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An open label, multicenter clinical trial that investigated the efficacy and safety of leuprorelin treatment of central precocious puberty in Chinese children
BACKGROUND: Leuprorelin is an analog of gonadotropin-releasing hormone that is used for the therapy of central precocious puberty (CPP). The aims of this prospective, open label, multicenter clinical trial were to establish its efficacy and safety during long-term use. METHODS: Patients, who were al...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8702188/ https://www.ncbi.nlm.nih.gov/pubmed/34941067 http://dx.doi.org/10.1097/MD.0000000000028158 |
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author | Luo, Xiaoping Hou, Ling Zhong, Yan You, Cheng Yang, Yu Wu, Xian Li, Pin Zhou, Shasha Qiu, Wenjuan Zhang, Huiwen Liu, Ying Qian, Ye Luo, Feihong Cheng, Ruoqian Hu, Yuhua Gong, Haihong Wang, Qing Xu, Zhuangjian Du, Hongwei Lu, Feiyu Fu, Junfen Chen, Xuefeng Wang, Winston Guo, Ziheng |
author_facet | Luo, Xiaoping Hou, Ling Zhong, Yan You, Cheng Yang, Yu Wu, Xian Li, Pin Zhou, Shasha Qiu, Wenjuan Zhang, Huiwen Liu, Ying Qian, Ye Luo, Feihong Cheng, Ruoqian Hu, Yuhua Gong, Haihong Wang, Qing Xu, Zhuangjian Du, Hongwei Lu, Feiyu Fu, Junfen Chen, Xuefeng Wang, Winston Guo, Ziheng |
author_sort | Luo, Xiaoping |
collection | PubMed |
description | BACKGROUND: Leuprorelin is an analog of gonadotropin-releasing hormone that is used for the therapy of central precocious puberty (CPP). The aims of this prospective, open label, multicenter clinical trial were to establish its efficacy and safety during long-term use. METHODS: Patients, who were all children, were treated with 1.88 to 3.75 mg leuprorelin subcutaneously once every 4 weeks for a total of 96 weeks between 2015 and 2018. The primary endpoint was the rate of occurrence of adverse events (AEs) and the secondary endpoint was no progression in the Tanner stage or regression by week 96 compared to baseline. RESULTS: A total of 307 CPP patients, 305 (99.3%) females and 2 males (0.7%), completed the 96-weeks of treatment. Due to limited data for male patients, they are not discussed in the efficacy results. Treatment-emergent AEs (TEAEs) were reported for 252 (82.1%) patients, mostly (79.5%) being mild or moderate and only 33 (10.7%) of patients experienced TEAEs related to leuprorelin therapy. The most frequent (>2%) drug-related TEAEs were injection site induration (4.6%, 14/307) and vaginal bleeding (2.3%, 7/305). After treatment, 83.5% of patients had regression or no progression in the Tanner stage (95% confidence interval: 78.68%, 87.62%) and the majority had decreased gonadotropin-releasing hormone-stimulated peak luteinizing hormone and follicle-stimulating hormone concentrations, as well as reduced sex hormone concentrations and a reduction in the bone age/chronological age ratio compared to baseline. CONCLUSIONS: The trial revealed that CPP was effectively treated in most patients who received leuprorelin for nearly 2 years. Any drug-related AEs were reported with low incidence (<5%) and were consistent with the known safety profile of leuprorelin. TRIAL REGISTRATION: The trial was registered at ClinicalTrials.gov (registration number: NCT02427958). |
format | Online Article Text |
id | pubmed-8702188 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-87021882021-12-27 An open label, multicenter clinical trial that investigated the efficacy and safety of leuprorelin treatment of central precocious puberty in Chinese children Luo, Xiaoping Hou, Ling Zhong, Yan You, Cheng Yang, Yu Wu, Xian Li, Pin Zhou, Shasha Qiu, Wenjuan Zhang, Huiwen Liu, Ying Qian, Ye Luo, Feihong Cheng, Ruoqian Hu, Yuhua Gong, Haihong Wang, Qing Xu, Zhuangjian Du, Hongwei Lu, Feiyu Fu, Junfen Chen, Xuefeng Wang, Winston Guo, Ziheng Medicine (Baltimore) 6200 BACKGROUND: Leuprorelin is an analog of gonadotropin-releasing hormone that is used for the therapy of central precocious puberty (CPP). The aims of this prospective, open label, multicenter clinical trial were to establish its efficacy and safety during long-term use. METHODS: Patients, who were all children, were treated with 1.88 to 3.75 mg leuprorelin subcutaneously once every 4 weeks for a total of 96 weeks between 2015 and 2018. The primary endpoint was the rate of occurrence of adverse events (AEs) and the secondary endpoint was no progression in the Tanner stage or regression by week 96 compared to baseline. RESULTS: A total of 307 CPP patients, 305 (99.3%) females and 2 males (0.7%), completed the 96-weeks of treatment. Due to limited data for male patients, they are not discussed in the efficacy results. Treatment-emergent AEs (TEAEs) were reported for 252 (82.1%) patients, mostly (79.5%) being mild or moderate and only 33 (10.7%) of patients experienced TEAEs related to leuprorelin therapy. The most frequent (>2%) drug-related TEAEs were injection site induration (4.6%, 14/307) and vaginal bleeding (2.3%, 7/305). After treatment, 83.5% of patients had regression or no progression in the Tanner stage (95% confidence interval: 78.68%, 87.62%) and the majority had decreased gonadotropin-releasing hormone-stimulated peak luteinizing hormone and follicle-stimulating hormone concentrations, as well as reduced sex hormone concentrations and a reduction in the bone age/chronological age ratio compared to baseline. CONCLUSIONS: The trial revealed that CPP was effectively treated in most patients who received leuprorelin for nearly 2 years. Any drug-related AEs were reported with low incidence (<5%) and were consistent with the known safety profile of leuprorelin. TRIAL REGISTRATION: The trial was registered at ClinicalTrials.gov (registration number: NCT02427958). Lippincott Williams & Wilkins 2021-12-23 /pmc/articles/PMC8702188/ /pubmed/34941067 http://dx.doi.org/10.1097/MD.0000000000028158 Text en Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) |
spellingShingle | 6200 Luo, Xiaoping Hou, Ling Zhong, Yan You, Cheng Yang, Yu Wu, Xian Li, Pin Zhou, Shasha Qiu, Wenjuan Zhang, Huiwen Liu, Ying Qian, Ye Luo, Feihong Cheng, Ruoqian Hu, Yuhua Gong, Haihong Wang, Qing Xu, Zhuangjian Du, Hongwei Lu, Feiyu Fu, Junfen Chen, Xuefeng Wang, Winston Guo, Ziheng An open label, multicenter clinical trial that investigated the efficacy and safety of leuprorelin treatment of central precocious puberty in Chinese children |
title | An open label, multicenter clinical trial that investigated the efficacy and safety of leuprorelin treatment of central precocious puberty in Chinese children |
title_full | An open label, multicenter clinical trial that investigated the efficacy and safety of leuprorelin treatment of central precocious puberty in Chinese children |
title_fullStr | An open label, multicenter clinical trial that investigated the efficacy and safety of leuprorelin treatment of central precocious puberty in Chinese children |
title_full_unstemmed | An open label, multicenter clinical trial that investigated the efficacy and safety of leuprorelin treatment of central precocious puberty in Chinese children |
title_short | An open label, multicenter clinical trial that investigated the efficacy and safety of leuprorelin treatment of central precocious puberty in Chinese children |
title_sort | open label, multicenter clinical trial that investigated the efficacy and safety of leuprorelin treatment of central precocious puberty in chinese children |
topic | 6200 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8702188/ https://www.ncbi.nlm.nih.gov/pubmed/34941067 http://dx.doi.org/10.1097/MD.0000000000028158 |
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