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The diagnostic and therapeutic role of gene CDC73 in blood

Application of plasma exosome CDC73 in the diagnosis and treatment of lung adenocarcinoma

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400094769
Enrollment
Unknown
Registered
2024-12-27
Start date
2025-01-01
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

Lung adenocarcinoma

Interventions

Gold Standard:Pathological diagnosis
Index test:Western blot experiment
Immunohistochemistry experiment

Sponsors

Xuzhou Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Oncology research is for adults, so the lower age limit is 18 years old and the upper limit is 80 years old; 2. Patients with an ECOG score of less than 2 points; 3. Pathologically diagnosed with lung adenocarcinoma or healthy people; 4. Patients with lung adenocarcinoma are patients who have not undergone standard treatment; 5. The pathology report of patients with lung adenocarcinoma should have measurable lesions; 6. Expected survival>=3 months; 7. Blood routine, liver and kidney function, and some will also require normal urine protein, coagulation function and heart function; 8. Not during pregnancy and lactation. Signed: Subjects sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Have serious heart and brain diseases or other mental diseases; 2. Severe pulmonary fibrosis, especially drug-induced pulmonary fibrosis; 3. Patients with severe pulmonary dysfunction, pulmonary ventilation disorder, and multiple bullae in the past; 4. During pregnancy and lactation; Prior antineoplastic therapy received; 5. Those who have recently undergone major surgery or radiotherapy; 6. Patients who have recently used corticosteroids (glucocorticoids) or immunosuppressants; 7. In addition to the type of primary tumor studied, other primary tumors should be excluded; 8. Exclude active autoimmune disease; 9. Patients with uncontrollable pleural effusion, ascites, or pericardial effusion are excluded; 10. Exclude interstitial lung disease, uncontrollable hypertension, active infection, and cardiovascular and cerebrovascular diseases of great significance; 11. Grade 2/3 immune-related adverse events (irAEs) were excluded; 12. Exclude the presence of known or suspected inability to comply with the study protocol.

Design outcomes

Primary

MeasureTime frame
Tumor marker CDC73;

Countries

China

Contacts

Public ContactDong Hao

Xuzhou Central Hospital

1207673067@qq.com+86 19005227916

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026