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Objective Response by mRECIST to Initial Lenvatinib Therapy Is an Independent Factor Contributing to Deep Response in Hepatocellular Carcinoma Treated with Lenvatinib-Transcatheter Arterial Chemoembolization Sequential Therapy

OBJECTIVE: There is limited information regarding the benefits of Lenvatinib-transcatheter arterial chemoembolization (LEN-TACE) sequential therapy for unresectable hepatocellular carcinoma (u-HCC). We compared the efficacy and safety of LEN-TACE sequential therapy to LEN monotherapy and investigate...

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Autores principales: Kuroda, Hidekatsu, Oikawa, Takayoshi, Ninomiya, Masashi, Fujita, Masashi, Abe, Kazumichi, Okumoto, Kazuo, Katsumi, Tomohiro, Sato, Wataru, Igarashi, Go, Iino, Chikara, Endo, Tetsu, Tanabe, Nobukazu, Numao, Hiroshi, Fukuda, Shinsaku, Iijima, Katsunori, Masamune, Atsushi, Ohira, Hiromasa, Ueno, Yoshiyuki, Takikawa, Yasuhiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9294936/
https://www.ncbi.nlm.nih.gov/pubmed/35978602
http://dx.doi.org/10.1159/000522424
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author Kuroda, Hidekatsu
Oikawa, Takayoshi
Ninomiya, Masashi
Fujita, Masashi
Abe, Kazumichi
Okumoto, Kazuo
Katsumi, Tomohiro
Sato, Wataru
Igarashi, Go
Iino, Chikara
Endo, Tetsu
Tanabe, Nobukazu
Numao, Hiroshi
Fukuda, Shinsaku
Iijima, Katsunori
Masamune, Atsushi
Ohira, Hiromasa
Ueno, Yoshiyuki
Takikawa, Yasuhiro
author_facet Kuroda, Hidekatsu
Oikawa, Takayoshi
Ninomiya, Masashi
Fujita, Masashi
Abe, Kazumichi
Okumoto, Kazuo
Katsumi, Tomohiro
Sato, Wataru
Igarashi, Go
Iino, Chikara
Endo, Tetsu
Tanabe, Nobukazu
Numao, Hiroshi
Fukuda, Shinsaku
Iijima, Katsunori
Masamune, Atsushi
Ohira, Hiromasa
Ueno, Yoshiyuki
Takikawa, Yasuhiro
author_sort Kuroda, Hidekatsu
collection PubMed
description OBJECTIVE: There is limited information regarding the benefits of Lenvatinib-transcatheter arterial chemoembolization (LEN-TACE) sequential therapy for unresectable hepatocellular carcinoma (u-HCC). We compared the efficacy and safety of LEN-TACE sequential therapy to LEN monotherapy and investigated the factors contributing to the LEN-TACE sequential therapy deep response. METHODS: We enrolled a multicenter cohort of 247 patients with u-HCC treated with LEN between 2018 and 2020. Propensity score matching identified 63 matching pairs of patients with well-balanced characteristics. We retrospectively compared the clinical outcomes, including overall survival (OS), progression-free survival (PFS), and incidence of adverse events (AEs), between the LEN-TACE and LEN monotherapy groups. Additionally, we evaluated the tumor response, change in albumin-bilirubin (ALBI) score, factors affecting PFS and OS, and independent predictors contributing to the LEN-TACE sequential therapy deep response. In this study, at eight weeks after resumption of LEN after initial TACE, “deep response” was defined as achieving complete response or partial response (PR) on modified Response Evaluation Criteria in Solid Tumors (mRECIST), and at least a 30% decrease in the sum of diameters of target lesions, taking the baseline sum diameters as the reference. RESULTS: The OS and PFS in the LEN-TACE group were significantly higher than those in the LEN monotherapy group (p = 0.002 and p = 0.037, respectively). The incidence of AEs related to LEN was not significantly different between the two groups. In LEN-TACE sequential therapy, the objective response rate was 61.9%, and the disease control rate was 74.6%, according to the mRECIST criteria. No significant change in the ALBI score was observed during sequential LEN-TACE therapy. Multivariable analyses revealed that deep response was independently associated with the outcome of the initial response to LEN by mRECIST: PR (odds ratio: 5.176, 95% confidence interval: 1.528–17.537, p < 0.001). CONCLUSIONS: LEN-TACE sequential therapy may provide more clinical benefits than LEN monotherapy in u-HCC patients who responded to initial LEN treatment. Objective response according to mRECIST to initial LEN is an independent factor contributing to LEN-TACE sequential therapy deep response.
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spelling pubmed-92949362022-08-16 Objective Response by mRECIST to Initial Lenvatinib Therapy Is an Independent Factor Contributing to Deep Response in Hepatocellular Carcinoma Treated with Lenvatinib-Transcatheter Arterial Chemoembolization Sequential Therapy Kuroda, Hidekatsu Oikawa, Takayoshi Ninomiya, Masashi Fujita, Masashi Abe, Kazumichi Okumoto, Kazuo Katsumi, Tomohiro Sato, Wataru Igarashi, Go Iino, Chikara Endo, Tetsu Tanabe, Nobukazu Numao, Hiroshi Fukuda, Shinsaku Iijima, Katsunori Masamune, Atsushi Ohira, Hiromasa Ueno, Yoshiyuki Takikawa, Yasuhiro Liver Cancer Research Article OBJECTIVE: There is limited information regarding the benefits of Lenvatinib-transcatheter arterial chemoembolization (LEN-TACE) sequential therapy for unresectable hepatocellular carcinoma (u-HCC). We compared the efficacy and safety of LEN-TACE sequential therapy to LEN monotherapy and investigated the factors contributing to the LEN-TACE sequential therapy deep response. METHODS: We enrolled a multicenter cohort of 247 patients with u-HCC treated with LEN between 2018 and 2020. Propensity score matching identified 63 matching pairs of patients with well-balanced characteristics. We retrospectively compared the clinical outcomes, including overall survival (OS), progression-free survival (PFS), and incidence of adverse events (AEs), between the LEN-TACE and LEN monotherapy groups. Additionally, we evaluated the tumor response, change in albumin-bilirubin (ALBI) score, factors affecting PFS and OS, and independent predictors contributing to the LEN-TACE sequential therapy deep response. In this study, at eight weeks after resumption of LEN after initial TACE, “deep response” was defined as achieving complete response or partial response (PR) on modified Response Evaluation Criteria in Solid Tumors (mRECIST), and at least a 30% decrease in the sum of diameters of target lesions, taking the baseline sum diameters as the reference. RESULTS: The OS and PFS in the LEN-TACE group were significantly higher than those in the LEN monotherapy group (p = 0.002 and p = 0.037, respectively). The incidence of AEs related to LEN was not significantly different between the two groups. In LEN-TACE sequential therapy, the objective response rate was 61.9%, and the disease control rate was 74.6%, according to the mRECIST criteria. No significant change in the ALBI score was observed during sequential LEN-TACE therapy. Multivariable analyses revealed that deep response was independently associated with the outcome of the initial response to LEN by mRECIST: PR (odds ratio: 5.176, 95% confidence interval: 1.528–17.537, p < 0.001). CONCLUSIONS: LEN-TACE sequential therapy may provide more clinical benefits than LEN monotherapy in u-HCC patients who responded to initial LEN treatment. Objective response according to mRECIST to initial LEN is an independent factor contributing to LEN-TACE sequential therapy deep response. S. Karger AG 2022-02-15 /pmc/articles/PMC9294936/ /pubmed/35978602 http://dx.doi.org/10.1159/000522424 Text en Copyright © 2022 by The Author(s). Published by S. Karger AG, Basel https://creativecommons.org/licenses/by-nc/4.0/This article is licensed under the Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC). Usage and distribution for commercial purposes requires written permission. Drug Dosage: The authors and the publisher have exerted every effort to ensure that drug selection and dosage set forth in this text are in accord with current recommendations and practice at the time of publication. However, in view of ongoing research, changes in government regulations, and the constant flow of information relating to drug therapy and drug reactions, the reader is urged to check the package insert for each drug for any changes in indications and dosage and for added warnings and precautions. This is particularly important when the recommended agent is a new and/or infrequently employed drug. Disclaimer: The statements, opinions and data contained in this publication are solely those of the individual authors and contributors and not of the publishers and the editor(s). The appearance of advertisements or/and product references in the publication is not a warranty, endorsement, or approval of the products or services advertised or of their effectiveness, quality or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements.
spellingShingle Research Article
Kuroda, Hidekatsu
Oikawa, Takayoshi
Ninomiya, Masashi
Fujita, Masashi
Abe, Kazumichi
Okumoto, Kazuo
Katsumi, Tomohiro
Sato, Wataru
Igarashi, Go
Iino, Chikara
Endo, Tetsu
Tanabe, Nobukazu
Numao, Hiroshi
Fukuda, Shinsaku
Iijima, Katsunori
Masamune, Atsushi
Ohira, Hiromasa
Ueno, Yoshiyuki
Takikawa, Yasuhiro
Objective Response by mRECIST to Initial Lenvatinib Therapy Is an Independent Factor Contributing to Deep Response in Hepatocellular Carcinoma Treated with Lenvatinib-Transcatheter Arterial Chemoembolization Sequential Therapy
title Objective Response by mRECIST to Initial Lenvatinib Therapy Is an Independent Factor Contributing to Deep Response in Hepatocellular Carcinoma Treated with Lenvatinib-Transcatheter Arterial Chemoembolization Sequential Therapy
title_full Objective Response by mRECIST to Initial Lenvatinib Therapy Is an Independent Factor Contributing to Deep Response in Hepatocellular Carcinoma Treated with Lenvatinib-Transcatheter Arterial Chemoembolization Sequential Therapy
title_fullStr Objective Response by mRECIST to Initial Lenvatinib Therapy Is an Independent Factor Contributing to Deep Response in Hepatocellular Carcinoma Treated with Lenvatinib-Transcatheter Arterial Chemoembolization Sequential Therapy
title_full_unstemmed Objective Response by mRECIST to Initial Lenvatinib Therapy Is an Independent Factor Contributing to Deep Response in Hepatocellular Carcinoma Treated with Lenvatinib-Transcatheter Arterial Chemoembolization Sequential Therapy
title_short Objective Response by mRECIST to Initial Lenvatinib Therapy Is an Independent Factor Contributing to Deep Response in Hepatocellular Carcinoma Treated with Lenvatinib-Transcatheter Arterial Chemoembolization Sequential Therapy
title_sort objective response by mrecist to initial lenvatinib therapy is an independent factor contributing to deep response in hepatocellular carcinoma treated with lenvatinib-transcatheter arterial chemoembolization sequential therapy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9294936/
https://www.ncbi.nlm.nih.gov/pubmed/35978602
http://dx.doi.org/10.1159/000522424
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