Surgical Treatment of Hilar Cholangiocarcinoma: Minor or Major Liver Resection?

Sponsor
Huazhong University of Science and Technology (Other)
Overall Status
Completed
CT.gov ID
NCT00733200
Collaborator
Ministry of Health, China (Other), Hepatic Surgery Clinical Research Centre of Hubei, China (Other)
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Study Details

Study Description

Brief Summary

The investigators conducted a prospective study to determine the safety and efficacy of minor and major hepatectomy selected by predetermined criteria in 138 patients with hilar cholangiocarcinoma. In selected patients, minor liver resection was a good treatment.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Minor or Major Liver Resection
N/A

Detailed Description

Objective: To determine the safety and efficacy of minor and major hepatectomy selected by predetermined criteria in patients with hilar cholangiocarcinoma (HC).

Summary Background Data: For HC treated with hepatectomy, the extent of liver resection remains controversial despite extensive studies.

Methods: From January 2000 to December 2007, we prospectively studied patients who received surgical treatment for HC. Of the 187 patients who were surgically treated, 138 (73.8%) underwent resection with a curative intent. Minor hepatectomy was carried out in 93 patients who had Bismuth-Corlette types I, II and III HC without hepatic artery/portal vein invasion; and major hepatectomy in 45 patients who had type III HC with hepatic artery/portal vein invasion, or type IV HC.

Study Design

Study Type:
Interventional
Official Title:
Surgical Treatment of Hilar Cholangiocarcinoma: Minor or Major Liver Resection?

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Control group

Procedure: Minor or Major Liver Resection

Outcome Measures

Primary Outcome Measures

  1. On multivariate analysis, prognostic factors significantly impacted on long-term survival were UICC tumor stage and histopathologic grade. []

Eligibility Criteria

Criteria

Ages Eligible for Study:
26 Years to 72 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Criteria for resectability were absence of peritoneal or liver metastases, tumor extension to beyond secondary biliary branches bilaterally, tumor extension to secondary portal venous branches bilaterally
Exclusion Criteria:
  • not in accordance with the above criteria

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Huazhong University of Science and Technology
  • Ministry of Health, China
  • Hepatic Surgery Clinical Research Centre of Hubei, China

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00733200
Other Study ID Numbers:
  • chenxp002
First Posted:
Aug 12, 2008
Last Update Posted:
Dec 11, 2009
Last Verified:
Aug 1, 2008
Keywords provided by , ,
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 11, 2009