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Added Value of PET/CT in Assessment of Hepatocellular Malignancy Post Radiofrequency Ablation

T

Tanta University

Status

Completed

Conditions

Hepatocellular Malignancy
Radiofrequency Ablation
PET/CT

Treatments

Other: PET/CT technique

Study type

Observational

Funder types

Other

Identifiers

NCT06960031
36264PR1162/3/25

Details and patient eligibility

About

This study aims to assess the residual tumoral activity versus the well ablation of اepatocellular carcinoma (HCC) post radiofrequency ablation.

Full description

Hepatocellular carcinoma (HCC) is the most common primary liver malignancy and is a leading cause of cancer-related death worldwide. It is the third most common cause of death of cancer worldwide, also the sixth and fourth common cancer in worldwide and Egypt, respectively.

Radiofrequency ablation (RFA) is a technique that is recently developed for the ablation of liver tumours. It converts radio frequency waves into thermal energy, causing coagulation necrosis of the tumours. It has attracted great interest in recent years because of the excellent response rate with little morbidity. Compared with other local ablative modalities, RFA has been shown to be safer and more effective.

Positron emission tomography (PET) with 18F-fluoro-2- deoxy-D-glucose (18F-FDG) is a functional imaging tool that provides metabolic information of the lesion. It is effective for diagnosis, monitoring therapy and detection of recurrent tumours of various cancers because of its high sensitivity and specificity. However, it is less successful in the detection of primary HCC because of variable uptake. Even though the value of 18F-FDG PET for the detection of primary HCC remains controversial, 18F-FDG PET would seem to be appropriate for the follow-up of liver tumours.

Enrollment

70 patients

Sex

All

Ages

40 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age from 40 to 75 years.
  • Both sexes.
  • Patients with hepatocellular carcinoma (HCC) and underwent radiofrequency ablation (RFA) .

Exclusion criteria

  • Patients with past history of contrast allergy.
  • Patients with blood glucose level >200 mg/dl at the time of the study.
  • High serum creatinine> 2 mg / dl.
  • Small lesions < 10 mm.
  • Well differentiated hepatocellular carcinoma (HCC) lesions by pathology.

Trial design

70 participants in 1 patient group

PET/CT
Description:
Hybrid positron emission tomography (PET) and computed tomography (CT) images will be performed using Philips hybrid system equipped with a 16 MDCT scanner. The whole-body PET images from the skull vault down to the knee will be performed using several bed positions acquisition, each bed is approximately 15cm axial filed with 4mm special resolution. The time of acquisition of the emission scan is about 2 min for each bed, with a total time range between 12 and 17 min.
Treatment:
Other: PET/CT technique

Trial contacts and locations

1

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Central trial contact

Naglaa S Abou Taira, MD

Data sourced from clinicaltrials.gov

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