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临床试验/NCT06896552
NCT06896552尚未招募1 期

Investigating the Effect of Ketogenic Diet on Immunological Parameters in Advanced Cancer Patients Undergoing Immunotherapy

Rabin Medical Center1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年4月1日最近更新:
适应症

试验速览

阶段
1 期
状态
尚未招募
入组人数
60
试验地点
1
主要终点
Number of Participants Adhering to the Ketogenic Diet and Experiencing Treatment-Related Adverse Events as Assessed by CTCAE v5.0

研究概览

简要总结

This clinical trial aims to evaluate whether a ketogenic diet (KD), when combined with immunotherapy, can improve immune function and treatment outcomes in patients with advanced melanoma, cutaneous squamous cell carcinoma (cSCC), or renal cell carcinoma (RCC).

Why Is This Study Important? Immunotherapy is a promising cancer treatment, but not all patients respond well. Research suggests that diet, particularly a high-fat, low-carbohydrate ketogenic diet, may help boost the immune system and make treatments more effective.

What Will This Study Examine?

Researchers want to understand:

Is the ketogenic diet well-tolerated for cancer patients? Does the diet improve immune responses and treatment effectiveness?

How Will the Study Work?

Participants will be placed into one of two groups:

Ketogenic Diet (KD) Group: A structured high-fat, low-carb diet (intermittent schedule: 2 weeks on, 1 week off).

Standard Diet (SD) Group: A typical diet with no major changes. Throughout the study, a dietitian will closely support and guide you. Both groups will continue their standard immunotherapy treatment.

What Will Participants Do? Write their food intake three times a week to help assess dietary adherence Follow their assigned diet for 10 weeks Have weekly check-ins with a dietitian (in-person at the hospital or via phone) Have weekly blood glucose and ketone level checks using a home device. Provide monthly blood samples to measure immune response during routine immunotherapy infusions Provide stool samples for gut microbiome analysis at the start and end of the study Measure Monthly Weight, body composition, and resting calorie burn Complete quality-of-life questionnaires

What Are the Potential Benefits? Improved response to immunotherapy Better understanding of how diet influences cancer treatment Potential for a new supportive strategy for cancer care

This study may help uncover ways to enhance cancer treatment through personalized nutrition.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Sequential
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 100 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • • Males and females, age >= 18 years
  • Patients with a histologically confirmed melanoma or cSCC or RCC receiving first line treatment with combination nivolumab and ipilimumab /relatlimab or single agent ipilimumab, nivolumab, pembrolizumab, Cemiplimab.
  • Able to read, understand, and provide written informed consent
  • Willing and able to complete all study-specific procedures and visits
  • Patients with Eastern Cooperative Oncology Group (ECOG) performance status ≤
  • Blood tests:
  • Creatinine (Cr) < 1.5 mg/dL.
  • Magnesium normal range ( 1.5 -2,6 mg/dL)
  • Liver function tests (LFTs) 2.5x upper limit of normal (ULN).
  • Neutrophils ≥ 1,000/mm3, platelets ≥ 50,000/mm3, Hb>8 g/dL
  • Women of childbearing potential must have a negative β-HCG pregnancy test documented within 1 week of registration.

排除标准

  • • Individuals < 18 years of age
  • Unable or unwilling to provide consent
  • Other active malignancy (other than adequately treated and cured basal or squamous cell skin cancer, curatively treated in situ disease, or any other cancer from which the patient has been disease free >=2 years)
  • Currently consuming a low-carbohydrate (< 130 g/day) or KD or done so in the last 6-months
  • Patients currently participating in an interventional or therapeutic clinical trial involving the use of active anti-cancer therapy.
  • Active autoimmune diseases requiring active Immune suppressive medications
  • Systemic steroid therapy, excluding for replacement due to adrenal insufficiency
  • Major surgery within last 3 months
  • BMI <18 or >35
  • Medical contraindications to the intervention diet as determined by the treating physician.
  • Self-reported major dietary restrictions related to the intervention such as irritable bowel syndrome (IBS).
  • Patients with a history or active eating disorder
  • Uncontrolled Diabetes mellitus or patients receiving insulin
  • Known diagnosis of HIV
  • Known active hepatitis B or hepatitis C
  • Known inborn errors of lipid metabolism
  • Sever or uncontrolled Hyperlipidemia (total cholesterol over 400 mg / dL, low-density lipoprotein (LDL) above 300 mg / dL, triglycerides over 500 mg / dl.).
  • Pregnant or lactating.
  • Patients who have undergone a transplant

结局指标

主要结局

Number of Participants Adhering to the Ketogenic Diet and Experiencing Treatment-Related Adverse Events as Assessed by CTCAE v5.0

时间窗: From enrollment to the end of treatment at 10 weeks

This measure will assess the feasibility and tolerability of the ketogenic diet (KD) in cancer patients undergoing immunotherapy by evaluating: Diet Adherence: The number of participants who maintain KD for at least 80% of the study duration, based on dietary intake logs and ketone level measurements. Tolerability: The number of participants experiencing treatment-related adverse events (AEs), as assessed using the Common Terminology Criteria for Adverse Events (CTCAE) v5.0. The severity and frequency of AEs will be documented and categorized.

Change in Peripheral Blood Mononuclear Cell (PBMC) Composition at Baseline, During, and Post-Intervention

时间窗: Monthly (week 0, 4, 10 ±1 week).

This measure will evaluate changes in immune cell composition in response to the ketogenic diet (KD) and immunotherapy. PBMC Composition: Assessed using cytometry by time-of-flight (CyTOF) to characterize shifts in immune cell subsets (e.g., T cells, natural killer cells, monocytes). Data Analysis: Changes from the baseline will be reported as absolute values and fold-changes over time.

Serum Cytokine Levels at Baseline, During, and Post-Intervention

时间窗: Monthly (week 0, 4, 10 ±1 week).

This measure will evaluate changes in cytokine levels in response to the ketogenic diet (KD) and immunotherapy. Serum Cytokine Levels: Quantified using multiplex immunoassays to measure the concentrations of key cytokines, such as IL-2, IFN-γ, TNF-α, and IL-10. Data Analysis: Changes from baseline will be reported as absolute values and fold-changes over time.

次要结局

  • Overall response rate according to RECIST v1.(End of treatment at 10 weeks)
  • Adherence to Dietary Interventions - Ketone Level Measurements(Weekly from Baseline (Week 0) to Week 10)
  • Change in Body Weight (kg) Over the Study Period(Baseline (Week 0), Week 4, Week 10, and Week 14 (±1 week).)
  • Change in Quality of Life Score Assessed by the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30)(At enrollment (Baseline, Week 0) and at the end of treatment (Week 10).)
  • Fecal microbiome(At enrollment (baseline) and at the end of treatment at 10 weeks)
  • Sarcopenia(At enrollment (baseline) and at the end of treatment at 10 weeks)
  • Body composition-- Fat Mass and Lean Mass(Monthly (week 0, 4, 10 ±1 week).)
  • Resting Energy Expenditure (REE)(Monthly (week 0, 4, 10 ±1 week).)
  • The Rate of immune-related adverse events(From enrollment to the end of treatment at 10 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Gal Markel

MD Ph.D. MBA, Deputy Director of Rabin Medical Center, and Director of Davidoff Center Rabin Medical Center, Full Professor of Clinical Microbiology & Immunology at the Sackler Faculty of Medicine, Tel Aviv University.

Rabin Medical Center

研究点 (1)

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