Hepatocellular Carcinoma Clinical Trial
— TACEOfficial title:
A Prospective Randomized Trial Comparing Cytoreductive Surgery Followed by Transcatheter Arterial Chemoembolization (TACE) Versus TACE Alone for Multinodular Hepatocellular Carcinoma (MNHCC)
| Verified date | August 2013 |
| Source | Eastern Hepatobiliary Surgery Hospital |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
The aim of this study is to compare the surgical outcomes of cytoreductive surgery followed by Transarterial Chemoembolization (TACE) with TACE alone in patients with MNHCC so as to establish a treatment standard for MNHCC.
| Status | Completed |
| Enrollment | 120 |
| Est. completion date | December 2012 |
| Est. primary completion date | November 2010 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years to 70 Years |
| Eligibility |
Inclusion Criteria: - Male or female patients > 18 years and <=70 years of age. - at least 2 radiologic imaging showing characteristic features of HCC or one radiologic imaging associated with AFP >400 or cytologic/histologic evidence. - tumor number >3 and <=5,maximum diameter >5cm and <=15cm;without evidence of radiologically definable vascular invasion or extrahepatic metastasis. - Criteria of liver function: Child A-B level, serum bilirubin = 1.5 times the upper limit of normal value,alanine aminotransferase and aspartate aminotransferase = 2 times the upper limit of normal value. - No dysfunction in major organs; Blood routine, kidney function, cardiac function and lung function are basically normal. - Hb =90g/L,WBC =3.000 cells/mm³,platelets =80.000 cells/mm³ - Patients who can understand this trial and have signed information consent Exclusion Criteria: - Patients with apparent cardiac, pulmonary, cerebral and renal dysfunction,which may affect the treatment of liver cancer. - Patients with other diseases which may affect the treatment mentioned. - Patients with a medical history of other malignant tumors. - Subjects participating in other clinical trials. - Extrahepatic metastasis, portal vein or other major vascular involvement. - liver function:Child C. - no pathological evidence of HCC. |
| Country | Name | City | State |
|---|---|---|---|
| China | Eastern Hepatobiliary Surgery Hospital | Shanghai | Shanghai |
| Lead Sponsor | Collaborator |
|---|---|
| Eastern Hepatobiliary Surgery Hospital |
China,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | the overall survival rate of each group | 3 years | ||
| Secondary | the disease-free survival rate of each group | 3 years |
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