Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
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
_version_ 1784621187110797312
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
work_keys_str_mv AT luoxiaoping anopenlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT houling anopenlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT zhongyan anopenlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT youcheng anopenlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT yangyu anopenlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT wuxian anopenlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT lipin anopenlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT zhoushasha anopenlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT qiuwenjuan anopenlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT zhanghuiwen anopenlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT liuying anopenlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT qianye anopenlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT luofeihong anopenlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT chengruoqian anopenlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT huyuhua anopenlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT gonghaihong anopenlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT wangqing anopenlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT xuzhuangjian anopenlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT duhongwei anopenlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT lufeiyu anopenlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT fujunfen anopenlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT chenxuefeng anopenlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT wangwinston anopenlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT guoziheng anopenlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT luoxiaoping openlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT houling openlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT zhongyan openlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT youcheng openlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT yangyu openlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT wuxian openlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT lipin openlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT zhoushasha openlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT qiuwenjuan openlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT zhanghuiwen openlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT liuying openlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT qianye openlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT luofeihong openlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT chengruoqian openlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT huyuhua openlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT gonghaihong openlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT wangqing openlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT xuzhuangjian openlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT duhongwei openlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT lufeiyu openlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT fujunfen openlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT chenxuefeng openlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT wangwinston openlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren
AT guoziheng openlabelmulticenterclinicaltrialthatinvestigatedtheefficacyandsafetyofleuprorelintreatmentofcentralprecociouspubertyinchinesechildren