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Trial Title: Ate-Bev Early Response Prediction Model in Advanced HCC

NCT ID: NCT05763277

Condition: Hepatocellular Carcinoma
Atezolizumab-bevacizumab
Response Evaluation

Conditions: Official terms:
Carcinoma
Carcinoma, Hepatocellular

Study type: Observational [Patient Registry]

Overall status: Recruiting

Study design:

Time perspective: Prospective

Intervention:

Intervention type: Diagnostic Test
Intervention name: Early response evaluation
Description: Atezolizumab and bevacizumab are administered every three weeks, and before to the second treatment cycle, blood tests and imaging tests are conducted (week 5). This precedes the standard response evaluation (week 9-12).
Arm group label: Ate-Bev

Summary: The prognosis of hepatocellular carcinoma is poor compared to other carcinomas. Many drugs have recently been developed, and recently, atezolizumab-bevacizumab treatment was superior to sorafenib, the conventional treatment for advanced hepatocellular carcinoma. However, there is no information on the evaluation on the evaluation of treatment response for atezolizumab-bevacizumab combination therapy compared to atezolizumab alone or bevacizumab alone. Therefore, this study aimed to create a predictive model that can detect treatment response at an early stage.

Criteria for eligibility:

Study pop:
Patients who were diagnosed with advanced hepatocellular carcinoma and who were scheduled to receive atezolizumab-bevacizumab as the first-line therapy in a single tertiary hospital are included.

Sampling method: Non-Probability Sample
Criteria:
Inclusion Criteria: - Patients who were diagnosed with advanced hepatocellular carcinoma and who were scheduled to receive atezolizumab-bevacizumab as the first-line therapy - Patients willing to participate in this study Exclusion Criteria: - Individuals with a history of severe contrast allergy - Individuals with severe comorbidities (according to the American Society of Clinical Oncology-Friends of Cancer Research Organ Dysfunction.)

Gender: All

Minimum age: 18 Years

Maximum age: 80 Years

Healthy volunteers: Accepts Healthy Volunteers

Locations:

Facility:
Name: Seoul National University Hospital

Address:
City: Seoul
Country: Korea, Republic of

Status: Recruiting

Contact:
Last name: Jeong-Hoon Lee, M.D., Ph.D.
Email: pindra@empal.com

Start date: July 22, 2022

Completion date: May 22, 2025

Lead sponsor:
Agency: Seoul National University Hospital
Agency class: Other

Source: Seoul National University Hospital

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT05763277

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