Skip to content

Evaluating the effectiveness of autologous RAK cells combined with surgery in patients with primary liver cancer

Evaluating the effectiveness of autologous RAK cells combined with surgery in patients with primary liver cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800019336
Enrollment
Unknown
Registered
2018-11-06
Start date
2018-11-06
Completion date
Unknown
Last updated
2024-07-29

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

Conditions

Primary liver cancer

Interventions

Case series:Autologous RAK cells

Sponsors

Cancer Hospital Chinese Academy of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged 18-70 years old; 2. Patients with primary liver cancer were confirmed by histological examination; 3. No other combination treatment before and after operation (radiotherapy, chemotherapy, etc., except traditional Chinese medicine); In addition, if one of the following conditions is met, the group can be enrolled: 1) tumor greater than or equal to 5cm or involved/located in the middle of the liver or adjacent to the tumor ( 20ng/mL; 7) positive lymph nodes; 4. Effective methods of contraception from screening to the end of the trial should be agreed upon for women and men who are fertile; 5. Sign written informed consent.

Exclusion criteria

Exclusion criteria: 1. Pregnant or lactating women; 2. Patients who had received cytotoxic chemotherapy within 3 months, patients who had received targeted drug therapy within 2 months, patients who had received interferon and/or interleukin-2 within 3 months;I have received targeted drugs for immune nodes; 3. Have used immunosuppressive agents (including azathioprine, 6-mp, cyclosporin, tisirolimus, ivermox, rapamycin, etc.); Long-term use of corticosteroids; 4. Has previously been treated with dc-cik or CIK cells, autologous RAK/LAK cells or other adoptive immunotherapy; 5. Has a history of other malignant diseases in the last five years (with the exception of cured skin cancer and cervical carcinoma in situ).

Design outcomes

Primary

MeasureTime frame
Disease free survival rate;

Secondary

MeasureTime frame
total survival;

Countries

China

Contacts

Public ContactJie Ma

Beijing Hospital

majie1965@163.com+86 18611719186

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 8, 2026