<HashMap><database>ecrin-mdr-crc</database><scores/><additional><omics_type>Clinical</omics_type><study_start_year>2023</study_start_year><condition>Cancer-Bowel-Anal</condition><condition>Anal Cancer</condition><disease>Cancer-bowel-anal</disease><disease>Anal Cancer</disease><study_type>Interventional</study_type><full_dataset_link>https://newmdr.ecrin.org/Study/116890</full_dataset_link><location>Australia</location><study_start_month>12</study_start_month><repository>ECRIN MDR</repository><study_status>Not yet recruiting</study_status></additional><is_claimable>false</is_claimable><name>Investigating the role of interim Positron Emission Tomography (PET) and Magnetic Resonance Imaging (MRI) and blood markers to predict local and regional failure in patients with anal squamous cell carcinoma.</name><description>Interventions: FDG-PET, Biomarker testing with optional MRI will be administered to participants eligible and consenting to this study.
Patients will receive 5-6 weeks of CRT depending on their staging.
FDG- PET scans will be performed at 3 timepoints for all patients. PETpre is to be completed prior to commencement of CRT, PETinterim during the second week of CRT and PETpost at 3 months post CRT. If the PETpost at 3 months post-treatment FDG-PET reveals a partial response, and the patient does not have clinically progressive disease, a 4th FDG-PET (PETprogress) will be performed at 5 months after completion of CRT.
The scans will be performed in the Nuclear Medicine department at Liverpool Hospital on a digital PET scanner (GE Healthcare, Discovery MI) in 3D mode for a total acquisition time of 1.5 – 2.5 min per bed position, adjusted according to the patient weight, from mid brain to proximal femora at about 1 hour post injection of a radiotracer called fluorodeoxyglucose (3.4 MBq/Kg). PET images will be reconstructed using GE VUE Point FX (Time of Flight) algorithm into a 256 x 256 matrix size with a slice thickness of 3.75 to 4.0 mm, and GE Q.Clear iterative reconstruction and if required Q-static motion-corrected respiratory gated algorithm for measurement of SUV and other volumetric parameters. Transmission scans and attenuation corrections will be obtained by using a 128-slice CT, using helical mode without the use of a contrast medium. CT images are to be acquired at 3.75 to 5mm slice thickness and reconstructed to a transaxial matrix size of 512 x 512. The current (30-40 mAs) and voltage (120-140 kV) are varied according to the patient weight. All FDG PET images will be analysed by the consensus reading of a nuclear medicine physician and a radiation oncologist.
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Primary outcome(s): Locoregional failure will be assessed by using FDG PET, MRI imaging and HPV ctDNA biomarker testing.[ 6 months post chemoradiation treatment];MTV 2.5 will be assessed using FDG-PET imaging.[ 2 weeks during chemoradiation treatment, 3 and 6 months post chemoradiation treatment];Diffusion weighted images with B values 50, 400 and 800 will be assessed using MRI[ 2 weeks during Chemoradiation treatment]
Study Design: Purpose: Diagnosis; Allocation: Non-randomised trial; Masking: Open (masking not used);Assignment: Single group;Type of endpoint: Efficacy</description><dates><creation>2023-12-15</creation></dates><accession>116890</accession><cross_references><Australian New Zealand Clinical Trials Registry>ACTRN12623001098628</Australian New Zealand Clinical Trials Registry></cross_references></HashMap>