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阿糖胞苷和米托蒽醌联合去米替特治疗急性髓系白血病的 II 期临床试验。

Phase II trial of cytarabine and mitoxantrone with devimistat in acute myeloid leukemia.

机构信息

Section on Hematology and Oncology, Comprehensive Cancer Center of Atrium Health Wake Forest Baptist, Winston-Salem, NC, USA.

Department of Cancer Biology, Comprehensive Cancer Center of Atrium Health Wake Forest Baptist, Winston-Salem, NC, USA.

出版信息

Nat Commun. 2022 Mar 30;13(1):1673. doi: 10.1038/s41467-022-29039-4.

DOI:10.1038/s41467-022-29039-4
PMID:35354808
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8967916/
Abstract

Devimistat is a TCA cycle inhibitor. A previously completed phase I study of devimistat in combination with cytarabine and mitoxantrone in patients with relapsed or refractory AML showed promising response rates. Here we report the results of a single arm phase II study (NCT02484391). The primary outcome of feasibility of maintenance devimistat following induction and consolidation with devimistat in combination with high dose cytarabine and mitoxantrone was not met, as maintenance devimistat was only administered in 2 of 21 responders. The secondary outcomes of response (CR + CRi) and median survival were 44% (21/48) and 5.9 months respectively. There were no unexpected toxicities observed. An unplanned, post-hoc analysis of the phase I and II datasets suggests a trend of a dose response in older but not younger patients. RNA sequencing data from patient samples reveals an age-related decline in mitochondrial gene sets. Devimistat impairs ATP synthesis and we find a correlation between mitochondrial membrane potential and sensitivity to chemotherapy. Devimistat also induces mitochondrial reactive oxygen species and turnover consistent with mitophagy. We find that pharmacological or genetic inhibition of mitochondrial fission or autophagy sensitizes cells to devimistat. These findings suggest that an age related decline in mitochondrial quality and autophagy may be associated with response to devimistat however this needs to be confirmed in larger cohorts with proper trial design.

摘要

地维司他是三羧酸(TCA)循环抑制剂。此前完成的一项地维司他联合阿糖胞苷和米托蒽醌治疗复发/难治性急性髓系白血病(AML)的 I 期研究显示出有前景的缓解率。在此,我们报告了一项单臂 II 期研究(NCT02484391)的结果。诱导和巩固治疗后使用地维司他维持治疗的可行性是主要终点,未达到,因为只有 21 名缓解者中的 2 人接受了地维司他维持治疗。次要终点为缓解率(完全缓解+部分缓解)和中位总生存期,分别为 44%(21/48)和 5.9 个月。未观察到意外毒性。对地维司他 I 期和 II 期数据集的计划外事后分析表明,老年患者而非年轻患者存在剂量反应趋势。来自患者样本的 RNA 测序数据显示,线粒体基因集随年龄增长而下降。地维司他会损害 ATP 合成,我们发现线粒体膜电位与对化疗的敏感性之间存在相关性。地维司他还会诱导与线粒体自噬一致的线粒体活性氧和周转率。我们发现,抑制线粒体分裂或自噬的药理学或遗传学方法可使细胞对地维司他敏感。这些发现表明,线粒体质量和自噬随年龄增长而下降可能与对地维司他的反应相关,但这需要在具有适当试验设计的更大队列中得到证实。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba98/8967916/e75dce2b0243/41467_2022_29039_Fig6_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba98/8967916/8b0ae09e4f95/41467_2022_29039_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba98/8967916/e75dce2b0243/41467_2022_29039_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba98/8967916/d419be7961a1/41467_2022_29039_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba98/8967916/7d75626d3767/41467_2022_29039_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba98/8967916/b75a953db535/41467_2022_29039_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba98/8967916/f80fa7a5aa52/41467_2022_29039_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba98/8967916/8b0ae09e4f95/41467_2022_29039_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba98/8967916/e75dce2b0243/41467_2022_29039_Fig6_HTML.jpg

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