Effectiveness of Drug Eluting TACE in Primary HCC
Primary Purpose
Hepatic Cell Carcinoma
Status
Unknown status
Phase
Early Phase 1
Locations
Study Type
Interventional
Intervention
HepaSphere Microspheres/Doxorubicin Hydrochloride
Lipiodol
Sponsored by
About this trial
This is an interventional treatment trial for Hepatic Cell Carcinoma
Eligibility Criteria
Inclusion Criteria:
- patients must be 18 to 75 years old.
- patients must be diagnosed as primary Hepatocellular carcinoma (HCC) by radiologic imaging revealed angiogenicity pattern .
- All of the patient have Child-Pugh status A or B .
- All of the patient have BCLC stage A or B.
- patients must have adequate renal and liver function accepting the maneuver.
- patients must have adequate coagulation profile (platelets count ≥ 80 000), (prothrombin concentration ≥ 70 %).
- patients must haven't previous history of resection of other ablation (alcohol, radio frequency or micro wave ablation).
Exclusion Criteria:
- patients have previous history of resection of other ablation (alcohol, radio frequency or micro wave ablation).
- patients with impaired coagulation profile (platelets count < 80 000), (prothrombin concentration < 70 %).
- patients with decompensated liver cell failure having ascites which impedes the maneuver .
- patients with past history of reaction to the drug used in maneuver
- patients with poor image quality.
- patients with lost follow up .
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
drug eluting bead trans arterial chemo embolization
conventional trans arterial chemo embolization
Arm Description
the international arm is the patients embolized with drug eluting bead trans arterial chemo embolization using Hepasphere
the control arm is the patients embolized with drug eluting bead trans arterial chemo embolization using Lipiodol
Outcomes
Primary Outcome Measures
Evaluate the effectiveness of drug-eluting bead trans-arterial chemo-embolization in patients of hepatocellular carcinoma
Evaluate the efficacy and safety of drug-eluting bead trans-arterial chemo-embolization in management of HCC patients in comparison of conventional chemo-embolization in 75 stable patients by evaluating the response of embolized lesions for each drug with modified RECIST criteria.
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04048317
Brief Title
Effectiveness of Drug Eluting TACE in Primary HCC
Official Title
Effectiveness of Drug Eluting & Conventional Trans-arterial Chemo-embolization in Treatment of Primary Hepatic Cell Carcinoma
Study Type
Interventional
2. Study Status
Record Verification Date
August 2019
Overall Recruitment Status
Unknown status
Study Start Date
September 1, 2019 (Anticipated)
Primary Completion Date
September 1, 2020 (Anticipated)
Study Completion Date
December 1, 2020 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Assiut University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
the aim of this work to compare effectiveness of drug-eluting bead trans-arterial chemo-embolization and conventional trans-arterial chemo-embolization of hepatic cell carcinoma in the aspect of (Tumor response via m-RECIST criteria), (liver injury via Liver function tests and tumor markers) and (survival outcome) of patients treated in Assiut university .
Detailed Description
Hepatocellular carcinoma (HCC) is the sixth most common cancer in the world and the third most common cause of cancer-related death .. With improved surveillance of patients with chronic liver disease and advances in imaging, more patients are diagnosed with early-stage HCC . For the treatment of early stage HCC, curative therapies including liver transplantation, hepatic resection, and radio frequency ablation (RFA) are recommended. Liver transplantation is the treatment option especially for patients with decompensated cirrhosis, but potential recipients outnumber donors. Hepatic resection is widely used as the main choice of treatment for resectable HCC. However, the risk of postoperative hepatic dysfunction often precludes surgery.
For unresectable patient, trans-arterial chemo-embolization (TACE) was the treatment of choice .
At 2014, Yang et al. compared the treatment effects of hepatic resection, RFA, and conventional TACE on long-term survival. It was found that the range of patients treated by TACE in clinical practice reported survivals widely range from 8-26% at 5-years. which was similar to that with hepatic resection and RFA in patients with single-nodule HCC of 3 cm or smaller without vascular invasion when the underlying liver status was balanced among the patients receiving each treatment. In addition, most of the patients initially treated with c-TACE achieved a complete response, which was one of the independent prognostic factors of survival, although some should receive repeated treatments. However, when c-TACE is used as an initial treatment, special care should be taken to obtain a complete response, and surveillance for tumor recurrence should be undertaken. These results are consistent with those of cohort studies demonstrating that TACE provided overall survival similar to hepatic resection in early-stage HCC .
Conventional (Lipiodol) TACE Base on technique with emulsified combination of chemotherapy such as Doxorubicin and Lipiodol administrate via arterial feeder.
Less in systemic chemotherapy and increase overall survival rate were the most concern in treatment but many studies reported side effects from conventional (Lipiodol) TACE significantly among an improvement of overall survival rate .
Conventional TACE may cause side effects because it can damage healthy cells as it kills cancer cells. Side effects can develop any time during, immediately after or a few days or weeks after chemotherapy . in addition to the patient needed frequent ablation after a short time .
The most commonly Side Effect of TACE is (Post embolization syndrome) which is a group of symptoms . include : fever, Right upper quadrant pain, nausea, vomiting and fatigue .
Other side effects may occur include bruising or bleeding at the catheter site, hair loss, abnormal liver functions, lung infections, gall bladder inflammation and tumor lysis syndrome .
Drug-eluting bead TACE is the new method of delivering chemotherapy during TACE which uses special beads that already have the chemotherapy drug in them . after these are injected into the arteries of the liver , they slowly sustained releasing the drug to treat the tumor .
The studies showed that TACE with (Hepasphere) less systemic side effect in patient than TACE with (Lipiodol) but no definite statistical difference in treatment and survival outcome.
This study compares effectiveness of those methods in treatment of Hepatocellular carcinoma in Assiut university
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatic Cell Carcinoma
7. Study Design
Primary Purpose
Treatment
Study Phase
Early Phase 1
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
75 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
drug eluting bead trans arterial chemo embolization
Arm Type
Experimental
Arm Description
the international arm is the patients embolized with drug eluting bead trans arterial chemo embolization using Hepasphere
Arm Title
conventional trans arterial chemo embolization
Arm Type
Placebo Comparator
Arm Description
the control arm is the patients embolized with drug eluting bead trans arterial chemo embolization using Lipiodol
Intervention Type
Drug
Intervention Name(s)
HepaSphere Microspheres/Doxorubicin Hydrochloride
Intervention Description
evaluation the tumor (size, location and pattern of enhancement) ;and ensure portal vein patency; then evaluation of hepatic arterial anatomy, after that we determine the tumor arterial feeders and the arteries that should be avoided during the maneuver.
Selective celiac and superior mesenteric angiograms were performed using 5 Fr. Catheter then superselective angiogram were used microcatheter. then injection of drug-eluting microsphere (25 mg Hepasphere 50-100 micron) loaded with 50 mg doxorubicin solution for 2 hours.
Intervention Type
Drug
Intervention Name(s)
Lipiodol
Intervention Description
evaluation the tumor (size, location and pattern of enhancement) ;and ensure portal vein patency; then evaluation of hepatic arterial anatomy, after that we determine the tumor arterial feeders and the arteries that should be avoided during the maneuver.
Selective celiac and superior mesenteric angiograms were performed using 5 Fr. Catheter then superselective angiogram were used microcatheter. then injection of prepared mixture of Lipiodol and (Doxorubicin or 5-FU) vary in dosage depend on operator consideration
Primary Outcome Measure Information:
Title
Evaluate the effectiveness of drug-eluting bead trans-arterial chemo-embolization in patients of hepatocellular carcinoma
Description
Evaluate the efficacy and safety of drug-eluting bead trans-arterial chemo-embolization in management of HCC patients in comparison of conventional chemo-embolization in 75 stable patients by evaluating the response of embolized lesions for each drug with modified RECIST criteria.
Time Frame
baseline
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
patients must be 18 to 75 years old.
patients must be diagnosed as primary Hepatocellular carcinoma (HCC) by radiologic imaging revealed angiogenicity pattern .
All of the patient have Child-Pugh status A or B .
All of the patient have BCLC stage A or B.
patients must have adequate renal and liver function accepting the maneuver.
patients must have adequate coagulation profile (platelets count ≥ 80 000), (prothrombin concentration ≥ 70 %).
patients must haven't previous history of resection of other ablation (alcohol, radio frequency or micro wave ablation).
Exclusion Criteria:
patients have previous history of resection of other ablation (alcohol, radio frequency or micro wave ablation).
patients with impaired coagulation profile (platelets count < 80 000), (prothrombin concentration < 70 %).
patients with decompensated liver cell failure having ascites which impedes the maneuver .
patients with past history of reaction to the drug used in maneuver
patients with poor image quality.
patients with lost follow up .
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ahmed M. Abdurabou, resident
Phone
00201149112036
Email
ahmedabdurabou@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Haisam A. Atta, professor
Phone
00201005017866
Email
haisamasa@gmail.com
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
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25220842
Citation
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Results Reference
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Citation
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Links:
URL
https://www.journalacs.org/article/S1072-7515(11)00896-9/abstract
Description
Hepatic Arterial Infusion of Doxorubicin-Loaded Microsphere for Treatment of Hepatocellular Cancer: A Multi-Institutional Registry
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Effectiveness of Drug Eluting TACE in Primary HCC
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