Radiofrequency Ablation Accompanied With Spontaneous Sorafenib in Early to Intermediate Stage HCC

Army Medical University

Status: Unknown

Conditions: HCC

Treatments: Procedure: Radiofrequency ablation; Procedure: radiofrequency ablation plus Sorafenib

Study type: Interventional

Funder types: Other

Identifiers

NCT02187081

SWHB008

Details and patient eligibility

About

Radiofrequency ablation (RFA)can be curative with small localized HCCs up to 5 cm in diameter. However, the long-term prognosis is not satisfactory due to the high incidence of recurrence.Multimodality treatments are needed to prevent recurrences，but only useful with locoregional disease. Sorafenib is an oral multi-kinase inhibitor and the only systemic drug associated with improved overall survival (OS) in patients with advanced HCC. Retrospective and randomized studies have suggested that the combined use of Sorafenib may be useful in patients with unresectable HCC. Based on these information and the multiple actions of Sorafenib, we hypothesized that Sorafenib plus RFA may be useful in patients with early to Mid term HCC. In this investigation, we evaluated the safety and efficacy of a combination Sorafenib and RFA therapy in patients with Barcelona Clinic Liver Cancer (BCLC) Stage 0 -B1 HCC in a multicenter prospective cohort study.

Full description

Radiofrequency ablation (RFA) has been used as a minimally invasive option to eradicate tumors and preserve liver function in patients with impaired function or with a postoperative tumor recurrence. RFA can be curative with small localized HCCs up to 5 cm in diameter. However, the long-term prognosis for HCC patients treated with RFA is not satisfactory due to the high incidence of recurrence including local tumor recurrence and multicentric carcinogenesis.

Multimodality treatments are needed to prevent recurrences. Although there is a potential benefit with this strategy, it is only useful with locoregional disease. Sorafenib is an oral multi-kinase inhibitor and the only systemic drug associated with improved overall survival (OS) in patients with advanced HCC.

Retrospective and randomized studies have suggested that the combined use of Sorafenib, TACE, and RFA may be useful in patients with unresectable HCC. Based on these information and the multiple actions of Sorafenib, we hypothesized that Sorafenib plus RFA may be useful in patients with early HCC or recurrent HCC. Although no supportive data from clinical trials is available, this hypothesis is supported by recent animal studies. Inadequate RFA has been shown to promote rapid progression of residual tumors. Adjuvant Sorafenib postponed time to recurrence by inhibition of hypoxia inducible factor-1and vascular endothelial growth factor A (VEGFA). In a multifocal tumor model of HCC, RFA and Sorafenib alone resulted in a significant volume reduction of non-RFA-targeted tumors, but this effect was enhanced when both modalities were combined. This phenomenon was also demonstrated by more recent study on human subject.

Besides the advantages, Sorafenib initially promoted necrosis, delayed tissue repair after RFA and adversely affected normal liver parenchyma, which could result in increased RFA toxicity and limit its use in patients with HCC who have undergone RFA. Thus, the overall advantages of RFA plus Sorafenib need to be weighed against its adverse effects. In this investigation, we evaluated the safety and efficacy of a combination Sorafenib and RFA therapy in patients with Barcelona Clinic Liver Cancer (BCLC) Stage 0 -B1 HCC in a multicenter prospective cohort study.

Outcome measures: Post-RFA tumor recurrence

Enrollment: 380 estimated patients

Sex: All

Ages: 18 to 70 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Authorization of Informed Consent
• HCC diagnosed by biopsy or Image findings
• BCLC stage 0 to B1
• This time was the primary treatment of HCC. Had no history of any tumor specific therapy,including RFA,Hepatectomy,TACE,HIFU,and Transplantation
• Child Pugh A or B
• ECOG 0 to 2
• single lesion less than or equal to 5 cm,2 to 3 nodules, maximal size less than equal to 3cm
• Male or female (without pregnancy)
• Ages between 18 to 70 years
• Capable of take medicines
• anticipate at least survival of 12 weeks
• Unwilling to receive surgical resection or liver transplantation
• Potentially curable disease by RFA
• Sorafenib administrated less than 4 weeks before or after RFA procedures
• For any excuse,subject should take Sorafenib at least for 4 weeks

Exclusion criteria

• A cancer embolus in major hepatic vessels or extrahepatic metastases
• Tumor number more than 4 or tumor size larger than 5 cm
• A present or past history of uncontrollable ascites, hepatic encephalopathy or variceal bleeding
• A history of a secondary malignancy
• Severe dysfunction of the heart, kidney or other organs
• Active infection except viral hepatitis
• Any treatment history of target lesion including chemotherapy and TACE
• Pregnancy
• received other trials on gene therapy
• have received operation less than 4 weeks

Trial design

Primary purpose: Treatment

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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380 participants in 2 patient groups

Sorafenib+RFA

Experimental group

Description:

We give radiofrequency ablation plus Sorafenib for the treatment of HCC

Treatment:

Procedure: radiofrequency ablation plus Sorafenib

RFA alone

Active Comparator group

Description:

We give Radiofrequency ablation alone for the treatment of HCC

Treatment:

Procedure: Radiofrequency ablation