Dual Energy CT - a Tool for Delineation of Tumor and Organs at Risk in Radiotherapy

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorAalborg University Hospital

About this trial

The primary aim of this clinical study, 'Dual Energy CT - a tool for delineation of tumor and organs at risk in radiotherapy' (DART) is to evaluate whether dual-energy CT (DECT) is at least as effective as magnetic resonance imaging (MRI) in delineating both tumors and organs at risk (OARs) in patients referred for radiotherapy (RT). This primary aim will be explored in patient groups where the performance of DECT for RT has been described in the literature (but mostly based on signal-to-noise ratio and/or contrast-to-noise ratio), such as brain metastases (sub-cohort 'DART Brain') and head and neck cancer (sub-cohort 'DART H\&N'). Additionally, DART will explore diagnoses not yet studied in the literature, such as bone metastases (sub-cohort 'DART Bone'). If DECT could be demonstrated to achieve delineations for RT in both tumors and OARs that are equally accurate as those based on MRI, it could offer significant advantages by being faster and more cost-effective, making DECT a valuable alternative to MRI in clinical practice. As a secondary aim, the study will evaluate whether DART offers benefits when added to standard RT imaging for tumor and OAR delineation: (1) For lung cancer patients (sub-cohort 'DART Lung'), where MRI scans are typically not valuable due to tumor motion caused by breathing, 'DART Lung' will assess whether DECT performed in breath-hold provides added value compared to the single-energy CT (SECT) scan conducted during free breathing, as used in current clinical practice. (2) For head and neck cancer patients, 'DART H\&N' will evaluate whether DECT offers added value compared to the positron emission tomography (PET)/CT scan currently used in clinical practice.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

ECOG performance status (PS) 0-2

Assessed to be able to complete the protocol scanning regime

Referred for RT

For head and neck cancer patients, a PET/CT scan must have been performed during the diagnostic evaluation for cancer

Disqualifiers

Pregnancy

Previous RT in the same anatomical area now referred for RT

Previous surgery in the same anatomical area now referred for RT

Participation in conflicting protocols

Trial population

Cancer patients referred for radiotherapy at Aalborg University Hospital, Denmark. For the 'DART Bone (SBRT)' cohort, patients are also referred for radiotherapy at Odense University Hospital and Copenhagen University Hospital, Herlev and Gentofte, Denmark

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Dual-energy CT (DECT)

    Diagnostic test

    Additional DECT scan performed for tumor and OAR delineation.

  • Iodine-based contrast agent

    Drug

    Administered intravenously with DECT for enhanced imaging.

  • Magnetic Resonance Imaging (MRI)

    Diagnostic test

    Additional MRI scan performed for tumor and OAR delineation.

  • Gadolinium-based contrast agent

    Drug

    Administered intravenously with MRI for enhanced imaging.

Treatment groups

80 Participants
are divided into 6 treatment groups

6

Treatment groups

See each treatment group below.

Group A: DART Brain (whole)4 interventions
Group B: DART Brain (SRS)2 interventions
Group C: DART Bone (pall)3 interventions
Group D: DART Bone (SBRT)2 interventions
Group E: DART H&N1 intervention
Group F: DART Lung1 intervention

Trial outcomes

Primary outcomes

1

Inter-observer variability (geometric differences in volume and surface) of manual tumor and OAR delineations on DECT compared with SECT/MRI.

For patients enrolled in cohorts 'DART Brain', 'DART Bone' and 'DART H\&N', the accuracy of manual delineations of tumors and OARs on DECT scans will be compared to those manually performed on a combination of SECT and MRI scans for each patient. For patients enrolled in 'DART H\&N' the comparison will also be done to the PET/CT scan. A reduction in inter-observer variability in delineations will serve as an indicator of improved contour accuracy for both tumors and OARs. Inter-observer variability for tumor and OAR delineations on DECT and SECT/MRI scans, respectively, will be measured as geometric differences between individual manual delineations and consensus structures for each tumor and OAR. Consensus structures will be generated on both DECT and SECT/MRI scans using the STAPLE function with a 50% agreement threshold. Variations relative to the consensus structures will be reported using various metrics, including volume and surface differences.

Time frame
Baseline (time of imaging before radiotherapy planning)

Secondary outcomes

1

Qualitative image-quality assessment of tumors and OARs using a Likert scale (or comparable method) for DECT compared with SECT/MRI.

The secondary outcome will be measured in all patient cohorts ('DART Brain', 'DART Bone', 'DART H\&N', and 'DART Lung'). Image-quality for tumors and OARs will be evaluated qualitatively by experienced oncologists using a Likert scale or comparable method, and evaluations will be made and reported between DECT and SECT/MRI scans (and, for patients enrolled in 'DART H\&N', also PET/CT scans).

Time frame
Baseline (time of imaging before radiotherapy planning)

Other outcomes

Sponsors and contacts

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Aalborg University Hospital

Lead sponsor

Copenhagen University Hospital at Herlev

Collaborator

Odense University Hospital

Collaborator

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