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Recruiting NCT06604533

NCT06604533 Magnetic Resonance Imaging (MRI) Guided Stereotactic Adaptive Radiotherapy for Targeting Abdominal Cancer

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Clinical Trial Summary
NCT ID NCT06604533
Status Recruiting
Phase
Sponsor Australasian Gastro-Intestinal Trials Group
Condition Abdominal Cancer
Study Type INTERVENTIONAL
Enrollment 30 participants
Start Date 2025-07-07
Primary Completion 2030-01

Trial Parameters

Condition Abdominal Cancer
Sponsor Australasian Gastro-Intestinal Trials Group
Study Type INTERVENTIONAL
Phase N/A
Enrollment 30
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2025-07-07
Completion 2030-01
Interventions
Intervention: MRI-Linac SABR

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Brief Summary

The aim of this study is to investigate the effect of MRI-guided adaptive stereotactic radiotherapy on local control, survival, and toxicity in the treatment of oligometastatic cancer to the abdomen.

Eligibility Criteria

Inclusion Criteria: * Aged 18 years or older * Patients with diagnosis of oligometastatic disease from primary colorectal, upper gastrointestinal (e.g. gastric, oesophagus, pancreatic), breast, non-small cell lung, renal cell, or gynaecological malignancy. Oligometastatic disease with controlled primary disease\* and maximum total of 5 metastatic lesions in a maximum of 2 different organ systems in any of the following sites: 1. Liver 2. Adrenal 3. Abdomino-pelvic lymph node 4. Other abdominal site e.g. pancreatic, renal. 5. Other pelvic site 6. Bony or lung is allowed only if in conjunction with an abdominal site above * De novo or metachronous oligometastatic disease where the original tumour site has been treated with curative intent. * Controlled primary disease in metachronous oligometastastic disease defined as at least 3 months since original tumour treated with curative intent and no progression at primary site * Controlled primary disease in de novo oligometastatic disease def

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