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NCT Number: NCT07584291

Liquid Biopsy Multi-Omics and Biomarker Development in Melanoma

This prospective, observational cohort study aims to explore the multi-omics profiles of liquid biopsies and develop clinical biomarkers in melanoma. Two hundred participants with pathologically confirmed acral or cutaneous melanoma who are scheduled to receive standard first-line immunotherapy will be enrolled. Blood samples will be collected at baseline and every 3 weeks during treatment, along with radiological assessments every 12 weeks. Tumor tissue will be obtained at surgery after approximately 3 months of therapy. Using microfluidic-based circulating tumor cell isolation, exosome enrichment, ctDNA analysis, and integrative multi-omics approaches, the study will compare molecular features across primary tumors, metastases, and liquid biopsy components. The primary outcomes are progression-free survival and overall survival, assessed up to 36 months. Secondary outcomes include changes in circulating tumor cell counts, ctDNA concentrations, exosomal biomarker levels, pathological response rate at surgery, and the predictive accuracy of a multi-omics model for treatment response. The findings are expected to provide a basis for personalized monitoring and treatment strategies in melanoma.

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Xijing Hospital, Air Force Medical University

Xi'an, Shaanxi, China

Location status: Recruiting

Location contact

Weinan Guo

CONTACT

[email protected]

+86-29-84775406

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Diagnosed with acral or cutaneous melanoma according to the "Melanoma Diagnosis and Treatment Guidelines."
  • Underwent sentinel lymph node biopsy with complete information available.
  • Archived melanoma tissue samples available with complete information.
  • Complete basic demographic and clinical information.
  • Age 18-80 years, any sex.

Exclusion criteria

  • Patients with severe organic diseases, immunodeficiency disorders, organ absence, or organ transplantation.
  • Patients diagnosed with mucosal melanoma according to the "Melanoma Diagnosis and Treatment Guidelines."
  • Patients with other concurrent malignant tumors (e.g., basal cell carcinoma, lung cancer).
  • Incomplete patient information or pathological sample data.

Treatment and study plan

Primary outcomes

  1. Progression-free survival (PFS)

    Time frame: From date of enrollment until date of progression or death, assessed up to 36 months.

    PFS is defined as the time from enrollment to the first occurrence of disease progression (assessed by RECIST 1.1) or death from any cause, whichever occurs first.

  2. Overall survival (OS)

    Time frame: From date of enrollment until date of death, assessed up to 36 months.

    OS is defined as the time from enrollment to death from any cause.

Secondary outcomes

  1. Circulating tumor cell (CTC) count

    Time frame: Baseline and after completion of treatment (up to 3 months)

    Number of CTCs isolated from peripheral blood using surface antigen-independent microfluidic separation and enumerated.

  2. Circulating tumor DNA (ctDNA) concentration

    Time frame: Baseline and after completion of treatment (up to 3 months)

    Concentration of ctDNA in plasma, quantified by digital PCR or next-generation sequencing.

  3. Exosomal PD-L1 expression level

    Time frame: Baseline and after completion of treatment (up to 3 months)

    Concentration of PD-L1 on exosomes isolated by ultracentrifugation and quantified by immuno-multiplex fluorescence analysis.

  4. Sum of diameters of target lesions

    Time frame: Baseline and every 12 weeks through study completion (up to 36 months)

    Sum of the longest diameters for non-nodal target lesions and short-axis diameters for nodal target lesions, assessed by CT or MRI per RECIST 1.1.

  5. Pathological response rate

    Time frame: At surgery after approximately 3 months of treatment.

    Number of participants with pathological response (partial or complete) in resected tissue after approximately 3 months of treatment, as determined by histopathological analysis.

  6. Predictive accuracy of multi-omics model for treatment response

    Time frame: At 3months after treatment initiation.

    Area under the receiver operating characteristic (ROC) curve of an integrated multi-omics model (combining clinical, imaging, and liquid biopsy features) for predicting objective response (complete or partial response per RECIST 1.1) at 6 months.

Study contacts

Contact information is provided by the study sponsor or research team.

Weinan Guo

CONTACT

[email protected]

+86-29-84775406

Sponsors and collaborators

Lead sponsor

Xijing Hospital

Other

Collaborators

  • Southern University of Science and Technology

Registry information

Official study title

Multi-Omics Analysis of Liquid Biopsy and Development of Clinical Biomarkers in Melanoma: A Prospective Cohort Study

Important dates

Study start
2025
Primary completion
2027
Study completion
2028
First posted
May 13, 2026
Registry last updated
May 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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