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Clinical Trials/NCT05117957
NCT05117957
Completed
Phase 2

Efficacy and Safety of Sorafenib in Previously Treated Advanced Hepatocellular Carcinoma: SOPT Study

Bo Hyun Kim1 site in 1 country50 target enrollmentStarted: March 8, 2022Last updated:

Overview

Phase
Phase 2
Status
Completed
Sponsor
Bo Hyun Kim
Enrollment
50
Locations
1
Primary Endpoint
Progression-free survival (PFS)

Overview

Brief Summary

To investigate the efficacy and safety of sorafenib administered as later lines of treatment in patients with advanced HCC.

Detailed Description

Sorafenib (Soranib Tablet) will be administered orally at a dose of 600mg daily without food for patients who have been treated with prior systemic therapy for advanced HCC. The study drug is continued until disease progression, unacceptable toxicity, withdrawal of consent, or study closure.

Response to sorafenib should be assessed at least every 8 weeks (± 7 days) by either CT scan or MRI.

After the treatment phase, subjects will undergo follow up for survival and the use of other anticancer treatments and/or therapies every 12 weeks (± 7 days) from the last dose and the survival follow up will be performed for at least 12 months after the enrollment of the last subject.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
20 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Signed written informed consent
  • Age of 20 or more
  • Histological or clinical diagnosis of HCC based on the guidelines of the Korean Liver Cancer Association-National Cancer Center
  • Locally advanced unresectable or metastatic disease not amenable to curative surgical and/or locoregional therapies
  • Intolerant to or progressed on at least 1 prior systemic treatment for HCC
  • Having at least one measurable target lesion (per RECIST v1.1)
  • \- Patients who received prior local therapy (e.g., radiofrequency ablation, transarterial chemoembolization, transarterial embolization, radiation therapy etc.) are eligible provided that other target lesion(s) have not been previously treated with local therapy or the target lesion(s) within the field of local therapy have subsequently progressed in accordance with RECIST 1.
  • Child-Pugh class A or B7
  • Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0-1
  • Life expectancy of at least 16 weeks

Exclusion Criteria

  • Fibrolamellar carcinoma or sarcomatoid carcinoma
  • Having active brain metastasis or leptomeningeal metastasis
  • Moderate to severe or intractable ascites
  • Presence of hepatic encephalopathy
  • Presence of active bacterial infection
  • Uncontrolled severe medical comorbidity
  • Other malignant disease (a history of treated malignancy -other than HCC- is allowable if the patient's malignancy has been in complete remission, off chemotherapy and without additional surgical intervention, during the preceding two years)
  • Other patients judged by the investigator or sub-investigator to be inappropriate as subjects of this study

Arms & Interventions

Sorafenib

Experimental

Sorafenib will be administered orally at a dose of 600mg (3 tablets; 400mg orally in the morning and 200mg orally in the evening about 12 hours apart or 200mg orally in the morning and 400mg orally in the evening about 12 hours apart) daily without food (at least 1 hour before or 2 hours after a meal).

Intervention: Sorafenib (Drug)

Outcomes

Primary Outcomes

Progression-free survival (PFS)

Time Frame: Until 12 months after the last patient was enrolled

Progression-free survival (PFS) is defined as the time from the date of treatment initiation to the date of the first observation of progressive disease (PD) by independent radiologic review according to RECIST criteria (version 1.1) or death from any cause.

Safety (Adverse events)

Time Frame: Until 12 months after the last patient was enrolled

Incidence of adverse events will be evaluated.

Secondary Outcomes

  • Overall survival (OS)(Until 12 months after the last patient was enrolled)
  • Time to progression (TTP)(Until 12 months after the last patient was enrolled)
  • Objective response rate (ORR)(Until 12 months after the last patient was enrolled)
  • Disease control rate (DCR)(Until 12 months after the last patient was enrolled)

Investigators

Sponsor
Bo Hyun Kim
Sponsor Class
Other Gov
Responsible Party
Sponsor Investigator
Principal Investigator

Bo Hyun Kim

Adjunct Associate Professor, Senior Scientist

National Cancer Center, Korea

Study Sites (1)

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