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The FuSion Program: A Prospective and Multicenter Cohort Study of Pan-Cancer Screening in Chinese Population

A Prospective, Multicenter, Noninterventional Cohort Study of Muti-Omics Models for Pan-Cancer Screening

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05159544
Enrollment
60000
Registered
2021-12-16
Start date
2021-07-06
Completion date
2024-12-07
Last updated
2024-04-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer

Keywords

Muti-omics, Pan-cancer screening, Early detection

Brief summary

The integrative study by Fudan and Singlera for cancer early detection(The FuSion Program ) will evaluate sensitivity,specificity and positive/negative predictive value of the screening model jointly developed by FuDan University and Singlera in a 2-year follow-up corhort including 10,000 persons in routine annual physicals from dozens of hospitals. The multi-omics model for pan-cancer screening will be developed in a 3-year follow-up corhort including 50,000 natural persons in community containing genetic information of tumor families, assessment of epidemiological risk factors, tumor markers, proteomics, genomics and DNA methylation. After optimizing, the ability of this model will be validated in the Taizhou corhort in reality.

Interventions

None listed

Sponsors

Fudan University
CollaboratorOTHER
Singlera Genomics Inc.
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
40 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

1. Take physical examinations in our research centers and have no cancer history; 2. Population Health tracking Survey - simplified version of the questionnaire must be filled according to the research program and an annual physical examination can be received as follow-up ; 3. Timely feed back the information related to tumor diagnosis in other hospitals to the investigator during the program; 4. Have no birth plan for the last 3 years; 5. Fully understand the study and voluntarily sign the informed consent.

Exclusion criteria

1. Have been diagnosed with esophageal cancer, gastric cancer, colorectal cancer, liver cancer, lung cancer, pancreatic cancer, breast cancer (including non-primary, such as recurrence, metastasis or other complications) and other malignant tumors; 2. Received blood transfusion, transplantation and other major operations within 3 months; 3. Participated in other interventional clinical researchs within 3 months; 4. Pregnant or lactating women; 5. Patients with autoimmune diseases, genetic diseases, mental diseases/disabilities and other diseases considered unsuitable for the study by the investigator; 6. Due to poor compliance, the researcher judged that the study could not be completed.

Design outcomes

Primary

MeasureTime frameDescription
To develop a multi-omics model for pan-cancer screening integrating the markers of ctDNA mutation, DNA fragmentation and methylation et al.assessed up to 36 monthsTo construct a multi-dimensional ensembled stacked machine learning approach, employing several different base models on ctDNA mutation, DNA fragmentation and mehylation, to provide an effective model for cancer early detection.
To evaluate sensitivity,specificity,positive/negative predictive value of the screening model in participants taking routine annual physicalsassessed up to 24 monthsSensitivity: the ability of a test to correctly identify patients with a disease. Specificity: the ability of a test to correctly identify people without the disease. Positive predictive value refers to the probability of the person having the disease when the test is positive. Negative predictive value refers to the probability of the person not having the disease when the test is negative.
To validate model's efficacy and clinical value in the diagnosis of cancers in Taizhou cohort.assessed up to 12 monthsCancer early detection could increase detection of cancer at early stages, when survival outcomes are better and treatment costs are lower. we will explore whether this model with high specificity could potentially improve long-term health outcomes and reduce cancer treatment costs.

Countries

China

Contacts

Primary ContactWen Zou, Ph.D
zouwen@fdtzihs.org.cn+8615152621812
Backup ContactRui Liu, Ph.D
rliu@singleragenomics.com

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026