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

Radiofrequency Ablation Accompanied With Spontaneous Sorafenib Administration in the Treatment of Early to Intermediate Stage Hepatocellular Carcinoma: a Prospective Multicenter Cohort Study.(REASSESS)

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02187081
Enrollment
380
Registered
2014-07-10
Start date
2017-03-15
Completion date
2018-12-31
Last updated
2017-03-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HCC

Keywords

HCC, RFA, Sorafenib, Tumor recurrence, Overall survival

Brief summary

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.

Detailed 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

Interventions

PROCEDUREradiofrequency ablation plus Sorafenib

To treat HCC with the combination of radiofrequency ablation and sorafenib

PROCEDURERadiofrequency ablation

To treat HCC with radiofrequency ablation alone.

Sponsors

Southwest Hospital, China
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
2-year incidence of tumor recurrence2 yearto calculate the incidence of tumor recurrence of experiment and control group at two year after complete treatment.

Secondary

MeasureTime frameDescription
1-year incidence of recurrence1-year1-year incidence of recurrence
3-year incidence of recurrence3 year3-year incidence of recurrence
5-year incidence of recurrence5 year5-year incidence of recurrence
Overall survival5 yearsOverall survival
Disease Control Rateaverage 2 yearsDisease Control Rate
complications and adverse effect1 yearto sum all the complications and adverse effect for all the eligible enrolled patients during 1 year of a complete treatment.
Time to progressionaverage 2 yearsTime to progression

Countries

China

Contacts

Primary ContactXiaobin Feng, Docter
fengxiaobin200708@aliyun.com86-23-68765297

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026