Actively Recruiting

Age: 18Years +
All Genders
ID06787053

Selecting Hypoxic Tumours for Treatment Modification in Bladder, Prostate, and Cervical Cancers

Led by University of Manchester · Updated on 2026-05-12

30

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating whether personalized treatment guided by hypoxia biomarkers can improve outcomes for patients with certain solid tumors, including bladder, prostate, and cervical cancers. Hypoxic tumors, which have low oxygen levels, tend to respond poorly to radiotherapy and are linked to worse prognosis. This study focuses on demonstrating that gene-expression signature biomarkers can identify hypoxic tumors and predict which patients will benefit from hypoxia modification treatments during radiotherapy in real-time. The study includes patients diagnosed with bladder, prostate, or cervical cancer who are receiving radiotherapy and can undergo MRI scans. The research integrates gene-expression biomarkers from tumor tissue with advanced MRI techniques to assess tumor hypoxia more accurately. This personalized approach aims to guide treatment modifications such as oxygen-enriched air breathing, nicotinamide administration, chemoradiosensitisation, or radiation dose escalation. The study also explores combining radiological data with biomarkers and evaluating blood-based biomarkers as early indicators of treatment response. Participants will undergo MRI imaging and provide tumor tissue samples for gene-expression analysis to assess hypoxia status before and during radiotherapy. Researchers will monitor treatment response and survival outcomes up to May 2028, integrating imaging and biomarker data to personalize therapy. Safety assessments include screening for MRI contraindications and pregnancy status. The study is observational and involves regular follow-up and data collection to evaluate the predictive value of hypoxia biomarkers and imaging in guiding cancer treatment.

CONDITIONS

Brief Title

Selecting Hypoxic Tumours for Treatment Modification

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Diagnosed with bladder, prostate, or cervical cancer
  • Scheduled to have radiotherapy at the Christie NHS Foundation Trust
  • Suitable for imaging on an MRI scanner
  • Able to give informed consent
Not Eligible

You will not qualify if you...

  • Any contraindications to MRI after safety screening
  • Unable to tolerate MRI scans
  • Pregnant (for bladder and cervical cancer patients)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Up to 1 month

Participants undergo MRI scans and tissue sample analysis to assess tumour hypoxia using gene-expression signatures and imaging biomarkers.

1 to 2 visits depending on imaging and sample collection schedules

Long-term Monitoring

Duration - Up to study completion in May 2028

Participants are observed over time to assess cancer outcomes and the effectiveness of personalised hypoxia-targeted treatment strategies.

Periodic monitoring visits throughout the study duration

Trial Site Locations

Total: 1 location

1

The Christie NHS Foundation Trust

Manchester, United Kingdom

Actively Recruiting

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Research Team

R

Rachel Reed, MSc

K

Kimberley Reeves, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

3

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Published Research Related To This Trial

Correlation and colocalization of HIF-1α and pimonidazole staining for hypoxia in laryngeal squamous cell carcinomas: A digital, single-cell-based analysis.

Justin E Swartz, Hilde J G Smits, Marielle E P Philippens...

https://pubmed.ncbi.nlm.nih.gov/35447566

Lack of predictive tools for conventional and targeted cancer therapy: Barriers to biomarker development and clinical translation.

Nikolaos Batis, Jill M Brooks, Karl Payne...

https://pubmed.ncbi.nlm.nih.gov/34192550

A Gene Signature for Selecting Benefit from Hypoxia Modification of Radiotherapy for High-Risk Bladder Cancer Patients.

Lingjian Yang, Janet Taylor, Amanda Eustace...

https://pubmed.ncbi.nlm.nih.gov/28400426

Technical development and validation of a clinically applicable microenvironment classifier as a biomarker of tumour hypoxia for soft tissue sarcoma.

Laura J Forker, Becky Bibby, Lingjian Yang...

https://pubmed.ncbi.nlm.nih.gov/37085598

A 26-gene hypoxia signature predicts benefit from hypoxia-modifying therapy in laryngeal cancer but not bladder cancer.

Amanda Eustace, Navin Mani, Paul N Span...

https://pubmed.ncbi.nlm.nih.gov/23820108