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NCT Number: NCT05994859

SIRT for Potentially Resectable HCC

This study is conducted to evaluate the efficacy and safety of Y-90 selective internal radiation therapy (SIRT) in patients with potentially resectable hepatocellular carcinoma (HCC).

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

The Second Affiliated Hospital of Guangzhou Medical University

Guangzhou, Guangdong, 510260, China

Location status: Recruiting

Location contact

Kangshun Zhu, Dr.

CONTACT

[email protected]

+86-20-34156205

Kangshun Zhu, Dr.

PRINCIPAL_INVESTIGATOR

Mingyue Cai, Dr.

SUB_INVESTIGATOR

About this study

This is a bi-center, prospective study to evaluate the efficacy and safety of SIRT in patient with potentially resectable HCC.

35 patients with potentially resectable (initially unresectable) HCC will be enrolled in this study. The patients will receive 1-2 sessions of SIRT. If the patients have invasive tumors, extensive liver involvement or vascular invasion, systematic treatment will be added. If the patients are evaluated as resectable during follw-up, liver resection will be recommended.

The primary end point of this study is success rate of conversion to resection. The secondary endpoints are objective response rate (ORR), disease control rate (DCR), progression-free survival (PFS), time to progression (TTP), duration of response (DOR), overall survival (OS) and adverse events (AEs).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • HCC with diagnosis confirmed pathologically or clinically
  • No pervious treatment for HCC
  • At least one measurable intrahepatic target lesion
  • Potentially resectable HCC: tumor(s) confined to the left/right hemiliver, with/without invasion to the unilateral branch of the portal vein and/or hepatic vein
  • Disease amenable to SIRT (after evaluation)
  • Child-Pugh Class A or without cirrhosis
  • Eastern Cooperative Oncology Group performance status (ECOG PS) of 0 or 1
  • Patients with active hepatitis B are allowed, but they need to receive antiviral treatment to achieve a HBV DNA<10^3 IU/mL
  • Patients with hepatitis C need to finish the anti-HCV treatment
  • Adequate organ and bone marrow function; the blood biochemical examination: platelet count ≥75×10^9/L, white blood cell count >3.0×10^9/L, absolute value of neutrophils >1.5×10^9/L, hemoglobin ≥85 g/L, ASL and AST≤5×ULN, creatinine≤1.5×ULN, INR<1.5 or PT/APTT normal range
  • Life expectancy of at least 6 months

Exclusion criteria

  • Tumor involving main portal vein, bilateral branches of portal vein, or vena cava
  • tumor extention beyond one lobe of the liver
  • Bilobar tumor distribution
  • Extrahepatic metastasis
  • Decompensated liver function, including ascites, bleeding from esophageal and gastric varices, and/or hepatic encephalopathy
  • Organ (heart, kidney) dysfunction
  • HBsAg and anti-HCV antibody positive concurrently
  • History of malignancy other than HCC
  • Uncontrolled infection
  • History of HIV
  • History of organ and cell transplantation
  • Patients with bleeding tendency

Treatment and study plan

SIRT

Procedure

The patients will receive 1-2 sessions of SIRT. If the patients have invasive tumors, extensive liver involvement or vascular invasion, systematic treatment will be added.

Primary outcomes

  1. Success rate of conversion to resection

    Time frame: 3 years

    The proportion of patients with initially unresectable HCC who were evaluated by the surgical team as suitable for second-stage surgical resection after SIRT

Secondary outcomes

  1. Objective response rate (ORR)

    Time frame: 3 years

    The percentage of patients who have a best overall tumor response rating of complete response (CR) or partial response (PR)

  2. Disease control rate (DCR)

    Time frame: 3 years

    The percentage of patients who have a tumor response rating of CR, PR, or stable disease (SD)

  3. Progression-free survival (PFS)

    Time frame: 3 years

    The time between the first treatment and the first occurrence of disease progression (PD) or death from any cause, whichever occurs first

  4. Time to progression (TTP)

    Time frame: 3 years

    the time interval from first treatment to the first occurrence of disease progression

  5. Duration of response (DOR)

    Time frame: 3 years

    the time from initial objective response (CR or PR) until PD or death, whichever occurs first

  6. Overall survival (OS)

    Time frame: 3 years

    The time from initiation of treatment until the date of death from any cause

  7. Adverse Events (AEs)

    Time frame: 3 years

    Number of patients with AEs assessed by NCI CTCAE v5.0.

Study contacts

Contact information is provided by the study sponsor or research team.

Kangshun Zhu, Dr.

CONTACT

[email protected]

+86-20-34156205

Mingyue Cai, Dr.

CONTACT

[email protected]

+86-20-34156205

Sponsors and collaborators

Lead sponsor

Second Affiliated Hospital of Guangzhou Medical University

Other

Registry information

Official study title

Y-90 Selective Internal Radiation Therapy for Potentially Resectable Hepatocellular Carcinoma: a Prospective, Single Arm Trial

Important dates

Study start
2023
Primary completion
2026
Study completion
2027
First posted
Aug 16, 2023
Registry last updated
Sep 14, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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