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Does first‐line treatment have prognostic impact for unresectable HCC?—Atezolizumab plus bevacizumab versus lenvatinib
BACKGROUND/AIM: A comparison of therapeutic efficacy between atezolizumab plus bevacizumab (Atez/Bev) and lenvatinib treatment given as first‐line therapy for unresectable hepatocellular carcinoma (u‐HCC) in regard to progression‐free survival (PFS) overall survival (OS) has not been reported. We ai...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9844603/ https://www.ncbi.nlm.nih.gov/pubmed/35666040 http://dx.doi.org/10.1002/cam4.4854 |
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author | Hiraoka, Atsushi Kumada, Takashi Tada, Toshifumi Hirooka, Masashi Kariyama, Kazuya Tani, Joji Atsukawa, Masanori Takaguchi, Koichi Itobayashi, Ei Fukunishi, Shinya Tsuji, Kunihiko Ishikawa, Toru Tajiri, Kazuto Ochi, Hironori Yasuda, Satoshi Toyoda, Hidenori Ogawa, Chikara Nishimura, Takashi Hatanaka, Takeshi Kakizaki, Satoru Shimada, Noritomo Kawata, Kazuhito Naganuma, Atsushi Kosaka, Hisashi Shibata, Hiroshi Aoki, Tomoko Tanaka, Takaaki Ohama, Hideko Nouso, Kazuhiro Morishita, Asahiro Tsutsui, Akemi Nagano, Takuya Itokawa, Norio Okubo, Tomomi Arai, Taeang Imai, Michitaka Koizumi, Yohei Nakamura, Shinichiro Joko, Kouji Iijima, Hiroko Kaibori, Masaki Hiasa, Yoichi Kudo, Masatoshi |
author_facet | Hiraoka, Atsushi Kumada, Takashi Tada, Toshifumi Hirooka, Masashi Kariyama, Kazuya Tani, Joji Atsukawa, Masanori Takaguchi, Koichi Itobayashi, Ei Fukunishi, Shinya Tsuji, Kunihiko Ishikawa, Toru Tajiri, Kazuto Ochi, Hironori Yasuda, Satoshi Toyoda, Hidenori Ogawa, Chikara Nishimura, Takashi Hatanaka, Takeshi Kakizaki, Satoru Shimada, Noritomo Kawata, Kazuhito Naganuma, Atsushi Kosaka, Hisashi Shibata, Hiroshi Aoki, Tomoko Tanaka, Takaaki Ohama, Hideko Nouso, Kazuhiro Morishita, Asahiro Tsutsui, Akemi Nagano, Takuya Itokawa, Norio Okubo, Tomomi Arai, Taeang Imai, Michitaka Koizumi, Yohei Nakamura, Shinichiro Joko, Kouji Iijima, Hiroko Kaibori, Masaki Hiasa, Yoichi Kudo, Masatoshi |
author_sort | Hiraoka, Atsushi |
collection | PubMed |
description | BACKGROUND/AIM: A comparison of therapeutic efficacy between atezolizumab plus bevacizumab (Atez/Bev) and lenvatinib treatment given as first‐line therapy for unresectable hepatocellular carcinoma (u‐HCC) in regard to progression‐free survival (PFS) overall survival (OS) has not been reported. We aimed to elucidate which of those given as initial treatment for u‐HCC has greater prognostic impact on PFS and OS of affected patients, retrospectively. MATERIALS/METHODS: From 2020 to January 2022, 251 u‐HCC (Child–Pugh A, ECOG PS 0/1, BCLC‐B/C) treated were enrolled (Atez/Bev‐group, n = 194; lenvatinib‐group, n = 57). PFS and OS were analyzed following adjustment based on inverse probability weighting (IPW). RESULTS: There was a greater number of patients with macro‐vascular invasion in Atez/Bev‐group (22.7% vs. 8.8%, p = 0.022). In lenvatinib‐group, the frequencies of appetite loss (38.6% vs. 19.6%, p = 0.002), hypothyroidism (21.1% vs. 6.7%, p = 0.004), hand foot skin reaction (19.3% vs. 1.0%, p < 0.001), and diarrhea (10.5% vs. 4.6%, p = 0.012) were greater, while that of general fatigue was lower (22.8% vs. 26.3%, p = 0.008). Comparisons of therapeutic best response using modified response evaluation criteria in solid tumors (mRECIST) did not show significant differences between the present groups (Atez/Bev vs. lenvatinib: CR/PR/SD/PD = 6.1%/39.1%/39.1%/15.6% vs. 0%/48.0%/38.0%/14.0%, p = 0.285). In patients of discontinuation of treatments, 48.2% switched to lenvatinib, 10.6% continued beyond PD, 8.2% received another systemic treatment, 5.9% underwent transcatheter arterial chemoembolization (TACE), 3.5% received hepatic arterial infusion chemotherapy (HAIC), and 1.2% underwent surgical resection in Atez/Bev‐group, while 42.2% switched to Atez/Bev, 4.4% continued beyond PD, 4.4% received another systemic treatment, 2.2% nivolumab, 6.7% received TACE, and 2.2% received HAIC in lenvatinib‐group. Following adjustment with inverse probability weighting (IPW), Atez/Bev‐group showed better PFS (0.5−/1−/1.5‐years: 56.6%/31.6%/non‐estimable vs. 48.6%/20.4%/11.2%, p < 0.0001) and OS rates (0.5−/1−/1.5‐years: 89.6%/67.2%/58.1% vs. 77.8%/66.2%/52.7%, p = 0.002). CONCLUSION: The present study showed that u‐HCC patients who received Atez/Bev as a first‐line treatment may have a better prognosis than those who received lenvatinib. |
format | Online Article Text |
id | pubmed-9844603 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98446032023-01-23 Does first‐line treatment have prognostic impact for unresectable HCC?—Atezolizumab plus bevacizumab versus lenvatinib Hiraoka, Atsushi Kumada, Takashi Tada, Toshifumi Hirooka, Masashi Kariyama, Kazuya Tani, Joji Atsukawa, Masanori Takaguchi, Koichi Itobayashi, Ei Fukunishi, Shinya Tsuji, Kunihiko Ishikawa, Toru Tajiri, Kazuto Ochi, Hironori Yasuda, Satoshi Toyoda, Hidenori Ogawa, Chikara Nishimura, Takashi Hatanaka, Takeshi Kakizaki, Satoru Shimada, Noritomo Kawata, Kazuhito Naganuma, Atsushi Kosaka, Hisashi Shibata, Hiroshi Aoki, Tomoko Tanaka, Takaaki Ohama, Hideko Nouso, Kazuhiro Morishita, Asahiro Tsutsui, Akemi Nagano, Takuya Itokawa, Norio Okubo, Tomomi Arai, Taeang Imai, Michitaka Koizumi, Yohei Nakamura, Shinichiro Joko, Kouji Iijima, Hiroko Kaibori, Masaki Hiasa, Yoichi Kudo, Masatoshi Cancer Med RESEARCH ARTICLES BACKGROUND/AIM: A comparison of therapeutic efficacy between atezolizumab plus bevacizumab (Atez/Bev) and lenvatinib treatment given as first‐line therapy for unresectable hepatocellular carcinoma (u‐HCC) in regard to progression‐free survival (PFS) overall survival (OS) has not been reported. We aimed to elucidate which of those given as initial treatment for u‐HCC has greater prognostic impact on PFS and OS of affected patients, retrospectively. MATERIALS/METHODS: From 2020 to January 2022, 251 u‐HCC (Child–Pugh A, ECOG PS 0/1, BCLC‐B/C) treated were enrolled (Atez/Bev‐group, n = 194; lenvatinib‐group, n = 57). PFS and OS were analyzed following adjustment based on inverse probability weighting (IPW). RESULTS: There was a greater number of patients with macro‐vascular invasion in Atez/Bev‐group (22.7% vs. 8.8%, p = 0.022). In lenvatinib‐group, the frequencies of appetite loss (38.6% vs. 19.6%, p = 0.002), hypothyroidism (21.1% vs. 6.7%, p = 0.004), hand foot skin reaction (19.3% vs. 1.0%, p < 0.001), and diarrhea (10.5% vs. 4.6%, p = 0.012) were greater, while that of general fatigue was lower (22.8% vs. 26.3%, p = 0.008). Comparisons of therapeutic best response using modified response evaluation criteria in solid tumors (mRECIST) did not show significant differences between the present groups (Atez/Bev vs. lenvatinib: CR/PR/SD/PD = 6.1%/39.1%/39.1%/15.6% vs. 0%/48.0%/38.0%/14.0%, p = 0.285). In patients of discontinuation of treatments, 48.2% switched to lenvatinib, 10.6% continued beyond PD, 8.2% received another systemic treatment, 5.9% underwent transcatheter arterial chemoembolization (TACE), 3.5% received hepatic arterial infusion chemotherapy (HAIC), and 1.2% underwent surgical resection in Atez/Bev‐group, while 42.2% switched to Atez/Bev, 4.4% continued beyond PD, 4.4% received another systemic treatment, 2.2% nivolumab, 6.7% received TACE, and 2.2% received HAIC in lenvatinib‐group. Following adjustment with inverse probability weighting (IPW), Atez/Bev‐group showed better PFS (0.5−/1−/1.5‐years: 56.6%/31.6%/non‐estimable vs. 48.6%/20.4%/11.2%, p < 0.0001) and OS rates (0.5−/1−/1.5‐years: 89.6%/67.2%/58.1% vs. 77.8%/66.2%/52.7%, p = 0.002). CONCLUSION: The present study showed that u‐HCC patients who received Atez/Bev as a first‐line treatment may have a better prognosis than those who received lenvatinib. John Wiley and Sons Inc. 2022-06-03 /pmc/articles/PMC9844603/ /pubmed/35666040 http://dx.doi.org/10.1002/cam4.4854 Text en © 2022 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | RESEARCH ARTICLES Hiraoka, Atsushi Kumada, Takashi Tada, Toshifumi Hirooka, Masashi Kariyama, Kazuya Tani, Joji Atsukawa, Masanori Takaguchi, Koichi Itobayashi, Ei Fukunishi, Shinya Tsuji, Kunihiko Ishikawa, Toru Tajiri, Kazuto Ochi, Hironori Yasuda, Satoshi Toyoda, Hidenori Ogawa, Chikara Nishimura, Takashi Hatanaka, Takeshi Kakizaki, Satoru Shimada, Noritomo Kawata, Kazuhito Naganuma, Atsushi Kosaka, Hisashi Shibata, Hiroshi Aoki, Tomoko Tanaka, Takaaki Ohama, Hideko Nouso, Kazuhiro Morishita, Asahiro Tsutsui, Akemi Nagano, Takuya Itokawa, Norio Okubo, Tomomi Arai, Taeang Imai, Michitaka Koizumi, Yohei Nakamura, Shinichiro Joko, Kouji Iijima, Hiroko Kaibori, Masaki Hiasa, Yoichi Kudo, Masatoshi Does first‐line treatment have prognostic impact for unresectable HCC?—Atezolizumab plus bevacizumab versus lenvatinib |
title | Does first‐line treatment have prognostic impact for unresectable HCC?—Atezolizumab plus bevacizumab versus lenvatinib |
title_full | Does first‐line treatment have prognostic impact for unresectable HCC?—Atezolizumab plus bevacizumab versus lenvatinib |
title_fullStr | Does first‐line treatment have prognostic impact for unresectable HCC?—Atezolizumab plus bevacizumab versus lenvatinib |
title_full_unstemmed | Does first‐line treatment have prognostic impact for unresectable HCC?—Atezolizumab plus bevacizumab versus lenvatinib |
title_short | Does first‐line treatment have prognostic impact for unresectable HCC?—Atezolizumab plus bevacizumab versus lenvatinib |
title_sort | does first‐line treatment have prognostic impact for unresectable hcc?—atezolizumab plus bevacizumab versus lenvatinib |
topic | RESEARCH ARTICLES |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9844603/ https://www.ncbi.nlm.nih.gov/pubmed/35666040 http://dx.doi.org/10.1002/cam4.4854 |
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