Smith Kris A, Hendricks Benjamin K, DiDomenico Joseph D, Conway Beth N, Smith Tracy L, Azadi Amir, Fonkem Ekokobe
Neurosurgery, Barrow Neurological Institute, Phoenix, USA.
Nutrition, Custom Nutrition Consultants, Phoenix, USA.
Cureus. 2022 Jun 30;14(6):e26457. doi: 10.7759/cureus.26457. eCollection 2022 Jun.
This study describes a retrospective case series of patients with glioma who received ketogenic metabolic therapy through dietary adherence and intermittent fasting.
A retrospective chart review of a single surgeon's clinic records was performed to identify patients who maintained nutritional ketosis for at least four months between January 2015 and October 2020.
Sixteen patients who met the inclusion criteria constituted a heterogeneous population of patients with diagnoses including eight World Health Organization (WHO) grade IV gliomas (seven glioblastoma, one gliosarcoma), seven WHO grade III gliomas (three oligodendroglioma, four astrocytoma), and one WHO grade II oligodendroglioma. mutation status was present for 12 patients, and methylation status was present for eight patients. The mean (standard deviation [SD]) duration of ketogenic metabolic therapy was 20.6 (13.8) months. The Response Assessment in Neuro-oncology Criteria was applied during the ketogenic metabolic therapy interval, indicating a complete response in eight patients and partial response in eight patients. The mean (SD) progression-free survival while patients maintained ketogenic metabolic therapy was 20.0 (14.4) months.
Ketogenic metabolic therapy appears to convey a survival advantage within this patient series, which highlights the possibility that this therapy, when strictly applied, can augment the standard of care. Further exploration of this modality in a prospective series is warranted to formally explore this therapy.
本研究描述了一组通过饮食依从性和间歇性禁食接受生酮代谢疗法的胶质瘤患者的回顾性病例系列。
对一位外科医生的临床记录进行回顾性图表审查,以确定在2015年1月至2020年10月期间维持营养性酮症至少四个月的患者。
符合纳入标准的16名患者构成了一个异质性患者群体,诊断包括8例世界卫生组织(WHO)IV级胶质瘤(7例胶质母细胞瘤,1例胶质肉瘤)、7例WHO III级胶质瘤(3例少突胶质细胞瘤,4例星形细胞瘤)和1例WHO II级少突胶质细胞瘤。12例患者有突变状态记录,8例患者有甲基化状态记录。生酮代谢疗法的平均(标准差[SD])持续时间为20.6(13.8)个月。在生酮代谢疗法期间应用了神经肿瘤学疗效评估标准,显示8例患者完全缓解,8例患者部分缓解。患者维持生酮代谢疗法时的平均(SD)无进展生存期为20.0(14.4)个月。
在该患者系列中,生酮代谢疗法似乎具有生存优势,这突出了这种疗法在严格应用时可提高护理标准的可能性。有必要在前瞻性系列中进一步探索这种治疗方式,以正式研究这种疗法。