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二甲双胍联合替莫唑胺治疗新诊断的胶质母细胞瘤:I期研究结果及相关研究简要综述

Metformin with Temozolomide for Newly Diagnosed Glioblastoma: Results of Phase I Study and a Brief Review of Relevant Studies.

作者信息

Ohno Makoto, Kitanaka Chifumi, Miyakita Yasuji, Tanaka Shota, Sonoda Yukihiko, Mishima Kazuhiko, Ishikawa Eiichi, Takahashi Masamichi, Yanagisawa Shunsuke, Ohashi Ken, Nagane Motoo, Narita Yoshitaka

机构信息

Department of Neurosurgery and Neuro-Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan.

Department of Molecular Cancer Science, Faculty of Medicine, Yamagata University, Yamagata 990-9585, Japan.

出版信息

Cancers (Basel). 2022 Aug 30;14(17):4222. doi: 10.3390/cancers14174222.

DOI:10.3390/cancers14174222
PMID:36077758
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9454846/
Abstract

Glioblastoma (GBM) inevitably recurs due to a resistance to current standard therapy. We showed that the antidiabetic drug metformin (MF) can induce the differentiation of stem-like glioma-initiating cells and suppress tumor formation through AMPK-FOXO3 activation. In this study, we design a phase I/II study to examine the clinical effect of MF. We aim to determine a recommended phase II MF dose with maintenance temozolomide (TMZ) in patients with newly diagnosed GBM who completed standard concomitant radiotherapy and TMZ. MF dose-escalation was planned using a 3 + 3 design. Dose-limiting toxicities (DLTs) were assessed during the first six weeks after MF initiation. Three patients were treated with 1500 mg/day MF and four patients were treated with 2250 mg/day MF between February 2021 and January 2022. No DLTs were observed. The most common adverse effects were appetite loss, nausea, and diarrhea, all of which were manageable. Two patients experienced tumor progression at 6.0 and 6.1 months, and one died 12.2 months after initial surgery. The other five patients remained stable at the last follow-up session. The MF dose of up to 2250 mg/day combined with maintenance TMZ appeared to be well tolerated, and we proceeded to a phase II study with 2250 mg/day MF.

摘要

胶质母细胞瘤(GBM)由于对当前标准治疗产生耐药性而不可避免地复发。我们发现抗糖尿病药物二甲双胍(MF)可通过激活AMPK-FOXO3诱导干细胞样胶质瘤起始细胞分化并抑制肿瘤形成。在本研究中,我们设计了一项I/II期研究以检验MF的临床疗效。我们旨在确定在完成标准同步放疗和替莫唑胺(TMZ)治疗的新诊断GBM患者中,联合维持性TMZ使用时MF的推荐II期剂量。计划采用3 + 3设计进行MF剂量递增。在开始使用MF后的前六周评估剂量限制性毒性(DLT)。在2021年2月至2022年1月期间,3例患者接受1500 mg/天的MF治疗,4例患者接受2250 mg/天的MF治疗。未观察到DLT。最常见的不良反应是食欲减退、恶心和腹泻,所有这些反应均可控制。2例患者分别在6.0个月和6.1个月时出现肿瘤进展,1例在初次手术后12.2个月死亡。其他5例患者在最后一次随访时病情保持稳定。高达2250 mg/天的MF剂量联合维持性TMZ似乎耐受性良好,我们随后开展了一项使用2250 mg/天MF的II期研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5982/9454846/96a3e0f5850e/cancers-14-04222-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5982/9454846/a5fa61a75fbb/cancers-14-04222-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5982/9454846/96a3e0f5850e/cancers-14-04222-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5982/9454846/a5fa61a75fbb/cancers-14-04222-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5982/9454846/96a3e0f5850e/cancers-14-04222-g002.jpg

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