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PTPRZ1-METFUsion GENe (ZM-FUGEN) trial: study protocol for a multicentric, randomized, open-label phase II/III trial.
Bao, Zhaoshi; Li, Shouwei; Wang, Liang; Zhang, Bisi; Zhang, Peilong; Shi, Hepeng; Qiu, Xiaoguang; Jiang, Tao.
Afiliação
  • Bao Z; Department of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, 100070, China.
  • Li S; Chinese Glioma Genome Atlas Network (CGGA) and Asian Glioma Genome Atlas Network (AGGA), Beijing, China.
  • Wang L; Chinese Glioma Genome Atlas Network (CGGA) and Asian Glioma Genome Atlas Network (AGGA), Beijing, China.
  • Zhang B; Department of Neurosurgery, Sanbo Brain Hospital, Capital Medical University, Beijing, 100093, China.
  • Zhang P; Chinese Glioma Genome Atlas Network (CGGA) and Asian Glioma Genome Atlas Network (AGGA), Beijing, China.
  • Shi H; Department of Neurosurgery, Tangdu Hospital, Fourth Military Medical University, Xi'an, China.
  • Qiu X; Beijing Pearl Biotechnology Limited Liability Company, Beijing, China.
  • Jiang T; Beijing Pearl Biotechnology Limited Liability Company, Beijing, China.
Chin Neurosurg J ; 9(1): 21, 2023 Jul 14.
Article em En | MEDLINE | ID: mdl-37443050
ABSTRACT

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).
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Guideline Idioma: En Revista: Chin Neurosurg J Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Guideline Idioma: En Revista: Chin Neurosurg J Ano de publicação: 2023 Tipo de documento: Article