• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

D,L-美沙酮与化疗联合应用于胶质瘤患者的安全性和耐受性

Safety and Tolerance of D,L-Methadone in Combination with Chemotherapy in Patients with Glioma.

作者信息

Onken Julia, Friesen Claudia, Vajkoczy Peter, Misch Martin

机构信息

Department of Neurosurgery, Charité University of Berlin, Berlin, Germany

Berlin Institute of Health, Berlin, Germany.

出版信息

Anticancer Res. 2017 Mar;37(3):1227-1235. doi: 10.21873/anticanres.11438.

DOI:10.21873/anticanres.11438
PMID:28314286
Abstract

BACKGROUND/AIM: D,L-Methadone increases sensitivity toward chemotherapy of different tumor cell populations. We evaluated the safety and tolerance of additional use of D,L-methadone in patients with glioma in combination with chemotherapy.

PATIENTS AND METHODS

The dosage, duration of therapy and side-effects related to D,L-methadone were recorded in 27 patients. Toxicity was assessed accordingly to the Common Toxicity Criteria (CTC) of the National Cancer Institute. Progression-free survival at 6 months (PFS-6) was assessed.

RESULTS

A total of 13 patients reported grade 1-3 nausea at the beginning of the D,L-methadone therapy. Four patients reported persistent side-effects of nausea (CTC Grade 2, n=1) and obstipation (CTC grade 2-3, n=3). PFS-6 of patients with glioblastoma was 80% in those with non-methylated O-methylguanine-DNA methyltransferase (MGMT) (n=5) and 100% in those with MGMT methylation (n=7).

CONCLUSION

D,L-methadone can be safely combined with standard glioma chemotherapy without increasing the risk of toxicity or vegetative symptoms such as tachycardia, sweating and restlessness. PFS-6 in patients with primary glioblastoma treated this way seems to be at least comparable to that of historic controls.

摘要

背景/目的:消旋美沙酮可提高不同肿瘤细胞群体对化疗的敏感性。我们评估了消旋美沙酮联合化疗在胶质瘤患者中额外使用的安全性和耐受性。

患者与方法

记录了27例患者使用消旋美沙酮的剂量、治疗持续时间及相关副作用。根据美国国立癌症研究所的通用毒性标准(CTC)评估毒性。评估了6个月时的无进展生存期(PFS-6)。

结果

共有13例患者在消旋美沙酮治疗开始时报告有1-3级恶心。4例患者报告有持续性恶心副作用(CTC 2级,n = 1)和便秘(CTC 2-3级,n = 3)。胶质母细胞瘤患者中,O-甲基鸟嘌呤-DNA甲基转移酶(MGMT)未甲基化者(n = 5)的PFS-6为80%,MGMT甲基化者(n = 7)的PFS-6为100%。

结论

消旋美沙酮可安全地与标准胶质瘤化疗联合使用,而不会增加毒性风险或出现如心动过速、出汗和烦躁不安等植物神经症状。以这种方式治疗的原发性胶质母细胞瘤患者的PFS-6似乎至少与历史对照相当。

相似文献

1
Safety and Tolerance of D,L-Methadone in Combination with Chemotherapy in Patients with Glioma.D,L-美沙酮与化疗联合应用于胶质瘤患者的安全性和耐受性
Anticancer Res. 2017 Mar;37(3):1227-1235. doi: 10.21873/anticanres.11438.
2
Long-term therapy with temozolomide is a feasible option for newly diagnosed glioblastoma: a single-institution experience with as many as 101 temozolomide cycles.替莫唑胺长期治疗是新诊断胶质母细胞瘤的一种可行选择:一家机构多达101个替莫唑胺疗程的经验。
Neurosurg Focus. 2014 Dec;37(6):E4. doi: 10.3171/2014.9.FOCUS14502.
3
NOA-04 randomized phase III trial of sequential radiochemotherapy of anaplastic glioma with procarbazine, lomustine, and vincristine or temozolomide.NOA-04 间变性胶质瘤序贯放化疗(采用丙卡巴肼、洛莫司汀和长春新碱或替莫唑胺)的随机 III 期试验
J Clin Oncol. 2009 Dec 10;27(35):5874-80. doi: 10.1200/JCO.2009.23.6497. Epub 2009 Nov 9.
4
MGMT Promoter Methylation Is a Strong Prognostic Biomarker for Benefit from Dose-Intensified Temozolomide Rechallenge in Progressive Glioblastoma: The DIRECTOR Trial.MGMT 启动子甲基化是预测剂量强化替莫唑胺再挑战获益的强预后生物标志物:DIRECTOR 试验。
Clin Cancer Res. 2015 May 1;21(9):2057-64. doi: 10.1158/1078-0432.CCR-14-2737. Epub 2015 Feb 5.
5
MGMT promoter methylation correlates with survival benefit and sensitivity to temozolomide in pediatric glioblastoma.O6-甲基鸟嘌呤-DNA甲基转移酶(MGMT)启动子甲基化与儿童胶质母细胞瘤的生存获益及对替莫唑胺的敏感性相关。
Pediatr Blood Cancer. 2007 Apr;48(4):403-7. doi: 10.1002/pbc.20803.
6
Two cilengitide regimens in combination with standard treatment for patients with newly diagnosed glioblastoma and unmethylated MGMT gene promoter: results of the open-label, controlled, randomized phase II CORE study.两种西仑吉肽方案联合标准治疗新诊断的胶质母细胞瘤且MGMT基因启动子未甲基化患者:开放标签、对照、随机II期CORE研究结果
Neuro Oncol. 2015 May;17(5):708-17. doi: 10.1093/neuonc/nou356. Epub 2015 Mar 11.
7
MGMT promoter methylation status can predict the incidence and outcome of pseudoprogression after concomitant radiochemotherapy in newly diagnosed glioblastoma patients.O-6-甲基鸟嘌呤-DNA甲基转移酶(MGMT)启动子甲基化状态可预测新诊断的胶质母细胞瘤患者同步放化疗后假性进展的发生率及预后。
J Clin Oncol. 2008 May 1;26(13):2192-7. doi: 10.1200/JCO.2007.14.8163.
8
Predictive impact of MGMT promoter methylation in glioblastoma of the elderly.MGMT 启动子甲基化对老年胶质母细胞瘤的预测影响。
Int J Cancer. 2012 Sep 15;131(6):1342-50. doi: 10.1002/ijc.27385. Epub 2012 Jan 11.
9
MGMT gene promoter methylation as a potent prognostic factor in glioblastoma treated with temozolomide-based chemoradiotherapy: a single-institution study.MGMT 基因启动子甲基化作为替莫唑胺为基础的放化疗治疗胶质母细胞瘤的一种潜在预后因素:单机构研究。
Int J Radiat Oncol Biol Phys. 2012 Nov 1;84(3):661-7. doi: 10.1016/j.ijrobp.2011.12.086. Epub 2012 Mar 11.
10
Phase II study of protracted daily temozolomide for low-grade gliomas in adults.成人低级别胶质瘤每日持续使用替莫唑胺的II期研究。
Clin Cancer Res. 2009 Jan 1;15(1):330-7. doi: 10.1158/1078-0432.CCR-08-0888.

引用本文的文献

1
PKA inhibition is a central step in D,L-methadone-induced ER Ca release and subsequent apoptosis in acute lymphoblastic leukemia.蛋白激酶A(PKA)抑制是D,L-美沙酮诱导急性淋巴细胞白血病内质网钙释放及随后凋亡的关键步骤。
Front Cell Dev Biol. 2024 Apr 24;12:1388745. doi: 10.3389/fcell.2024.1388745. eCollection 2024.
2
Use of complementary therapies and supportive measures of patients with intracranial gliomas-a prospective evaluation in an outpatient clinic.颅内胶质瘤患者的补充治疗和支持措施的使用-门诊的前瞻性评估。
J Neurooncol. 2024 Jul;168(3):507-513. doi: 10.1007/s11060-024-04696-1. Epub 2024 May 6.
3
Mapping the Evidence for Opioid-Mediated Changes in Malignancy and Chemotherapeutic Efficacy: Protocol for a Scoping Review.
绘制阿片类药物介导的恶性肿瘤变化和化疗疗效证据图谱:一项范围综述方案
JMIR Res Protoc. 2023 May 22;12:e38167. doi: 10.2196/38167.
4
Cytotoxic and Senolytic Effects of Methadone in Combination with Temozolomide in Glioblastoma Cells.美沙酮联合替莫唑胺对胶质母细胞瘤细胞的细胞毒性和衰老作用。
Int J Mol Sci. 2020 Sep 23;21(19):7006. doi: 10.3390/ijms21197006.
5
Against Repurposing Methadone for Glioblastoma Therapy.反对将美沙酮重新用于治疗胶质母细胞瘤。
Biomolecules. 2020 Jun 17;10(6):917. doi: 10.3390/biom10060917.
6
Methadone does not potentiate the effect of doxorubicin in canine tumour cell lines.美沙酮不会增强阿霉素在犬肿瘤细胞系中的作用。
Vet Med Sci. 2020 Aug;6(3):283-289. doi: 10.1002/vms3.266. Epub 2020 Apr 19.
7
Safety aspects of opioid-naïve patients with high-grade glioma treated with D,L-Methadone: an observational case series.D,L-美沙酮治疗高级别脑胶质瘤的阿片类药物初治患者的安全性:一项观察性病例系列研究。
Neurosurg Rev. 2021 Feb;44(1):579-586. doi: 10.1007/s10143-020-01250-1. Epub 2020 Feb 14.
8
Efficacy of D,L-methadone in the treatment of glioblastoma in vitro.消旋美沙酮在体外治疗胶质母细胞瘤的疗效
CNS Oncol. 2018 Jul 1;7(3):CNS18. doi: 10.2217/cns-2018-0006. Epub 2018 Jun 19.
9
Methadone as anticancer treatment: hype, hope, or hazard? : A series of case reports and a short review of the current literature and recommendations of the societies.美沙酮作为抗癌治疗手段:炒作、希望还是危害?:一系列病例报告以及对当前文献和学会建议的简要综述
Wien Med Wochenschr. 2018 May;168(7-8):159-167. doi: 10.1007/s10354-018-0623-5. Epub 2018 Feb 19.
10
Methadone as a "Tumor Theralgesic" against Cancer.美沙酮作为一种抗癌“肿瘤镇痛药”。
Front Pharmacol. 2017 Oct 31;8:733. doi: 10.3389/fphar.2017.00733. eCollection 2017.