DECIMA: Dual-Energy Computed Tomography for Improving Imaging Assessment of Multiple Myeloma

Sponsor
Guy's and St Thomas' NHS Foundation Trust (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05353907
Collaborator
(none)
78
54

Study Details

Study Description

Brief Summary

Up to 30% of patients with newly diagnosed/suspected myeloma cannot undergo or do not tolerate whole body MRI (WB-MRI). A number of factors may be contributory. First, WB-MRI protocols can take in excess of 1 hour. Patients must remain still within a narrow bore scanner with multiple MRI coils that can be claustrophobic. Second, there is significant acoustic noise that can be heard despite the use of ear protection. Third, 80% of patients will experience bone pain or fracture at some point during their illness, affecting their comfort within the scanner. Fourth, patients also have higher anxiety. One review reported up to 30% of patients experienced considerable apprehension and up to 10% severe psychological distress when undergoing MRI. Finally, myeloma is predominantly an illness of the elderly and co-morbid conditions decrease patients' ability to tolerate a long scan. When WB-MRI cannot be performed, NICE recommend whole-body computed tomography (WB-CT), which the investigators know offers decreased diagnostic performance in terms of marrow assessment and focal lesion detection. The investigators believe that using a novel CT technique - dual-energy CT (DECT)

  • may offer better diagnostic performance over standard WB-CT in myeloma patients.

What the investigators seek to do in this study is to evaluate the sensitivity and specificity of DECT in a cohort of untreated patients; and compare the performance of DECT to simulated standard CT (data simulated from the DECT) and also to WB-MRI (reference standard alongside bone marrow biopsy results. The investigators will assess both subjective visual analysis of DECT images as well as CT quantitative values for the bone marrow.

Secondary objectives include assessment of patient experience across both imaging tests and assessment of intra & inter observer variability in subjective visual analysis

Condition or Disease Intervention/Treatment Phase
  • Radiation: Whole Body MRI

Study Design

Study Type:
Observational
Anticipated Enrollment :
78 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Dual-Energy Computed Tomography for Improving Imaging Assessment of Multiple Myeloma
Anticipated Study Start Date :
Jun 1, 2022
Anticipated Primary Completion Date :
Dec 1, 2025
Anticipated Study Completion Date :
Dec 1, 2026

Outcome Measures

Primary Outcome Measures

  1. Sensitivity and specificity of WB-DECT [Baseline (both scans acquired at the same time point)]

    Sensitivity and specificity of whole body dual-energy CT (WB-DECT) to detect focal lesions and marrow infiltration compared to WB-MRI (gold standard) and WB-CT.

Secondary Outcome Measures

  1. Qualitatively measure patient experience of WB-DECT compared to WB-MRI . [Baseline (both scans acquired at the same time point)]

    Pre and post scan questionnaire administered for both WB-MRI and WB-DECT. Thematic analysis will be used.

  2. Intra & inter observer variability in subjective visual analysis and quantitative analysis of WB-DECT [Baseline (both scans acquired at the same time point)]

    Measured by Kappa statistic.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Adults with suspected or newly diagnosed myeloma
Exclusion Criteria:
  • No previous treatment for myeloma

  • No concurrent cancer elsewhere

  • No contraindications to CT or MRI scans

  • Routine, standard of care cut-off for minimum renal function (eGFR > 40 ml/min/1.73 m2) in order to receive IV gadolinium-based contrast media.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Guy's and St Thomas' NHS Foundation Trust

Investigators

  • Principal Investigator: Vicky Goh, King's College London

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Guy's and St Thomas' NHS Foundation Trust
ClinicalTrials.gov Identifier:
NCT05353907
Other Study ID Numbers:
  • 274302
First Posted:
Apr 29, 2022
Last Update Posted:
Apr 29, 2022
Last Verified:
Apr 1, 2022
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 Apr 29, 2022