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Assessment of Hypoxia Before Radioembolization Treatment With 18F-FMISO PET (ARTE-MISO)

A

Ankara University

Status

Completed

Conditions

Radioembolization
Radiotherapy
Cancer
Positron Emission Tomography

Treatments

Diagnostic Test: 18F-Fluoromisonidazole PET

Study type

Observational

Funder types

Other

Identifiers

NCT06027021
ARTE-MISO

Details and patient eligibility

About

Hypoxia is a known factor for resistance to radiotherapy in tumors. Response to transarterial radioembolization is known to be variable between different patients even if the same dose of radiation was delivered. In this study the investigators aim to quantify the hypoxia in the primary and secondary tumors of liver with 18F-FMISO PET before radioembolization and to prove any effect of the hypoxia, if present, on the dose that should be delivered to tumor to ensure treatment response.

Enrollment

64 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosed with colorectal carcinoma with liver metastasis or hepatocellular carcinoma.
  • Is not eligible for surgery
  • Above 18 years old
  • The patients who are referred for transarterial radioembolization treatment to Ankara University School of Medicine Department of Nuclear Medicine.

Exclusion criteria

  • Patients with ECOG performance score >1
  • Claustrophobia
  • Life expectancy shorter than 3 months
  • Pregnant or breast-feeding patients

Trial design

64 participants in 1 patient group

Treatment group
Description:
Patients received radioembolization with hepatocellular cancer or colorectal cancer liver metastases
Treatment:
Diagnostic Test: 18F-Fluoromisonidazole PET

Trial contacts and locations

1

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Central trial contact

Cigdem Soydal, MD

Data sourced from clinicaltrials.gov

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