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Clinical observation of autologous NK cells in preventing cancer recurrence

Clinical observation of autologous NK cells in preventing cancer recurrence

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100048409
Enrollment
Unknown
Registered
2021-07-06
Start date
2021-07-01
Completion date
Unknown
Last updated
2022-03-14

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

Conditions

Primary liver cancer, lung cancer

Interventions

experimental group:Intravenous infusion of autologous NK cells

Sponsors

The First People's Hospital of Hefei
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-70 years; 2. Gender is not limited; 3. Diagnosed with hepatocellular carcinoma or lung cancer; 4. Patients who have received tumor interventional therapy in the past or received iodine 125 seed implantation for lung cancer at least 6 months ago, and have achieved complete remission by pathological/radiological examination; 5. The vital organs function normally; 6. The remaining life should be at least 3 months; 7. The patients or their guardians are willing to sign the informed consent; 8. Hepatocellular carcinoma patients: Child-Pugh score 60.

Exclusion criteria

Exclusion criteria: 1. The preparation of autologous NK cell preparations failed; 2. Accept other treatments other than tumor intervention; 3. ECOG score > 2; 4. Serum bilirubin>3mg/dl; 5. GFR<40ml/min/1.73MW; 6. Heart left ventricular ejection fraction <40%; 7. Severe asthma; 8. Uncontrolled infection; 9. HIV, HTLV-1, syphilis positive, or other infectious diseases; 10. Currently receiving or may need systemic immunosuppressive therapy; 11. Have taken anticancer drugs before clinical trials; 12. Pregnant patients or patients who are planning to become pregnant or breastfeeding; 13. Have a history of severe allergies; 14. Suffering from serious mental illness; 15. Participating in other clinical trials; 16. The researchers believe that other reasons are not suitable for clinical trials.

Design outcomes

Primary

MeasureTime frame
Incidence of treatment-related adverse events;

Secondary

MeasureTime frame
Relapse-free survival;

Countries

China

Contacts

Public ContactHe Kewu

The First People's Hospital of Hefei

kewu_he3145@163.com+86 13855151343

Outcome results

None listed

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