Tumor biopsy and patient enrollment in clinical trials for advanced hepatocellular carcinoma
Author
Rimassa, LorenzaReig, Maria
Abbadessa, Giovanni
Peck-Radosavljevic, Markus
Harris, William
Zagonel, Vittorina
Pastorelli, Davide
Rota Caremoli, Elena
Porta, Camillo
Damjanov, Nevena
Patel, Hitendra
Daniele, Bruno
Lamar, Maria
Schwartz, Brian
Goldberg, Terri
Santoro, Armando
Bruix, Jordi
Affiliation
Univ Arizona, Ctr Canc, Dept MedIssue Date
2017
Metadata
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BAISHIDENG PUBLISHING GROUP INCCitation
Tumor biopsy and patient enrollment in clinical trials for advanced hepatocellular carcinoma 2017, 23 (13):2448 World Journal of GastroenterologyRights
Copyright © The Author(s) 2017. Published by Baishideng Publishing Group Inc. All rights reserved. This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license.Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Tumor biopsies may help to reliably distinguish hepatocellular carcinoma (HCC) from other tumors, mostly cholangiocarcinoma as well as to identify the patient populations who most benefit from target-driven HCC treatments, in order to improve the success rate of experimental therapies. Clarifying tumor biology may also lead to identify biomarkers with prognostic role and/or enabling to predict response or resistance to therapies. Recently, clinical trials have more efficiently included biomarker endpoints and increasingly collected tumor tissue from enrolled patients. Due to their frail status and sometimes fast-progressing disease, the performance status of patients with HCC progressing on first-line therapy can deteriorate quickly, preventing their enrollment in clinical trials. However, the challenge of identifying the proper patient at the proper time can be overcome by periodic inter-department meetings involving the key specialists taking care of HCC patients, and solid networks between research centers and referring institutions. An early planned biopsy would also facilitate timely inclusion of patients in biology-driven clinical trials. Ultimately, institution of multidisciplinary teams can optimize treatment choice, biopsy timing, and quick enrollment of patients in clinical trials, before their performance status deteriorates.Note
Open Access Publication.ISSN
1007-9327PubMed ID
28428725Version
Final published versionAdditional Links
http://www.wjgnet.com/1007-9327/full/v23/i13/2448.htmae974a485f413a2113503eed53cd6c53
10.3748/wjg.v23.i13.2448
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Except where otherwise noted, this item's license is described as Copyright © The Author(s) 2017. Published by Baishideng Publishing Group Inc. All rights reserved. This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license.
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