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Therapeutic effectiveness of anlotinib combined with etoposide in extensive-stage small-cell lung cancer: a single-arm, phase II trial

BACKGROUND: Anlotinib plus chemotherapy as first-line treatment for extensive-stage small-cell lung cancer (ES-SCLC) achieves good efficacy, but there is still room for improvement. This clinical study examined the effectiveness of anlotinib plus etoposide for maintenance therapy in ES-SCLC. METHODS...

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Autores principales: Wu, Yuan, Zhou, Xuefeng, Zhao, Weiqing, Wang, Qiong, Han, Zhengxiang, Wang, Lifeng, Zhou, Wenjie, Zhou, Tong, Song, Haizhu, Chen, Yong, Yang, Kaihua, Shi, Lin, Pan, Banzhou, Guo, Renhong, Zhou, Guoren, Jiang, Feng, Feng, Jifeng, Shen, Bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10663256/
https://www.ncbi.nlm.nih.gov/pubmed/37837490
http://dx.doi.org/10.1007/s10637-023-01398-9
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author Wu, Yuan
Zhou, Xuefeng
Zhao, Weiqing
Wang, Qiong
Han, Zhengxiang
Wang, Lifeng
Zhou, Wenjie
Zhou, Tong
Song, Haizhu
Chen, Yong
Yang, Kaihua
Shi, Lin
Pan, Banzhou
Guo, Renhong
Zhou, Guoren
Jiang, Feng
Feng, Jifeng
Shen, Bo
author_facet Wu, Yuan
Zhou, Xuefeng
Zhao, Weiqing
Wang, Qiong
Han, Zhengxiang
Wang, Lifeng
Zhou, Wenjie
Zhou, Tong
Song, Haizhu
Chen, Yong
Yang, Kaihua
Shi, Lin
Pan, Banzhou
Guo, Renhong
Zhou, Guoren
Jiang, Feng
Feng, Jifeng
Shen, Bo
author_sort Wu, Yuan
collection PubMed
description BACKGROUND: Anlotinib plus chemotherapy as first-line treatment for extensive-stage small-cell lung cancer (ES-SCLC) achieves good efficacy, but there is still room for improvement. This clinical study examined the effectiveness of anlotinib plus etoposide for maintenance therapy in ES-SCLC. METHODS: The current single-arm, prospective phase II study was performed at Jiangsu Cancer Hospital (March 2019 to March 2022). After successful primary etoposide-based therapy, anlotinib was administered at 12 mg/day on days 1 to 14 of 21-day cycles until disease progression or consent withdrawal. All patients also received etoposide at 50 mg/day on days 1 to 14 of 21-day cycles for a maximum of six cycles. Progression-free survival (PFS) constituted the primary study endpoint. Secondary endpoints were overall survival (OS), objective remission rate (ORR), disease control rate (DCR), and safety. In addition, adverse events (AEs) were assessed. RESULTS: Twenty-eight patients were treated. Median PFS and OS were 8.02 (95%CI 5.36–10.67) and 11.04 (95%CI 10.37–11.68) months, respectively. Totally 9 and 18 participants showed a partial response and stable disease, respectively; ORR and DCR were 32.14% and 96.43%, respectively. The commonest all-grade AEs were fatigue (n = 11, 39.28%), hypertension (n = 11, 39.28%), loss of appetite (n = 9, 32.14%), oral mucositis (n = 7, 25.00%) and proteinuria (n = 6, 21.40%). Grade 3–4 AEs included fatigue (n = 4, 14.28%), hypertension (n = 2, 7.14%), hand and foot syndrome (n = 2, 7.14%), oral mucositis (n = 1, 3.57%), hemoptysis (n = 1, 3.57%), proteinuria (n = 1, 3.57%), gingival bleeding (n = 1, 3.57%), and serum creatinine elevation (n = 1, 3.57%). CONCLUSION: Maintenance anlotinib plus etoposide achieves promising PFS and OS in clinical ES-SCLC. REGISTRATION NUMBER: ChiCTR1800019421. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10637-023-01398-9.
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spelling pubmed-106632562023-10-14 Therapeutic effectiveness of anlotinib combined with etoposide in extensive-stage small-cell lung cancer: a single-arm, phase II trial Wu, Yuan Zhou, Xuefeng Zhao, Weiqing Wang, Qiong Han, Zhengxiang Wang, Lifeng Zhou, Wenjie Zhou, Tong Song, Haizhu Chen, Yong Yang, Kaihua Shi, Lin Pan, Banzhou Guo, Renhong Zhou, Guoren Jiang, Feng Feng, Jifeng Shen, Bo Invest New Drugs Research BACKGROUND: Anlotinib plus chemotherapy as first-line treatment for extensive-stage small-cell lung cancer (ES-SCLC) achieves good efficacy, but there is still room for improvement. This clinical study examined the effectiveness of anlotinib plus etoposide for maintenance therapy in ES-SCLC. METHODS: The current single-arm, prospective phase II study was performed at Jiangsu Cancer Hospital (March 2019 to March 2022). After successful primary etoposide-based therapy, anlotinib was administered at 12 mg/day on days 1 to 14 of 21-day cycles until disease progression or consent withdrawal. All patients also received etoposide at 50 mg/day on days 1 to 14 of 21-day cycles for a maximum of six cycles. Progression-free survival (PFS) constituted the primary study endpoint. Secondary endpoints were overall survival (OS), objective remission rate (ORR), disease control rate (DCR), and safety. In addition, adverse events (AEs) were assessed. RESULTS: Twenty-eight patients were treated. Median PFS and OS were 8.02 (95%CI 5.36–10.67) and 11.04 (95%CI 10.37–11.68) months, respectively. Totally 9 and 18 participants showed a partial response and stable disease, respectively; ORR and DCR were 32.14% and 96.43%, respectively. The commonest all-grade AEs were fatigue (n = 11, 39.28%), hypertension (n = 11, 39.28%), loss of appetite (n = 9, 32.14%), oral mucositis (n = 7, 25.00%) and proteinuria (n = 6, 21.40%). Grade 3–4 AEs included fatigue (n = 4, 14.28%), hypertension (n = 2, 7.14%), hand and foot syndrome (n = 2, 7.14%), oral mucositis (n = 1, 3.57%), hemoptysis (n = 1, 3.57%), proteinuria (n = 1, 3.57%), gingival bleeding (n = 1, 3.57%), and serum creatinine elevation (n = 1, 3.57%). CONCLUSION: Maintenance anlotinib plus etoposide achieves promising PFS and OS in clinical ES-SCLC. REGISTRATION NUMBER: ChiCTR1800019421. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10637-023-01398-9. Springer US 2023-10-14 2023 /pmc/articles/PMC10663256/ /pubmed/37837490 http://dx.doi.org/10.1007/s10637-023-01398-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research
Wu, Yuan
Zhou, Xuefeng
Zhao, Weiqing
Wang, Qiong
Han, Zhengxiang
Wang, Lifeng
Zhou, Wenjie
Zhou, Tong
Song, Haizhu
Chen, Yong
Yang, Kaihua
Shi, Lin
Pan, Banzhou
Guo, Renhong
Zhou, Guoren
Jiang, Feng
Feng, Jifeng
Shen, Bo
Therapeutic effectiveness of anlotinib combined with etoposide in extensive-stage small-cell lung cancer: a single-arm, phase II trial
title Therapeutic effectiveness of anlotinib combined with etoposide in extensive-stage small-cell lung cancer: a single-arm, phase II trial
title_full Therapeutic effectiveness of anlotinib combined with etoposide in extensive-stage small-cell lung cancer: a single-arm, phase II trial
title_fullStr Therapeutic effectiveness of anlotinib combined with etoposide in extensive-stage small-cell lung cancer: a single-arm, phase II trial
title_full_unstemmed Therapeutic effectiveness of anlotinib combined with etoposide in extensive-stage small-cell lung cancer: a single-arm, phase II trial
title_short Therapeutic effectiveness of anlotinib combined with etoposide in extensive-stage small-cell lung cancer: a single-arm, phase II trial
title_sort therapeutic effectiveness of anlotinib combined with etoposide in extensive-stage small-cell lung cancer: a single-arm, phase ii trial
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10663256/
https://www.ncbi.nlm.nih.gov/pubmed/37837490
http://dx.doi.org/10.1007/s10637-023-01398-9
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