PTPRZ1-METFUsion基因(ZM-FUGEN)试验:一项多中心、随机、开放标签II/III期试验的研究方案。

Zhaoshi Bao, Shouwei Li, Liang Wang, Bisi Zhang, Peilong Zhang, Hepeng Shi, Xiaoguang Qiu, Tao Jiang
{"title":"PTPRZ1-METFUsion基因(ZM-FUGEN)试验:一项多中心、随机、开放标签II/III期试验的研究方案。","authors":"Zhaoshi Bao,&nbsp;Shouwei Li,&nbsp;Liang Wang,&nbsp;Bisi Zhang,&nbsp;Peilong Zhang,&nbsp;Hepeng Shi,&nbsp;Xiaoguang Qiu,&nbsp;Tao Jiang","doi":"10.1186/s41016-023-00329-0","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>PTPRZ1-MET fusion was reported to associate with glioma progression from low-grade to high-grade glioma, which was a target by a MET inhibitor vebreltinib. However, little is known about the further efficacy of vebreltinib among more glioma patients. This trial aims to evaluate the safety and efficacy of vebreltinib enteric-coated capsules in the treatment of sGBM/IDH mutant glioblastoma patients with the ZM fusion gene.</p><p><strong>Methods: </strong>This multicentric, randomized, open-label, controlled trial plans to include 19 neurosurgical centers and recruit 84 sGBM or IDH mutant glioblastoma patients with the ZM fusion gene. This trial enrolls sGBM or IDH mutant glioblastoma patients with the inclusion criteria and without the exclusion criteria. It was registered with chinadrugtrials.org.cn (CTR20181664). The primary efficacy endpoint is overall survival (OS). The secondary endpoints are progression-free survival (PFS) and objective response rate (ORR).</p><p><strong>Discussion: </strong>If proven effective, this targeted multifaceted intervention protocol will be extended for more glioma patients as a protocol to evaluate the safety and efficacy of MET inhibitors.</p><p><strong>Trial registration: </strong>It was registered with chinadrugtrials.org.cn (CTR20181664).</p>","PeriodicalId":36700,"journal":{"name":"Chinese Neurosurgical Journal","volume":"9 1","pages":"21"},"PeriodicalIF":0.0000,"publicationDate":"2023-07-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10347714/pdf/","citationCount":"0","resultStr":"{\"title\":\"PTPRZ1-METFUsion GENe (ZM-FUGEN) trial: study protocol for a multicentric, randomized, open-label phase II/III trial.\",\"authors\":\"Zhaoshi Bao,&nbsp;Shouwei Li,&nbsp;Liang Wang,&nbsp;Bisi Zhang,&nbsp;Peilong Zhang,&nbsp;Hepeng Shi,&nbsp;Xiaoguang Qiu,&nbsp;Tao Jiang\",\"doi\":\"10.1186/s41016-023-00329-0\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>PTPRZ1-MET fusion was reported to associate with glioma progression from low-grade to high-grade glioma, which was a target by a MET inhibitor vebreltinib. However, little is known about the further efficacy of vebreltinib among more glioma patients. This trial aims to evaluate the safety and efficacy of vebreltinib enteric-coated capsules in the treatment of sGBM/IDH mutant glioblastoma patients with the ZM fusion gene.</p><p><strong>Methods: </strong>This multicentric, randomized, open-label, controlled trial plans to include 19 neurosurgical centers and recruit 84 sGBM or IDH mutant glioblastoma patients with the ZM fusion gene. This trial enrolls sGBM or IDH mutant glioblastoma patients with the inclusion criteria and without the exclusion criteria. It was registered with chinadrugtrials.org.cn (CTR20181664). The primary efficacy endpoint is overall survival (OS). The secondary endpoints are progression-free survival (PFS) and objective response rate (ORR).</p><p><strong>Discussion: </strong>If proven effective, this targeted multifaceted intervention protocol will be extended for more glioma patients as a protocol to evaluate the safety and efficacy of MET inhibitors.</p><p><strong>Trial registration: </strong>It was registered with chinadrugtrials.org.cn (CTR20181664).</p>\",\"PeriodicalId\":36700,\"journal\":{\"name\":\"Chinese Neurosurgical Journal\",\"volume\":\"9 1\",\"pages\":\"21\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-07-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10347714/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chinese Neurosurgical Journal\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1186/s41016-023-00329-0\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chinese Neurosurgical Journal","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1186/s41016-023-00329-0","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

摘要

背景:据报道,PTPRZ1-MET融合与胶质瘤从低级别到高级别的进展有关,这是MET抑制剂vebreltinib的靶点。然而,对于vebreltinib在更多神经胶质瘤患者中的进一步疗效知之甚少。本试验旨在评价vebreltinib肠溶胶囊治疗ZM融合基因的sGBM/IDH突变型胶质母细胞瘤患者的安全性和有效性。方法:这项多中心、随机、开放标签、对照试验计划纳入19个神经外科中心,招募84例具有ZM融合基因的sGBM或IDH突变胶质母细胞瘤患者。该试验招募了sGBM或IDH突变胶质母细胞瘤患者,有纳入标准,没有排除标准。注册号为chinadrutrials.org.cn (CTR20181664)。主要疗效终点是总生存期(OS)。次要终点是无进展生存期(PFS)和客观缓解率(ORR)。讨论:如果证明有效,这种靶向多方面干预方案将扩展到更多的胶质瘤患者,作为评估MET抑制剂安全性和有效性的方案。试验注册:注册号为chinadrutrials.org.cn (CTR20181664)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
PTPRZ1-METFUsion GENe (ZM-FUGEN) trial: study protocol for a multicentric, randomized, open-label phase II/III trial.

Background: PTPRZ1-MET fusion was reported to associate with glioma progression from low-grade to high-grade glioma, which was a target by a MET inhibitor vebreltinib. However, little is known about the further efficacy of vebreltinib among more glioma patients. This trial aims to evaluate the safety and efficacy of vebreltinib enteric-coated capsules in the treatment of sGBM/IDH mutant glioblastoma patients with the ZM fusion gene.

Methods: This multicentric, randomized, open-label, controlled trial plans to include 19 neurosurgical centers and recruit 84 sGBM or IDH mutant glioblastoma patients with the ZM fusion gene. This trial enrolls sGBM or IDH mutant glioblastoma patients with the inclusion criteria and without the exclusion criteria. It was registered with chinadrugtrials.org.cn (CTR20181664). The primary efficacy endpoint is overall survival (OS). The secondary endpoints are progression-free survival (PFS) and objective response rate (ORR).

Discussion: If proven effective, this targeted multifaceted intervention protocol will be extended for more glioma patients as a protocol to evaluate the safety and efficacy of MET inhibitors.

Trial registration: It was registered with chinadrugtrials.org.cn (CTR20181664).

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
2.70
自引率
0.00%
发文量
224
审稿时长
10 weeks
期刊最新文献
Nonadjustable state of programmable shunt valve: obstruction of middle cranial fossa arachnoid cyst-peritoneal shunt. Emergency neurosurgical hybrid operating platform for acute intracranial hemorrhage (E-HOPE). Extubation timing and risk of extubation failure in aneurysmal subarachnoid hemorrhage patients. Radiographic predictors of peritumoral brain edema in intracranial meningiomas: a review of current controversies and illustrative cases. Comparison of ketorolac intravenous versus acetaminophen intravenous in treating headache following head trauma: a semi-experimental study.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1