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Conference Paper: Living donor versus deceased donor liver transplantation for early unresectable hepatocellular carcinoma: same criteria, different outcome

TitleLiving donor versus deceased donor liver transplantation for early unresectable hepatocellular carcinoma: same criteria, different outcome
Authors
Issue Date2005
PublisherInforma Healthcare. The Journal's web site is located at http://www.tandf.co.uk/journals/titles/1365182X.asp
Citation
The 6th Congress of the European Hepato-Pancreato-Biliary Association (EHPBA 2005), Heidelberg, Germany, 25-28 May 2005. In HPB, 2005, v. 7 suppl. 1, p. 54, abstract no. 33 How to Cite?
AbstractINTRODUCTIONANDAIM: Hypothetical studies that supported the role of living donor liver transplantation (LDLT) for early unresectable hepatocellular carcinoma (HCC) assumed the same outcome as deceased donor liver transplantation (DDLT).Wetested this assumption with a clinical study. PATIENTS AND METHODS: We studied 60 consecutive patients who met the Milan or UCSF criteria on pretransplant imaging and underwent LDLT (LD group, n=43) or DDLT (DD group, n=17). RESULTS: Compared to the DD group, the LD group had fewer incidental tumors or pretransplant transarterial chemoembolization but more salvage transplantation for recurrence. There was a shorter waiting time and lower graft-weight-to-standard-liver-weight (GW/SLW) ratio. The perioperative course was the same in terms of transfusion, morbidity, mortality and hospital stay. Histopathologic analysis showed similar tumor size, number, grade, and stage. At a median follow-up of 28 months (range: 4–111), 7 (16%) patients of the LD group and none (0%) of the DD group recurred. The 1-, and 5-year cumulative recurrence rate was 9%, and 25%, respectively, for the LD group, and all 0%, for the DD group (p=0.05). The corresponding patient survival was 97% and 55%, respectively, for the LD group, and 94% and 94%, respectively, for the DD group (p=0.279). Apart from tumor factors including vascular permeation, tumor nodules 43, and a pathologic stage beyond UCSF criteria, GW/SLW ratio 50.6 and salvage transplantation were also risk factors for recurrence. CONCLUSION: Despite standard selection criteria, patients who undergo LDLT for early unresectable HCC have different clinical characteristics and inferior oncologic outcome.
DescriptionInvited lecture
Persistent Identifierhttp://hdl.handle.net/10722/88589
ISSN
2022 Impact Factor: 2.9
2020 SCImago Journal Rankings: 1.577

 

DC FieldValueLanguage
dc.contributor.authorLo, CMen_HK
dc.contributor.authorFan, STen_HK
dc.contributor.authorLiu, CLen_HK
dc.contributor.authorChan, SCen_HK
dc.contributor.authorNg, IOLen_HK
dc.contributor.authorWong, Jen_HK
dc.date.accessioned2010-09-06T09:45:22Z-
dc.date.available2010-09-06T09:45:22Z-
dc.date.issued2005en_HK
dc.identifier.citationThe 6th Congress of the European Hepato-Pancreato-Biliary Association (EHPBA 2005), Heidelberg, Germany, 25-28 May 2005. In HPB, 2005, v. 7 suppl. 1, p. 54, abstract no. 33en_HK
dc.identifier.issn1365-182Xen_HK
dc.identifier.urihttp://hdl.handle.net/10722/88589-
dc.descriptionInvited lecture-
dc.description.abstractINTRODUCTIONANDAIM: Hypothetical studies that supported the role of living donor liver transplantation (LDLT) for early unresectable hepatocellular carcinoma (HCC) assumed the same outcome as deceased donor liver transplantation (DDLT).Wetested this assumption with a clinical study. PATIENTS AND METHODS: We studied 60 consecutive patients who met the Milan or UCSF criteria on pretransplant imaging and underwent LDLT (LD group, n=43) or DDLT (DD group, n=17). RESULTS: Compared to the DD group, the LD group had fewer incidental tumors or pretransplant transarterial chemoembolization but more salvage transplantation for recurrence. There was a shorter waiting time and lower graft-weight-to-standard-liver-weight (GW/SLW) ratio. The perioperative course was the same in terms of transfusion, morbidity, mortality and hospital stay. Histopathologic analysis showed similar tumor size, number, grade, and stage. At a median follow-up of 28 months (range: 4–111), 7 (16%) patients of the LD group and none (0%) of the DD group recurred. The 1-, and 5-year cumulative recurrence rate was 9%, and 25%, respectively, for the LD group, and all 0%, for the DD group (p=0.05). The corresponding patient survival was 97% and 55%, respectively, for the LD group, and 94% and 94%, respectively, for the DD group (p=0.279). Apart from tumor factors including vascular permeation, tumor nodules 43, and a pathologic stage beyond UCSF criteria, GW/SLW ratio 50.6 and salvage transplantation were also risk factors for recurrence. CONCLUSION: Despite standard selection criteria, patients who undergo LDLT for early unresectable HCC have different clinical characteristics and inferior oncologic outcome.-
dc.languageengen_HK
dc.publisherInforma Healthcare. The Journal's web site is located at http://www.tandf.co.uk/journals/titles/1365182X.aspen_HK
dc.relation.ispartofHPBen_HK
dc.rightsHPB. Copyright © Informa Healthcare.en_HK
dc.titleLiving donor versus deceased donor liver transplantation for early unresectable hepatocellular carcinoma: same criteria, different outcomeen_HK
dc.typeConference_Paperen_HK
dc.identifier.openurlhttp://library.hku.hk:4550/resserv?sid=HKU:IR&issn=1365-182X&volume=7&issue=Suppl 1&spage=54 Abstract no. 33&epage=&date=2005&atitle=Living+donor+versus+deceased+donor+liver+transplantation+for+early+unresectable+hepatocellular+carcinoma:+same+criteria,+different+outcomeen_HK
dc.identifier.emailLo, CM: chungmlo@hkucc.hku.hken_HK
dc.identifier.emailFan, ST: stfan@hku.hken_HK
dc.identifier.emailLiu, CL: clliu@hkucc.hku.hken_HK
dc.identifier.emailNg, IOL: iolng@hkucc.hku.hken_HK
dc.identifier.emailWong, J: jwong@hkucc.hku.hken_HK
dc.identifier.authorityLo, CM=rp00412en_HK
dc.identifier.authorityFan, ST=rp00355en_HK
dc.identifier.authorityNg, IOL=rp00335en_HK
dc.identifier.authorityWong, J=rp00322-
dc.identifier.hkuros98166en_HK
dc.identifier.hkuros99504-
dc.identifier.volume7-
dc.identifier.issuesuppl. 1-
dc.identifier.spage54, abstract no. 33-
dc.identifier.epage54, abstract no. 33-
dc.identifier.issnl1365-182X-

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