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Neo-TACE-HAIC for PVTT-HCC (NeoconceptC)

Primary Purpose

Hepatocellular Carcinoma, Portal Vein Thrombosis

Status
Recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
neo-TACE-HAIC+Surgery
Surgery alone
Sponsored by
Sun Yat-sen University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hepatocellular Carcinoma

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 18-75 years;
  • Patients with resectable primary hepatocellular carcinoma and portal vein tumor thrombus, which was not located in main portal vein;
  • Child-Pugh A or B (7 score) liver function;
  • With more than 3 months expected survival;
  • The volume of residual liver more than 30%

Exclusion Criteria:

  • Patients with primary hepatocellular carcinoma and major portal vein tumor thrombus
  • With extrahepatic metastasis or unresectable HCC
  • Pregnant woman or sucking period;
  • With other malignant cancer;
  • Received chemotherapy, target therapy or immunosuppressive drugs therapy before this study.

Sites / Locations

  • Sun Yat-sen University Cancer CenterRecruiting
  • Sun Yat-sen University Cancer CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

neo-TACE-HAIC with surgery

surgery alone

Arm Description

neoadjuvant TACE-HAIC with surgery for HCC patients with PVTT

surgery alone for HCC patients with PVTT

Outcomes

Primary Outcome Measures

Progression-free survival, PFS
PFS was calculated from the date of starting treatment to the date of progression, of disease or death.

Secondary Outcome Measures

Overall survival, OS
OS was calculated from the date of starting treatment to the date of death.

Full Information

First Posted
November 25, 2019
Last Updated
October 22, 2020
Sponsor
Sun Yat-sen University
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1. Study Identification

Unique Protocol Identification Number
NCT04181931
Brief Title
Neo-TACE-HAIC for PVTT-HCC
Acronym
NeoconceptC
Official Title
Neoadjuvant Transartery Chemoembolization Plus Artery Infusion Chemotherapy With Surgery Versus Surgery Alone for Hepatocellular Carcinoma Patients With Portal Vein Tumor Thrombus: a Randomized Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
October 2020
Overall Recruitment Status
Recruiting
Study Start Date
December 16, 2019 (Actual)
Primary Completion Date
December 30, 2022 (Anticipated)
Study Completion Date
December 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Sun Yat-sen University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Hepatocellular carcinoma (HCC) patients is a common disease in the East Asia. During the disease course, 20%-50% patients suffered portal vein tumor thrombus (PVTT), which is characterized with poor outcome and low response for treatments. Although BCLC (Barcelona clinical liver cancer) system recommend to palliative targeted treatment, the East Asian countries recommend to resection or transartery chemoembolization (TACE). Recently, FOLFOX (Oxaliplatin and 5-fluorouracil) based hepatic artery infusion chemotherapy (HAIC) exhibited high response rate for advanced HCC. Pilot study showed TACE combined HAIC (TACE-HAIC) had better tumor response, with low progression disease rate. Whether TACE-HAIC would improve survival for patients with PVTT is need to further to study. A randomized clinical trial compared neo-TACE-HAIC with surgery versus surgery alone is aimed to answer this question.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatocellular Carcinoma, Portal Vein Thrombosis

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
320 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
neo-TACE-HAIC with surgery
Arm Type
Experimental
Arm Description
neoadjuvant TACE-HAIC with surgery for HCC patients with PVTT
Arm Title
surgery alone
Arm Type
Active Comparator
Arm Description
surgery alone for HCC patients with PVTT
Intervention Type
Procedure
Intervention Name(s)
neo-TACE-HAIC+Surgery
Intervention Description
transartery chemoembolization with lipiodol and EADM, FOLFOX (Oxa 85mg/m2 2h+CF 400mg/m2 2h+5FU 400mg/m2 10min+5FU 1200mg/m2 23h)-based artery infusion chemotherapy, followed by hepatic resection
Intervention Type
Procedure
Intervention Name(s)
Surgery alone
Intervention Description
hepatic resection remove the liver tumor and portal vein tumor thrombus
Primary Outcome Measure Information:
Title
Progression-free survival, PFS
Description
PFS was calculated from the date of starting treatment to the date of progression, of disease or death.
Time Frame
36 months
Secondary Outcome Measure Information:
Title
Overall survival, OS
Description
OS was calculated from the date of starting treatment to the date of death.
Time Frame
60 months

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: Age 18-75 years; Patients with resectable primary hepatocellular carcinoma and portal vein tumor thrombus, which was not located in main portal vein; Child-Pugh A or B (7 score) liver function; With more than 3 months expected survival; The volume of residual liver more than 30% Exclusion Criteria: Patients with primary hepatocellular carcinoma and major portal vein tumor thrombus With extrahepatic metastasis or unresectable HCC Pregnant woman or sucking period; With other malignant cancer; Received chemotherapy, target therapy or immunosuppressive drugs therapy before this study.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jiliang Qiu, MD.
Phone
862087343114
Email
qiujl@sysucc.org.cn
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yunfei Yuan, MD.
Organizational Affiliation
Sun Yat-sen University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sun Yat-sen University Cancer Center
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510060
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yunfei Yuan
Phone
+862087343118
Email
yuanyf@mail.sysu.edu.cn
Facility Name
Sun Yat-sen University Cancer Center
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510060
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jiliang Qiu, MD.
Phone
862087343114
Email
qiujl@sysucc.org.cn

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Neo-TACE-HAIC for PVTT-HCC

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