Skip to content

Epstein-Barr Virus and Cancer Risks

Prospective Cohort Study on Epstein-Barr Virus Antibody and Cancer Risks

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06203314
Acronym
EBVCR
Enrollment
100000
Registered
2024-01-12
Start date
2008-08-01
Completion date
2030-12-31
Last updated
2024-01-12

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

Conditions

Cancer

Keywords

EBV, Prospective study, Cancer

Brief summary

The goal of this prospective cohort study is to investigate the associations between Epstein-Barr Virus (EBV) antibody levels and the risk of overall and site-specific cancer types in Southern China. The main questions it aims to answer are: Question 1: In addition to the established EBV-associated cancer types, such as lymphomas, nasopharyngeal carcinoma, and stomach cancer, whether EBV is associated with other cancer types? Question 2: What's the cancer burden attributed to EBV in Southern China?

Detailed description

Growing molecular evidence suggests the involvement of EBV in various cancers, however, comprehensive epidemiological evidence is still lacking. In this study, researchers conducted a population-based prospective cohort study to investigate the associations between EBV antibodies and the risk of overall and site-specific cancer types in Southern China. All the participants underwent EBV antibody tests at enrollment and were subsequently followed up annually for cancer incidence, vital status, and immigration status. The primary objective of this study was to provide prospective evidence for the role of EBV in multiple cancers, shedding light on the etiology of a broad range of common EBV-associated cancers.

Interventions

OTHERDiagnostic test: EBV antibody tests

Participants underwent several EBV antibody tests, including VCA-IgA, EBNA1-IgA, etc.

Sponsors

Wuzhou Red Cross Hospital
CollaboratorOTHER
Zhongshan People's Hospital, Guangdong, China
CollaboratorOTHER
Sun Yat-sen University
Lead SponsorOTHER

Study design

Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
30 Years to 69 Years
Healthy volunteers
Yes

Inclusion criteria

* Subject residents in Zhongshan or Wuzhou City; * Subject has no medical record of prevalent cancer; * Subject has psychical condition and well consciousness, and willingness to accept and cooperate with the study's follow-up procedures.

Exclusion criteria

* Subject has heavy cardiovascular, liver, or kidney disease; * Subject has prevalent cancer.

Design outcomes

Primary

MeasureTime frameDescription
Cancer incidence10 yearsThe primary outcome of the study was the diagnosis of any type of cancer. The cancer type for each participant was defined as their initial and primary cancer diagnosis.

Secondary

MeasureTime frameDescription
All-cause mortality10 yearsThe participants were followed up annually for cancer incidence, vital status and immigration status through the Cancer Registry, Death Registry, and Population Registry of local regions.

Countries

China

Contacts

Primary ContactWei-Hua Jia
jiawh@sysucc.org.cn86+020-87342327
Backup ContactYong-Qiao He
heyq@sysucc.org.cn86+020-87342410

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026