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Second-line treatment of advanced hepatocellular carcinoma: Time for more individualized treatment options?

Hepatocellular carcinoma (HCC) is the most frequently diagnosed primary tumor of the liver and is usually detected as advanced disease. It is an aggressive disease that often progresses rapidly when it fails to respond to treatment. As such, patients have limited opportunities to try different subse...

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Autores principales: Rajappa, Senthil, Rau, Kun-Ming, Dattatreya, Palanki Satya, Ramaswamy, Anant, Fernandes, Philana, Pruthi, Aarohan, Cheng, Rebecca, Lukanowski, Mariusz, Huang, Yi-Hsiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9258252/
https://www.ncbi.nlm.nih.gov/pubmed/35978665
http://dx.doi.org/10.4254/wjh.v14.i6.1074
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author Rajappa, Senthil
Rau, Kun-Ming
Dattatreya, Palanki Satya
Ramaswamy, Anant
Fernandes, Philana
Pruthi, Aarohan
Cheng, Rebecca
Lukanowski, Mariusz
Huang, Yi-Hsiang
author_facet Rajappa, Senthil
Rau, Kun-Ming
Dattatreya, Palanki Satya
Ramaswamy, Anant
Fernandes, Philana
Pruthi, Aarohan
Cheng, Rebecca
Lukanowski, Mariusz
Huang, Yi-Hsiang
author_sort Rajappa, Senthil
collection PubMed
description Hepatocellular carcinoma (HCC) is the most frequently diagnosed primary tumor of the liver and is usually detected as advanced disease. It is an aggressive disease that often progresses rapidly when it fails to respond to treatment. As such, patients have limited opportunities to try different subsequent-line treatment regimens. In the last 5 years, the number of agents and/or regimens available for the treatment of advanced HCC has significantly increased, which has made treatment choices for this patient population increasingly complex. In the second-line setting, several phase III trials of regorafenib (RESORCE), ramucirumab (REACH/REACH-2), and cabozantinib (CELESTIAL) have demonstrated clinically meaningful survival benefits in patients with the disease. However, the median overall survival of patients with advanced HCC remains unchanged at approximately 12 mo from the start of systemic second-line therapy, with a limited duration of response. Evidence from the REACH/REACH-2 trials demonstrated for the first time that baseline alpha-fetoprotein (AFP) levels can be used as an identification factor to select those who are likely to benefit the most from ramucirumab treatment. Ramucirumab is both well tolerated and efficacious and has a clinically acceptable safety profile. Therefore, it should be considered an option for patients with AFP levels ≥ 400 ng/mL.
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spelling pubmed-92582522022-08-16 Second-line treatment of advanced hepatocellular carcinoma: Time for more individualized treatment options? Rajappa, Senthil Rau, Kun-Ming Dattatreya, Palanki Satya Ramaswamy, Anant Fernandes, Philana Pruthi, Aarohan Cheng, Rebecca Lukanowski, Mariusz Huang, Yi-Hsiang World J Hepatol Minireviews Hepatocellular carcinoma (HCC) is the most frequently diagnosed primary tumor of the liver and is usually detected as advanced disease. It is an aggressive disease that often progresses rapidly when it fails to respond to treatment. As such, patients have limited opportunities to try different subsequent-line treatment regimens. In the last 5 years, the number of agents and/or regimens available for the treatment of advanced HCC has significantly increased, which has made treatment choices for this patient population increasingly complex. In the second-line setting, several phase III trials of regorafenib (RESORCE), ramucirumab (REACH/REACH-2), and cabozantinib (CELESTIAL) have demonstrated clinically meaningful survival benefits in patients with the disease. However, the median overall survival of patients with advanced HCC remains unchanged at approximately 12 mo from the start of systemic second-line therapy, with a limited duration of response. Evidence from the REACH/REACH-2 trials demonstrated for the first time that baseline alpha-fetoprotein (AFP) levels can be used as an identification factor to select those who are likely to benefit the most from ramucirumab treatment. Ramucirumab is both well tolerated and efficacious and has a clinically acceptable safety profile. Therefore, it should be considered an option for patients with AFP levels ≥ 400 ng/mL. Baishideng Publishing Group Inc 2022-06-27 2022-06-27 /pmc/articles/PMC9258252/ /pubmed/35978665 http://dx.doi.org/10.4254/wjh.v14.i6.1074 Text en ©The Author(s) 2022. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Minireviews
Rajappa, Senthil
Rau, Kun-Ming
Dattatreya, Palanki Satya
Ramaswamy, Anant
Fernandes, Philana
Pruthi, Aarohan
Cheng, Rebecca
Lukanowski, Mariusz
Huang, Yi-Hsiang
Second-line treatment of advanced hepatocellular carcinoma: Time for more individualized treatment options?
title Second-line treatment of advanced hepatocellular carcinoma: Time for more individualized treatment options?
title_full Second-line treatment of advanced hepatocellular carcinoma: Time for more individualized treatment options?
title_fullStr Second-line treatment of advanced hepatocellular carcinoma: Time for more individualized treatment options?
title_full_unstemmed Second-line treatment of advanced hepatocellular carcinoma: Time for more individualized treatment options?
title_short Second-line treatment of advanced hepatocellular carcinoma: Time for more individualized treatment options?
title_sort second-line treatment of advanced hepatocellular carcinoma: time for more individualized treatment options?
topic Minireviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9258252/
https://www.ncbi.nlm.nih.gov/pubmed/35978665
http://dx.doi.org/10.4254/wjh.v14.i6.1074
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