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

NCT05602974 | Not Yet Recruiting

• 1 other identifier: 2022-0908
• Study Type: interventional
• Target: 140
• Locations: 1 country
• Sites: 1

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.

Conditions

Hepatocellular Carcinoma; Narrow Margin; Adjuvant Stereotactic Body Radiotherapy; Hepatectomy

Keywords

Hepatocellular carcinoma; Narrow margin; Adjuvant Stereotactic Body Radiotherapy; Hepatectomy

Outcome Measures

Primary Outcomes (1)

• marginal recurrence rate

  1-year marginal recurrence rate

  from date of enrollment to date of first documented marginal recurrence. Assessed up to 12 months

Secondary Outcomes (5)

• Overall survival

  from date of enrollment to the date of death from any cause. Assessed up to 36 months

• Recurrence free survival

  from date of enrollment to the date of first documented recurrence. Assessed up to 36 months

• 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]

  6 months after SBRT

• Quality of life by EORTC QLQ-C30

  through study completion, an average of 3 year

Study Arms (2)

adjuvant stereotactic body radiation therapy

EXPERIMENTAL

adjuvant stereotactic body radiation therapy after hepatectomy with narrow margin

Radiation: stereotactic body radiation therapy

regular follow-up

ACTIVE COMPARATOR

regular follow-up after hepatectomy with narrow margin

Other: regular follow-up

Interventions

stereotactic body radiation therapy RADIATION

adjuvant stereotactic body radiation therapy

adjuvant stereotactic body radiation therapy

regular follow-up OTHER

regular follow-up

regular follow-up

Eligibility Criteria

• Age: 18 Years - 75 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• 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:
• )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.

You may not qualify if:

• 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.

Sponsors & Collaborators

• Second Affiliated Hospital, School of Medicine, Zhejiang University: lead

Study Sites (1)

the second affiliated hospital of Zhejiang University

Hangzhou, Zhejiang, 310009, China

Location

MeSH Terms

Conditions

Carcinoma, Hepatocellular

Interventions

Radiosurgery

Condition Hierarchy (Ancestors)

Adenocarcinoma; Carcinoma; Neoplasms, Glandular and Epithelial; Neoplasms by Histologic Type; Neoplasms; Liver Neoplasms; Digestive System Neoplasms; Neoplasms by Site; Digestive System Diseases; Liver Diseases

Intervention Hierarchy (Ancestors)

Radiotherapy; Therapeutics; Stereotaxic Techniques; Neurosurgical Procedures; Surgical Procedures, Operative; Investigative Techniques

Study Officials

• Qichun Wei, MD/PhD

  Zhejiang University

  PRINCIPAL INVESTIGATOR

• Weilin Wang, MD/PhD

  Zhejiang University

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Yongjie Shui, MM

CONTACT

+8657187783521; shui-yongjie@zju.edu.cn

Lihong Liu, MM

CONTACT

+8657187783521; lihong_liu@zju.edu.cn

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Model Details: Experimental: adjuvant stereotactic body radiation therapy after hepatectomy with narrow margin Control: regular follow-up after hepatectomy with narrow margin

Study Record Dates

• First Submitted: October 29, 2022
• First Posted: November 2, 2022
• Study Start: March 1, 2023
• Primary Completion: December 1, 2025
• Study Completion (Estimated): December 1, 2027
• Last Updated: February 17, 2023

Record last verified: 2022-10

Locations

CN (1)