Hepatobiliary Tumors Tissue Samples Acquisition

NCT04445532 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 450

Last updated 2023-07-07

No results posted yet for this study

Summary

Hepatobiliary tumors have a poor prognosis and high individual heterogeneity, so it is of great significance to find important prognostic markers and then screen out specific subgroups of people; meanwhile, chronic hepatitis, cirrhosis, and healthy control participants also need to show the evolution of tumors and discover specific diagnostic markers as a control group. Moreover, targeted therapy and immunotherapy make cancer treatment enter a new field, but only part of patients achieve response rates and reach clinical benefit. However, these drugs are expensive and can cause treatment-related adverse events. Therefore, reliable biomarkers identification is needed to help predict the response to these treatment options in order to screen patients with better responsiveness and avoid wasting money. Multi-omics research can reveal the characteristics of hepatobiliary tumors more deeply and find meaningful therapeutic targets.

Therefore, 450 patients at least 18 years of age with hepatobiliary tumors were included in this study.

Conditions

Interventions

OTHER

Gene expression analysis

Gene expression analysis

OTHER

Genomic analysis

Genomic analysis

OTHER

Protein expression analysis

Protein expression analysis

OTHER

Proteomic profiling

Proteomic profiling

OTHER

Polymerase chain reaction

Polymerase chain reaction

OTHER

Mass spectrometry

Mass spectrometry

OTHER

Immunohistochemistry

Immunohistochemistry

OTHER

Metabolomics profiling

Metabolomics profiling

OTHER

Methylation and epigenetic analysis

Methylation and epigenetic analysis

OTHER

Liquid biopsy analysis

Liquid biopsy analysis, such as cell-free DNA or circulating tumor cell analysis

OTHER

Laboratory biomarker analysis

Laboratory biomarker analysis (such as AFP, CA19-9, CEA)

Sponsors & Collaborators

  • OrigiMed

    collaborator INDUSTRY
  • GeneCast Biotechnology Co., Ltd.

    collaborator INDUSTRY
  • YuceBio Technology Co., Ltd.

    collaborator UNKNOWN
  • Geneplus-Beijing Co. Ltd.

    collaborator INDUSTRY
  • Peking Union Medical College Hospital

    lead OTHER

Principal Investigators

  • Haitao Zhao, MD · Peking Union Medical College Hospital

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-10-11
Primary Completion
2025-06-01
Completion
2025-06-01

Countries

  • China

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04445532 on ClinicalTrials.gov