RecruitingNCT06363123

Plasma Metabolic Biomarkers for Multi-Cancer Diagnosis

Identification and Validation of Plasma Diagnostic Biomarkers for Multi-Cancer Based on Metabolomics: A Multi-Center Clinical Research and Validation Trial


Sponsor

Beijing Friendship Hospital

Enrollment

2,700 participants

Start Date

Mar 29, 2024

Study Type

OBSERVATIONAL

Conditions

Summary

The aim of this observational study is to comprehensively analyze the metabolites in plasma samples from multi-cancer patients using advanced mass spectrometry detection technology, in conjunction with metabolomics approaches. The goal is to construct a plasma metabolite database for multi-cancer patients. Simultaneously, we will delve into the exploration and validation of a series of metabolic biomarkers for early multi-cancer diagnosis. The objective is to establish a safer, more convenient, and more sensitive early screening method, thereby providing a reliable scientific foundation and critical evidence for improving the early diagnostic process for individuals at high risk of multi-cancer.


Eligibility

Inclusion Criteria8

  • Multi-Cancer Group:
  • Patients with a confirmed diagnosis based on the clinical "gold standard".
  • Collection of plasma samples prior to treatment.
  • Availability of complete clinical data.
  • Control Group:
  • Individuals with no abnormalities in routine physical examinations and relevant clinical tests.
  • Age ≥ 45 years.
  • Availability of complete clinical data.

Exclusion Criteria12

  • Previous reception of anti-tumor treatments (including radiotherapy, chemotherapy, etc.) before blood collection.
  • Coexistence of other systemic tumors.
  • Absence of plasma sample collection before treatment.
  • Pregnancy status.
  • No clear evidence of histopathological diagnosis (not applicable to the control group based on this criterion).
  • Patients with severe acute infections.
  • Patients with severe anemia.
  • Patients with severe liver or kidney dysfunction.
  • Patients with autoimmune deficiency diseases.
  • Patients with Hyperlipidemia.
  • Patients received contrast agent injection before blood draw.
  • Patients with psychiatric disorders.

Locations(4)

Cancer Hospital Chinese Academy of Medical Sciences

Beijing, Beijing Municipality, China

Beijing Friendship Hospital, Capital Medical University

Beijing, Beijing Municipality, China

Hebei Tumor Hospital

Shijiazhuang, Hebei, China

Zhejiang Cancer Hospital

Hangzhou, Zhejiang, China

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06363123


Related Trials