Development and Application of Accurate Detection Technology Based on Multimodal Data of Breast Cancer Comobid Depression

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

This study is a prospective, observational clinical research aimed at establishing a multimodal database encompassing clinical information and gut microbiome data from a sample of over 1,000 breast cancer patients comorbid with depression. The research involves collecting cohort sample information from breast cancer patients with comorbid depression, as well as fecal, blood, and saliva specimens for metagenomic sequencing, untargeted metabolite detection, and cortisol level analysis, respectively. Based on the collected multimodal data, diagnostic, efficacy prediction, and prognostic survival prediction models for breast cancer with comorbid depression will be developed. Additionally, a precision prediction cloud platform will be designed and deployed to support data upload, model prediction, and result visualization.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 80
Healthy Volunteers: f
View:

• Pathologically confirmed primary breast cancer; Aged 18-80 years; No prior history of malignancy other than breast cancer; Awareness of their breast cancer diagnosis; Karnofsky Performance Status (KPS) score \>70; Willing to provide blood, fecal, and saliva samples with signed informed consent.

Locations
Other Locations
China
Xiangya Hospital of Central South University
RECRUITING
Changsha
Contact Information
Primary
Jun Huang,doctor
404369@csu.edu.cn
86-18229944886
Time Frame
Start Date: 2025-03-11
Estimated Completion Date: 2027-04-01
Participants
Target number of participants: 1000
Treatments
Neoadjuvant therapy breast cancer patient cohort
HR-positive breast cancer cohort under adjuvant treatment
Advanced triple-negative immunotherapy and HR-positive endocrine therapy cohorts
Related Therapeutic Areas
Sponsors
Leads: Xiangya Hospital of Central South University

This content was sourced from clinicaltrials.gov