Assessment of Hypoxia Before Radioembolization Treatment With 18F-FMISO PET

NCT ID: NCT06027021

Last Updated: 2024-07-30

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

64 participants

Study Classification

OBSERVATIONAL

Study Start Date

2023-08-15

Study Completion Date

2024-07-15

Brief Summary

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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.

Detailed Description

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Conditions

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Radioembolization Radiotherapy Cancer Positron Emission Tomography

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Treatment group

Patients received radioembolization with hepatocellular cancer or colorectal cancer liver metastases

18F-Fluoromisonidazole PET

Intervention Type DIAGNOSTIC_TEST

Imaging of hypoxia before radioembolization with 18F-Fluoromisonidazole PET.

Interventions

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18F-Fluoromisonidazole PET

Imaging of hypoxia before radioembolization with 18F-Fluoromisonidazole PET.

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Ankara University

OTHER

Sponsor Role lead

Responsible Party

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Cigdem Soydal

Asc Prof

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Cigdem Soydal, MD

Role: PRINCIPAL_INVESTIGATOR

Ankara University

Locations

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Ankara University

Ankara, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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ARTE-MISO

Identifier Type: -

Identifier Source: org_study_id

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