A perioperative study of Safusidenib in patients with IDH1-mutated glioma

被引:1
作者
Cain, Sarah A. [1 ]
Topp, Monique [2 ]
Rosenthal, Mark [2 ]
Tobler, Robert [3 ]
Freytag, Saskia [3 ,4 ]
Best, Sarah A. [3 ,4 ]
Whittle, James R. [2 ,3 ,4 ]
Drummond, Katharine J. [1 ,5 ]
机构
[1] Royal Melbourne Hosp, Dept Neurosurg, Parkville 3052, Australia
[2] Peter MacCallum Canc Ctr, Dept Med Oncol, Melbourne 3000, Australia
[3] Walter & Eliza Hall Inst Med Res, Personalised Oncol Div, Parkville 3052, Australia
[4] Univ Melbourne, Dept Med Biol, Parkville 3052, Australia
[5] Univ Melbourne, Royal Melbourne Hosp, Fac Med Dent & Hlth Sci, Melbourne Med Sch,Dept Surg, Parkville 3052, Australia
关键词
AB-218; isocitrate dehydrogenase 1; IDH1; low grade glioma; Phase; 0; safusidenib; window of opportunity; LOW-GRADE GLIOMA; ISOCITRATE DEHYDROGENASE 1; CENTRAL-NERVOUS-SYSTEM; RESPONSE ASSESSMENT; SURGICAL RESECTION; MUTATIONS; IDH1; GLIOBLASTOMA; RADIATION; EXTENT;
D O I
10.1080/14796694.2024.2383064
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This is a single arm, open label perioperative trial to assess the feasibility, pharmacokinetics and pharmacodynamics of treatment with safusidenib following biopsy, and prior to surgical resection in patients with IDH1 mutated glioma who have not received radiation therapy or chemotherapy. Fifteen participants will receive treatment in two parts. First, biopsy followed by one cycle (28 days) of safusidenib, an orally available, small molecular inhibitor of mutated IDH1, then maximal safe resection of the tumor (Part A). Second, after recovery from surgery, safusidenib until disease progression or unacceptable toxicity (Part B). This research will enable objective measurement of biological activity of safusidenib in patients with IDH1 mutated glioma. Anti-tumor activity will be assessed by progression free survival and time to next intervention. Plain language summary: Adult low-grade gliomas (aLGG) are primary brain cancers, defined by mutations in IDH1 or IDH2. When the IDH gene becomes abnormal (mutated), production of a metabolite that causes cancer cells to grow is increased. These tumors grow slowly but invade the normal functioning brain, making them nearly impossible to cure. The current standard of care treatment includes surgery, followed by radiation therapy and chemotherapy, the timing of which depends on the risk of cancer regrowth. Some patients may be suitable for monitoring with MRI scans alone, however recurrences will inevitably occur. Recently developed targeted mutant IDH inhibitors for aLGG patients may be beneficial both at diagnosis and recurrence. Notably, early treatment prior to radiation therapy and chemotherapy delays growth of aLGG and the need for subsequent radiation therapy and chemotherapy. Nevertheless, most patients will eventually suffer further tumor growth and the optimal timing and sequencing of these therapies remains an area of active research. This research investigates the mutant IDH1 inhibitor safusidenib. The researchers are conducting an innovative clinical trial where patients with aLGG, who have not received radiation therapy or chemotherapy, are treated with safusidenib following a biopsy and prior to surgical removal of their tumor. In this study they investigate whether this trial design is safe and feasible, and how safusidenib works; with the goal to better understand the optimal use of IDH inhibitors for patients with aLGG.
引用
收藏
页码:2533 / 2545
页数:13
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