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

Sun Yat-sen University logo

Sun Yat-sen University

Status and phase

Unknown
Phase 1

Conditions

Hepatocellular Carcinoma

Treatments

Biological: Normal Dose NK cells ×4 times
Biological: Normal Dose NK cells ×8 times
Biological: Low Dose NK cells ×4 times

Study type

Interventional

Funder types

Other

Identifiers

NCT02399735
(2014)2-126

Details and patient eligibility

About

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

Full 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.

Enrollment

18 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

18 participants in 3 patient groups

Arm A
Experimental group
Description:
Received conventional treatment and NK cells once per two-week for the first two-month, at a dose of 5×10E9 NK cells.
Treatment:
Biological: Low Dose NK cells ×4 times
Arm B
Experimental group
Description:
Received conventional treatment and NK cells once per two-week for the first two-month, at a dose of 1×10E10 NK cells.
Treatment:
Biological: Normal Dose NK cells ×4 times
Arm C
Experimental group
Description:
Received conventional treatment and NK cells once per two-week for the first four-month, at a dose of 1×10E10 NK cells.
Treatment:
Biological: Normal Dose NK cells ×8 times

Trial contacts and locations

1

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Central trial contact

Wang Guoying, MD; Wang Guoying, MD

Data sourced from clinicaltrials.gov

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