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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02654028
Other study ID # AT/HCC
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 5, 2019
Est. completion date December 30, 2021

Study information

Verified date January 2023
Source Guangxi Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This prospective non-randomized controlled trial aims to determine whether autotransfusion of red blood cells salvaged before liver resection is associated with the recurrence-free survival in patients with hepatocellular carcinoma.


Description:

Preoperative and intraoperative blood salvage autotransfusion is used in various surgical procedures. However, because of the risk of reinfusion of salvaged blood contaminated by tumor cells, the use of autotransfusion in hepatocellular carcinoma (HCC) patients undergoing liver resection is controversial. The critical points include whether tumor cells can be cleared by autotransfusion, whether autotransfusion increases the risk of recurrence or metastasis, and what are the indications for autotransfusion. Moreover, some other issues are still not addressed. For example, is it warranted to take the risk of tumor dissemination by using autotransfusion to avoid allogeneic blood transfusion? Do the remaining tumor cells after additional filtration by leukocyte depletion filters still possess potential tumorigenicity?


Recruitment information / eligibility

Status Completed
Enrollment 618
Est. completion date December 30, 2021
Est. primary completion date December 30, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: - Patients who underwent liver resection; - Diagnosis of hepatocellular carcinoma confirmed by postoperative histopathology; - Level of preoperative hemoglobin =110 g/L; - Child-Pugh class A or B liver function; - Eastern Cooperative Oncology Group performance status (ECOG PS) of 0 or 1. Exclusion Criteria: - A history of other malignancies; - History of active autoimmune or immunodeficiency diseases; - Concurrent cardiac, pulmonary, cerebral, or renal dysfunction; - Loss to follow-up.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Autotransfusion
These group of patients will receive autotransfusion before liver resection.
Other:
Control group
These group of patients will not receive autotransfusion before liver resection.

Locations

Country Name City State
China Affiliated Tumor Hospital of Guangxi Medical University Nanning Guangxi

Sponsors (1)

Lead Sponsor Collaborator
Guangxi Medical University

Country where clinical trial is conducted

China, 

References & Publications (3)

Han S, Kim G, Ko JS, Sinn DH, Yang JD, Joh JW, Lee SK, Gwak MS. Safety of the Use of Blood Salvage and Autotransfusion During Liver Transplantation for Hepatocellular Carcinoma. Ann Surg. 2016 Aug;264(2):339-43. doi: 10.1097/SLA.0000000000001486. — View Citation

Kwon JH, Han S, Kim D, Kuk JH, Cho H, Kim S, Yang JD, Kim C, Kim JM, Choi GS, Joh JW, Ko JS, Gwak MS, Kim G. Blood Salvage and Autotransfusion With Single Leukoreduction Does Not Increase the Risk of Tumor Recurrence After Liver Transplantation for Advanced Hepatocellular Carcinoma. Ann Surg. 2022 Dec 1;276(6):e842-e850. doi: 10.1097/SLA.0000000000004866. Epub 2021 Mar 18. — View Citation

Tomimaru Y, Eguchi H, Wada H, Hama N, Kawamoto K, Kobayashi S, Umeshita K, Doki Y, Mori M, Nagano H. Predicting the necessity of autologous blood collection and storage before surgery for hepatocellular carcinoma. J Surg Oncol. 2013 Dec;108(7):486-91. doi: 10.1002/jso.23426. Epub 2013 Sep 5. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Number of participants with tumor recurrence The 1-year tumor recurrence will be compared between the two groups 1-year
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