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Extra scans to adapt radiation plans in children with tumors outside the brain

Tests extra imaging scans during radiation treatment in children with non-brain tumors.

Plain-language title generated from the registry record
Registry title: Hypersight and Ethos In Pediatric Radiotherapy

Key facts

Where
Toronto, CanadaSee the site

AI summary: who the study is looking for

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for children and teenagers aged 18 or under who are getting radiation therapy for a tumour outside the head. They will have extra scans twice a week.

Age
18 years or under
Sex
All sexes can join.
Disease stage
Non-cranial tumours (tumours that are not in the skull or brain). The record gives no stage.

Main reasons for not taking part

  • Primary cranial tumours (tumours that start in the skull or brain)
  • Fewer than 5 days of radiation therapy

Read by machine on 12 November 2026.

Where in Canada

  • Princess Margaret Cancer CentreToronto, CanadaContact: Dana Keilty, MDTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Trial details

Who runs it
University Health Network, Toronto
Trial code
NCT07528547
Record updated
15 April 2026
Original description
This is a single-center, prospective pilot study evaluating the utility of HyperSight CBCT imaging and Ethos adaptive radiation planning in pediatric patients receiving radiation therapy for non-cranial tumors.Read full original descriptionShow less

Hypersight and Ethos In Pediatric Radiotherapy (Peds Ethos)

This is a single-center, prospective pilot study evaluating the utility of HyperSight CBCT imaging and Ethos adaptive radiation planning in pediatric patients receiving radiation therapy for non-cranial tumors.

Twenty patients aged 18 or under will be enrolled. Participants will receive standard-of-care radiation therapy, with the addition of twice-weekly HyperSight CBCT scans. These scans will be used to assess anatomical changes and generate adapted radiation plans using the Ethos platform. Radiation oncologists and radiation therapists will independently evaluate the need for adaptation, and adapted vs. scheduled plans will be compared using dosimetric and anatomical similarity metrics.

An optional sub-study will allow anonymized imaging and planning data to be shared with Varian Medical Systems. The study duration will match the patient's treatment course, typically 1-6 weeks, with no additional follow-up beyond standard care.

Inclusion: Patient (paediatric or adolescent) age 18 or under receiving at least 5 days of radiation therapy; Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 3.

Exclusion: Patients with primary cranial tumours will be excluded due to the low expected utility of non-contrast CT scans in the delineation of brain edema and brain substructures.

ClinicalTrials.gov NCT07528547