CClinicalTrials.gg
Status unknownNCT00728078LDT-RFAUpdated Feb 9, 2009

Low-Dose Thalidomide as Adjuvant Therapy After Radiofrequency Ablation for Hepatocellular Carcinoma

A Phase 2/3 interventional study of thalidomide in Hepatocellular Carcinoma and Liver Cancer, sponsored by Sun Yat-sen University. Status unknown at 1 site in China. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2009-02-09.

Sponsored by Sun Yat-sen University · Phase 2/3, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Feb 2009), so the status shown — last known as Recruiting — may be out of date.
Phase
Phase 2/3
Study type
Interventional
Enrollment
200
Allocation
Randomized
Ages
18 Years to 75 Years
Sex
All
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Study summary

The purpose of the investigators' study is to prospectively evaluate whether low-dose thalidomide adjuvant therapy will improve the outcome of radiofrequency ablation for hepatocellular carcinoma (HCC).

Read the detailed description

Our previous studies showed that radiofrequency ablation (RFA) was as effective as liver resection for small hepatocellular carcinoma (HCC), but the recurrence rates after RFA were relatively high. Adjuvant therapies maybe reduce the recurrence rate. Phase 1 and 2 studies showed that thalidomide was a safety and effective treatment for HCC, especially for small HCC with liver cirrhosis. So we proposed that low-dose thalidomide adjuvant therapy will improve the disease progress free survivals and overall survivals after RFA for HCC.

02

Conditions studied

  • Hepatocellular Carcinoma
  • Liver Cancer

Keywords

  • hepatocellular carcinoma
  • liver cancer
  • radiofrequency ablation
  • thalidomide
03

In context

Carcinoma

6,741 studies on the registry are indexed under Carcinoma; 1,161 are open to participants now.

This study's planned enrollment of 200 is above the median of 45 across 5,170 interventional studies indexed under Carcinoma.

Browse Carcinoma studies →

Lead sponsor

Sun Yat-sen University is the lead sponsor of 1,644 studies on the registry; 602 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Age 18 - 75 years, who refused surgery or first recurrence after hepatectomy
  • A solitary HCC 3.1-7.0cm in diameter, or 2-3 lesions, sums of diameters ≤ 7.0cm
  • Lesions being visible on ultrasound (US) and with an acceptable/safe path between the lesion and the skin as shown on US
  • No extrahepatic metastasis
  • No imaging evidence of invasion into the major portal/hepatic vein branches
  • No history of encephalopathy, ascites refractory to diuretics or variceal bleeding
  • A platelet count of > 40,000/mm3
  • No previous treatment of HCC except liver resection

Exclusion criteria

Exclusion Criteria:

  • Patient compliance is poor
  • Previous or concurrent cancer that is distinct in primary site or histology from HCC, EXCEPT cervical carcinoma in situ, treated basal cell carcinoma, superficial bladder tumors (Ta, Tis \& T1). Any cancer curatively treated > 3 years prior to entry is permitted
  • History of cardiac disease:

    • congestive heart failure > New York Heart Association (NYHA) class 2
    • active coronary artery disease (myocardial infarction more than 6 months prior to study entry is permitted)
    • cardiac arrhythmias requiring anti-arrhythmic therapy other than beta blockers, *calcium channel blocker or digoxin
    • uncontrolled hypertension (failure of diastolic blood pressure to fall below 90 mmHg, despite the use of 3 antihypertensive drugs)
  • Active clinically serious infections (> grade 2 National Cancer Institute [NCI]-Common Terminology Criteria for Adverse Events [CTCAE] version 3.0)
  • Known history of human immunodeficiency virus (HIV) infection
  • Known Central Nervous System tumors including metastatic brain disease
  • Patients with clinically significant gastrointestinal bleeding within 30 days prior to study entry
  • Distantly extrahepatic metastasis
05

Study design

Phase
Phase 2 / Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
200 participants (estimated)

Study arms

  • Experimental
    1

    low-dose thalidomide adjuvant therapy after RFA for HCC

    Drug: thalidomide

  • No intervention
    2

    control group

Interventions

  • Drugthalidomide

    thalidomide 50mg tid for 6 months

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What researchers measure

Primary outcomes

  1. progress free survival

    Time frame: 1,3,5-year

  2. morbility

    Time frame: one month

Secondary outcomes

  1. overall survival

    Time frame: 1,3,5-year

  2. recurrence rate

    Time frame: 1,3,5-year

07

Study locations

1 of 1 sites recruiting
  • Cancer Center, Sun Yat-sen University
    Guangzhou, Guangdong 510060, China
    • min-shan chen, MD · Contact · Chminsh@mail.sysu.edu.cn · 86-20-87343117
    • min-shan chen, MD · Principal investigator
    • yao-jun zhang, Doctor · Sub investigator
    Recruiting
08

References and documents

Publications

  • Chen MS, Li JQ, Zheng Y, Guo RP, Liang HH, Zhang YQ, Lin XJ, Lau WY. A prospective randomized trial comparing percutaneous local ablative therapy and partial hepatectomy for small hepatocellular carcinoma. Ann Surg. 2006 Mar;243(3):321-8. doi: 10.1097/01.sla.0000201480.65519.b8. PubMed 16495695 ↗
  • Buscarini L, Buscarini E, Di Stasi M, Vallisa D, Quaretti P, Rocca A. Percutaneous radiofrequency ablation of small hepatocellular carcinoma: long-term results. Eur Radiol. 2001;11(6):914-21. doi: 10.1007/s003300000659. PubMed 11419162 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 9, 2009, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT00728078
Lead sponsor
Sun Yat-sen University
First posted
Aug 5, 2008
Start date
Jul 2008
Primary completion
Jul 2009 (estimated)
Completion
Jul 2011 (estimated)
Last update
Feb 9, 2009

Study contacts

min-shan chen, MD
Contact
Chminsh@mail.sysu.edu.cn
86-20-87343117 ext. 86-20-87343117
min-shan chen, MD
principal investigator · Department of Hepatobilliary Surgery, Cancer Center, Sun Yat-sen University

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Feb 2009. You cannot join it, but the record below documents what was studied.

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