Literature DB >> 33546234

Identification of Clinical Phenotypes and Related Survival in Patients with Large HCCs.

Brian I Carr1, Vito Guerra2, Rossella Donghia2, Fabio Farinati3, Edoardo G Giannini4, Luca Muratori5, Gian Ludovico Rapaccini6, Maria Di Marco7, Eugenio Caturelli8, Marco Zoli9, Rodolfo Sacco10, Ciro Celsa11, Claudia Campani12, Andrea Mega13, Maria Guarino14, Antonio Gasbarrini15, Gianluca Svegliati-Baroni16, Francesco Giuseppe Foschi17, Elisabetta Biasini18, Alberto Masotto19, Gerardo Nardone20, Giovanni Raimondo21, Francesco Azzaroli22, Gianpaolo Vidili23, Maurizia Rossana Brunetto24, Franco Trevisani25.   

Abstract

BACKGROUND: Hepatocellular carcinoma (HCC) factors, especially maximum tumor diameter (MTD), tumor multifocality, portal vein thrombosis (PVT), and serum alpha-fetoprotein (AFP), influence survival. AIM: To examine patterns of tumor factors in large HCC patients.
METHODS: A database of large HCC patients was examined.
RESULTS: A multiple Cox proportional hazard model on death identified low serum albumin levels and the presence of PVT and multifocality, with each having a hazard ratio ≥2.0. All combinations of these three parameters were examined in relation to survival. Using univariate Cox analysis, the combination of albumin >3.5 g/dL and the absence of both PVT and multifocality had the best survival rate, while all combinations that included the presence of PVT had poor survival and hazard ratios. We identified four clinical phenotypes, each with a distinct median survival: patients with or without PVT or multifocality plus serum albumin ≥3.5 (g/dL), with each subgroup displaying high (≥100 IU/mL) or low (<100 IU/mL) blood AFP levels. Across a range of MTDs, we identified only two significant trends, blood AFP and platelets.
CONCLUSIONS: Patients with large HCCs have distinct phenotypes and survival, as identified by the combination of PVT, multifocality, and blood albumin levels.

Entities:  

Keywords:  HCC; PVT; albumin; large; multifocality; phenotypes

Year:  2021        PMID: 33546234      PMCID: PMC7913341          DOI: 10.3390/cancers13040592

Source DB:  PubMed          Journal:  Cancers (Basel)        ISSN: 2072-6694            Impact factor:   6.639


  37 in total

1.  Alpha-fetoprotein: a new member of intracellular signal molecules in regulation of the PI3K/AKT signaling in human hepatoma cell lines.

Authors:  Mengsen Li; Hui Li; Chaoying Li; Shanshan Wang; Wei Jiang; Zhongmin Liu; Sheng Zhou; Xinhua Liu; Michael A McNutt; Gang Li
Journal:  Int J Cancer       Date:  2011-02-01       Impact factor: 7.396

2.  Fifty years of discovery of alpha-fetoprotein as the first tumor marker.

Authors:  Dina Nikulina; Alexander Terentyev; Khalil Galimzyanov; Vladimir Jurišić
Journal:  Srp Arh Celok Lek       Date:  2015 Jan-Feb       Impact factor: 0.207

Review 3.  Molecular signatures of noncancerous liver tissue can predict the risk for late recurrence of hepatocellular carcinoma.

Authors:  Tohru Utsunomiya; Mitsuo Shimada; Satoru Imura; Yuji Morine; Tetsuya Ikemoto; Masaki Mori
Journal:  J Gastroenterol       Date:  2009-12-08       Impact factor: 7.527

4.  Macrotrabecular-massive hepatocellular carcinoma: A distinctive histological subtype with clinical relevance.

Authors:  Marianne Ziol; Nicolas Poté; Giuliana Amaddeo; Alexis Laurent; Jean-Charles Nault; Frédéric Oberti; Charlotte Costentin; Sophie Michalak; Mohamed Bouattour; Claire Francoz; Georges Philippe Pageaux; Jeanne Ramos; Thomas Decaens; Alain Luciani; Boris Guiu; Valérie Vilgrain; Christophe Aubé; Jonathan Derman; Cécile Charpy; Jessica Zucman-Rossi; Nathalie Barget; Olivier Seror; Nathalie Ganne-Carrié; Valérie Paradis; Julien Calderaro
Journal:  Hepatology       Date:  2018-05-09       Impact factor: 17.425

5.  Effects of AFP-activated PI3K/Akt signaling pathway on cell proliferation of liver cancer.

Authors:  Lu Zheng; Wei Gong; Ping Liang; XiaoBing Huang; Nan You; Ke Qiang Han; Yu Ming Li; Jing Li
Journal:  Tumour Biol       Date:  2014-01-15

6.  Hepatocellular carcinoma size: platelets, γ-glutamyl transpeptidase, and alkaline phosphatase.

Authors:  Brian I Carr; Vito Guerra
Journal:  Oncology       Date:  2013-08-29       Impact factor: 2.935

7.  Alpha fetoprotein antagonises benzyl isothiocyanate inhibition of the malignant behaviors of hepatocellular carcinoma cells.

Authors:  Mingyue Zhu; Wei Li; Junli Guo; Yan Lu; Xu Dong; Bo Lin; Yi Chen; Xueer Zhang; Mengsen Li
Journal:  Oncotarget       Date:  2016-11-15

Review 8.  Platelets and Hepatocellular Cancer: Bridging the Bench to the Clinics.

Authors:  Quirino Lai; Alessandro Vitale; Tommaso M Manzia; Francesco G Foschi; Giovanni B Levi Sandri; Martina Gambato; Fabio Melandro; Francesco P Russo; Luca Miele; Luca Viganò; Patrizia Burra; Edoardo G Giannini
Journal:  Cancers (Basel)       Date:  2019-10-15       Impact factor: 6.639

9.  Platelet extracts induce growth, migration and invasion in human hepatocellular carcinoma in vitro.

Authors:  Brian I Carr; Aldo Cavallini; Rosalba D'Alessandro; Maria Grazia Refolo; Catia Lippolis; Antonio Mazzocca; Caterina Messa
Journal:  BMC Cancer       Date:  2014-01-27       Impact factor: 4.430

10.  Alpha-fetoprotein inhibits autophagy to promote malignant behaviour in hepatocellular carcinoma cells by activating PI3K/AKT/mTOR signalling.

Authors:  Shanshan Wang; Mingyue Zhu; Qiaoyun Wang; Yuli Hou; Lei Li; Honglei Weng; Yan Zhao; Dexi Chen; Huiguo Ding; Junli Guo; Mengsen Li
Journal:  Cell Death Dis       Date:  2018-10-09       Impact factor: 8.469

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