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Combined Treatment of RFA and Sorafenib on Recurrent HCC

Radiofrequency Ablation Plus Sorafenib Administration in Early Recurrent Hepatocellular Carcinoma: a Prospective Multicenter Cohort Trial (Repeat) Tumors for BCLC B Stage HCC Undergone Curative Hepatectomy

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01470495
Acronym
REPEAT
Enrollment
430
Registered
2011-11-11
Start date
2015-01-31
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, Radiofrequency Ablation, Sorafenib

Brief summary

RFA is a routaine treatment of recurrent HCC. Recently Sorafenib was reported to be a promising drug to treat late stage HCC. But few studies were related with its effectiveness on recurrent HCC. So the investigators hypothesized that combined RFA and Sorafenib might reduce the frequency of recurrence and improve the overall survival and disease free survial.

Interventions

OTHERRFA + Sorafenib

combined RFA and Sorafenib to treat recurrent HCC

OTHERRFA

treat Recurrent HCC with RFA

Sponsors

Hunan Province Tumor Hospital
CollaboratorOTHER
Tang-Du Hospital
CollaboratorOTHER
Xijing Hospital
CollaboratorOTHER
First Affiliated Hospital of Guangxi Medical University
CollaboratorOTHER
First Affiliated Hospital Xi'an Jiaotong University
CollaboratorOTHER
Anhui Provincial Hospital
CollaboratorOTHER_GOV
Xiangya Hospital of Central South University
CollaboratorOTHER
Xinqiao Hospital of Chongqing
CollaboratorOTHER
Xinjiang Tumor Hospital
CollaboratorUNKNOWN
People's Hospital of Guangxi Zhuang Autonomous Region
CollaboratorOTHER
Henan Cancer Hospital
CollaboratorOTHER_GOV
People's Hospital of Sichuan
CollaboratorUNKNOWN
Huaxi Hospital
CollaboratorOTHER
Southwest Hospital, China
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
DOUBLE (Caregiver, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* recurrent HCC after curative resection * without gender restriction * age between 18 to 75 years * The liver function showed no worse than Child-Pugh B * tumor nodes were less than 5cm and no more than 3 nodules

Exclusion criteria

* Pregnancy patients * With extrahepatic tumor or lymphnode metastasis * Tumor invasion or thrombosis in portal vein,hepatic vein or inferior vena cava

Design outcomes

Primary

MeasureTime frame
time interval between new lessions emerging after the first HCC recurrence3 year

Secondary

MeasureTime frame
3-year overrall survival3 year

Countries

China

Contacts

Primary ContactXiaobin Feng, MD
fengxiaobin200708@aliyun.com+86-2368765297

Outcome results

None listed

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