• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

戈谢病患者在酶替代疗法和底物减少疗法之间的转换:来自戈谢病结果调查(GOS)的数据。

Switching between Enzyme Replacement Therapies and Substrate Reduction Therapies in Patients with Gaucher Disease: Data from the Gaucher Outcome Survey (GOS).

作者信息

Hughes Derralynn A, Deegan Patrick, Giraldo Pilar, Göker-Alpan Özlem, Lau Heather, Lukina Elena, Revel-Vilk Shoshana, Scarpa Maurizio, Botha Jaco, Gadir Noga, Zimran Ari

机构信息

LSD Unit, Royal Free London NHS Foundation Trust, University College London, London NW3 2QG, UK.

Addenbrookes Hospital, Cambridge CB2 0QQ, UK.

出版信息

J Clin Med. 2022 Aug 31;11(17):5158. doi: 10.3390/jcm11175158.

DOI:10.3390/jcm11175158
PMID:36079085
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9457166/
Abstract

Switching between enzyme replacement therapies (ERT) and substrate reduction therapies (SRT) in patients with type 1 Gaucher disease (GD1) is not uncommon; however, the reasons for switchng treatments have not been explored in detail. Data from the Gaucher Outcome Survey (GOS), an international registry for patients with confirmed GD, were used to evaluate the reasons for, and consequences of, switching between these treatment types. Of the 1843 patients enrolled in GOS on 25 February 2020, 245 had undergone a treatment switch: 222 from initial ERT to SRT (of whom 88 later switched back to ERT) and 23 from initial SRT to ERT. The most common reasons for ERT-SRT switching were duration of infusion (25.4%), drug shortage (22.0%), and adverse events (AEs; 11.9%), and for SRT-ERT switching, AEs (63.6%), lack of beneficial effect (16.4%), and participation in a clinical trial (9.1%). Bodyweight and hematologic parameters largely remained stable before and after switching between ERT and SRT, although with substantial variation between patients. These findings contribute to understanding why treatment switching occurs in patients with GD, and may help physicians recognize the real-world impact of treatment switching between ERT and SRT for patients with GD.

摘要

在1型戈谢病(GD1)患者中,在酶替代疗法(ERT)和底物减少疗法(SRT)之间切换并不罕见;然而,切换治疗的原因尚未得到详细探讨。来自戈谢病结果调查(GOS)的数据,这是一个针对确诊戈谢病患者的国际登记处,被用于评估在这两种治疗类型之间切换的原因及后果。在2020年2月25日登记参加GOS的1843名患者中,有245名患者进行了治疗切换:222名从初始的ERT切换到SRT(其中88名后来又切换回ERT),23名从初始的SRT切换到ERT。从ERT切换到SRT的最常见原因是输液时间(25.4%)、药物短缺(22.0%)和不良事件(AE;11.9%),而从SRT切换到ERT的原因是AE(63.6%)、缺乏有益效果(16.4%)和参与临床试验(9.1%)。尽管患者之间存在很大差异,但在ERT和SRT之间切换前后,体重和血液学参数大体上保持稳定。这些发现有助于理解为什么戈谢病患者会发生治疗切换,并可能帮助医生认识到ERT和SRT之间的治疗切换对戈谢病患者的实际影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46dd/9457166/1526b5845117/jcm-11-05158-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46dd/9457166/38ed88940cc9/jcm-11-05158-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46dd/9457166/8619e9ada36f/jcm-11-05158-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46dd/9457166/7e8edfe2ff44/jcm-11-05158-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46dd/9457166/1526b5845117/jcm-11-05158-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46dd/9457166/38ed88940cc9/jcm-11-05158-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46dd/9457166/8619e9ada36f/jcm-11-05158-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46dd/9457166/7e8edfe2ff44/jcm-11-05158-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46dd/9457166/1526b5845117/jcm-11-05158-g004.jpg

相似文献

1
Switching between Enzyme Replacement Therapies and Substrate Reduction Therapies in Patients with Gaucher Disease: Data from the Gaucher Outcome Survey (GOS).戈谢病患者在酶替代疗法和底物减少疗法之间的转换:来自戈谢病结果调查(GOS)的数据。
J Clin Med. 2022 Aug 31;11(17):5158. doi: 10.3390/jcm11175158.
2
Impact on bone microarchitecture and failure load in a patient with type I Gaucher disease who switched from Imiglucerase to Eliglustat.一名从伊米苷酶转换为依利格鲁司他的I型戈谢病患者的骨微结构和破坏载荷受到的影响。
Mol Genet Metab Rep. 2020 May 30;24:100606. doi: 10.1016/j.ymgmr.2020.100606. eCollection 2020 Sep.
3
Incremental biomarker and clinical outcomes after switch from enzyme therapy to eliglustat substrate reduction therapy in Gaucher disease.戈谢病从酶替代疗法转换为依洛尤单抗底物减少疗法后的增量生物标志物与临床结局
Mol Genet Metab Rep. 2021 Aug 28;29:100798. doi: 10.1016/j.ymgmr.2021.100798. eCollection 2021 Dec.
4
Characteristics of 26 patients with type 3 Gaucher disease: A descriptive analysis from the Gaucher Outcome Survey.26例3型戈谢病患者的特征:来自戈谢病结局调查的描述性分析
Mol Genet Metab Rep. 2017 Dec 27;14:73-79. doi: 10.1016/j.ymgmr.2017.10.011. eCollection 2018 Mar.
5
Real-Life Experience with Oral Eliglustat in Patients with Gaucher Disease Previously Treated with Enzyme Replacement Therapy.口服 eliglustat 治疗既往接受过酶替代疗法的戈谢病患者的真实生活经验。
J Clin Med. 2022 Oct 24;11(21):6265. doi: 10.3390/jcm11216265.
6
Long-Term Treatment of Gaucher Disease with Velaglucerase Alfa in ERT-Naïve Patients from the Gaucher Outcome Survey (GOS) Registry.来自戈谢病结局调查(GOS)登记处的初治患者使用阿加糖酶α进行戈谢病的长期治疗。
J Clin Med. 2024 May 9;13(10):2782. doi: 10.3390/jcm13102782.
7
High-Dose Ambroxol Therapy in Type 1 Gaucher Disease Focusing on Patients with Poor Response to Enzyme Replacement Therapy or Substrate Reduction Therapy.高剂量氨溴索治疗 1 型戈谢病:重点关注对酶替代疗法或底物减少疗法反应不佳的患者。
Int J Mol Sci. 2023 Apr 4;24(7):6732. doi: 10.3390/ijms24076732.
8
Osteonecrosis in Gaucher disease in the era of multiple therapies: Biomarker set for risk stratification from a tertiary referral center.戈谢病中的骨坏死:来自三级转诊中心的风险分层生物标志物集。
Elife. 2023 May 30;12:e87537. doi: 10.7554/eLife.87537.
9
Long-Term Evaluation of Biomarkers in the Czech Cohort of Gaucher Patients.捷克戈谢病患者队列的生物标志物长期评估。
Int J Mol Sci. 2023 Sep 22;24(19):14440. doi: 10.3390/ijms241914440.
10
Changes of bone metabolism in seven patients with Gaucher disease treated consecutively with imiglucerase and miglustat.七例接受伊米苷酶和米格列醇序贯治疗的戈谢病患者的骨代谢变化
Calcif Tissue Int. 2008 Jul;83(1):43-54. doi: 10.1007/s00223-008-9143-4. Epub 2008 Jun 14.

引用本文的文献

1
Eliglustat and cardiac comorbidities in Gaucher disease: a pharmacogenomic approach to safety and efficacy.依利格鲁司他与戈谢病的心脏合并症:一种关于安全性和疗效的药物基因组学方法
Front Med (Lausanne). 2025 Mar 17;12:1535099. doi: 10.3389/fmed.2025.1535099. eCollection 2025.
2
Safety analysis of self-administered enzyme replacement therapy using data from the Fabry Outcome and Gaucher Outcome Surveys.利用法布里病结局和戈谢病结局调查的数据对自我给药酶替代疗法进行安全性分析。
Orphanet J Rare Dis. 2025 Mar 28;20(1):145. doi: 10.1186/s13023-024-03416-2.
3
Targeting Glucosylceramide Synthase: Innovative Drug Repurposing Strategies for Lysosomal Diseases.

本文引用的文献

1
Incremental biomarker and clinical outcomes after switch from enzyme therapy to eliglustat substrate reduction therapy in Gaucher disease.戈谢病从酶替代疗法转换为依洛尤单抗底物减少疗法后的增量生物标志物与临床结局
Mol Genet Metab Rep. 2021 Aug 28;29:100798. doi: 10.1016/j.ymgmr.2021.100798. eCollection 2021 Dec.
2
Real-world effectiveness of eliglustat in treatment-naïve and switch patients enrolled in the International Collaborative Gaucher Group Gaucher Registry.真实世界中依利格鲁司他在国际协作 Gaucher 小组 Gaucher 注册研究中初治和换药患者中的疗效。
Am J Hematol. 2020 Sep;95(9):1038-1046. doi: 10.1002/ajh.25875. Epub 2020 Jun 24.
3
靶向葡萄糖神经酰胺合酶:溶酶体疾病的创新药物再利用策略
Int J Mol Sci. 2025 Feb 28;26(5):2195. doi: 10.3390/ijms26052195.
4
Reply to Mistry et al. The Two Substrate Reduction Therapies for Type 1 Gaucher Disease Are Not Equivalent. Comment on "Hughes et al. Switching between Enzyme Replacement Therapies and Substrate Reduction Therapies in Patients with Gaucher Disease: Data from the Gaucher Outcome Survey (GOS). 2022, , 5158".对米斯特里等人的回复。1型戈谢病的两种底物还原疗法并不等效。对“休斯等人。戈谢病患者酶替代疗法和底物还原疗法之间的转换:来自戈谢病结局调查(GOS)的数据。2022年,,5158”的评论。
J Clin Med. 2023 Jun 13;12(12):4017. doi: 10.3390/jcm12124017.
5
Osteonecrosis in Gaucher disease in the era of multiple therapies: Biomarker set for risk stratification from a tertiary referral center.戈谢病中的骨坏死:来自三级转诊中心的风险分层生物标志物集。
Elife. 2023 May 30;12:e87537. doi: 10.7554/eLife.87537.
6
The Two Substrate Reduction Therapies for Type 1 Gaucher Disease Are Not Equivalent. Comment on Hughes et al. Switching between Enzyme Replacement Therapies and Substrate Reduction Therapies in Patients with Gaucher Disease: Data from the Gaucher Outcome Survey (GOS). 2022, , 5158.1型戈谢病的两种底物还原疗法并不等效。对休斯等人的评论。戈谢病患者在酶替代疗法和底物还原疗法之间的转换:来自戈谢病结果调查(GOS)的数据。2022年,,5158。
J Clin Med. 2023 May 4;12(9):3269. doi: 10.3390/jcm12093269.
7
Case report: Multidisciplinary collaboration in diagnosis and treatment of child gaucher disease.病例报告:儿童戈谢病诊断与治疗中的多学科协作
Front Pediatr. 2023 Mar 30;11:1057574. doi: 10.3389/fped.2023.1057574. eCollection 2023.
8
High-Dose Ambroxol Therapy in Type 1 Gaucher Disease Focusing on Patients with Poor Response to Enzyme Replacement Therapy or Substrate Reduction Therapy.高剂量氨溴索治疗 1 型戈谢病:重点关注对酶替代疗法或底物减少疗法反应不佳的患者。
Int J Mol Sci. 2023 Apr 4;24(7):6732. doi: 10.3390/ijms24076732.
9
Gene Therapy of Sphingolipid Metabolic Disorders.鞘脂代谢障碍的基因治疗。
Int J Mol Sci. 2023 Feb 11;24(4):3627. doi: 10.3390/ijms24043627.
Real-World Patient Experience of Switching Biologic Treatment in Inflammatory Arthritis and Ulcerative Colitis - A Systematic Literature Review.
炎症性关节炎和溃疡性结肠炎患者转换生物治疗的真实世界体验——一项系统文献综述
Patient Prefer Adherence. 2020 Feb 17;14:309-320. doi: 10.2147/PPA.S238843. eCollection 2020.
4
Reasons to switch: a noninterventional study evaluating immunotherapy switches in a large German multicentre cohort of patients with relapsing-remitting multiple sclerosis.换药原因:一项非干预性研究,评估德国一个大型多中心复发缓解型多发性硬化症患者队列中的免疫治疗换药情况。
Ther Adv Neurol Disord. 2019 Dec 19;12:1756286419892077. doi: 10.1177/1756286419892077. eCollection 2019.
5
Long-term adverse event profile from four completed trials of oral eliglustat in adults with Gaucher disease type 1.来自四项已完成的口服 eliglustat 治疗 1 型戈谢病成人患者的长期不良事件概况。
Orphanet J Rare Dis. 2019 Jun 7;14(1):128. doi: 10.1186/s13023-019-1085-6.
6
Enzyme Replacement Therapy: A Review and Its Role in Treating Lysosomal Storage Diseases.酶替代疗法:综述及其在治疗溶酶体贮积症中的作用
Pediatr Ann. 2018 May 1;47(5):e191-e197. doi: 10.3928/19382359-20180424-01.
7
Pharmacotherapy of Gaucher Disease: Current and Future Options.戈谢病的药物治疗:现状与未来选择
P T. 2018 May;43(5):274-309.
8
Attitudes of Individuals with Gaucher Disease toward Substrate Reduction Therapies.戈谢病患者对底物减少疗法的态度。
J Genet Couns. 2018 Feb;27(1):169-176. doi: 10.1007/s10897-017-0137-0. Epub 2017 Aug 13.
9
Outcomes after 18 months of eliglustat therapy in treatment-naïve adults with Gaucher disease type 1: The phase 3 ENGAGE trial.18个月依利格鲁司他治疗初治1型戈谢病成年患者的疗效:3期ENGAGE试验。
Am J Hematol. 2017 Nov;92(11):1170-1176. doi: 10.1002/ajh.24877. Epub 2017 Oct 3.
10
Long-term safety and efficacy of taliglucerase alfa in pediatric Gaucher disease patients who were treatment-naïve or previously treated with imiglucerase.对于初治或曾接受过伊米苷酶治疗的戈谢病儿科患者,taliglucerase alfa的长期安全性和疗效。
Blood Cells Mol Dis. 2018 Feb;68:163-172. doi: 10.1016/j.bcmd.2016.10.005. Epub 2016 Oct 20.