Liquid Biopsy Multi-Omics and Biomarker Development in Melanoma

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-80
SponsorXijing Hospital

About this trial

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.

Eligibility criteria

Qualifiers

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.

Disqualifiers

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.

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

200 Participants
are grouped into 1 trial group

Sponsors and collaborators

Xijing Hospital

Lead sponsor

Southern University of Science and Technology

Collaborator