Promoting Response to IMmunotherapy by Exercise in Patients With Advanced Renal Cell Carcinoma (PRIMER)
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.
調査の概要
詳細な説明
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.
研究の種類
入学 (推定)
段階
- 適用できない
連絡先と場所
研究連絡先
- 名前:Laurien Buffart, PhD
- 電話番号:+31 24 3667310
- メール:laurien.buffart@radboudumc.nl
研究場所
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Gelderland
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Arnhem、Gelderland、オランダ
- 募集
- Rijnstate
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Nijmegen、Gelderland、オランダ
- 募集
- Radboudumc
-
コンタクト:
- Laurien M Buffart, PhD
- 電話番号:+31 24 3667310
- メール:laurien.buffart@radboudumc.nl
-
-
参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
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
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:支持療法
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的:High Intensity Interval Training (HIIT)
High intensity aerobic interval training during dual immunotherapy
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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.
|
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介入なし:Usual care control (UC)
The control group will receive usual care and will be receive a folder about physical activity recommendations.
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この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Participation rate
時間枠:Study enrolment period (approximately 24 months)
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Calculated by the proportion of eligible patients that participate.
An accrual rate lower than 20% will be defined as not feasible.
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Study enrolment period (approximately 24 months)
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Exercise intervention adherence
時間枠:12 weeks (during intervention period)
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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
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12 weeks (during intervention period)
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Immune-related and exercise-related adverse events
時間枠:24 weeks (during intervention period of 12 weeks, and 12 weeks post intervention)
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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.
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24 weeks (during intervention period of 12 weeks, and 12 weeks post intervention)
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Body composition
時間枠:12 weeks (Baseline, post-intervention)
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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
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12 weeks (Baseline, post-intervention)
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Estimated aerobic fitness
時間枠:12 weeks (Baseline, post-intervention)
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Steep ramp test
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12 weeks (Baseline, post-intervention)
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Lower body muscle function
時間枠:12 weeks (Baseline, post-intervention)
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Lower body muscle function will be assessed using a sit-to-stand test
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12 weeks (Baseline, post-intervention)
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Physical activity
時間枠:12 weeks (Baseline, post-intervention)
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Modified Godin Leisure-Time Exercise Questionnaire, Fitbit continuously
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12 weeks (Baseline, post-intervention)
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Health-related quality of life (HRQoL)
時間枠:12 weeks (Baseline, post-intervention)
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European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire-Core 30 (EORTC QLQ-C30) questionnaire
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12 weeks (Baseline, post-intervention)
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Fatigue
時間枠:12 weeks (Baseline, post-intervention)
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European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Fatigue Module (EORTC QLQ FA12) questionnaire
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12 weeks (Baseline, post-intervention)
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Anxiety and depression
時間枠:12 weeks (Baseline, post-intervention)
|
Hospital Anxiety and Depression Scale (HADS) questionnaire
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12 weeks (Baseline, post-intervention)
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Sleep
時間枠:12 weeks (Baseline, post-intervention)
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Pittsburgh Sleep Quality Index (PSQI) questionnaire
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12 weeks (Baseline, post-intervention)
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Diet
時間枠:12 weeks (Baseline, post-intervention)
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World Cancer Research Fund / American Institute for Cancer Research (WCRF/AICR) Cancer Prevention Recommendations Questionnaire
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12 weeks (Baseline, post-intervention)
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ctDNA
時間枠:12 weeks (baseline, 6 weeks, and post-intervention)
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Venous blood sampling, concetration ctDNA (ng/mL) next-generation sequencing
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12 weeks (baseline, 6 weeks, and post-intervention)
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Immune cell phenotype and function, and inflammatory markers
時間枠:12 weeks (baseline, 6 weeks, and post-intervention)
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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).
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12 weeks (baseline, 6 weeks, and post-intervention)
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Gut microbiome composition
時間枠:12 weeks (baseline and post-intervention)
|
Taxonomic features and alpha and beta diversity via 16S rRNA marker gene sequencing of feces samples
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12 weeks (baseline and post-intervention)
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協力者と研究者
捜査官
- 主任研究者:Laurien M Buffart, PhD、Radboud University Medical Center
- 主任研究者:Sasja F Mulder, MD, PhD、Radboud University Medical Center
- 主任研究者:Theo van Voorthuizen, MD、Rijnstate
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
- NL-011443 (その他の識別子:Medical Ethical Committee)
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
IPD プランの説明
IPD 共有サポート情報タイプ
- CSR
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
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