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ivosidenib:晚期胆管癌治疗的研究进展。

Ivosidenib: A Review in Advanced Cholangiocarcinoma.

机构信息

Springer Nature, Mairangi Bay, Private Bag 65901, Auckland, 0754, New Zealand.

出版信息

Target Oncol. 2023 Nov;18(6):973-980. doi: 10.1007/s11523-023-01002-3. Epub 2023 Oct 19.

Abstract

Ivosidenib (Tibsovo), a first-in-class, oral small molecule, potent and selective inhibitor of mutant isocitrate dehydrogenase 1 (mIDH1), is approved in the EU and USA for the treatment of adults with pretreated, advanced, mIDH1 cholangiocarcinoma (CCA). It is presumed to exert its cytostatic effects in this setting by suppressing 2-hydroxyglutarate, an oncometabolite produced by mIDH1 that impairs cellular differentiation and promotes tumorigenesis. In the multinational phase 3 ClarIDHy study in patients with pretreated, advanced mIDH1 CCA, monotherapy with ivosidenib once daily significantly prolonged progression-free survival (PFS) and almost doubled the disease control rate compared with placebo. Moreover, it had a favourable effect on overall survival (OS), which was also significantly prolonged after correcting for a high rate of crossover from the placebo group (permitted by the trial protocol). Ivosidenib treatment preserved health-related quality of life (HRQOL) relating to physical function, pain and appetite loss/eating and was generally well tolerated, with the most common treatment-emergent adverse events being low-grade diarrhoea, nausea and fatigue. Thus, ivosidenib represents a novel and valuable targeted therapy for the subset of patients with pretreated, advanced CCA tumors harbouring mIDH1.

摘要

依维莫司(Tibsovo),一种首创的、口服小分子、强效且选择性的突变型异柠檬酸脱氢酶 1(mIDH1)抑制剂,在欧盟和美国获批用于治疗先前治疗过的、晚期的 mIDH1 胆管癌(CCA)成人患者。它被认为通过抑制 2-羟基戊二酸发挥其细胞抑制作用,2-羟基戊二酸是 mIDH1 产生的致癌代谢物,会损害细胞分化并促进肿瘤发生。在多国、三期 ClarIDHy 研究中,在先前治疗过的、晚期的 mIDH1 CCA 患者中,每日一次的依维莫司单药治疗与安慰剂相比,显著延长了无进展生存期(PFS),并使疾病控制率几乎翻倍。此外,它对总生存期(OS)也有积极影响,在按试验方案允许的安慰剂组交叉率较高进行校正后,OS 也显著延长。依维莫司治疗保持了与身体功能、疼痛和食欲丧失/进食相关的健康相关生活质量(HRQOL),并且总体耐受性良好,最常见的治疗相关不良事件为低级别腹泻、恶心和疲劳。因此,依维莫司代表了一种新型、有价值的针对先前治疗过的、晚期 CCA 肿瘤且携带 mIDH1 的患者的靶向治疗药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6f4/11467016/28af484c62c8/11523_2023_1002_Fig1_HTML.jpg

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