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Adjuvant Stereotactic Body Radiotherapy (SBRT) for Hepatocellular Carcinoma After Hepatectomy With Narrow Margin: a Prospective, Multi-center, Randomized Controlled, Open-labelled, Phase III Study

Primary Purpose

Hepatocellular Carcinoma, Narrow Margin, Adjuvant Stereotactic Body Radiotherapy

Status
Not yet recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
stereotactic body radiation therapy
regular follow-up
Sponsored by
Second Affiliated Hospital, School of Medicine, Zhejiang University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hepatocellular Carcinoma focused on measuring Hepatocellular carcinoma, Narrow margin, Adjuvant Stereotactic Body Radiotherapy, Hepatectomy

Eligibility Criteria

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

Inclusion Criteria: Aged ≥18 years; Confirmed diagnosis of HCC. The diagnosis can be established radiographically by the criteria of the American Association for the Study of the Liver (AASLD), or by histologic diagnosis from the core biopsy; Pathologically confirmed as narrow margin (the shortest distance from the edge of the tumor to the surface of liver transection <1cm) ; Child-Pugh class A and B7; ECOG (Eastern Cooperative Oncology Group) performance status 0 or 1; Willing to provide tissue from an excisional biopsy of a tumor lesion; For patients with active HBV: HBV DNA < 2000 IU/mL during screening, and have initiated anti-HBV treatment at least 7 days prior to SBRT and willingness to continue anti-HBV treatment during the study; Adequate organ and marrow function as defined below: 1)Marrow: absolute neutrophil count ≥1.5×109/L; platelets ≥50×109/L; hemoglobin ≥90g/L; 2)Liver: total bilirubin ≤3× institutional upper limit of normal (ULN); AST(aspartate aminotransferase) or ALT(alanine aminotransferase) ≤ 5× institutional ULN; albumin ≥29g/L; 3)Kidney: creatinine ≤ 1.5× institutional ULN or estimated glomerular filtration rate (GFR) ≥50 mL/min/1.73 m2 (according to the Cockcroft-Gault formula); 9. Women of childbearing potential must be willing to use a highly effective method of contraception for the course of the study through 30 days after radiotherapy. Female patient of childbearing potential should have a negative serum pregnancy test before 72h of her first treatment. Sexually active males must agree to use an adequate method of contraception starting with the treatment through 4 months after radiotherapy. Exclusion Criteria: Have received radiotherapy for the area to be treated in the past; Severe bleeding tendency or coagulation dysfunction within the previous 6 months; Extrahepatic metastasis; Known history of active Bacillus Tuberculosis (TB) Known additional malignancy that is progressing or requires active treatment. Exceptions include basal cell carcinoma of the skin or squamous cell carcinoma of the skin that has undergone potentially curative therapy, or in situ cervical cancer. Active infection requiring systemic therapy; Diagnosis of immunodeficiency or is receiving systemic steroid therapy or any other form of immunosuppressive therapy; Known psychiatric or substance abuse disorders ; Pregnant or breastfeeding; Known history of human immunodeficiency virus (HIV: HIV 1/2 antibodies); Received a live vaccine within 30 days before radiotherapy.

Sites / Locations

  • the second affiliated hospital of Zhejiang University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

adjuvant stereotactic body radiation therapy

regular follow-up

Arm Description

adjuvant stereotactic body radiation therapy after hepatectomy with narrow margin

regular follow-up after hepatectomy with narrow margin

Outcomes

Primary Outcome Measures

marginal recurrence rate
1-year marginal recurrence rate

Secondary Outcome Measures

Overall survival
3-year Overall survival
Recurrence free survival
3-year Recurrence free survival
Time to Progress
from date of enrollment to the date of progress. Assessed up to 36 months
Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability]
Incidence of Treatment-Emergent Adverse events (CTCAE v5.0)
Quality of life by EORTC QLQ-C30
Quality of life by EORTC QLQ-C30

Full Information

First Posted
October 29, 2022
Last Updated
February 16, 2023
Sponsor
Second Affiliated Hospital, School of Medicine, Zhejiang University
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1. Study Identification

Unique Protocol Identification Number
NCT05602974
Brief Title
Adjuvant Stereotactic Body Radiotherapy (SBRT) for Hepatocellular Carcinoma After Hepatectomy With Narrow Margin: a Prospective, Multi-center, Randomized Controlled, Open-labelled, Phase III Study
Official Title
Adjuvant Stereotactic Body Radiotherapy (SBRT) for Hepatocellular Carcinoma After Hepatectomy With Narrow Margin: a Prospective, Multicenter, Randomized Controlled, Open-labelled, Phase III Study
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
March 1, 2023 (Anticipated)
Primary Completion Date
December 1, 2025 (Anticipated)
Study Completion Date
December 1, 2027 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Second Affiliated Hospital, School of Medicine, Zhejiang 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
Hepatocellular carcinoma (HCC) is the sixth prevalent malignancy worldwide. Although surgical excision is considered the standard treatment for resectable HCC, a high rate of postoperative recurrence was observed after partial hepatectomy, with a marginal recurrence rate up to 30%. Narrow margin resection may be the most appropriate procedure for centrally located HCC or HCC located near liver capsule because the premise for survival is the conservation of more normal liver parenchyma. Unfortunately, narrow margin resection has been reported to contribute to poor survival outcomes. However, no adjuvant therapy after hepatectomy is generally considered to be effective in reducing post-operative recurrence. Radiotherapy (RT) has been well used in many solid malignant tumors as an (neo)adjuvant to surgical treatment, including HCC. SBRT has shown encouraging rates of local control for HCC. Compared with standard fractionation radiation, SBRT can achieve more precise delivery of high-dose radiation beams to the lesion, obtaining a much smaller target volume. Meanwhile, it could be finished in a short period which can bring more convenience to patients. Recently, several study and randomized controlled trials revealed the survival benefit of adjuvant RT (IMRT and SBRT) in patients with HCC. A large-sample and high-quality multi-center, randomized controlled, prospective study is warranted to further confirm the efficacy of adjuvant radiotherapy in patients with narrow margin resection, considering the small sample size of above-mentioned studies.
Detailed Description
Hepatocellular carcinoma (HCC) is the sixth prevalent malignancy worldwide. Although surgical excision is considered the standard treatment for resectable HCC, a high rate of postoperative recurrence was observed after partial hepatectomy, with a marginal recurrence rate up to 30%. Narrow margin resection may be the most appropriate procedure for centrally located HCC or HCC located near liver capsule because the premise for survival is the conservation of more normal liver parenchyma. Unfortunately, narrow margin resection has been reported to contribute to poor survival outcomes. However, no adjuvant therapy after hepatectomy is generally considered to be effective in reducing post-operative recurrence. Radiotherapy (RT) has been well used in many solid malignant tumors as an (neo)adjuvant to surgical treatment, including HCC. SBRT has shown encouraging rates of local control for HCC. Compared with standard fractionation radiation, SBRT can achieve more precise delivery of high-dose radiation beams to the lesion, obtaining a much smaller target volume. Meanwhile, it could be finished in a short period which can bring more convenience to patients. Recently, several study and randomized controlled trials revealed the survival benefit of adjuvant RT (IMRT and SBRT) in patients with HCC. A large-sample and high-quality multi-center, randomized controlled, prospective study is warranted to further confirm the efficacy of adjuvant radiotherapy in patients with narrow margin resection, considering the small sample size of above-mentioned studies.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatocellular Carcinoma, Narrow Margin, Adjuvant Stereotactic Body Radiotherapy, Hepatectomy
Keywords
Hepatocellular carcinoma, Narrow margin, Adjuvant Stereotactic Body Radiotherapy, Hepatectomy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Experimental: adjuvant stereotactic body radiation therapy after hepatectomy with narrow margin Control: regular follow-up after hepatectomy with narrow margin
Masking
None (Open Label)
Allocation
Randomized
Enrollment
140 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
adjuvant stereotactic body radiation therapy
Arm Type
Experimental
Arm Description
adjuvant stereotactic body radiation therapy after hepatectomy with narrow margin
Arm Title
regular follow-up
Arm Type
Active Comparator
Arm Description
regular follow-up after hepatectomy with narrow margin
Intervention Type
Radiation
Intervention Name(s)
stereotactic body radiation therapy
Intervention Description
adjuvant stereotactic body radiation therapy
Intervention Type
Other
Intervention Name(s)
regular follow-up
Intervention Description
regular follow-up
Primary Outcome Measure Information:
Title
marginal recurrence rate
Description
1-year marginal recurrence rate
Time Frame
from date of enrollment to date of first documented marginal recurrence. Assessed up to 12 months
Secondary Outcome Measure Information:
Title
Overall survival
Description
3-year Overall survival
Time Frame
from date of enrollment to the date of death from any cause. Assessed up to 36 months
Title
Recurrence free survival
Description
3-year Recurrence free survival
Time Frame
from date of enrollment to the date of first documented recurrence. Assessed up to 36 months
Title
Time to Progress
Description
from date of enrollment to the date of progress. Assessed up to 36 months
Time Frame
from date of enrollment to the date of progress. Assessed up to 36 months
Title
Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability]
Description
Incidence of Treatment-Emergent Adverse events (CTCAE v5.0)
Time Frame
6 months after SBRT
Title
Quality of life by EORTC QLQ-C30
Description
Quality of life by EORTC QLQ-C30
Time Frame
through study completion, an average of 3 year

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: Aged ≥18 years; Confirmed diagnosis of HCC. The diagnosis can be established radiographically by the criteria of the American Association for the Study of the Liver (AASLD), or by histologic diagnosis from the core biopsy; Pathologically confirmed as narrow margin (the shortest distance from the edge of the tumor to the surface of liver transection <1cm) ; Child-Pugh class A and B7; ECOG (Eastern Cooperative Oncology Group) performance status 0 or 1; Willing to provide tissue from an excisional biopsy of a tumor lesion; For patients with active HBV: HBV DNA < 2000 IU/mL during screening, and have initiated anti-HBV treatment at least 7 days prior to SBRT and willingness to continue anti-HBV treatment during the study; Adequate organ and marrow function as defined below: 1)Marrow: absolute neutrophil count ≥1.5×109/L; platelets ≥50×109/L; hemoglobin ≥90g/L; 2)Liver: total bilirubin ≤3× institutional upper limit of normal (ULN); AST(aspartate aminotransferase) or ALT(alanine aminotransferase) ≤ 5× institutional ULN; albumin ≥29g/L; 3)Kidney: creatinine ≤ 1.5× institutional ULN or estimated glomerular filtration rate (GFR) ≥50 mL/min/1.73 m2 (according to the Cockcroft-Gault formula); 9. Women of childbearing potential must be willing to use a highly effective method of contraception for the course of the study through 30 days after radiotherapy. Female patient of childbearing potential should have a negative serum pregnancy test before 72h of her first treatment. Sexually active males must agree to use an adequate method of contraception starting with the treatment through 4 months after radiotherapy. Exclusion Criteria: Have received radiotherapy for the area to be treated in the past; Severe bleeding tendency or coagulation dysfunction within the previous 6 months; Extrahepatic metastasis; Known history of active Bacillus Tuberculosis (TB) Known additional malignancy that is progressing or requires active treatment. Exceptions include basal cell carcinoma of the skin or squamous cell carcinoma of the skin that has undergone potentially curative therapy, or in situ cervical cancer. Active infection requiring systemic therapy; Diagnosis of immunodeficiency or is receiving systemic steroid therapy or any other form of immunosuppressive therapy; Known psychiatric or substance abuse disorders ; Pregnant or breastfeeding; Known history of human immunodeficiency virus (HIV: HIV 1/2 antibodies); Received a live vaccine within 30 days before radiotherapy.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yongjie Shui, MM
Phone
+8657187783521
Email
shui-yongjie@zju.edu.cn
First Name & Middle Initial & Last Name or Official Title & Degree
Lihong Liu, MM
Phone
+8657187783521
Email
lihong_liu@zju.edu.cn
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Qichun Wei, MD/PhD
Organizational Affiliation
Zhejiang University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Weilin Wang, MD/PhD
Organizational Affiliation
Zhejiang University
Official's Role
Principal Investigator
Facility Information:
Facility Name
the second affiliated hospital of Zhejiang University
City
Hangzhou
State/Province
Zhejiang
ZIP/Postal Code
310009
Country
China

12. IPD Sharing Statement

Plan to Share IPD
Undecided

Learn more about this trial

Adjuvant Stereotactic Body Radiotherapy (SBRT) for Hepatocellular Carcinoma After Hepatectomy With Narrow Margin: a Prospective, Multi-center, Randomized Controlled, Open-labelled, Phase III Study

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