HCC: Predictive Biomarkers in Patients With Advanced Hepatocellular Carcinoma Treated With Systemic Therapy

Sponsor
CHA University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05197504
Collaborator
(none)
100
1
36.4
2.7

Study Details

Study Description

Brief Summary

Hepatocellular carcinoma (HCC) is the third most common cause of cancer-related deaths worldwide, and HCC is more frequently observed in Asia, including South Korea. As HCC is often accompanied by chronic hepatitis B or C virus and liver cirrhosis, treatment of HCC consider not only the tumor but also various factors such as liver function and the patient's performance status. Local treatment and surgery are possible in the early stages of HCC. However, it has a high recurrence rate even after curative surgeries due to underlying cirrhosis and the tumor microenvironment.

Although several studies have investigated gene mutations and differences in treatment response in advanced HCC through next-generation sequencing (NGS), studies on transcriptome analysis of advanced HCC through RNA-sequencing are hard to find, with a need for future research into precise classification and clinical significance of HCC based on multi-omics data.

Condition or Disease Intervention/Treatment Phase
  • Drug: atezolizumab plus bevacizumab

Detailed Description

to establish multi-omics data and discover biomarkers highly associated with treatment response in HCC patients

Study Design

Study Type:
Observational
Anticipated Enrollment :
100 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
Biomarker Discovery Through Multiomics Study in Advanced Hepatocellular Carcinoma Patients Who Received Atezolizumab and Bevacizumab Combination Therapy
Actual Study Start Date :
Dec 20, 2021
Anticipated Primary Completion Date :
Dec 31, 2024
Anticipated Study Completion Date :
Dec 31, 2024

Arms and Interventions

Arm Intervention/Treatment
intervention

atezolizumab + bevacizumab

Drug: atezolizumab plus bevacizumab
1200 mg of atezolizumab plus 15 mg/kg of body weight of bevacizumab intravenously every 3 weeks

Outcome Measures

Primary Outcome Measures

  1. collected tumor samples [through study completion, an average of 3 years]

    tumor samples from patients with hepatobiliary cancers (incidence of genetic alteration, association with treatment response and survival duration)

  2. collected blood samples [through study completion, an average of 3 years]

    blood samples from patients with hepatobiliary cancers (incidence of genetic alteration, association with treatment response and survival duration)

Secondary Outcome Measures

  1. Multi-omics analysis [3 years]

    Multi-omics analysis to further subtype and find therapeutic targets of HCC

  2. Biomarkers on the efficacy of Atezolizumab+Bevacizumab for advanced HCC [3 years]

    Molecular biomarker associated with overall survival, progression-free survival and objective response rate in patients who receive atezolizumab plus bevacizumab

Eligibility Criteria

Criteria

Ages Eligible for Study:
19 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Those above the age of 20 who understand the purpose of the study and agree to participate in the collection of samples during the study.

  • Patients who have been diagnosed with unresectable advanced HCC through imaging, histological, or cytological tests.

  • Patients who underwent an NGS test with advanced HCC tissues

  • Patients who are scheduled to receive systemic treatment

  • Patients with measurable lesions based on RECIST v1.1

  • ECOG performance status 0 or 1

  • Patients with a life expectancy of at least three months

Exclusion Criteria:
  • Patients who have systemic conditions accompanied by instability of vital signs, such as infections or organ failure

  • Those with mental/neurological conditions or dementia who have difficulties understanding and completing the consent form

  • Those who are assessed as not suitable for this study, at the discretion of the researcher

Contacts and Locations

Locations

Site City State Country Postal Code
1 CHA Bundang Medical Center Seongnam-si Gyeonggi-do Korea, Republic of 13496

Sponsors and Collaborators

  • CHA University

Investigators

  • Principal Investigator: Hongjae Chon, MD,PhD, Principal Investigator

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Hong Jae Chon, Assistant professor, Department of Medical Oncology, CHA University
ClinicalTrials.gov Identifier:
NCT05197504
Other Study ID Numbers:
  • 2021-11-019
First Posted:
Jan 19, 2022
Last Update Posted:
Jan 19, 2022
Last Verified:
Jan 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Hong Jae Chon, Assistant professor, Department of Medical Oncology, CHA University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 19, 2022