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Safety Study of NK Cells From Sibship to Treat the Recurrence of HCC After Liver Transplantation

Safety Study of Nature Killer Cells From Sibship to Treat the Recurrence of Hepatocellular Carcinoma After Liver Transplantation

Status
UNKNOWN
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02399735
Enrollment
18
Registered
2015-03-26
Start date
2014-10-31
Completion date
2018-06-30
Last updated
2016-07-21

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

Conditions

Hepatocellular Carcinoma

Keywords

NK cells, Liver Transplantation, Hepatocellular Carcinoma Recurrence

Brief summary

The purpose of this study is to explore the safety of NK cells from Sibship in patients with recurrent hepatocellular carcinoma after liver transplantation.

Detailed description

Hepatocellular carcinoma (HCC) is one of the indications for the liver transplantation. With the advancement of liver transplantation associated science and technology, the recurrence of tumor posttransplantation has become the principal contradiction to worsen the prognosis and therefore the prevention of recurrence of HCC is the key to improve the efficacy of liver transplantation. Adoptive cellular immunotherapy has been applied in various malignant tumors including HCC and has obtained significant effects. But for patients with liver transplant in immunosuppressed states, to successfully apply the immune cells to prevent and treat HCC relapse after liver transplantation must balance immunosuppression and anti-tumor immunity. It is necessary to consider the safety of adoptive cellular immunotherapy,and it is also necessary to consider the effectiveness of treatment that the immune cells in the immunosuppression state can exert anti-tumor effects. Natural killer cells (NK cells) have MHC-unrestricted killing effect on malignant tumor cells and are not major mediating cells for GVHD, and might be an optimum choice to meet the above requirements. Patients with confirmed recurrence of hepatocellular carcinoma after liver transplantation at the Third Affiliated Hospital of Sun Yat-sen University were enrolled.Participants in the study will be assigned to one of three treatment arms: Arm A: Participants will received conventional treatment and low dose of NK cells treatment for 4 times. Arm B: Participants will received conventional treatment and normal dose of NK cells treatment for 4 times. Arm C: Participants will received conventional treatment and normal dose of NK cells treatment for 8 times. The cultured NK cells from the peripheral blood of the same blood type were taken and infused at intervals of two weeks. Periodic liver function recheck and imaging examination were conducted for 6 months after the last NK cells infusion.

Interventions

BIOLOGICALLow Dose NK cells ×4 times

Received conventional treatment and NK cells once per two-week for the first two-month, at a dose of 5×10E9 NK cells.

BIOLOGICALNormal Dose NK cells ×4 times

Received conventional treatment and NK cells once per two-week for the first two-month, at a dose of 1×10E10 NK cells.

BIOLOGICALNormal Dose NK cells ×8 times

Received conventional treatment and NK cells once per two-week for the first four-month, at a dose of 1×10E10 NK cells.

Sponsors

Third Affiliated Hospital, Sun Yat-Sen University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Proved hepatocellular carcinoma histologically after liver transplantation. * Confirmed recurrence of hepatocellular carcinoma by CT/MRI. * The same blood type relatives with blood transmitted diseases negative. * Written informed consent.

Exclusion criteria

* Autoimmune diseases require long-term of glucocorticoid. * Other candidates who are judged to be not applicable to this study by investigators. * Poor compliance.

Design outcomes

Primary

MeasureTime frameDescription
GVHD6 monthsRash, fever, diarrhea, jaundice etc. leukocyte, platelet, red blood cells reduce, abnormal liver function.Pathological biopsy if necessary.

Secondary

MeasureTime frameDescription
Acute rejection6 monthsabnormal liver function,pathological biopsy if necessary.

Countries

China

Contacts

Primary ContactWang Guoying, MD
wanggy3@126.com086-13632407313
Backup ContactWang Guoying, MD

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026