IDH1抑制剂Ivosidenib用于复发性IDH1突变胶质母细胞瘤患者:来自I期研究的病例报告

Q1 Medicine
CNS Oncology Pub Date : 2020-09-01 Epub Date: 2020-07-27 DOI:10.2217/cns-2020-0014
Dalissa Tejera, Marina Kushnirsky, Sakir H Gultekin, Min Lu, Lori Steelman, Macarena I de la Fuente
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引用次数: 18

摘要

胶质母细胞瘤是最常见、侵袭性最强的原发性脑肿瘤。尽管标准的多模式治疗,中位总生存率仍然很低,大多数研究的5年生存率约为5%(范围为4.7% -13.0%)。针对IDH突变的强烈兴趣导致了血液恶性肿瘤和实体肿瘤的各种研究,并批准了IDH抑制剂,如IDH1抑制剂ivosidenib,用于血液恶性肿瘤。在这里,我们提出了第一例复发性idh1突变胶质母细胞瘤患者的病例研究,该患者在接受伊沃西迪尼治疗后,癫痫发作控制得到改善,放射学上病情稳定超过4年。这些发现支持进一步开发IDH抑制剂作为单一药物和/或联合治疗IDH突变胶质瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Ivosidenib, an IDH1 inhibitor, in a patient with recurrent, <i>IDH1</i>-mutant glioblastoma: a case report from a Phase I study.

Ivosidenib, an IDH1 inhibitor, in a patient with recurrent, <i>IDH1</i>-mutant glioblastoma: a case report from a Phase I study.

Ivosidenib, an IDH1 inhibitor, in a patient with recurrent, IDH1-mutant glioblastoma: a case report from a Phase I study.

Glioblastoma is the most common and aggressive primary brain tumor. Despite standard multimodality therapy, median overall survival remains poor with a 5-year survival rate of approximately 5% in most studies (range 4.7-13.0%). Strong interest in targeting IDH mutations has led to a variety of studies in both hematologic malignancies and solid tumors and to the approval of IDH inhibitors such as ivosidenib, an IDH1 inhibitor, in hematologic malignancies. Here, we present the first case study of a patient with a recurrent IDH1-mutant glioblastoma who experienced improved seizure control and radiographic stable disease for more than 4 years while treated with ivosidenib. Such findings support the further development of IDH inhibitors as single agents and/or in combination for the treatment of IDH-mutant glioma.

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来源期刊
CNS Oncology
CNS Oncology Medicine-Neurology (clinical)
CiteScore
3.80
自引率
0.00%
发文量
12
审稿时长
13 weeks
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