators will use Whole Body MRI (WB-MRI) scans that have already been acquired in myeloma patients. They will also include 50 new scans obtained at RMH from healthy volunteer scans which will be used to 'teach' the computer to distinguish between healthy and diseased tissues. Research Design: The research will be divided into three parts: Development of the Machine Learning (ML) tool to detect active myeloma Measurement of the ability of the ML tool to improve the radiologists' interpretation of WB-MRI scans using a set of scans from patients with active and inactive myeloma and new scans obtained from healthy volunteers Development of the ML tool to quantify disease burden and changes between pre- and post-treatment WB-MRI scans in order to identify response to treatment The main outcome measure for this study will be the improvement in the detection of active disease and disease burden and the reduction in radiology reading time. The investigators will assess the reduction in reading time in both experienced specialist and non-specialist radiologists.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Myeloma
Keywords
Whole Body Diffusion Weighted, Magnetic Resonance Imaging, Machine Learning, Reading Time, Convolutional Neural Network, Algorithm, Diagnostic performance

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Cross-sectional diagnostic test accuracy design: development of a machine-based algorithm to augment expert classification of disease status and response to treatment in myeloma patients using retrospective interpretation of WB-MRI scans and disease-free (healthy volunteers) for comparison purposes.
Masking
Outcomes Assessor
Masking Description
The assessors interpretation of disease status using WB-MRI scans will be fully blinded to the reference standard (i.e. the Expert Panel's interpretation of the same scan).
Allocation
Non-Randomized
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Phase 1 - Mixed Scan Data Training Set
Arm Type
Other
Arm Description
Machine learning (ML): A mixed data set of 200 WB-MRI scans comprising scans obtained from 40 healthy volunteers (scanned for the purposes of the study), 40 previously acquired inactive myeloma WB-MRI scans and 120 previously acquired active myeloma WB-MRI scans, in which machine learning and convolutional neural networks will be trained to recognise healthy marrow, treated inactive previous myeloma and active myeloma. An algorithm will be developed for testing in phase 2.
Arm Title
Phase 2 - Mixed Scan Data Validation Set
Arm Type
Other
Arm Description
Machine Learning (ML): A mixed data set of 353 WB-MRI scans as that comprising 50 healthy volunteers (scanned for the purposes of the study), and previously acquired scans from 303 myeloma patients, 100 of whom have inactive disease and 203 of whom have active myeloma. The scans will be read by radiologists in random order either with or without the support of for the detection of active myeloma. The diagnostic performance of the radiology reads with or without the machine learning support will be measured against an expert panel reference standard.
Arm Title
Phase 3 - Disease Burden Paired Data Set
Arm Type
Other
Arm Description
Machine Learning (ML): Approximately 200 paired WB-MRI scans from 100 patients (scanned at baseline with active disease and then post treatment) will be used to develop a machine learning tool to quantify the burden of disease. The machine learning algorithm will then be tested on a further additional set of 60 patients who previously had two WB-MRI scans comprising paired baseline (with active disease) and post treatment scans. The agreement of radiology readers to evaluate the burden of disease will be measured against the reference standard (expert panel) with and without machine learning support.
Intervention Type
Other
Intervention Name(s)
Machine Learning (ML)
Other Intervention Name(s)
Algorithm, Software, Decision support tool, Convolutional neural network
Intervention Description
Application of ML support algorithm to accelerate and enhance human interpretation of WB-MRI scans in patients with myeloma
Primary Outcome Measure Information:
Title
Sensitivity of Machine Learning Algorithm to detect Myeloma
Description
Sensitivity for the detection of active myeloma on WB-MRI with and without ML support versus the reference standard
Time Frame
20 months
Secondary Outcome Measure Information:
Title
Level of Agreement in Assessment of Disease Burden
Description
Agreement between readers and reference standard in scoring overall disease burden with and without ML intervention
Time Frame
5 months
Title
Level of Agreement to Classify Disease Spread
Description
Agreement of machine learning algorithm with reference standard to classify disease spread assessed as percentage accuracy
Time Frame
20 months
Title
Quantification of Improvements to Correctly Identify Disease by Site and Reading Time
Description
Per site sensitivity to diagnose active disease
Time Frame
20 months
Title
Difference in Reading Time with and without Machine Learning
Description
Difference in reading time assessed in minutes
Time Frame
20 months
Title
Specificity for Identification of Active Disease with and without Machine Learning
Description
Per site specificity to diagnose active disease
Time Frame
20 months
Title
Sensitivity to detect Active Disease in non-Experienced Readers with and without Machine Learning
Description
Per site sensitivity to diagnose active disease
Time Frame
20 months
Title
Agreement in Categorisation of Active Disease
Description
Percentage agreement
Time Frame
20 months
Title
Difference in Reading Time for scoring Disease Burden with and without Machine Learning
Description
Difference in reading time assessed in minutes
Time Frame
5 months
Title
Agreement in Categorisation of Disease Responders and non-Responders with Reference Standard
Description
Percentage Agreement
Time Frame
5 months
Title
Agreement in Categorisation of Disease Responders and non-Responders in non-Experienced Readers
Description
Percentage Agreement
Time Frame
5 months
Title
Agreement in Assessment of Disease Burden in non-Experienced Readers
Description
Percentage Agreement
Time Frame
5 months
Title
Difference in Costs of Radiology Reading Time with and without Machine Learning
Description
Selected denominations
Time Frame
20 months
Other Pre-specified Outcome Measures:
Title
Predicting Segmentation Performance of the Machine Learning Algorithm
Description
Percentage Agreement
Time Frame
20 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
100 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Andrea G Rockall, FRCR
Organizational Affiliation
The Royal Marsden NHS Foundation Trust and Imperial College London
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Christina Messiou, MD, FRCR
Organizational Affiliation
The Royal Marsden NHS Foundation Trust and Institute of Cancer Research
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Radiology, The Royal Marsden NHS Foundation Trust
City
Sutton
State/Province
Surrey
ZIP/Postal Code
SM2 5PT
Country
United Kingdom
Facility Name
Institute of Cancer Research, London
City
London
ZIP/Postal Code
SW3 6JB
Country
United Kingdom
Facility Name
Imperial College, London
City
London
ZIP/Postal Code
W12 0NN
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
36198471
Citation
Satchwell L, Wedlake L, Greenlay E, Li X, Messiou C, Glocker B, Barwick T, Barfoot T, Doran S, Leach MO, Koh DM, Kaiser M, Winzeck S, Qaiser T, Aboagye E, Rockall A. Development of machine learning support for reading whole body diffusion-weighted MRI (WB-MRI) in myeloma for the detection and quantification of the extent of disease before and after treatment (MALIMAR): protocol for a cross-sectional diagnostic test accuracy study. BMJ Open. 2022 Oct 5;12(10):e067140. doi: 10.1136/bmjopen-2022-067140.
Results Reference
derived

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Machine Learning in Myeloma Response

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