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Evaluation of Novel Cone-Beam CT for Guidance and Adaptation of Precision Radiotherapy

V

Varian

Status

Completed

Conditions

Breast Cancer
Other Cancer
Lung Cancer
Liver Cancer

Treatments

Device: CBCT Imaging

Study type

Interventional

Funder types

Industry

Identifiers

NCT05176860
VAR-2021-12

Details and patient eligibility

About

This is a feasibility study investigating the image quality of a new, high-performance cone beam CT (CBCT) used for on-couch imaging during radiotherapy treatments.

Full description

This study focuses on potential benefits of a high performance cone beam CT (CBCT) image guidance system for improved precision in the delivery of radiotherapy. CBCT is currently used during radiation therapy to align the patient to their original treatment plan to increase the precision of radiation delivery. Current CBCT imaging technology requires approximately a minute to acquire an image. In order to acquire images with sufficient quality to allow accurate targeting, the patient may need to perform multiple breath hold maneuvers to "freeze" the motion of tumors that move with the breathing cycle (e.g. lung, liver, and breast tumors). The new high-performance CBCT can acquire an image in approximately 6 seconds, potentially enabling acquisition of images with a single breath hold. Improved motion compensation algorithms used in image reconstruction may allow acquisition of good quality images even while a patient is not holding their breath.

The methodology for the subject's treatment setup, CT simulation, treatment planning, image guidance and treatment delivery will be determined by the subject's treatment team and is not specified by this study. Enrollment in the study may occur after treatment delivery has started but must be prior to the fifth fraction.

Following completion of informed consent to participate in this study, high-performance CBCT imaging will be scheduled immediately before or after one of the subject's first five scheduled radiation treatment fractions. Two research CBCT images will be acquired, one with breath hold, the other with free breathing.

With minimal disruption for participating patients, this study will enable a comparison of (i) the subject's treatment planning fan-beam CT and (ii) the conventional CBCT acquired on an existing treatment unit with (iii) the high-performance CBCT. Image quality of the high performance CBCT image data will thereby be compared to both a best-case standard (fan-beam) and the status-quo for on-couch imaging to isolate and identify improvements.

Enrollment

30 patients

Sex

All

Ages

19+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Subject is scheduled for treatment on one of the five TrueBeam platforms at the NS Health QE2 site.
  • Subject is receiving radiation therapy using a breath-hold technique (for example, lung, liver and left breast cancers).

Exclusion criteria

  • Patient is pregnant or has plans for pregnancy during the period of treatment.
  • Patient is unwilling to consent to participating to the study, or for whom informed consent is not possible.

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

30 participants in 1 patient group

High-performance CBCT imaging
Experimental group
Description:
Two additional study imaging sets are acquired.
Treatment:
Device: CBCT Imaging

Trial contacts and locations

1

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Central trial contact

Sean Davidson; Claire McCann

Data sourced from clinicaltrials.gov

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