此页面是自动翻译的,不保证翻译的准确性。请参阅 英文版 对于源文本。

Promoting Response to IMmunotherapy by Exercise in Patients With Advanced Renal Cell Carcinoma (PRIMER)

2026年8月27日 更新者:Radboud University Medical Center

The primary aim of this study is to evaluate the feasibility of a supervised high intensity interval training (HIIT) program during first-line dual immune checkpoint inhibitor (ICI) therapy (nivolumab plus ipilimumab) in patients with advanced renal cell carcinoma (RCC). The second aim is to generate preliminary data on the effects of exercise on the immune cell phenotype and function, gut microbiota composition, physical fitness, patient-reported outcomes and clinical outcomes.

This is a two-arm randomized controlled pilot trial in which 30 patients with advanced RCC scheduled to receive first-line nivolumab plus ipilimumab will be randomized in 1:1 ratio to an exercise intervention group or usual care group. The exercise intervention consists of two 60-minute supervised HIIT sessions per week, delivered by oncology-trained physiotherapists and one additional home-based moderate-intensity aerobic exercise sessions per week. The intervention starts with the first cycle of immunotherapy and continues for four treatment cycles. Participants in both groups will receive usual care and general exercise guidelines. Measurements include blood and stool sampling for microbiome and immune parameters analysis, physical fitness assessments, physical fitness monitoring, body composition measurements, and patient-reported outcomes related to quality of life, fatigue, depression, sleep and diet.

研究概览

地位

招聘中

条件

干预/治疗

详细说明

There is strong evidence from randomized controlled trials that exercise during cancer treatment can maintain physical fitness, limit fatigue, and enhance health-related quality of life (HRQoL). Some studies also showed that exercise may help patients to better tolerate their treatment. However, most exercise trials have been conducted in patients receiving chemotherapy or radiotherapy, and little is known about the feasibility or effects of exercise during immunotherapy, particularly in patients with advanced RCC.

First-line treatment for patients with advanced RCC often consists of dual ICI treatment with nivolumab plus ipilimumab. While this combination has shown to improve survival, a substantial proportion of patients do not respond, and approximately 44% experience any grade immune-related adverse events. Tumor hypoxia, an immunosuppressive tumor microenvironment, and insufficient infiltration of cytotoxic immune cells are key factors believed to contribute to treatment resistance.

Preclinical studies in mice have shown that aerobic exercise can positively influence the tumor microenvironment through reduced tumor hypoxia, enhanced tumor perfusion, and increased activity and infiltration of cytotoxic immune cells such as CD8+ T cells and natural killer (NK) cells, while reducing immunosuppressive cell populations. In addition, preclinical studies in mice suggested that exercise-induced changes in the gut microbiome can further support immune activation and improve responses to immunotherapy. Despite this promising biological rationale, no clinical studies have evaluated whether supervised exercise is feasible or beneficial in patients with advanced RCC.

The primary objective of this pilot randomized controlled trial is to evaluate the feasibility of a supervised exercise program during first-line dual ICI therapy in patients with advanced RCC. Secondary objectives are to explore the preliminary effects of exercise on immune phenotype and function, inflammatory markers, circulating tumor (ct)DNA, gut microbiome composition, body composition, aerobic fitness, muscle function, physical activity, and patient reported outcomes including HRQoL, fatigue, anxiety, depression, sleep, and diet. In addition, changes in immune function, gut microbiome composition and clinical outcomes will also be explored.

This study is a two-arm randomized controlled trial including 30 adult patients with advanced RCC. Participants will be randomized to the intervention arm that receives a supervised HIIT program in addition to usual care or to a usual care control arm. The intervention consists of two supervised 60-minute HIIT-exercise sessions per week, delivered by oncology trained physiotherapists, combined with one additional home-based moderate intensity exercise session of at least 30 min per week. The intervention starts with the first cycle of immunotherapy and continues for four treatment cycles. Blood and stool samples will be collected at baseline and at 6 weeks and 12 weeks during treatment to assess immune and microbiome changes. In addition, in participants allocated to the exercise intervention group, to evaluate the acute effects of exercise on the immune response, blood samples will be collected immediately before and after a supervised exercise session.

Physical fitness tests, questionnaires and Fitbit to monitor physical activity will be used to evaluate functional and patient-reported outcomes.

This pilot study will provide important information on the feasibility of exercise during immunotherapy and generate preliminary data on potential immunological effects. These findings will inform the design of future larger trials aimed to optimize supportive care and improve treatment outcomes for patients with advanced RCC.

研究类型

介入性

注册 (估计的)

30

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

学习地点

    • Gelderland
      • Arnhem、Gelderland、荷兰
        • 招聘中
        • Rijnstate
      • Nijmegen、Gelderland、荷兰

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

描述

Inclusion Criteria:

  • Age ≥18 years.
  • Diagnosed with advanced RCC with indication for standard-of-care dual ICI treatment.
  • Able and willing to give written informed consent.

Exclusion Criteria:

  • Life expectancy <6 months.
  • Unable to perform basic activities of daily living such as walking.
  • Presence of cognitive impairment or severe emotional instability (e.g. schizophrenia, Alzheimer's disease, alcohol addiction), at the discretion of the investigator.
  • Presence of other disabling comorbidities that may interfere with the ability to perform physical exercise (e.g., heart failure, chronic obstructive pulmonary disease (COPD, GOLD stage 3 or 4), orthopaedic conditions, or neurological disorders such as hernia, paresis, amputation or active rheumatoid arthritis), at the discretion of the investigator.
  • Current participation in structured vigorous aerobic and/or resistance exercise ≥ 2 times per week at a level comparable to the intervention

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:支持治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:High Intensity Interval Training (HIIT)
High intensity aerobic interval training during dual immunotherapy
The intervention group will be offered a supervised exercise program consisting of two 60-minute sessions per week, including continuous aerobic exercise and HIIT. Sessions will be supervised by physiotherapists specialized in oncology, and the training load will be tailored to a patient's individual fitness levels throughout the intervention. Following a short warm-up, participants will perform repeated high-intensity cycling intervals targeting 85-95% of their estimated peak heart rate corresponding to a Borg Rating of Perceived Exertion (RPE) 16-18), interspersed with periods of active recovery at light intensity. The HIIT component will be followed by moderate-intensity aerobic exercise at approximately 70% of the estimated heart rate (Borg RPE 13-14), and a cool-down period. In addition, participants will be asked to be physically active for at least 30 minutes at moderate intensity, in accordance with the American College of Sports Medicine (ACSM) guidelines.
无干预:Usual care control (UC)
The control group will receive usual care and will be receive a folder about physical activity recommendations.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Participation rate
大体时间:Study enrolment period (approximately 24 months)
Calculated by the proportion of eligible patients that participate. An accrual rate lower than 20% will be defined as not feasible.
Study enrolment period (approximately 24 months)
Exercise intervention adherence
大体时间:12 weeks (during intervention period)
Adherence will be assesed by attendance and exercise relative dose intensity (ExRDI). Attendence will be assessed by dividing the number of attended sessions by the number of prescribed sessions. ExRDI will be calculated as the percentage of the exercise intensity achieved during the performed sessions relative to the total prescribed exercise intensity expressed as a percentage. The information will be collected using questionnaires and exercise-logs registered by the physical therapists. These logs will be collected by the researcher
12 weeks (during intervention period)
Immune-related and exercise-related adverse events
大体时间:24 weeks (during intervention period of 12 weeks, and 12 weeks post intervention)
Immune related adverse events will be assessed using Common Terminology Criteria for Adverse Events (CTCAE) v5.0 based on medical records and the patient reported outcomes (PRO)-CTCAE completed by patients before each immunotherapy cycle and at 3-month follow up.
24 weeks (during intervention period of 12 weeks, and 12 weeks post intervention)

次要结果测量

结果测量
措施说明
大体时间
Body composition
大体时间:12 weeks (Baseline, post-intervention)
Bioelectrical Impedance Analysis (BIA), Length (cm), Body weight (kg), Muscle mass (kg), Body fat percentage (%). Weight and height will be combined to report BMI in kg/m²
12 weeks (Baseline, post-intervention)
Estimated aerobic fitness
大体时间:12 weeks (Baseline, post-intervention)
Steep ramp test
12 weeks (Baseline, post-intervention)
Lower body muscle function
大体时间:12 weeks (Baseline, post-intervention)
Lower body muscle function will be assessed using a sit-to-stand test
12 weeks (Baseline, post-intervention)
Physical activity
大体时间:12 weeks (Baseline, post-intervention)
Modified Godin Leisure-Time Exercise Questionnaire, Fitbit continuously
12 weeks (Baseline, post-intervention)
Health-related quality of life (HRQoL)
大体时间:12 weeks (Baseline, post-intervention)
European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire-Core 30 (EORTC QLQ-C30) questionnaire
12 weeks (Baseline, post-intervention)
Fatigue
大体时间:12 weeks (Baseline, post-intervention)
European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Fatigue Module (EORTC QLQ FA12) questionnaire
12 weeks (Baseline, post-intervention)
Anxiety and depression
大体时间:12 weeks (Baseline, post-intervention)
Hospital Anxiety and Depression Scale (HADS) questionnaire
12 weeks (Baseline, post-intervention)
Sleep
大体时间:12 weeks (Baseline, post-intervention)
Pittsburgh Sleep Quality Index (PSQI) questionnaire
12 weeks (Baseline, post-intervention)
Diet
大体时间:12 weeks (Baseline, post-intervention)
World Cancer Research Fund / American Institute for Cancer Research (WCRF/AICR) Cancer Prevention Recommendations Questionnaire
12 weeks (Baseline, post-intervention)
ctDNA
大体时间:12 weeks (baseline, 6 weeks, and post-intervention)
Venous blood sampling, concetration ctDNA (ng/mL) next-generation sequencing
12 weeks (baseline, 6 weeks, and post-intervention)
Immune cell phenotype and function, and inflammatory markers
大体时间:12 weeks (baseline, 6 weeks, and post-intervention)
Venous blood sampling and flow cytometry to determine frequency (%) of circulating immune cells, functional characteristics of circulating immune cells will be determined using functional assays, inflammatory marker concentrations will measured (pg/mL or ng/mL).
12 weeks (baseline, 6 weeks, and post-intervention)
Gut microbiome composition
大体时间:12 weeks (baseline and post-intervention)
Taxonomic features and alpha and beta diversity via 16S rRNA marker gene sequencing of feces samples
12 weeks (baseline and post-intervention)

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Laurien M Buffart, PhD、Radboud University Medical Center
  • 首席研究员:Sasja F Mulder, MD, PhD、Radboud University Medical Center
  • 首席研究员:Theo van Voorthuizen, MD、Rijnstate

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2026年7月22日

初级完成 (估计的)

2028年7月1日

研究完成 (估计的)

2028年9月1日

研究注册日期

首次提交

2026年6月17日

首先提交符合 QC 标准的

2026年6月25日

首次发布 (实际的)

2026年7月2日

研究记录更新

最后更新发布 (实际的)

2026年8月28日

上次提交的符合 QC 标准的更新

2026年8月27日

最后验证

2026年6月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

是的

IPD 计划说明

IPD will be shared via the POLARIS consortium see PROSPERO registry CRD42013003805 or paper: Buffart et al. Systematic Reviews 2013; 2: 75.

IPD 共享支持信息类型

  • 企业社会责任

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

订阅