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NCT06787053Recruiting

Selecting Hypoxic Tumours for Treatment Modification

Source: ClinicalTrials.gov · Last updated 12 May 2026

Brief summary (registry, in English)

Approximately 50% of cancer patients with solid tumours will be treated with radiotherapy. A significant proportion (\>25%) of patients have hypoxic tumours which respond poorly to radiotherapy. Hypoxic tumours have a poor prognosis. This can be improved with treatment intensification. Treatment intensification can be modification with CON (breathing O2-enriched air + oral administration of nicotinamide), chemoradiosensitisation, radiation dose-escalation or additional systemic treatments, significantly improving response of the tumours to radiotherapy. However, there are currently no clinically approved biomarkers to identify hypoxic tumours. Our group has developed and validated gene-expression signature-based biomarkers that identify patients with hypoxic bladder, head and neck , prostate, sarcoma and lung cancers. The bladder cancer gene-expression hypoxia signature has been shown to predict benefit from hypoxia modification using RNA from archived tumour tissue. The main purpose of this study is to demonstrate in at least two cancer types that the hypoxia biomarker predicts benefit from hypoxia modification in real-time.

Status (registry)
Recruiting
Study type
Observational
Enrollment
30 (estimated)
First submitted
13 Dec 2024
Start date
16 Oct 2024
Primary completion date
30 May 2028
Lead sponsor
University of Manchester
NCT number
NCT06787053

What you commit to

  • Study type: Observational
  • Planned participants: 30
  • From 16 Oct 2024 to the primary completion date, 30 May 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • This will be tumour site dependent
  • Bladder:
  • Any contraindications to MRI identified after MRI safety screening including completion of an MRI Safety Screening Form.
  • Unable to tolerate MRI scans.
  • Pregnancy.
    • Cervix:
  • Any contraindications to MRI identified after MRI safety screening including completion of an MRI Safety Screening Form.
  • Unable to tolerate MRI scans.
  • Pregnancy.
    • Prostate:
  • Any contraindications to MRI identified after MRI safety screening including completion of an MRI Safety Screening Form.
  • Unable to tolerate MRI scans

Who the study is looking for

  • This will be tumour site dependent.
  • Bladder:
  • Older than age 18 years.
  • Patients having radiotherapy at the Christie NHS Foundation Trust suitable for imaging on an MRI scanner.
  • Able to give informed consent.
    • Cervix:
  • Older than age 18 years.
  • Patients having radiotherapy at the Christie NHS Foundation Trust suitable for imaging on an MRI scanner.
  • Able to give informed consent.
    • Prostate:
  • Older than age 18 years.
  • Patients having radiotherapy at the Christie NHS Foundation Trust suitable for imaging on an MRI scanner.
  • Able to give informed consent.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
The Christie NHS Foundation Trust
Coordinator of this site? Confirm its status
ManchesterUnited KingdomRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.