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Clinical impact of amrubicin monotherapy in patients with relapsed small cell lung cancer: a multicenter retrospective study

BACKGROUND: Topoisomerase is an essential enzyme for deoxyribonucleic acid replication, and its inhibitors suppress tumor progression. Amrubicin, a topoisomerase II inhibitor, is mainly used in the second-line treatment of patients with extensive-stage small cell lung cancer (ES-SCLC). However, the...

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Autores principales: Uda, Sayaka, Yamada, Tadaaki, Yoshimura, Akihiro, Goto, Yasuhiro, Yoshimine, Kohei, Nakamura, Yoichi, Shiotsu, Shinsuke, Yokoi, Takashi, Tamiya, Nobuyo, Kimura, Hideharu, Chihara, Yusuke, Umeda, Yukihiro, Izumi, Miiru, Takeda, Takayuki, Yamada, Takahiro, Hibino, Makoto, Hiranuma, Osamu, Ito, Kazuhiro, Okada, Asuka, Osugi, Shuji, Takemura, Yoshizumi, Ishii, Hiroshi, Chibana, Kenji, Hasegawa, Isao, Morimoto, Yoshie, Iwasaku, Masahiro, Tokuda, Shinsaku, Takayama, Koichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9554692/
https://www.ncbi.nlm.nih.gov/pubmed/36248326
http://dx.doi.org/10.21037/tlcr-22-160
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author Uda, Sayaka
Yamada, Tadaaki
Yoshimura, Akihiro
Goto, Yasuhiro
Yoshimine, Kohei
Nakamura, Yoichi
Shiotsu, Shinsuke
Yokoi, Takashi
Tamiya, Nobuyo
Kimura, Hideharu
Chihara, Yusuke
Umeda, Yukihiro
Izumi, Miiru
Takeda, Takayuki
Yamada, Takahiro
Hibino, Makoto
Hiranuma, Osamu
Ito, Kazuhiro
Okada, Asuka
Osugi, Shuji
Takemura, Yoshizumi
Ishii, Hiroshi
Chibana, Kenji
Hasegawa, Isao
Morimoto, Yoshie
Iwasaku, Masahiro
Tokuda, Shinsaku
Takayama, Koichi
author_facet Uda, Sayaka
Yamada, Tadaaki
Yoshimura, Akihiro
Goto, Yasuhiro
Yoshimine, Kohei
Nakamura, Yoichi
Shiotsu, Shinsuke
Yokoi, Takashi
Tamiya, Nobuyo
Kimura, Hideharu
Chihara, Yusuke
Umeda, Yukihiro
Izumi, Miiru
Takeda, Takayuki
Yamada, Takahiro
Hibino, Makoto
Hiranuma, Osamu
Ito, Kazuhiro
Okada, Asuka
Osugi, Shuji
Takemura, Yoshizumi
Ishii, Hiroshi
Chibana, Kenji
Hasegawa, Isao
Morimoto, Yoshie
Iwasaku, Masahiro
Tokuda, Shinsaku
Takayama, Koichi
author_sort Uda, Sayaka
collection PubMed
description BACKGROUND: Topoisomerase is an essential enzyme for deoxyribonucleic acid replication, and its inhibitors suppress tumor progression. Amrubicin, a topoisomerase II inhibitor, is mainly used in the second-line treatment of patients with extensive-stage small cell lung cancer (ES-SCLC). However, the impact of different types of topoisomerase inhibitors for first-line chemotherapy on the efficacy of amrubicin remains unclear. In the present study, we aimed to evaluate the efficacy of second-line amrubicin in patients with relapsed SCLC who were previously treated with platinum-based chemotherapy, including topoisomerase I and II inhibitors. METHODS: This study retrospectively analyzed patients with ES-SCLC who experienced recurrence and were treated with amrubicin at 22 institutions in Japan between April 2015 and November 2020. The progression-free survival of amrubicin monotherapy was investigated using the Kaplan-Meier method. RESULTS: A total of 320 patients were enrolled in this study, with 59 (18%) receiving platinum plus topoisomerase I inhibitor irinotecan and 261 (82%) receiving platinum plus topoisomerase II inhibitor etoposide as first-line treatment. The progression-free survival of amrubicin was significantly longer in the irinotecan group than in the etoposide group (3.2 vs. 2.5 months; P=0.034). CONCLUSIONS: These results showed that different types of topoisomerase inhibitors could affect the efficacy of amrubicin monotherapy in the second-line treatment of patients with relapsed ES-SCLC.
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spelling pubmed-95546922022-10-13 Clinical impact of amrubicin monotherapy in patients with relapsed small cell lung cancer: a multicenter retrospective study Uda, Sayaka Yamada, Tadaaki Yoshimura, Akihiro Goto, Yasuhiro Yoshimine, Kohei Nakamura, Yoichi Shiotsu, Shinsuke Yokoi, Takashi Tamiya, Nobuyo Kimura, Hideharu Chihara, Yusuke Umeda, Yukihiro Izumi, Miiru Takeda, Takayuki Yamada, Takahiro Hibino, Makoto Hiranuma, Osamu Ito, Kazuhiro Okada, Asuka Osugi, Shuji Takemura, Yoshizumi Ishii, Hiroshi Chibana, Kenji Hasegawa, Isao Morimoto, Yoshie Iwasaku, Masahiro Tokuda, Shinsaku Takayama, Koichi Transl Lung Cancer Res Original Article BACKGROUND: Topoisomerase is an essential enzyme for deoxyribonucleic acid replication, and its inhibitors suppress tumor progression. Amrubicin, a topoisomerase II inhibitor, is mainly used in the second-line treatment of patients with extensive-stage small cell lung cancer (ES-SCLC). However, the impact of different types of topoisomerase inhibitors for first-line chemotherapy on the efficacy of amrubicin remains unclear. In the present study, we aimed to evaluate the efficacy of second-line amrubicin in patients with relapsed SCLC who were previously treated with platinum-based chemotherapy, including topoisomerase I and II inhibitors. METHODS: This study retrospectively analyzed patients with ES-SCLC who experienced recurrence and were treated with amrubicin at 22 institutions in Japan between April 2015 and November 2020. The progression-free survival of amrubicin monotherapy was investigated using the Kaplan-Meier method. RESULTS: A total of 320 patients were enrolled in this study, with 59 (18%) receiving platinum plus topoisomerase I inhibitor irinotecan and 261 (82%) receiving platinum plus topoisomerase II inhibitor etoposide as first-line treatment. The progression-free survival of amrubicin was significantly longer in the irinotecan group than in the etoposide group (3.2 vs. 2.5 months; P=0.034). CONCLUSIONS: These results showed that different types of topoisomerase inhibitors could affect the efficacy of amrubicin monotherapy in the second-line treatment of patients with relapsed ES-SCLC. AME Publishing Company 2022-09 /pmc/articles/PMC9554692/ /pubmed/36248326 http://dx.doi.org/10.21037/tlcr-22-160 Text en 2022 Translational Lung Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Uda, Sayaka
Yamada, Tadaaki
Yoshimura, Akihiro
Goto, Yasuhiro
Yoshimine, Kohei
Nakamura, Yoichi
Shiotsu, Shinsuke
Yokoi, Takashi
Tamiya, Nobuyo
Kimura, Hideharu
Chihara, Yusuke
Umeda, Yukihiro
Izumi, Miiru
Takeda, Takayuki
Yamada, Takahiro
Hibino, Makoto
Hiranuma, Osamu
Ito, Kazuhiro
Okada, Asuka
Osugi, Shuji
Takemura, Yoshizumi
Ishii, Hiroshi
Chibana, Kenji
Hasegawa, Isao
Morimoto, Yoshie
Iwasaku, Masahiro
Tokuda, Shinsaku
Takayama, Koichi
Clinical impact of amrubicin monotherapy in patients with relapsed small cell lung cancer: a multicenter retrospective study
title Clinical impact of amrubicin monotherapy in patients with relapsed small cell lung cancer: a multicenter retrospective study
title_full Clinical impact of amrubicin monotherapy in patients with relapsed small cell lung cancer: a multicenter retrospective study
title_fullStr Clinical impact of amrubicin monotherapy in patients with relapsed small cell lung cancer: a multicenter retrospective study
title_full_unstemmed Clinical impact of amrubicin monotherapy in patients with relapsed small cell lung cancer: a multicenter retrospective study
title_short Clinical impact of amrubicin monotherapy in patients with relapsed small cell lung cancer: a multicenter retrospective study
title_sort clinical impact of amrubicin monotherapy in patients with relapsed small cell lung cancer: a multicenter retrospective study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9554692/
https://www.ncbi.nlm.nih.gov/pubmed/36248326
http://dx.doi.org/10.21037/tlcr-22-160
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