Regorafenib After Treatment Failure of First Line Immune Checkpoint Inhibitor Treatment in Advanced Hepatocellular Carcinoma Patients

Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age19-80
SponsorJu Hyun Shim

About this trial

Immune checkpoint inhibitor (ICI)-based regimens (atezolizumab+bevacizumab, durvalumab+tremelimumab, nivolumab+ipilimumab) are now a first-line standard for advanced hepatocellular carcinoma (HCC). For Child-Pugh (CP) A patients, regorafenib, cabozantinib, and ramucirumab are approved second-line agents, but there is no approved second-line systemic therapy for CP-B. In CP-B historical controls treated with best supportive care, median progression free survival (PFS) was \~1.4 months in a REACH trial subgroup analysis and \~1.9 months in a CELESTIAL trial subgroup analysis. Regorafenib demonstrated benefit as a post-sorafenib second-line therapy in CP-A patients in the RESORCE trial, but prospective evidence in CP-B is lacking. A multicenter retrospective study of CP-B patients receiving second-line regorafenib after sorafenib reported a median PFS of 1.8 months, and prospective data after ICI-based first-line therapy are not available.

This study will evaluate the efficacy and safety of regorafenib as second-line therapy in CP-B patients with disease progression after first-line ICI-based treatment. The primary objective is to demonstrate superiority over historical controls, with PFS as the primary endpoint.

After written informed consent, all participants will receive regorafenib. Regorafenib will be administered at 120 mg orally once daily at the same time each day, after a meal with water, for 3 consecutive weeks followed by 1 week off (4-week cycle). Treatment must start within 3 days after screening and will continue until disease progression, unacceptable toxicity, withdrawal of consent, or study termination, whichever occurs first. After treatment discontinuation, patients will be followed every 12 week (+/-7 days) for survival status and subsequent anticancer therapies, and survival follow-up will continue for at least 12 months after enrollment of the last participant.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Voluntarily signed written informed consent form.

Age ≥19 years at the time of signing the informed consent form.

Histologically or clinically diagnosed hepatocellular carcinoma (HCC) according to the Korean Liver Cancer Association-National Cancer Center (KLCA-NCC) guidelines.

Disease progression or treatment discontinuation due to toxicity during first-line immune checkpoint inhibitor-based combination therapy (atezolizumab plus bevacizumab, durvalumab plus tremelimumab, or nivolumab plus ipilimumab).

Disqualifiers

ALBI (Albumin-Bilirubin) grade 3.

Fibrolamellar carcinoma or sarcomatoid carcinoma.

Prior treatment with regorafenib.

Within 2 weeks since the last administration of an immune checkpoint inhibitor.

Trial design

Design model

Single group

Treatments tested in this trial

  • Regorafenib (BAY 73-4506)

    Drug

    Oral regorafenib 120 mg once daily, taken at the same time each day after a meal with water. The study drug is administered on a 28-day cycle, consisting of 3 consecutive weeks of daily dosing followed by 1 week off. Treatment will continue until disease progression, unacceptable toxicity, withdrawal of consent, or study termination.

Treatment groups

20 Participants
are divided into 1 treatment group
Group A: RegorafenibExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Progression Free Survival

Time frame
From treatment initiation until the date of first documented progression or death from any cause, whichever comes first, assessed up to 36 months.

Secondary outcomes

1

Overall survival

Time frame
From treatment initiation until the date of death from any cause, assessed up to 36 months.
2

time to progression

Time frame
From treatment initiation until the date of first documented progression, assessed up to 36 months.
3

objective response rate

Time frame
From treatment initiation until first documented progression or start of subsequent systemic anticancer therapy, assessed up to 36 months.
4

disease control rate

Time frame
From treatment initiation until first documented progression or start of subsequent systemic anticancer therapy, assessed up to 36 months.

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Ju Hyun Shim

Lead sponsor

Asan Medical Center

Sponsor institution

Boryung Pharmaceutical Co., Ltd

Collaborator

National Cancer Center, Korea

Collaborator

Seoul National University Hospital

Collaborator

Seoul National University Bundang Hospital

Collaborator

Samsung Medical Center

Collaborator

Hanyang University Guri Hospital

Collaborator

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