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OpenTrials
Completed

NCT Number: NCT07225452

An Exosomal miRNA-based Liquid Biopsy for ICC Detection

Intrahepatic cholangiocarcinoma (ICC) is a malignant liver tumor with poor prognosis and limited curative treatment options. Early and accurate detection remains an unmet clinical need.

The LUMIC study aims to develop a non-invasive liquid biopsy platform based on both exosomal microRNAs (exo-miRNAs) to detect intrahepatic cholangiocarcinoma with high sensitivity and specificity.

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Key information

About this study

Intrahepatic cholangiocarcinoma (ICC) is the second most common primary liver malignancy after hepatocellular carcinoma, accounting for approximately 10-15% of all primary liver cancers. Despite improvements in surgical techniques and imaging modalities, ICC is often diagnosed at advanced stages, resulting in dismal outcomes with a 5-year overall survival rate of 25-30%.

Traditional imaging approaches such as CT and MRI have limited sensitivity for detecting early or small ICC lesions. Blood-based biomarkers, including CA19-9, also lack adequate specificity.

Recent advances in liquid biopsy have demonstrated that exosomal microRNAs (exo-miRNAs) can serve as promising, minimally invasive biomarkers reflecting tumor biology and microenvironmental changes.

The LUMIC study (Liquid biopsy Using exosomal miRNA for Intrahepatic Cholangiocarcinoma detection) aims to identify and validate miRNA signatures capable of distinguishing ICC from benign biliary or non-cancerous liver conditions.

Blood samples are collected before treatment, and exo-miRNA expression profiles are analyzed using RT-qPCR and bioinformatic pipelines. Diagnostic performance (AUC, sensitivity, specificity) will be evaluated through training and validation cohorts.

This study provides a foundation for integrating liquid biopsy-based diagnostics into ICC clinical workflows to enable earlier detection and improved treatment stratification.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Age ≥ 18 years
  • Histologically confirmed intrahepatic cholangiocarcinoma
  • Availability of pre-treatment plasma sample
  • Informed consent provided

Exclusion criteria

  • Extrahepatic cholangiocarcinoma
  • History of other malignancy within 5 years
  • Active infection, autoimmune disease, or pregnancy
  • Inadequate clinical data or poor sample quality

Treatment and study plan

Small RNA sequencing

Diagnostic Test

Small RNA sequencing of serum/plasma RNA to identify ICC-specific upregulated miRNAs

LUMIC assay

Diagnostic Test

RT-qPCR validation of selected miRNAs

Primary outcomes

  1. Sensitivity

    Time frame: Through study completion (~1 year)

    The proportion of true positive ICC cases correctly identified by the LUMIC assay.

Secondary outcomes

  1. Specificity

    Time frame: Through study completion (~1 year)

    The proportion of true negative cases correctly classified as non-ICC.

  2. Diagnostic accuracy (AUC)

    Time frame: Through study completion (~1 year)

    The overall discriminative ability of the exo-miRNA panel for ICC detection.

Sponsors and collaborators

Lead sponsor

City of Hope Medical Center

Other

Registry information

Official study title

Liquid Biopsy Using Exosomal miRNA for Intrahepatic Cholangiocarcinoma Detection

Acronym: LUMIC

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Nov 6, 2025
Registry last updated
Mar 13, 2026

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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