Impact of tumor size, number of tumors and neutrophil‐to‐lymphocyte ratio in liver transplantation for recurrent hepatocellular carcinoma. Issue 7 (29th November 2012)
- Record Type:
- Journal Article
- Title:
- Impact of tumor size, number of tumors and neutrophil‐to‐lymphocyte ratio in liver transplantation for recurrent hepatocellular carcinoma. Issue 7 (29th November 2012)
- Main Title:
- Impact of tumor size, number of tumors and neutrophil‐to‐lymphocyte ratio in liver transplantation for recurrent hepatocellular carcinoma
- Authors:
- Yoshizumi, Tomoharu
Ikegami, Toru
Yoshiya, Shohei
Motomura, Takashi
Mano, Yohei
Muto, Jun
Ikeda, Tetsuo
Soejima, Yuji
Shirabe, Ken
Maehara, Yoshihiko - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="hepr12016-sec-0001" sec-type="section"> <title>Aim</title> <p>Hepatocellular carcinoma (HCC) is primarily treated with hepatic resection and/or locoregional therapy. When HCC recurs and further treatment is no longer possible owing to poor liver function, liver transplantation (LT) or living‐donor LT (LDLT) is considered. The aim of this study was to clarify risk factors for tumor recurrence after LDLT in patients with recurrent HCC.</p> </sec> <sec id="hepr12016-sec-0002" sec-type="section"> <title>Methods</title> <p>The study comprised 104 patients who had undergone LDLT because of end‐stage liver disease with recurrent HCC. The recurrence‐free survival rates after the LDLT were calculated. Risk factors for tumor recurrence were identified.</p> </sec> <sec id="hepr12016-sec-0003" sec-type="section"> <title>Results</title> <p>The 1‐, 3‐ and 5‐year recurrence‐free survival rates were 89.6%, 80.3% and 78.4%, respectively. By univariate analysis, the factors affecting recurrence‐free survival were the sum of the largest tumor size and number of tumors of 8 or more (<italic>P</italic> &lt; 0.0001), des‐γ‐carboxy prothrombin of more than 300 mAU/mL (<italic>P</italic> = 0.0001), and a neutrophil‐to‐lymphocyte ratio (NLR) of 4 or more (<italic>P</italic> = 0.0002), α‐fetoprotein of more than 400 ng/mL (<italic>P</italic> = 0.0001) and bilobar tumor distribution<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="hepr12016-sec-0001" sec-type="section"> <title>Aim</title> <p>Hepatocellular carcinoma (HCC) is primarily treated with hepatic resection and/or locoregional therapy. When HCC recurs and further treatment is no longer possible owing to poor liver function, liver transplantation (LT) or living‐donor LT (LDLT) is considered. The aim of this study was to clarify risk factors for tumor recurrence after LDLT in patients with recurrent HCC.</p> </sec> <sec id="hepr12016-sec-0002" sec-type="section"> <title>Methods</title> <p>The study comprised 104 patients who had undergone LDLT because of end‐stage liver disease with recurrent HCC. The recurrence‐free survival rates after the LDLT were calculated. Risk factors for tumor recurrence were identified.</p> </sec> <sec id="hepr12016-sec-0003" sec-type="section"> <title>Results</title> <p>The 1‐, 3‐ and 5‐year recurrence‐free survival rates were 89.6%, 80.3% and 78.4%, respectively. By univariate analysis, the factors affecting recurrence‐free survival were the sum of the largest tumor size and number of tumors of 8 or more (<italic>P</italic> &lt; 0.0001), des‐γ‐carboxy prothrombin of more than 300 mAU/mL (<italic>P</italic> = 0.0001), and a neutrophil‐to‐lymphocyte ratio (NLR) of 4 or more (<italic>P</italic> = 0.0002), α‐fetoprotein of more than 400 ng/mL (<italic>P</italic> = 0.0001) and bilobar tumor distribution (<italic>P</italic> = 0.046). A multivariate analysis identified independent risk factors for post‐LDLT tumor recurrence including the sum of tumor size and number of tumors of 8 or more (<italic>P</italic> = 0.0004) and an NLR of 4 or more (<italic>P</italic> = 0.01). The 1‐ and 3‐ year recurrence‐free survival rates in the recipients who had both risk factors were 30.0% and 15.0%, respectively.</p> </sec> <sec id="hepr12016-sec-0004" sec-type="section"> <title>Conclusion</title> <p>LDLT should not be performed for patients who have both independent risk factors after any treatments for HCC.</p> </sec> </abstract> … (more)
- Is Part Of:
- Hepatology research. Volume 43:Issue 7(2013:Jul.)
- Journal:
- Hepatology research
- Issue:
- Volume 43:Issue 7(2013:Jul.)
- Issue Display:
- Volume 43, Issue 7 (2013)
- Year:
- 2013
- Volume:
- 43
- Issue:
- 7
- Issue Sort Value:
- 2013-0043-0007-0000
- Page Start:
- 709
- Page End:
- 716
- Publication Date:
- 2012-11-29
- Subjects:
- Liver -- Diseases -- Periodicals
Liver Diseases -- Periodicals
Foie -- Maladies -- Périodiques
616.362 - Journal URLs:
- http://www.sciencedirect.com/science/journal/09284346 ↗
http://firstsearch.oclc.org/journal=1386-6346;screen=info;ECOIP ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1872-034X ↗
http://www.sciencedirect.com/science/journal/13866346 ↗
http://www3.interscience.wiley.com/journal/118507311/home ↗
http://www.blackwell-synergy.com/rd.asp?goto=journal&code=hep ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/hepr.12016 ↗
- Languages:
- English
- ISSNs:
- 1386-6346
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4295.845000
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- 4238.xml