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Early Prediction of Response Focused on Tumor Markers in Atezolizumab plus Bevacizumab Therapy for Hepatocellular Carcinoma

SIMPLE SUMMARY: The combination of atezolizumab and bevacizumab was introduced as a first-line therapy for patients with unresectable hepatocellular carcinoma in 2020. Although some patients have shown a treatment response, there have also been those with disease progression. Such cases should be ap...

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Autores principales: Tanabe, Norikazu, Saeki, Issei, Aibe, Yuki, Matsuda, Takashi, Hanazono, Tadasuke, Nishi, Maiko, Hidaka, Isao, Kuwashiro, Shinya, Shiratsuki, Shogo, Matsuura, Keiji, Egusa, Maho, Nishiyama, Natsuko, Fujioka, Tsuyoshi, Kawamoto, Daiki, Sasaki, Ryo, Nishimura, Tatsuro, Oono, Takashi, Hisanaga, Takuro, Matsumoto, Toshihiko, Ishikawa, Tsuyoshi, Yamasaki, Takahiro, Takami, Taro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10251947/
https://www.ncbi.nlm.nih.gov/pubmed/37296889
http://dx.doi.org/10.3390/cancers15112927
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author Tanabe, Norikazu
Saeki, Issei
Aibe, Yuki
Matsuda, Takashi
Hanazono, Tadasuke
Nishi, Maiko
Hidaka, Isao
Kuwashiro, Shinya
Shiratsuki, Shogo
Matsuura, Keiji
Egusa, Maho
Nishiyama, Natsuko
Fujioka, Tsuyoshi
Kawamoto, Daiki
Sasaki, Ryo
Nishimura, Tatsuro
Oono, Takashi
Hisanaga, Takuro
Matsumoto, Toshihiko
Ishikawa, Tsuyoshi
Yamasaki, Takahiro
Takami, Taro
author_facet Tanabe, Norikazu
Saeki, Issei
Aibe, Yuki
Matsuda, Takashi
Hanazono, Tadasuke
Nishi, Maiko
Hidaka, Isao
Kuwashiro, Shinya
Shiratsuki, Shogo
Matsuura, Keiji
Egusa, Maho
Nishiyama, Natsuko
Fujioka, Tsuyoshi
Kawamoto, Daiki
Sasaki, Ryo
Nishimura, Tatsuro
Oono, Takashi
Hisanaga, Takuro
Matsumoto, Toshihiko
Ishikawa, Tsuyoshi
Yamasaki, Takahiro
Takami, Taro
author_sort Tanabe, Norikazu
collection PubMed
description SIMPLE SUMMARY: The combination of atezolizumab and bevacizumab was introduced as a first-line therapy for patients with unresectable hepatocellular carcinoma in 2020. Although some patients have shown a treatment response, there have also been those with disease progression. Such cases should be appropriately transitioned to second-line or later treatment. Thus, this study investigated early predictors of response and disease progression categorized into two groups based on a baseline alpha-fetoprotein (AFP) of 20 ng/mL. As a result, we found that changes in AFP and baseline des-gamma-carboxy prothrombin levels were useful predictors of treatment response. Tumor markers are useful in predicting treatment response and prognosis. ABSTRACT: Despite the promising efficacy of atezolizumab plus bevacizumab (atezo/bev), some patients with unresectable hepatocellular carcinoma (HCC) experience disease progression. This retrospective study, which included 154 patients, aimed to evaluate predictors of treatment efficacy of atezo/bev for unresectable HCC. Factors associated with treatment response were examined, focusing on tumor markers. In the high-alpha-fetoprotein (AFP) group (baseline AFP ≥ 20 ng/mL), a decrease in AFP level > 30% was an independent predictor of objective response (odds ratio, 5.517; p = 0.0032). In the low-AFP group (baseline AFP < 20 ng/mL), baseline des-gamma-carboxy prothrombin (DCP) level < 40 mAU/mL was an independent predictor of objective response (odds ratio, 3.978; p = 0.0206). The independent predictors of early progressive disease were an increase in AFP level ≥ 30% at 3 weeks (odds ratio, 4.077; p = 0.0264) and the presence of extrahepatic spread (odds ratio, 3.682; p = 0.0337) in the high-AFP group and up-to-seven criteria, OUT (odds ratio, 15.756; p = 0.0257) in the low-AFP group. In atezo/bev therapy, focusing on early AFP changes, baseline DCP, and tumor burden of up-to-seven criteria are useful in predicting response to treatment.
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spelling pubmed-102519472023-06-10 Early Prediction of Response Focused on Tumor Markers in Atezolizumab plus Bevacizumab Therapy for Hepatocellular Carcinoma Tanabe, Norikazu Saeki, Issei Aibe, Yuki Matsuda, Takashi Hanazono, Tadasuke Nishi, Maiko Hidaka, Isao Kuwashiro, Shinya Shiratsuki, Shogo Matsuura, Keiji Egusa, Maho Nishiyama, Natsuko Fujioka, Tsuyoshi Kawamoto, Daiki Sasaki, Ryo Nishimura, Tatsuro Oono, Takashi Hisanaga, Takuro Matsumoto, Toshihiko Ishikawa, Tsuyoshi Yamasaki, Takahiro Takami, Taro Cancers (Basel) Article SIMPLE SUMMARY: The combination of atezolizumab and bevacizumab was introduced as a first-line therapy for patients with unresectable hepatocellular carcinoma in 2020. Although some patients have shown a treatment response, there have also been those with disease progression. Such cases should be appropriately transitioned to second-line or later treatment. Thus, this study investigated early predictors of response and disease progression categorized into two groups based on a baseline alpha-fetoprotein (AFP) of 20 ng/mL. As a result, we found that changes in AFP and baseline des-gamma-carboxy prothrombin levels were useful predictors of treatment response. Tumor markers are useful in predicting treatment response and prognosis. ABSTRACT: Despite the promising efficacy of atezolizumab plus bevacizumab (atezo/bev), some patients with unresectable hepatocellular carcinoma (HCC) experience disease progression. This retrospective study, which included 154 patients, aimed to evaluate predictors of treatment efficacy of atezo/bev for unresectable HCC. Factors associated with treatment response were examined, focusing on tumor markers. In the high-alpha-fetoprotein (AFP) group (baseline AFP ≥ 20 ng/mL), a decrease in AFP level > 30% was an independent predictor of objective response (odds ratio, 5.517; p = 0.0032). In the low-AFP group (baseline AFP < 20 ng/mL), baseline des-gamma-carboxy prothrombin (DCP) level < 40 mAU/mL was an independent predictor of objective response (odds ratio, 3.978; p = 0.0206). The independent predictors of early progressive disease were an increase in AFP level ≥ 30% at 3 weeks (odds ratio, 4.077; p = 0.0264) and the presence of extrahepatic spread (odds ratio, 3.682; p = 0.0337) in the high-AFP group and up-to-seven criteria, OUT (odds ratio, 15.756; p = 0.0257) in the low-AFP group. In atezo/bev therapy, focusing on early AFP changes, baseline DCP, and tumor burden of up-to-seven criteria are useful in predicting response to treatment. MDPI 2023-05-26 /pmc/articles/PMC10251947/ /pubmed/37296889 http://dx.doi.org/10.3390/cancers15112927 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Tanabe, Norikazu
Saeki, Issei
Aibe, Yuki
Matsuda, Takashi
Hanazono, Tadasuke
Nishi, Maiko
Hidaka, Isao
Kuwashiro, Shinya
Shiratsuki, Shogo
Matsuura, Keiji
Egusa, Maho
Nishiyama, Natsuko
Fujioka, Tsuyoshi
Kawamoto, Daiki
Sasaki, Ryo
Nishimura, Tatsuro
Oono, Takashi
Hisanaga, Takuro
Matsumoto, Toshihiko
Ishikawa, Tsuyoshi
Yamasaki, Takahiro
Takami, Taro
Early Prediction of Response Focused on Tumor Markers in Atezolizumab plus Bevacizumab Therapy for Hepatocellular Carcinoma
title Early Prediction of Response Focused on Tumor Markers in Atezolizumab plus Bevacizumab Therapy for Hepatocellular Carcinoma
title_full Early Prediction of Response Focused on Tumor Markers in Atezolizumab plus Bevacizumab Therapy for Hepatocellular Carcinoma
title_fullStr Early Prediction of Response Focused on Tumor Markers in Atezolizumab plus Bevacizumab Therapy for Hepatocellular Carcinoma
title_full_unstemmed Early Prediction of Response Focused on Tumor Markers in Atezolizumab plus Bevacizumab Therapy for Hepatocellular Carcinoma
title_short Early Prediction of Response Focused on Tumor Markers in Atezolizumab plus Bevacizumab Therapy for Hepatocellular Carcinoma
title_sort early prediction of response focused on tumor markers in atezolizumab plus bevacizumab therapy for hepatocellular carcinoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10251947/
https://www.ncbi.nlm.nih.gov/pubmed/37296889
http://dx.doi.org/10.3390/cancers15112927
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