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Macroscopic Portal Vein Thrombosis in HCC Patients
Author(s) -
Hikmet Akkız,
Brian I. Carr,
Sedef Kuran,
Ümit Karaoğullarından,
Oğuz Üsküdar,
Salih Tokmak,
Burcu Arslan,
Figen Doran,
Hüseyin Tuğsan Ballı,
Abdulalh Ülkü,
Tolga Atılgan Akçam,
Halil İbrahim Bahçeci,
Kâmil Yalçın Polat,
Necati Örmecı,
Cem Şimşek,
Abdullah Sonsuz,
Ali Rıza Demir,
Engin Altıntaş,
Mehmet Demir,
Kendal Yalçın,
Nazım Ekin,
Ayşegül Özakyol,
Mehmet Yücesoy,
Ahmet Uygun,
Vito Guerra,
Anıl Delik,
Yaman Tokat,
Sezai Yılmaz,
Ahmet Bektaş,
Murat Kılıç
Publication year - 2018
Publication title -
canadian journal of gastroenterology and hepatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.921
H-Index - 65
eISSN - 2291-2797
pISSN - 2291-2789
DOI - 10.1155/2018/3120185
Subject(s) - medicine , hepatocellular carcinoma , portal vein thrombosis , gastroenterology , logistic regression , odds ratio , portal vein , thrombosis , cohort , oncology
Macroscopic portal vein invasion (PVT) by hepatocellular carcinoma (HCC) in the liver is one of the most important negative prognostic factors for HCC patients. The characteristics of a large cohort of such patients were examined. We found that the percent of patients with PVT significantly increased with increasing maximum tumor diameter (MTD), from 13.7% with tumors of MTD <5cm to 56.4% with tumors of MTD >10cm. There were similar numbers of HCC patients with very large tumors with and without PVT. Thus, MTD alone was insufficient to explain the presence of PVT, as were high AFP levels, since less than 50% of high AFP patients had PVT. However, the percent of patients with PVT was also found to significantly increase with increasing blood alpha-fetoprotein (AFP) levels and tumor multifocality. A logistic regression model that included these 3 factors together showed an odds ratio of 17.9 for the combination of MTD>5.0cm plus tumor multifocality plus elevated AFP, compared to low levels of these 3 parameters. The presence or absence of macroscopic PVT may therefore represent different HCC aggressiveness phenotypes, as judged by a significant increase in tumor multifocality and AFP levels in the PVT positive patients. Factors in addition to MTD and AFP must also contribute to PVT development.

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