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CT Volume Measurement of Hepatocellular Carcinoma

Ct Volume Measurement of Hepatocellular Carcinoma After Transarterial Chemoembolization (TACE) or Microwave Ablation (MWA)

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07183566
Enrollment
66
Registered
2025-09-19
Start date
2025-10-01
Completion date
2027-11-01
Last updated
2025-09-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

CT, Hepatocellular Carcinoma (HCC)

Brief summary

The aim of this study is to evaluate the role of CT volumetric measurement in assessing treatment response of hepatocellular carcinoma (HCC) following trans arterial chemoembolization (TACE) or microwave ablation (MWA)

Detailed description

Hepatocellular carcinoma (HCC) is the predominant form of primary liver cancer and a major contributor to cancer-related mortality worldwide (1). Conventional curative interventions for HCC encompass liver transplantation, hepatic resection, and thermal ablation. Regrettably, fewer than 30% of patients qualify for surgery upon diagnosis, and many tumor-related characteristics, including size and location, may inhibit the application of thermal ablative methods . In these cases, locoregional therapies such as transarterial chemoembolization (TACE) and microwave ablation (MWA) play a pivotal role. Both techniques aim to achieve local tumor control and improve patient survival. TACE induces ischemic necrosis through targeted delivery of chemotherapeutic agents combined with arterial embolization, whereas MWA achieves tumor destruction by generating high-frequency electromagnetic waves that produce thermal coagulative necrosis. Accurate assessment of treatment response is essential for guiding clinical decisions and predicting outcomes. Conventional imaging-based response criteria, such as RECIST and mRECIST, primarily focus on changes in lesion diameter. However, these methods may not fully reflect the extent of tumor necrosis or viable residual tissue . In this context, CT-based volumetric measurements have emerged as a more objective and sensitive tool for evaluating therapeutic response after locoregional treatment. Volumetric analysis provides a three-dimensional assessment of tumor burden and may bet ter correlate with treatment efficacy and prognosis compared to traditional linear measurements. Therefore, this study aims to investigate the role of CT volumetric measurement of HCC after TACE or microwave ablation in evaluating treatment response and predicting clinical outcomes .

Interventions

DEVICECt

Ct volume measurement of HCC after TACE or MWA

Sponsors

Assiut University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* Adult patients (≥18 years) with a confirmed diagnosis of HCC based on AASLD or EASL criteria. * Patients deemed unresectable by the multidisciplinary tumor board. * Patients scheduled for TACE as the primary locoregional therapy. * Preserved liver function (Child-Pugh class A or B). * Adequate renal function to permit contrast-enhanced CT.

Exclusion criteria

* Patients with extrahepatic metastases or portal vein thrombosis. * Patients with contraindications to iodinated contrast or TACE. * Patients with severe comorbid illness that precludes participation. * Patients refuse to provide informed consent.

Design outcomes

Primary

MeasureTime frameDescription
Ct volume measurent of hepatocellular carcinoma after Transarterial chemoembolization or microwave ablationBaselineAt enrollment, all patients will undergo a comprehensive clinical assessment, including full medical history with emphasis on risk factors for hepatocellular carcinoma triphasic CT scan of the liver, which will serve as the reference for tumor volume (by cm3 or cc), number, and distribution prior to TACE or MWA.

Contacts

Primary ContactAhmes Saber Hamed, Master
Ahmed.17289721@med.aun.edu.eg+2001019545804

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026