Proton Beam Therapy in Hepatocellular Carcinoma With Portal Vein Tumor Thrombosis

Not Applicable

Completed

• Conditions: Proton Therapy; Liver Neoplasm; Portal Vein Tumor Thrombosis
• Interventions: Radiation: Proton beam therapy

• Registration Number: NCT02571946
• Lead Sponsor: Samsung Medical Center

Brief Summary

The standard treatment of advanced hepatocellular carcinoma (HCC) is sorafenib. Though the agent showed clear survival benefit in two randomized phase III trials, the benefit was modest and response rate was just a few percent. Therefore, other loco-regional modalities, like trans-arterial chemo-embolization (TACE), hepatic arterial infusion chemotherapy (HAIC), and radiotherapy (RT) were continuously tried, especially in locally advanced HCC including portal vein tumor thrombosis (PVTT).

With the advancement of conformal RT techniques, RT was actively applied in HCC, especially in PVTT combined HCC. Many researchers reported that there is a relationship between RT dose and tumor response rate. RT dose, however, is frequently limited because the complications (like radiation induced liver disease (RILD), radiation induced gastro-duodenal toxicity, etc.) are also closely related with higher exposed RT dose.

Proton beam has characteristic depth-dose distribution contrast to photon, the "Bragg peak". The advantage of this dose distribution could be more highlighted in HCC management, because of the weakness and maintenance importance of liver function itself in HCC patients. In fact, the superior results of proton beam therapy in HCC were constantly reported in several groups as prospectively as well as retrospectively.

In those background, the investigators planned the present study to evaluate the efficacy and safety of proton beam therapy in HCC patients combined with PVTT.

Detailed Description

Not available

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Study Start: 2015-08
• Study First Submitted: 2015-10-07
• Study First Submitted QC: 2015-10-07
• Study First Posted: 2015-10-08
• Primary Completion: 2021-09
• Study Completion: 2021-09
• Status Verified: 2023-11
• Last Update Submitted: 2023-11-20
• Last Update Posted: 2023-11-22

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 53

Inclusion Criteria

• Hepatocellular carcinoma (HCC) patients
• pathologically proven
• HCC diagnosed based on American Association for the Study of Liver Diseases (AASLD) guideline
• Portal vein tumor thrombosis (main, first branch, segmental)
• Discussion in tumor board including gastroenterologist, radiologist, radiation oncologist
• 20 or more age
• Eastern Cooperative Oncology Group performance status 0 to 2 within 1 week before participate
• Adequate bone marrow function (absolute neutrophil count ≥ 1.0 x 109/l, platelet ≥ 30 x 109/l, hemoglobin ≥ 8 g/dl)
• Adequate liver/renal function within 1 week before participate
• Child-Pugh class A, B, or early C (score ≤ 10)
• Total bilirubin <3.0 mg/dL, Prothrombin time/International normalized ratio <1.7, Albumin≥2.8g/dL, Aspartate aminotransferase/alanine aminotransferase<6 times of upper normal limit
• Serum creatinine < 1,5 x upper normal limit, glomerular filtration rate > 50 ml/min Informed consent
• Women of childbearing potential and male participants must agree to practice adequate contraception while on study and for at least 6 months following the last dose of RT and for at least 28 days following the last dose of sorafenib (whichever is later).

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Exclusion Criteria

• Uncontrolled hepatic encephalopathy
• Previous history of upper abdominal radiotherapy
• Status of pregnancy or breast feeding
• Less than 12 weeks of expected survival
• Uncontrolled ascites
• Combined with disease known as radiosensitive disorder (connective tissue disorder, Ataxia-telangiectasia)
• Hard to maintain stable respiration less than 5 minutes related with respiratory disease
• Combined with uncontrolled severe acute disease other than liver

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Proton beam therapy	Proton beam therapy	-

Primary Outcome Measures

Name	Time	Method
one-year overall survival	one-year after proton beam therapy

Secondary Outcome Measures

Name	Time	Method
6 month Quality of life assessment compared with baseline	6 month after proton beam therapy
1 year portal vein tumor thrombosis progression free survival	one-year after proton beam therapy
3 month objective response rate	3 months after proton beam therapy
Hepatobiliary phase signal change after proton beam therapy	3 month after proton beam therapy
1 month objective response rate	1 month after proton beam therapy
1 year local progression free survival	one-year after proton beam therapy
Adverse event	one-year after proton beam therapy
Indocyanine green test change compared with baseline	3 month after proton beam therapy
1 year progression free survival	one-year after proton beam therapy
1 month portal vein tumor thrombosis response rate	1 month after proton beam therapy
3 month portal vein tumor thrombosis response rate	3 month after proton beam therapy
1 month Quality of life assessment compared with baseline	1 month after proton beam therapy
3 month Quality of life assessment compared with baseline	3 month after proton beam therapy

Trial Locations

Locations (1)

Samsung Medical Center; 🇰🇷 Seoul, Korea, Republic of