Macroscopic Portal Vein Thrombosis in HCC Patients

Author:

Akkiz Hikmet1,Carr Brian I.2ORCID,Kuran Sedef1,Karaoğullarından Ümit1,Üsküdar Oguz1,Tokmak Salih1,Arslan Burcu1,Doran Figen1,Balli Hüseyin Tugsan1,Ülkü Abdulalh1,Akçam Tolga Atılgan1,Bahçeci Halil İbrahim3,Polat Kamil Yalçın4,Örmeci Necati5,Şimşek Halis6,Sonsuz Abdullah7,Demir Ali8,Altıntaş Engin9,Demir Mehmet10,Yalçın Kendal11,Ekinci Nazım11,Harmancı Özakyol Ayşegül12,Yücesoy Mehmet13,Uygun Ahmet14,Guerra Vito15,Delik Anıl1,Tokat Yaman16,Yilmaz Sezai17,Bektaş Ahmet18,Kılıç Murat19

Affiliation:

1. Çukurova University Gastroenterology Department, Adana, Turkey

2. İzmir Biomedicine and Genome Institute, Dokuz Eylül University, İzmir, Turkey

3. Fırat University, Turkey

4. İstanbul Memorial Hospital, Turkey

5. Ankara University, Turkey

6. Hacettepe University, Turkey

7. İstanbul Cerrahpaşa University, Turkey

8. Konya Necmettin Erbakan University, Turkey

9. Mersin University, Turkey

10. Hatay Mustafa Kemal University, Turkey

11. Dicle University, Turkey

12. Eskişehir Osmangazi University, Turkey

13. Erciyes University, Turkey

14. Haydarpaşa Sultan Abdülhamid Eğitim Araştırma Hospital, Turkey

15. Trials Centre, National Institute for Digestive Diseases, IRCCS “Saverio de Bellis”, Castellana, Bari, Italy

16. Florence Nightingale Hospital, İstanbul, Turkey

17. İnonu University, Malatya, Turkey

18. Ondokuz Mayıs University, Turkey

19. Izmir Kent Hospital, Turkey

Abstract

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.

Funder

National Institutes of Health

Publisher

Hindawi Limited

Subject

Gastroenterology,Hepatology,General Medicine

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