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Postoperative radiotherapy with concomitant temozolomide plus anlotinib for newly diagnosed glioblastoma: Study protocol for a multicenter, double-blind, randomized phase II trial

Authors :
Yuanyuan Chen
Baiqiang Dong
Guihong Liu
Pengfei Sun
Meihua Li
Xuejun Yang
Shiyu Feng
Liang Wang
Yonghong Hua
Ming Zhao
Yanhui Liu
Juntao Ran
Li Qiao
Xueguan Lu
Hao Jiang
Deqiang Mao
Junxin Wu
Xianming Li
Wei Zheng
Zhigang Liu
Song Lin
Meiling Deng
Qunying Yang
Chengcheng Guo
Jing Li
Zhong-ping Chen
Source :
Glioma, Vol 5, Iss 2, Pp 69-76 (2022)
Publication Year :
2022
Publisher :
Wolters Kluwer Medknow Publications, 2022.

Abstract

Background and Aim: Postoperative radiotherapy with concomitant temozolomide (TMZ) followed by ≤ six cycles of adjuvant TMZ chemotherapy (Stupp regimen) is the standard treatment for newly diagnosed glioblastoma (GBM); however, its effectiveness is limited. Anlotinib inhibits both tumor angiogenesis and tumor cell proliferation by targeting multiple kinases, and showing promising results in preclinical GBM models. We designed a Phase II trial to assess the efficacy and safety of the Stupp regimen plus anlotinib. Methods/Design: This is a multicenter, double-blind, randomized, placebo-controlled trial with an expected 150 patients randomly assigned 1:1 ratio to receive TMZ-based radiochemotherapy with anlotinib (Stupp regimen + anlotinib) or placebo (Stupp regimen + placebo). Postoperative patient recruitment will begin in July 2021, the analysis of primary outcome measures will be completed in July 2023, and the study will finish in July 2024. Major eligibility criteria include histologically confirmed newly diagnosed GBM and an Eastern Cooperative Oncology Group performance score ≤2. Other criteria for inclusion include age ≥18 years and lack of significant comorbidity. In this study, the primary endpoint will be the median progression-free survival (PFS). Secondary endpoints include 1-year overall survival rate, PFS at 6 months, overall response rate, duration of response, disease control rate, quality of life, and toxicity. The protocol has received approval from Sun Yat-sen University Cancer Center Ethics Committee (Approval No. B2021-073-01; approved on April 19, 2021). Discussion: Updated treatment modalities are required for newly diagnosed GBM. Our proposed treatment modality of the Stupp regimen combined with anlotinib therapy are waiting conclusion. Trial Registration: This study was registered with ClinicalTrials.gov under identifier NCT04959500 on July 13, 2021.

Details

Language :
English
ISSN :
25896113 and 25896121
Volume :
5
Issue :
2
Database :
Directory of Open Access Journals
Journal :
Glioma
Publication Type :
Academic Journal
Accession number :
edsdoj.957d382a6ece4f998758a2f022104d7f
Document Type :
article
Full Text :
https://doi.org/10.4103/glioma.glioma_17_22