Embolization with microspheres alone for hepatocellular carcinoma with portal vein tumor: analysis of outcome and liver function at disease progression.


Journal

HPB : the official journal of the International Hepato Pancreato Biliary Association
ISSN: 1477-2574
Titre abrégé: HPB (Oxford)
Pays: England
ID NLM: 100900921

Informations de publication

Date de publication:
04 2020
Historique:
received: 16 04 2019
revised: 08 07 2019
accepted: 07 08 2019
pubmed: 3 9 2019
medline: 28 9 2021
entrez: 3 9 2019
Statut: ppublish

Résumé

This retrospective study reviews long-term outcome of hepatic artery embolization (HAE) using microspheres alone in patients presenting with Hepatocellular Carcinoma (HCC) and portal vein tumor (PVT). From 2005 to 2015, 43 patients with HCC and PVT underwent HAE. Response to treatment, time-to-progression (TTP), local-tumor-progression (LTP), distant-hepatic-progression (DHP), PVT-progression (PVTP), and/or the development of extra-hepatic progression (EHP) were assessed on pre-HAE CT/MRI scans, within 4 weeks post-HAE and at quarterly intervals thereafter, along with liver function (Child-Pugh score, CP). Forty (40/43) patients progressed during a median follow-up of 10 months with a median TTP of 2.9 months. Eleven of the 40 patients (27.5%) developed EHP, with only 2 patients (5%) demonstrating solely LTP. Six patients (15%) developed PVTP only. At progression, 27 patients (27/40, 77%) maintained their initial CP status, including all 5 CP-B patients. Median survival was 12.5 (95% CI 8-23) months for the entire group; 17.3 (95% CI 10-33) months for the patients with segmental/lobar PVT, compared with 8.4 (95% CI 6-13) months for the patients with main PVT (p = 0.02). HAE can be used to treat patients with HCC and PVT with median survival of approximately a year and preserved liver function.

Sections du résumé

BACKGROUND
This retrospective study reviews long-term outcome of hepatic artery embolization (HAE) using microspheres alone in patients presenting with Hepatocellular Carcinoma (HCC) and portal vein tumor (PVT).
METHODS
From 2005 to 2015, 43 patients with HCC and PVT underwent HAE. Response to treatment, time-to-progression (TTP), local-tumor-progression (LTP), distant-hepatic-progression (DHP), PVT-progression (PVTP), and/or the development of extra-hepatic progression (EHP) were assessed on pre-HAE CT/MRI scans, within 4 weeks post-HAE and at quarterly intervals thereafter, along with liver function (Child-Pugh score, CP).
RESULTS
Forty (40/43) patients progressed during a median follow-up of 10 months with a median TTP of 2.9 months. Eleven of the 40 patients (27.5%) developed EHP, with only 2 patients (5%) demonstrating solely LTP. Six patients (15%) developed PVTP only. At progression, 27 patients (27/40, 77%) maintained their initial CP status, including all 5 CP-B patients. Median survival was 12.5 (95% CI 8-23) months for the entire group; 17.3 (95% CI 10-33) months for the patients with segmental/lobar PVT, compared with 8.4 (95% CI 6-13) months for the patients with main PVT (p = 0.02).
CONCLUSION
HAE can be used to treat patients with HCC and PVT with median survival of approximately a year and preserved liver function.

Identifiants

pubmed: 31474455
pii: S1365-182X(19)30689-6
doi: 10.1016/j.hpb.2019.08.004
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

588-594

Informations de copyright

Copyright © 2019 International Hepato-Pancreato-Biliary Association Inc. Published by Elsevier Ltd. All rights reserved.

Auteurs

Alessandra Borgheresi (A)

Department of Radiology, 1275 York Avenue, New York, NY, 10065, USA.

Anne Covey (A)

Department of Radiology, 1275 York Avenue, New York, NY, 10065, USA; Weil Cornell Medical College, 1300 York Avenue, New York, NY, 10065, USA.

Hooman Yarmohammadi (H)

Department of Radiology, 1275 York Avenue, New York, NY, 10065, USA; Weil Cornell Medical College, 1300 York Avenue, New York, NY, 10065, USA.

Franz E Boas (FE)

Department of Radiology, 1275 York Avenue, New York, NY, 10065, USA; Weil Cornell Medical College, 1300 York Avenue, New York, NY, 10065, USA.

Etay Ziv (E)

Department of Radiology, 1275 York Avenue, New York, NY, 10065, USA; Weil Cornell Medical College, 1300 York Avenue, New York, NY, 10065, USA.

George Getrajdman (G)

Department of Radiology, 1275 York Avenue, New York, NY, 10065, USA; Weil Cornell Medical College, 1300 York Avenue, New York, NY, 10065, USA.

Joseph Erinjeri (J)

Department of Radiology, 1275 York Avenue, New York, NY, 10065, USA; Weil Cornell Medical College, 1300 York Avenue, New York, NY, 10065, USA.

William Jarnagin (W)

Department of Surgery, 1275 York Avenue, New York, NY, 10065, USA; Weil Cornell Medical College, 1300 York Avenue, New York, NY, 10065, USA.

James J Harding (JJ)

Department of Medicine Memorial Sloan Kettering Cancer Center, 1275 York Avenue, New York, NY, 10065, USA; Weil Cornell Medical College, 1300 York Avenue, New York, NY, 10065, USA.

Michael D'Angelica (M)

Department of Surgery, 1275 York Avenue, New York, NY, 10065, USA; Weil Cornell Medical College, 1300 York Avenue, New York, NY, 10065, USA.

Mithat Gonen (M)

Department of Biostatistics, Memorial Sloan Kettering Cancer Center, 485 Lexington Avenue, New York, NY 10017, USA.

Karen T Brown (KT)

Department of Radiology, 1275 York Avenue, New York, NY, 10065, USA; Weil Cornell Medical College, 1300 York Avenue, New York, NY, 10065, USA. Electronic address: karen.brown@utah.edu.

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Classifications MeSH