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NCT Number: NCT05184400

Identification of New Biomarkers for Patients With Cholangiocarcinoma and Gallbladder Cancer

No validated biomarkers exist that can identify patients with biliary tract cancer at an early stage or predict treatment outcomes. The objective of the present study is to find diagnostic, prognostic and predictive biomarkers.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Herlev & Gentofte Hospital

Herlev, Copenhagen, 2700, Denmark

Location status: Recruiting

Location contact

Julia S Johansen, D.M.Sc. MD

CONTACT

[email protected]

+4538689241

Julia S Johansen, MD, D.M.Sc.

SUB_INVESTIGATOR

Ole Larsen, MD, PhD

PRINCIPAL_INVESTIGATOR

Troels D Christensen, MD

CONTACT

[email protected]

+4538681381

Troels D Christensen, MD

SUB_INVESTIGATOR

About this study

Biliary tract cancer (BTC) is a heterogeneous disease and includes both gallbladder cancer and cholangiocarcinoma. Combined BTC is the fifth most common gastrointestinal cancer. The prognosis is poor with a median overall survival of less than a year and estimated 5-year survival of about 20 % for all stages. The poor survival is related to aggressive malign nature, late diagnosis, and limited treatment options. Today, only CA 19-9 is used in routine practice but its use as a prognostic or diagnostic biomarker is very limited.

The objective of the present study is to find diagnostic, prognostic, and predictive biomarkers, which can be used to 1) diagnose BTC early in the disease course with high specificity and sensitivity, 2) improve prognostication, or 3) predict and monitor treatment effectiveness and tolerability for the individual patient.

CHOCA is an observational and translational open cohort study with a prospective collection of biological materials (blood samples and tissue) and clinical data in patients with BTC receiving standard or protocolized treatment. Blood samples (i.e. serum, EDTA plasma and buffy coat, and blood in PAXgeneRNA tubes) are collected from all patients before operation or start of chemotherapy and during treatment with blood sampling before the 2nd cycle of chemotherapy and longitudinally at the time of follow-up CT scan (about every 3 months) until disease progression. Tissue removed during routine diagnostic procedures or treatment will be requisitioned.

The patients are followed until death. The following data are collected: Demographics, disease characteristics, comorbidities and lifestyle factors, routine blood tests (i.e. hematology, creatinine, liver enzymes, bilirubin, carbohydrate antigen 19-9, C-reactive protein); type of operation; types of chemotherapy, reason for termination of therapy; date of disease recurrence in operated patients; date of disease progression for each line of chemotherapy; and date of death. Biomarker analyses will include a range of molecules with different characteristics such as DNA, Single Nucleotide Polymorphism (SNPs), RNA, microRNA, proteins, proteoglycans, and metabolites. Controls will be included from other studies in order to identify potential diagnostic biomarkers,. Controls include patients with other diseases or healthy subjects. Biomarkers will be analyzed using appropriate methods and statistical analysis following REMARK guidelines.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Histological or cytological diagnosis of BTC
  • Patients referred for treatment of BTC
  • Signed informed consent

Exclusion criteria

  • None

Treatment and study plan

Primary outcomes

  1. Diagnostic accuracy (sensitivity and specificity)

    Time frame: Baseline

    Outcome for diagnostic biomarkers. Case-control design.

  2. Overall survival (OS)

    Time frame: Baseline to death or lost to follow-up, an average of 1 year

    Outcome for prognostic and predictive biomarkers

Secondary outcomes

  1. Progression free survival (PFS)

    Time frame: Baseline to progression, death or lost to follow-up, an average of 1 year

    Outcome for prognostic and predictive biomarkers

  2. Incidence of adverse events

    Time frame: Baseline to progression, death or lost to follow-up, an average of 1 year

    Outcome for prognostic and predictive biomarkers related to treatment toxicity.

Sponsors and collaborators

Lead sponsor

Herlev and Gentofte Hospital

Other

Registry information

Official study title

Identification of New Biomarkers for Patients With Biliary Tract Cancer (Cholangiocarcinoma and Gallbladder Cancer) - do They Provide New Information Regarding Diagnosis, Treatment Efficacy, Side Effects, or Prognosis?

Acronym: CHOCA

Important dates

Study start
2015
Primary completion
2030
Study completion
2030
First posted
Jan 11, 2022
Registry last updated
Jan 11, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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