Amaral L J, Gresham Gillian, Kim Sungjin, Tighiouart Mourad, Nelson Thomas A, Welborn Amelia, Lockshon Laura, Noorvash Brandon, Rudnick Jeremy D, Irwin Scott A, Freedland Stephen J, Hu Jethro
Cedars-Sinai Cancer, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Center for Integrated Research in Cancer and Lifestyle, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Sci Rep. 2025 Jul 1;15(1):21064. doi: 10.1038/s41598-025-06675-6.
Despite great interest, there is limited clinical evidence to support the use of a ketogenic diet (KD) for cancer patients. We conducted a single-arm phase 1 trial of a KD among patients with recently diagnosed glioblastoma (GBM) receiving standard-of-care (SOC) treatment. Adults with GBM within 3 months of diagnosis followed a supervised 16-week intervention of a 3:1 KD (Fat(g): Carbohydrate + Protein(g)) plus SOC chemoradiation. The primary outcome was safety, evaluated by weekly assessments of weight and body mass index (BMI). Secondary outcomes included feasibility (pre-specified as > 50% of patients maintaining blood ketone levels > 0.3 mM over 50% of study days), progression-free survival (PFS), overall survival (OS), health-related quality-of-life, and cognitive function. Twice daily blood glucose and ketones, weight/BMI, physical activity, and sleep were assessed by remote monitoring. Seventeen patients were evaluable: 53% women, median age 55, median Karnofsky Performance Status 85. All subjects met the primary safety objective with no instances of excessive weight loss or related serious adverse events. Adherence was high: all 17 patients maintained nutritional ketosis (≥ 0.3 mM/dL) > 50% of study days. Median PFS and OS were 12.9 months and 29.4 months from KD initiation respectively. Quality of Life, symptom control, and cognitive function remained stable or improved, although these did not reach statistical significance. This phase 1 trial demonstrates that KD is safe and feasible for GBM patients receiving SOC, may improve outcomes, and provides a foundation for an NCI-funded multicenter randomized diet trial to assess efficacy that is currently underway.
尽管人们对此兴趣浓厚,但支持癌症患者采用生酮饮食(KD)的临床证据有限。我们对近期诊断为胶质母细胞瘤(GBM)并接受标准治疗(SOC)的患者进行了一项KD的单臂1期试验。诊断后3个月内的GBM成年患者接受了为期16周的3:1 KD(脂肪(克):碳水化合物+蛋白质(克))加SOC放化疗的监督干预。主要结局是安全性,通过每周评估体重和体重指数(BMI)来评估。次要结局包括可行性(预先设定为超过50%的患者在超过50%的研究天数内维持血酮水平>0.3 mM)、无进展生存期(PFS)、总生存期(OS)、健康相关生活质量和认知功能。通过远程监测评估每日两次的血糖和酮体、体重/BMI、身体活动和睡眠情况。17例患者可评估:53%为女性,中位年龄55岁,中位卡诺夫斯基功能状态为85。所有受试者均达到主要安全目标,无体重过度减轻或相关严重不良事件发生。依从性高:所有17例患者在超过50%的研究天数内维持营养性酮症(≥0.3 mM/dL)。从开始KD起,中位PFS和OS分别为12.9个月和29.4个月。生活质量、症状控制和认知功能保持稳定或有所改善,尽管这些未达到统计学显著性。这项1期试验表明,KD对于接受SOC的GBM患者是安全可行的,可能改善预后,并为目前正在进行的由美国国立癌症研究所资助的多中心随机饮食试验评估疗效奠定了基础。