...
首页> 外文期刊>Cancer & Metabolism >Treatment of glioma patients with ketogenic diets: report of two cases treated with an IRB-approved energy-restricted ketogenic diet protocol and review of the literature
【24h】

Treatment of glioma patients with ketogenic diets: report of two cases treated with an IRB-approved energy-restricted ketogenic diet protocol and review of the literature

机译:用生酮饮食治疗神经胶质瘤患者:两例接受IRB批准的能量受限生酮饮食治疗方案的报告并复习文献

获取原文
           

摘要

BackgroundBased on the hypothesis that cancer cells may not be able to metabolize ketones as efficiently as normal brain cells, the ketogenic diet (KD) has been proposed as a complementary or alternative therapy for treatment of malignant gliomas. Case presentationWe report here our experience in treating two glioma patients with an IRB-approved energy-restricted ketogenic diet (ERKD) protocol as monotherapy and review the literature on KD therapy for human glioma patients. An ERKD protocol was used in this pilot clinical study. In addition to the two patients who enrolled in this study, we also reviewed findings from 30 other patients, including 5 patients from case reports, 19 patients from a clinical trial reported by Rieger and 6 patients described by Champ. A total of 32 glioma patients have been treated using several different KD protocols as adjunctive/complementary therapy. The two patients who enrolled in our ERKD pilot study were monitored with twice daily measurements of blood glucose and ketones and daily weights. However, both patients showed tumor progression while on the ERKD therapy. Immunohistochemistry reactions showed that their tumors had tissue expression of at least one of the two critical mitochondrial ketolytic enzymes (succinyl CoA: 3-oxoacid CoA transferase, beta-3-hydroxybutyrate dehydrogenase 1). The other 30 glioma patients in the literature were treated with several different KD protocols with varying responses. Prolonged remissions ranging from more than 5 years to 4 months were reported in the case reports. Only one of these patients was treated using KD as monotherapy. The best responses reported in the more recent patient series were stable disease for approximately 6 weeks. No major side effects due to KD have been reported in any of these patients. ConclusionsWe conclude that 1. KD is safe and without major side effects; 2. ketosis can be induced using customary foods; 3. treatment with KD may be effective in controlling the progression of some gliomas; and 4. further studies are needed to determine factors that influence the effectiveness of KD, whether as a monotherapy, or as adjunctive or supplemental therapy in treating glioma patients. Trial registrationClinicalTrials.gov# NCT01535911
机译:背景基于基于癌细胞可能无法像正常脑细胞一样高效地代谢酮的假设,生酮饮食(KD)已被提议作为治疗恶性神经胶质瘤的补充或替代疗法。病例介绍我们在这里报告我们使用IRB批准的能量受限生酮饮食(ERKD)方案作为单药治疗两名神经胶质瘤患者的经验,并回顾了有关人类胶质瘤患者KD治疗的文献。在该试验性临床研究中使用了ERKD方案。除了参加本研究的两名患者外,我们还回顾了其他30例患者的发现,包括病例报告中的5例患者,Rieger报道的19例临床试验患者和Champ报道的6例患者。使用几种不同的KD方案作为辅助/补充疗法,共治疗了32位神经胶质瘤患者。参加我们ERKD初步研究的两名患者接受了每日两次血糖,酮和每日体重的监测。然而,两名患者在接受ERKD治疗时均显示出肿瘤进展。免疫组织化学反应表明,他们的肿瘤具有两种关键的线粒体酮分解酶(琥珀酰CoA:3-氧代酸CoA转移酶,β-3-羟基丁酸脱氢酶1)中至少一种的组织表达。文献中的其他30名神经胶质瘤患者接受了几种不同的KD方案,且反应不同。病例报告中报告的缓解期从5年以上到4个月不等。这些患者中只有一名接受KD单一疗法治疗。在最近的患者系列中报告的最佳反应是稳定疾病约6周。在这些患者中,均未见因KD引起的重大副作用。结论我们得出结论:1. KD安全且无重大副作用; 2.使用常规食物可诱发酮症; 3. KD治疗可能有效控制某些神经胶质瘤的进展; 4.需要进一步研究以确定影响KD有效性的因素,无论是作为单一疗法,还是辅助或补充疗法治疗神经胶质瘤患者。试用注册ClinicalTrials.gov#NCT01535911

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号