NCT02309788

Brief Summary

Hepatocellular carcinoma (HCC) is one of ten leading cancer types worldwide and also in Asia, but the five-year relative survival rate is relatively quite low1-3. As a common complication of HCC, portal vein tumor thrombosis (PVTT) have been reported with an occurrence of 34% \~ 50% in advanced HCC and it is now become an extremely pressing problem for hepatic surgeon. Nevertheless, the patients overall survival (OS) varies on their clinical features or liver function4. For HCC PVTT treatment, current options are surgical resection, embolization chemotherapy, radiation therapy, a variety of ablation therapy, biological and gene therapy,etc. Among them, the use of radiation therapy is getting more and more attention, and it is changing from the past palliative treatment to current curable treatment. From an oncologic point of view, a narrow margin \<1 cm is not safe and is often associated with higher rates of recurrence and shorter patient survival.On the other hand, it is also believed that most intrahepatic recurrences arise from multicentric carcinogenesis and are distant from the resection margin.To address this issue, the investigators are going to conduct a series of retrospective and prospective studies to investigate the effect of adjuvant RT for centrally located HCC after narrow margin (\<1 cm) hepatectomy on tumor recurrence.

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
100

participants targeted

Target at P50-P75 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 2, 2014

Completed
3 days until next milestone

First Posted

Study publicly available on registry

December 5, 2014

Completed
1.1 years until next milestone

Study Start

First participant enrolled

January 1, 2016

Completed
3.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2019

Completed
Last Updated

January 26, 2016

Status Verified

January 1, 2016

Enrollment Period

3.9 years

First QC Date

December 2, 2014

Last Update Submit

January 23, 2016

Conditions

Outcome Measures

Primary Outcomes (1)

  • overall survival

    1year

Study Arms (2)

RT

Resectable HCC patients adjuvant RT for PVT or NM

No RT

Resectable HCC patients adjuvant other treatment for PVT or NM

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Patients diagnosed with HCC at the Affiliated Tumor Hospital of Guangxi Medical University Science were considered for enrollment in the study. The diagnostic criteria for HCC used in the study were in accordance with the American Association for the Study of Liver Diseases' 2005 guidelines. All patients had preoperative serum a-fetoprotein (AFP) levels \>200 ng/mL or a typical enhancement pattern (arterial enhancement and portal/delayed washed out) on dynamic imaging of hepatic mass(es)\>2 cm, or cytologic/histologic evidence of HCC

You may qualify if:

  • HCC with no preoperative RT
  • resectable lesion that could be completely removed, at the same time retaining a sufficient residual liver tissue to maintain adequate function
  • compensated cirrhosis or no cirrhosis; Child-Pugh A
  • ECOG Performance Status of 0 or 1.
  • Patients who had undergone transarterial chemoembolization (TACE) were eligible for enrollment in the study, provided this form of therapy ended at least 4 weeks before study entry

You may not qualify if:

  • unresectable hepatocellular carcinoma patients
  • Hepatocellular carcinoma without portal vein tumor thrombus
  • Hepatectomy without narrow margin(more than 1cm)
  • presence of distant metastasis
  • palliative resection with tumor residual
  • non-HCC confirmed by postoperative pathology

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

TaoBai

Nanning, Guangxi, 530000, China

RECRUITING

MeSH Terms

Conditions

Carcinoma, Hepatocellular

Condition Hierarchy (Ancestors)

AdenocarcinomaCarcinomaNeoplasms, Glandular and EpithelialNeoplasms by Histologic TypeNeoplasmsLiver NeoplasmsDigestive System NeoplasmsNeoplasms by SiteDigestive System DiseasesLiver Diseases

Central Study Contacts

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Researcher

Study Record Dates

First Submitted

December 2, 2014

First Posted

December 5, 2014

Study Start

January 1, 2016

Primary Completion

December 1, 2019

Last Updated

January 26, 2016

Record last verified: 2016-01

Locations