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Clinical Trials in Australia / NCT06050707
Recruiting Phase 2

MR-Adaptive Radiation Therapy for Anal Cancer With EScalated-Treatment in a Risk-Optimized Approach

NCT06050707 · tracked via the Priya Life Science Australia tracker
Phase
Phase 2
Started
2023-09-29
Last updated
2026-06-10

Condition(s) studied

Anal Squamous Cell Carcinoma

Investigational drug(s) / intervention(s)

Radiotherapy - Low risk groupRadiotherapy - Standard risk groupRadiotherapy - Intermediate risk groupRadiotherapy - High risk group

Radiotherapy - Low risk group: 20 fractions completed in 4 weeks

Radiotherapy - Standard risk group: 25 fractions completed in 5 weeks

Radiotherapy - Intermediate risk group: 30 fractions completed in 6 weeks

Radiotherapy - High risk group: 35 fractions completed in 7 weeks

Study summary

The proposed study is a phase II, single arm, open-label trial of MR-guided radiation therapy (RT) with risk stratified RT dose selection in patients with anal cancer. Based on previous data, a risk adaptive treatment approached is proposed in 4 groups: Low risk, standard risk, intermediate risk, and high risk. Human papillomavirus (HPV) DNA will be analyzed to identify novel biomarkers that predict chemoradiotherapy (CRT) response and toxicity.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients with pathologically proven diagnosis of anal SCC. This may include tumors of non-keratinizing histology such as basoloid or cloacogenic histology. Individuals with squamous cell carcinoma of the anal margin are eligible. * Clinical stage T1-4 N0-1 M0 (the Union for International Cancer Control (UICC) / the American Joint Committee on Cancer (AJCC) 8th Ed) * Patients must be eligible for definitive RT or CRT * Must be ≥ 18 years of age * Must have an Eastern Cooperative Oncology Group (ECOG) performance status of 0-2 Exclusion Criteria: * Previous chemotherapy, RT or curative-intent surgical treatment (i.e. APR) for anal cancer. * Any previous RT to the abdomino-pelvic region that would result in overlap of RT volume for the current study. * Individuals with a history of a different malignancy except if they have been disease-free for at least 2 years and are deemed by the investigator to be at low risk for recurrence. Individuals with the following cancers are eligible if diagnosed and treated within the past 5 years: cervical cancer in situ, and basal cell or squamous cell carcinoma of the skin.

Primary outcome measure(s)

Trial sites (5)

FacilityCityRegionStatus
Allegheny Health Network Pittsburgh Pennsylvania Not Yet Recruiting
Medical College of Wisconsin Cancer Center Milwaukee Wisconsin Not Yet Recruiting
Austin Health Heidelberg Victoria Not Yet Recruiting
Princess Margaret Cancer Centre Toronto Ontario Recruiting
CHUM - Centre hospitalier de l'Université de Montréal Montreal Quebec Not Yet Recruiting

More University Health Network, Toronto trials in Australia

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06050707 on ClinicalTrials.gov ↗ ← All trials in Australia