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Evaluation of Cytokine-induced Killer (CIK) Cells as Therapy or Adjuvant Treatment for Advanced HCC

Primary Purpose

Liver Cancer

Status
Unknown status
Phase
Phase 3
Locations
Egypt
Study Type
Interventional
Intervention
CIK
TACE
Sponsored by
Sherief Abd-Elsalam
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Liver Cancer

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Patients with advanced HCC and not fit for resection or local ablative therapies stage B (according Barcelona Clinic Liver Cancer (BCLC) Staging system ).
  2. Patient with HCC and portal vein thrombosis stage C.
  3. Patients with HCC and lymphatic or distant metastases stage D.

Exclusion Criteria:

  1. Patients with HCC and fit for radical or local ablation (stage 0 and A) therapies.
  2. Platelet count below 50,000 / dl
  3. Prothrombin activity below 50%
  4. All patients will sign a written informed consent after explaining the details and possible hazards of the procedure to them. Those who will refuse to share in the study will be excluded.

Sites / Locations

  • Sherief Abd-ElsalamRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

No Intervention

Arm Label

CIK with TACE for HCC stage B

TACE only for HCC stage B

CIK in HCC stage C or D

Supportive treatment in HCC stage C or D

Arm Description

HCC patients stage B treated with TACE and CIK as adjuvant therapy.

HCC patients stage B treated with TACE without receiving CIK cells infusion

HCC stage C or D will receive supportive treatment in addition to CIK cells infusion

HCC stage C or D will receive supportive treatment only .

Outcomes

Primary Outcome Measures

Number of patients with ablated hcc
patients with ablated hcc

Secondary Outcome Measures

Full Information

First Posted
October 4, 2015
Last Updated
April 26, 2017
Sponsor
Sherief Abd-Elsalam
Collaborators
Tanta University
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1. Study Identification

Unique Protocol Identification Number
NCT02568748
Brief Title
Evaluation of Cytokine-induced Killer (CIK) Cells as Therapy or Adjuvant Treatment for Advanced HCC
Official Title
Evaluation of Cytokine-induced Killer (CIK) Cells as Therapy or Adjuvant Treatment for Patients With Advanced Hepatocelluler Carcinoma
Study Type
Interventional

2. Study Status

Record Verification Date
April 2017
Overall Recruitment Status
Unknown status
Study Start Date
October 2015 (undefined)
Primary Completion Date
June 2019 (Anticipated)
Study Completion Date
October 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Sherief Abd-Elsalam
Collaborators
Tanta University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Hepatocellular carcinoma (HCC) is the fifth most common malignancy in the world and the third most common cause of cancer-related deaths complicating liver cirrhosis in most cases. In Egypt, there has been a remarkable increase of the proportion of HCC among CLD patients from 4.0% to 7.2% over a decade. This rising proportion may be explained by the increasing risk factors such as the emergence of HCV over the same period of time, the contribution of HBV infection, improvement of the screening programs and diagnostic tools of HCC as well as the increased survival rate among patients with cirrhosis to allow time for some of them to develop HCC. The only curative treatment modalities for HCC are surgery, local ablation, and liver transplantation which have high recurrence rate either due to viral hepatitis infection or cirrhosis leading to low success rate and high economic burden. Unfortunately, the majority of patients have unresectable disease at diagnosis. So, patients search for palliative very expensive therapies including chemotherapy and radiotherapy which often fail to eradicate tumor lesions completely and tend to result in many adverse events.Thus, novel approaches for treatment options are needed for patients with advanced HCC . In recent years, immunotherapy has emerged as an efficacious treatment modality with encouraging efficacy and slight adverse events in cancer therapy [Stroncek 2010]. Cytokine-induced killer CIK cells therapy has been evaluated as an adoptive cell immunotherapy for cancer patients in a number of clinical trials and the promising efficacy of CIK cells on malignancies has been proved.
Detailed Description
Hepatocellular carcinoma (HCC) is the fifth most common malignancy in the world and the third most common cause of cancer-related deaths complicating liver cirrhosis in most cases. In Egypt, there has been a remarkable increase of the proportion of HCC among CLD patients from 4.0% to 7.2% over a decade. This rising proportion may be explained by the increasing risk factors such as the emergence of HCV over the same period of time, the contribution of HBV infection, improvement of the screening programs and diagnostic tools of HCC as well as the increased survival rate among patients with cirrhosis to allow time for some of them to develop HCC. The only curative treatment modalities for HCC are surgery, local ablation, and liver transplantation which have high recurrence rate either due to viral hepatitis infection or cirrhosis leading to low success rate and high economic burden.. Unfortunately, the majority of patients have unresectable disease at diagnosis. So, patients search for palliative very expensive therapies including chemotherapy and radiotherapy which often fail to eradicate tumor lesions completely and tend to result in many adverse events.Thus, novel approaches for treatment options are needed for patients with advanced HCC . In recent years, immunotherapy has emerged as an efficacious treatment modality with encouraging efficacy and slight adverse events in cancer therapy. Cytokine-induced killer CIK cells therapy has been evaluated as an adoptive cell immunotherapy for cancer patients in a number of clinical trials and the promising efficacy of CIK cells on malignancies has been proved. . Clinical studies have demonstrated that it is an excellent method to prevent tumor recurrence and has preliminarily shown its efficacy in inhibiting recurrence and metastasis of primary HCC -Peripheral blood mononuclear cells (PBMC)from patients with primary HCC were incubated in vitro and induced into CIK cells in the presence of various cytokines such as interferon-gamma (IFN-ã ), interleukin-1 (IL-1), IL-2, and monoclonal antibody (mAb) against CD3. CIK cells infusion will be performed Once every week, with a total of at least4infusions. Infusion will be given intrahepatic or via peripheral veins . The serial biological events following CIK cells administration to a cancer patient includes (a) immune activation and effective lymphocytes (mostly C D3+CD 5 6+Tlymphocytes) proliferation starting early after the first administration , ( b) clinically measurable antitumor effect mediated by activated immune cells over weeks to months ,and (c) potential delayed effect on patient survival several months or even longer after the first administration. Our team have many grants in field of HCC biomarkers discovery and managements from NIH as multicenter studies which got many international publication. As well as grant for the use of laboratory techniques in the cultivation of stem cells for specialized cells used in the treatment of different diseases which got publication in this era. we aim in this project to cultivate patients cells in vitro to get CIK cells and study the safety and efficacy of immunization with specific antihepatocellular carcinoma Cytokine -induced killer cells in Egyptian patients with advanced hepatocellular carcinoma as treatment or adjuvant treatment in comparison with traditional treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Liver Cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Masking Description
No Masking
Allocation
Non-Randomized
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
CIK with TACE for HCC stage B
Arm Type
Experimental
Arm Description
HCC patients stage B treated with TACE and CIK as adjuvant therapy.
Arm Title
TACE only for HCC stage B
Arm Type
Experimental
Arm Description
HCC patients stage B treated with TACE without receiving CIK cells infusion
Arm Title
CIK in HCC stage C or D
Arm Type
Experimental
Arm Description
HCC stage C or D will receive supportive treatment in addition to CIK cells infusion
Arm Title
Supportive treatment in HCC stage C or D
Arm Type
No Intervention
Arm Description
HCC stage C or D will receive supportive treatment only .
Intervention Type
Biological
Intervention Name(s)
CIK
Intervention Description
Cytokine -induced killer cells in Egyptian patients with advanced hepatocellular carcinoma as treatment or adjuvant treatment in comparison with traditional treatment.
Intervention Type
Procedure
Intervention Name(s)
TACE
Intervention Description
Trans-arterial chemoembolization
Primary Outcome Measure Information:
Title
Number of patients with ablated hcc
Description
patients with ablated hcc
Time Frame
1 year

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with advanced HCC and not fit for resection or local ablative therapies stage B (according Barcelona Clinic Liver Cancer (BCLC) Staging system ). Patient with HCC and portal vein thrombosis stage C. Patients with HCC and lymphatic or distant metastases stage D. Exclusion Criteria: Patients with HCC and fit for radical or local ablation (stage 0 and A) therapies. Platelet count below 50,000 / dl Prothrombin activity below 50% All patients will sign a written informed consent after explaining the details and possible hazards of the procedure to them. Those who will refuse to share in the study will be excluded.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sherief Abd-Elsalam, lecturer
Phone
00201095159522
Email
Sherif_tropical@yahoo.com
First Name & Middle Initial & Last Name or Official Title & Degree
Sherief Abd-Elsalam, lecturer
Phone
00201095159522
Email
Sheriefabdelsalam@yahoo.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dina H Ziada, Prof
Organizational Affiliation
Hepatology dept.-Tanta
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Hanan H Soliman, Prof
Organizational Affiliation
Hepatology dept.-Tanta
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Enas Arafa, Prof
Organizational Affiliation
Clinical pathology dept.
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Sherief Abd-Elsalam, lecturer
Organizational Affiliation
Hepatology dept.-Tanta
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Abdelrahman Zekri, Professor
Organizational Affiliation
Pathology dept.- Cairo university
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Amre Elbadry, Professor
Organizational Affiliation
Interventional radiology- Tanta university
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Marwa Salama, Ass.lecturer
Organizational Affiliation
Hepatology dept.- Tantauniversity
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Ahmed Elsharkawy, Ass.lecturer
Organizational Affiliation
Interventional radiology- Tanta university
Official's Role
Study Chair
Facility Information:
Facility Name
Sherief Abd-Elsalam
City
Cairo
State/Province
Tanta
Country
Egypt
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sherief Abd-elsalam, lecturer
Phone
00201000040794
Email
Sherif_tropical@yahoo.com
First Name & Middle Initial & Last Name & Degree
Ahmed Elsharkawy, Ass. lect.

12. IPD Sharing Statement

Plan to Share IPD
Undecided

Learn more about this trial

Evaluation of Cytokine-induced Killer (CIK) Cells as Therapy or Adjuvant Treatment for Advanced HCC

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