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Study of Liver Resection With Versus Without Hepatic Inflow Occlusion for the HBV-related HCC (OHx-NOHx)

Primary Purpose

Liver Cancer, Surgery

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
non-occlusion technique
Sponsored by
Chinese PLA General Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Liver Cancer focused on measuring liver resection, blood inflow control, ischemia-reperfusion injury, inflammatory response, randomized controlled trial

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Elective liver resection due to HBV-related HCC with Barcelona-Clinic Liver Cancer (BCLC) staging 0 or A;
  2. Child-Pugh classified A with or without cirrhosis, or reversed to A from B after conventional therapy;
  3. Tumors located either in the left or right hemiliver;
  4. Resection extent was a hemi-hepatectomy or less;
  5. Informed consent.

Exclusion Criteria:

  1. Having comorbidity that contraindicates surgery;
  2. Participation in concurrent interventional trials with interference to this study;
  3. Eligible for laparoscopic hepatectomy;
  4. Requiring concomitant procedures, such as digestive, vascular or biliary reconstruction;
  5. Lack of compliance for treatment or future follow-up.

Sites / Locations

  • Chinese PLA General HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Hx with hepatic inflow occlusion

Hx with non-occlusion technique

Arm Description

Hepatectomy is carried out using Pringle maneuver in cycles of 15 minutes clamping + 5 minutes unclamping of the hepatoduodenal ligament.

Hepatectomy without hepatic inflow occlusion (non-occlusion technique)

Outcomes

Primary Outcome Measures

Serum total bilirubin on postoperative day 5
Postoperative liver insufficiency characterized by the serum total bilirubin on POD 5.

Secondary Outcome Measures

Intraoperative blood loss
Total blood loss from the incision to the closure of abdomen
Requirement of blood transfusion
The amount of intraoperative blood transfusion
Operative time
The time from induction of anesthesia to the closure of abdomen
Postoperative intensive-care unit (ICU) stay
Duration of stay in ICU
Hospital stay
Duration of hospital stay
Total hospital expenditure
Total costs during hospital stay
Perioperative systemic inflammatory response
Perioperative systemic inflammatory response is characterized by elevated serum level of tumor necrosis factor-α (TNF-α), interleukins (IL)-1α, 2, 6, 8 and 10, procalcitonin (PCT) and C-reactive protein (CRP) at different time points.
Postoperative morbi-mortality
Postoperative morbi-mortality is characterized by postoperative complication and its severity based on Clavien-Dindo classification and in-hospital mortality
Long-term oncologic outcomes
1, 3, 5-year tumor recurrence rate
Long-term survival
1, 3, 5-year overall survival (OS) and disease (tumor)-free survival (DFS)

Full Information

First Posted
September 26, 2015
Last Updated
May 10, 2016
Sponsor
Chinese PLA General Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02563158
Brief Title
Study of Liver Resection With Versus Without Hepatic Inflow Occlusion for the HBV-related HCC
Acronym
OHx-NOHx
Official Title
Short- and Long-term Outcomes of Liver Resection With Versus Without Hepatic Inflow Occlusion for the Hepatitis B Virus-related Hepatocellular Carcinoma: a Prospective Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
May 2016
Overall Recruitment Status
Unknown status
Study Start Date
January 2016 (undefined)
Primary Completion Date
January 2019 (Anticipated)
Study Completion Date
January 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chinese PLA General Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The study aims to compare the perioperative and long-term outcomes of liver resection for HBV-related HCC with versus without hepatic inflow occlusion.
Detailed Description
High prevalence of hepatitis B virus (HBV) imposes a huge burden of hepatocellular carcinoma (HCC) in Asia. Liver resection remains the mainstay of treatment for HCC. Hepatic inflow occlusion, known as the Pringle maneuver, is most commonly used to reduce blood loss during liver parenchymal transection. A major issue about this maneuver is the ischemia-reperfusion injury to the remnant liver. And the hemodynamic disturbance to the tumor-bearing liver remains an oncologic concern. Given the technical advances in living donor liver transplantation, vascular occlusion can be avoided in liver resection by experienced hands. This study aims to compare the perioperative and long-term outcomes of liver resection for HBV-related HCC without versus with hepatic inflow occlusion. This study will include eligible patients with HBV-related HCC elected for liver resection. 57 patients will be enrolled in each randomized arm to detect a 20% difference in the serum level of total bilirubin on postoperative day 5 (80% power and α = 0.05). The secondary endpoints include procedural parameters, perioperative liver function and inflammatory response, postoperative morbidity and mortality, and long-term outcomes. Patients will be followed for up to five years. Data will be statistically analyzed on an intention-to-treat basis. This prospective randomized controlled trial is designed to evaluate the feasibility of liver resections for HBV-related HCC without vascular occlusion. Clinical implication of its outcomes may change the present surgical practice and fill the oncologic gaps therein.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Liver Cancer, Surgery
Keywords
liver resection, blood inflow control, ischemia-reperfusion injury, inflammatory response, randomized controlled trial

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
114 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Hx with hepatic inflow occlusion
Arm Type
No Intervention
Arm Description
Hepatectomy is carried out using Pringle maneuver in cycles of 15 minutes clamping + 5 minutes unclamping of the hepatoduodenal ligament.
Arm Title
Hx with non-occlusion technique
Arm Type
Experimental
Arm Description
Hepatectomy without hepatic inflow occlusion (non-occlusion technique)
Intervention Type
Procedure
Intervention Name(s)
non-occlusion technique
Other Intervention Name(s)
hepatectomy without hepatic inflow occlusion
Intervention Description
Hepatectomy is carried out without hepatic inflow control. (non-occlusion technique)
Primary Outcome Measure Information:
Title
Serum total bilirubin on postoperative day 5
Description
Postoperative liver insufficiency characterized by the serum total bilirubin on POD 5.
Time Frame
5 days
Secondary Outcome Measure Information:
Title
Intraoperative blood loss
Description
Total blood loss from the incision to the closure of abdomen
Time Frame
Entire operation duration
Title
Requirement of blood transfusion
Description
The amount of intraoperative blood transfusion
Time Frame
Entire operation duration
Title
Operative time
Description
The time from induction of anesthesia to the closure of abdomen
Time Frame
Entire operation duration
Title
Postoperative intensive-care unit (ICU) stay
Description
Duration of stay in ICU
Time Frame
Duration of stay in ICU
Title
Hospital stay
Description
Duration of hospital stay
Time Frame
Duration of hospital stay
Title
Total hospital expenditure
Description
Total costs during hospital stay
Time Frame
Duration of hospital stay
Title
Perioperative systemic inflammatory response
Description
Perioperative systemic inflammatory response is characterized by elevated serum level of tumor necrosis factor-α (TNF-α), interleukins (IL)-1α, 2, 6, 8 and 10, procalcitonin (PCT) and C-reactive protein (CRP) at different time points.
Time Frame
an expected average of 7 days
Title
Postoperative morbi-mortality
Description
Postoperative morbi-mortality is characterized by postoperative complication and its severity based on Clavien-Dindo classification and in-hospital mortality
Time Frame
an expected average of 12 days in hospital
Title
Long-term oncologic outcomes
Description
1, 3, 5-year tumor recurrence rate
Time Frame
5 years after operation
Title
Long-term survival
Description
1, 3, 5-year overall survival (OS) and disease (tumor)-free survival (DFS)
Time Frame
5 years after operation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Elective liver resection due to HBV-related HCC with Barcelona-Clinic Liver Cancer (BCLC) staging 0 or A; Child-Pugh classified A with or without cirrhosis, or reversed to A from B after conventional therapy; Tumors located either in the left or right hemiliver; Resection extent was a hemi-hepatectomy or less; Informed consent. Exclusion Criteria: Having comorbidity that contraindicates surgery; Participation in concurrent interventional trials with interference to this study; Eligible for laparoscopic hepatectomy; Requiring concomitant procedures, such as digestive, vascular or biliary reconstruction; Lack of compliance for treatment or future follow-up.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Shichun Lu, MD, PhD
Phone
+86 10 68160801
Email
sclu_301@163.com
First Name & Middle Initial & Last Name or Official Title & Degree
Yinzhe Xu, MD, PhD
Phone
+1 617 818 4081
Email
james_hbp@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shichun Lu, MD, PhD
Organizational Affiliation
Department of Hepatobiliary Surgery, Chinese PLA General Hospital, 28 Fuxing Road, Haidian, Beijing, 100853, China
Official's Role
Principal Investigator
Facility Information:
Facility Name
Chinese PLA General Hospital
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100853
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yinzhe Xu, M.D., Ph.D.
Phone
86-10-66936609
Email
james_hbp@163.com
First Name & Middle Initial & Last Name & Degree
Shichun Lu, M.D., Ph.D.

12. IPD Sharing Statement

Citations:
PubMed Identifier
14762851
Citation
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Results Reference
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PubMed Identifier
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Citation
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Results Reference
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PubMed Identifier
19094562
Citation
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Results Reference
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PubMed Identifier
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Citation
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Results Reference
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PubMed Identifier
20632273
Citation
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Results Reference
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PubMed Identifier
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Citation
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Results Reference
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PubMed Identifier
19300227
Citation
Katz SC, Shia J, Liau KH, Gonen M, Ruo L, Jarnagin WR, Fong Y, D'Angelica MI, Blumgart LH, Dematteo RP. Operative blood loss independently predicts recurrence and survival after resection of hepatocellular carcinoma. Ann Surg. 2009 Apr;249(4):617-23. doi: 10.1097/SLA.0b013e31819ed22f.
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Citation
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Citation
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Results Reference
derived

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Study of Liver Resection With Versus Without Hepatic Inflow Occlusion for the HBV-related HCC

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