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Palliative Treatments for Patients With Advanced Hepatocellular Carcinoma (HCC)

A Prospective Multicenter Non-randomized Controlled Study of Palliative Treatments for Patients With Advanced Hepatocellular Carcinoma

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01409499
Acronym
2011PTAHCC
Enrollment
180
Registered
2011-08-04
Start date
2011-01-31
Completion date
2018-01-31
Last updated
2018-09-11

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

Conditions

Hepatectomy, Hepatocellular Carcinoma, Sorafenib

Keywords

hepatocellular carcinoma, treatments, survival

Brief summary

The standard treatment choice for advanced hepatocellular carcinoma (HCC) is sorafenib, and its efficacy is limited. More active treatments were performed in patients with advanced HCC in China, which include radical hepatectomy or TACE. The study is to investigate whether the active treatment will profit survival of patients, and to evaluate the safety.

Detailed description

This is a prospective non-randomized controlled study. Patients with advanced hepatocellular carcinoma (BCLC C stage) who underwent palliative resection or TACE followed with Sorafenib or treated by sorafenib alone will be included. The patients will be divided to group A (palliative resection plus sorafenib), group B (palliative TACE plus sorafenib), and group C (sorafenib alone). The sample size will be about 200 cases altogether.

Interventions

PROCEDUREhepatic resection

palliative hepatectomy followed by sorafenib

PROCEDUREtranscatheter hepatic arterial chemoembolization

TACE followed by sorafenib

DRUGsorafenib

sorafenib monotherapy, 400mg Bid, continuously

Sponsors

Sun Yat-sen University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* Male or female patients \> 18 years of age. * Diagnosed to have advanced HCC (BCLC C stage). * Patients who have a life expectancy of at least 12 weeks. * Patients whose primary tumor can be resected. Definition of resectable in this study: * Tumor number \<=2. * If number of tumors \>= 3, then all tumors were located in the same lobe. * Without tumor invasion of the main trunk of the portal vein, or hepatic duct, or caval vein. * Hepatocellular carcinoma with histological diagnose or clinical diagnose according to AASLD. * No major post-operative complication. * Patients who have an ECOG PS of 0, or 1. * Cirrhotic status of Child-Pugh class A only. * The following laboratory parameters: Platelet count \> 60 x 109/L Hemoglobin \> 8.5 g/dL Albumin \> 3.5 g/dL Total bilirubin \< 25μmol/L Alanine transaminase (ALT) and AST \< 2.5 x upper limit of normal Serum creatinine \<1.5 x the upper limit of normal Prothrombin time (PT)\<3 seconds above control. • Patients who give written informed consent.

Exclusion criteria

* Previous or concurrent cancer that is distinct in primary site or histology from HCC. * History of cardiac disease. * 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. * History of organ allograft. * Known or suspected allergy to the investigational agent or any agent given in association with this trial. * Pregnant or breast-feeding patients. * Any condition that is unstable or which could jeopardize the safety of the patient and his/her compliance in the study. * Excluded therapies and medications, previous and concomitant: Systemic chemotherapy and target drug other than sorafenib. Antiviral treatment is allowed. * Radiotherapy except for which done for bone metastases palliatively.

Design outcomes

Primary

MeasureTime frameDescription
Overall survival (OS)anticipate 6-12 monthsdefined as the time from the first treatment to death

Secondary

MeasureTime frameDescription
Progression Free Survival (PFS)anticipate 3-6 monthsdefined as the time from the first treatment to the first progression disease is confirmed by radiological methods
AEs and SAEsanticipate 6-12 monthsaccording to CTC AE 3.0
cost of treatments3 months in averageto compare costs of different treatments

Countries

China

Outcome results

None listed

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