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Efficacy of killer NK / NKT cells in the treatment of several common malignancies

Efficacy of killer NK / NKT cells in the treatment of several common malignancies

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800014555
Enrollment
Unknown
Registered
2018-01-21
Start date
2018-03-01
Completion date
Unknown
Last updated
2018-01-29

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

Conditions

Lung cancer, stomach cancer, hepatocellular cancer, pancreatic cancer, colorectal cancer, breast cancer

Interventions

Experimental group:NK/NKT immunotherapy

Sponsors

Second People's Hospital of Shenzhen
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1) informed consent; 2) Age 18 to 70 years old; 3) pathological diagnosis of lung cancer, gastric cancer, hepatocellular carcinoma, pancreatic cancer, colorectal cancer, breast cancer; 4) Peripheral blood leukocytes> 3×10^9/L; Lymphocytes absolute> 1.0 × 10^9/L; Lymphocyte ratio> 18%; 5) survival expectation in more than 3 months.

Exclusion criteria

Exclusion criteria: 1) brain metastasis and macrovascular invasion; 2) highly allergic or have a history of serious allergies; 3) severe liver and kidney dysfunction; 4) patients with severe autoimmune disease or who are receiving immunosuppressive therapy; 5) serious infection uncontrolled or hyperthermia; 6) Organ transplant or organ transplant; 7) T-cell lymphoma, syphilis, AIDS patients or amalgamation; 8) shock, vital organ failure, unstable vital signs; 9) severe coagulation disorders (such as hemophilia) who; 10) the merger of mental or mental illness can not cooperate with the treatment and efficacy evaluation; 11) women of childbearing age during pregnancy or lactation, or women of childbearing age who refuse contraception during the study period; 12) drug or alcohol abusers; 13) The doctor thinks there are other reasons that can not be included in the treatment.

Design outcomes

Primary

MeasureTime frame
Tumor recurrence rate.;progression-free survival;overall survival;

Countries

China

Contacts

Public ContactZeqiang Zhou

Department of oncology,Second People's Hospital of Shenzhen

szchou123@163.com+86 13600166286

Outcome results

None listed

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