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A multicenter retrospective study on the detection of EBV-related antibody markers by chemiluminescence to assist in the early diagnosis of nasopharyngeal carcinoma

A multicenter retrospective study on the detection of EBV-related antibody markers by chemiluminescence to assist in the early diagnosis of nasopharyngeal carcinoma

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600120294
Enrollment
Unknown
Registered
2026-03-11
Start date
2026-04-01
Completion date
Unknown
Last updated
2026-03-16

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

Conditions

Nasopharyngeal Carcinoma

Interventions

Gold Standard:Nasopharyngeal biopsy
Index test:Detection of EBV-Related Antibody Markers Based on Chemiluminescence Method

Sponsors

Sun Yat-sen University Cancer Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Nasopharyngeal carcinoma (NPC) group 1.Cases initially diagnosed as Nasopharyngeal carcinoma through pathological examination; 2.No restrictions on age, gender or pathological stage; 3.No previous anti-tumor treatments such as surgery, chemotherapy, radiotherapy or immunotherapy have been received; 4.Primary tumors in other parts were ruled out through CT, MRI or PET-CT examinations combined with clinical symptoms; 5.Serum samples were collected before any clinical treatment was received, and the sample volume was no less than 600 µL; 6.The medical record information is complete and there is data from the last follow-up; Non-NPC control group: Follow-up for at least 2 years or more, with no clinical symptoms related to nasopharyngeal carcinoma, no solid tumors detected in chest CT scans, no history of other malignant tumors, and basic normal results in blood routine, blood biochemistry, and liver and kidney function tests.

Exclusion criteria

Exclusion criteria: 1.Concurrent other malignant tumors; 2.Have autoimmune system diseases; 3.The sample quality does not meet the operational requirements (such as improper sample collection, improper preservation, insufficient sample size, sample leakage, sample contamination, and abnormal sample). 4.Missing medical records;

Design outcomes

Primary

MeasureTime frame
Sensitivity;Specificity;Accuracy;

Secondary

MeasureTime frame
Positive predictive value;Negative predictive value;

Countries

China

Contacts

Public ContactQian Zhong

Sun Yat-sen University Cancer Center

zhongqian@sysucc.org.cn+86 20 8734 2662

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 20, 2026