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Radioembolization Followed by Transarterial Chemoembolization in Hepatocellular Carcinoma

Background and objective: In recent years, combination therapies for hepatocellular carcinoma (HCC) have been increasingly used with superior treatment responses compared to monotherapies. However, the safety and efficacy of the transarterial chemoembolization (TACE) and transarterial radioembolizat...

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Autores principales: Vardar, Baran U, Meram, Ece, Karaoglu, Kerim, Liang, Muxuan, Yu, Menggang, Laeseke, Paul, Ozkan, Orhan S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9063732/
https://www.ncbi.nlm.nih.gov/pubmed/35518553
http://dx.doi.org/10.7759/cureus.23783
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author Vardar, Baran U
Meram, Ece
Karaoglu, Kerim
Liang, Muxuan
Yu, Menggang
Laeseke, Paul
Ozkan, Orhan S
author_facet Vardar, Baran U
Meram, Ece
Karaoglu, Kerim
Liang, Muxuan
Yu, Menggang
Laeseke, Paul
Ozkan, Orhan S
author_sort Vardar, Baran U
collection PubMed
description Background and objective: In recent years, combination therapies for hepatocellular carcinoma (HCC) have been increasingly used with superior treatment responses compared to monotherapies. However, the safety and efficacy of the transarterial chemoembolization (TACE) and transarterial radioembolization (TARE) combinations for HCC patients have not been investigated in the literature. In this study, our aim was to evaluate the safety and outcomes of TACE after TARE in HCC patients. Materials and methods: All TARE procedures performed on HCC patients at a single institution between January 2008 and November 2016 were retrospectively reviewed. Seventy-three patients who did not receive any additional transarterial therapy in the areas targeted by TARE were assigned to the “TARE group,” while 27 patients who received TACE after TARE to the same target area were assigned to the “Combo group.” Post-procedural liver toxicity, tumor response, overall survival (OS), and time to progression (TTP) were evaluated. Results: Fewer patients in the Combo group had worsening liver function than the TARE group based on the change in bilirubin levels (19% vs. 40%; p=0.029) and Child-Pugh score increase (28% vs. 51%; p=0.056). The median OS time of all patients was 11.04 months. The Combo group had a significantly longer median OS of 36.8 months (vs. 10.6, p=0.003) and median TTP of 14.4 months (vs. 5.5, p=0.018). After accounting for selection bias, OS and TTP were still in favor of the Combo group, with hazard ratios of 0.651 (p<0.05) and 0.63 (p<0.05), respectively. Conclusion: The addition of TACE to TARE is a safe and effective treatment in unresectable HCC patients and can be considered in select patients with a lack of complete response or disease progression.
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spelling pubmed-90637322022-05-04 Radioembolization Followed by Transarterial Chemoembolization in Hepatocellular Carcinoma Vardar, Baran U Meram, Ece Karaoglu, Kerim Liang, Muxuan Yu, Menggang Laeseke, Paul Ozkan, Orhan S Cureus Radiology Background and objective: In recent years, combination therapies for hepatocellular carcinoma (HCC) have been increasingly used with superior treatment responses compared to monotherapies. However, the safety and efficacy of the transarterial chemoembolization (TACE) and transarterial radioembolization (TARE) combinations for HCC patients have not been investigated in the literature. In this study, our aim was to evaluate the safety and outcomes of TACE after TARE in HCC patients. Materials and methods: All TARE procedures performed on HCC patients at a single institution between January 2008 and November 2016 were retrospectively reviewed. Seventy-three patients who did not receive any additional transarterial therapy in the areas targeted by TARE were assigned to the “TARE group,” while 27 patients who received TACE after TARE to the same target area were assigned to the “Combo group.” Post-procedural liver toxicity, tumor response, overall survival (OS), and time to progression (TTP) were evaluated. Results: Fewer patients in the Combo group had worsening liver function than the TARE group based on the change in bilirubin levels (19% vs. 40%; p=0.029) and Child-Pugh score increase (28% vs. 51%; p=0.056). The median OS time of all patients was 11.04 months. The Combo group had a significantly longer median OS of 36.8 months (vs. 10.6, p=0.003) and median TTP of 14.4 months (vs. 5.5, p=0.018). After accounting for selection bias, OS and TTP were still in favor of the Combo group, with hazard ratios of 0.651 (p<0.05) and 0.63 (p<0.05), respectively. Conclusion: The addition of TACE to TARE is a safe and effective treatment in unresectable HCC patients and can be considered in select patients with a lack of complete response or disease progression. Cureus 2022-04-03 /pmc/articles/PMC9063732/ /pubmed/35518553 http://dx.doi.org/10.7759/cureus.23783 Text en Copyright © 2022, Vardar et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Radiology
Vardar, Baran U
Meram, Ece
Karaoglu, Kerim
Liang, Muxuan
Yu, Menggang
Laeseke, Paul
Ozkan, Orhan S
Radioembolization Followed by Transarterial Chemoembolization in Hepatocellular Carcinoma
title Radioembolization Followed by Transarterial Chemoembolization in Hepatocellular Carcinoma
title_full Radioembolization Followed by Transarterial Chemoembolization in Hepatocellular Carcinoma
title_fullStr Radioembolization Followed by Transarterial Chemoembolization in Hepatocellular Carcinoma
title_full_unstemmed Radioembolization Followed by Transarterial Chemoembolization in Hepatocellular Carcinoma
title_short Radioembolization Followed by Transarterial Chemoembolization in Hepatocellular Carcinoma
title_sort radioembolization followed by transarterial chemoembolization in hepatocellular carcinoma
topic Radiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9063732/
https://www.ncbi.nlm.nih.gov/pubmed/35518553
http://dx.doi.org/10.7759/cureus.23783
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