Somatic mutations as seen in myeloid malignancies can also be detected in healthy, elderly individuals (clonal hematopoiesis of indeterminate potential, CHIP), in patients with unex-plained cytopenia, that do not fulfill the criteria for myeloid malignancy (clonal cytopenia of un-determined significance, CCUS) It has been shown that these conditions predispose to hema-tological cancer. For patients with CCUS, it has been reported that in a 5-year period up to 50-90 % of the patients will progress to myelodysplastic syndrome (MDS) or acute myeloid leu-kemia (AML), both devastating diseases with poor outcomes, especially for the elderly popula-tion. There is currently no treatment available for patients with CCUS besides supporting agents. Since the somatic mutations can be detected up to 10 years before a diagnosis of MDS, it opens the potential for early intervention. Physical inactivity is associated with multiple solid cancers, and it has been suggested that exercise can prevent for example certain colon- or breast cancers. Studies in mice have shown that exercise can reduce tumor size and incidence of solid cancers, and different mechanisms have been suggested including increased immune cell infiltration, reduced systemic inflamma-tion, and metabolic changes. The mechanisms of disease progression of pre-leukemia and MDS are complex and probably multifactorial, but recent studies suggest that components such as natural killer cells, adipocytes, and inflammatory substances in the bone marrow mi-croenvironment play a crucial role; factors that exercise may modulate. In addition, recent stud-ies have shown that increased bone marrow adipose tissue (BMAT) may create a microenvi-ronment that supports the expansion of leukemic cells and thus may facilitate disease progres-sion, and earlier studies among healthy, younger individuals have shown that exercise can reduce the amount of BMAT significantly. Therefore, the investigators hypothesize that exercise may prevent or delay the progression from pre-leukemia to leukemia by altering the microenvironment in the bone marrow. The purpose with this clinical, pilot trial where patients with the preleukemic condition CCUS or early stage of leukemia (i.e., lower-risk MDS) will undergo an individualized exercise interven-tion, is to investigate: 1. whether an exercise intervention and the trial set-up, are feasible and safe in this cohort, 2. potential mechanisms in leukemogenesis affected by exercise in controlling dis-ease progression, 3. and the effect hereof on quality of life and activities of daily living. The above will inform the decision-making on designing a larger randomized, controlled trial.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Enrollment
36
Rigshospitalet
Copenhagen, Denmark, Denmark
NOT_YET_RECRUITINGRigshospitalet
Copenhagen, Denmark
RECRUITINGExercise feasibility: Exercise sessions attendance
The number of attended exercise training sessions relative to the number of planned exercise sessions
Time frame: From baseline until the end of12 weeks of supervised exercise. And after 12 weeks of no supervised exercise.
Exercise feasibility: Recruitment, refusal, and retention rates
The number of patients recruited to the study, the number of patients who refused to be enrolled in the study, the number of participants that completed the study
Time frame: From baseline until end of intervention (24 weeks)
Incidence of Adverse Events (AEs)
AE will be recorded during trial assessment visits and through medical records. This procedure will concern any AE during the trial period. We will collect patients' self-report of AEs for each trial visit and telephone interview, which may have occurred since the last trial visit and telephone interview.
Time frame: From baseline until the end of intervention (24 weeks)
Incidence of Serious Adverse Events (SAEs)
SAE will be recorded during trial assessment visits and through medical records. This procedure will concern any SAE during the trial period. We will collect patients' self-report of SAEs for each trial visit and telephone interview, which may have occurred since the last trial visit and telephone interview.
Time frame: From baseline until the end of intervention (24 weeks)
Changes in peak oxygen consumption (VO2 peak)
Changes in VO2peak assessed during an incremental exercise test to volitional exhaustion on a bicycle ergometer
Time frame: From baseline until the end of12 weeks of supervised exercise. And after 12 weeks of no supervised exercise.
Changes in Aerobic Capacity: Peak power output
Changes in peak power output assessed during an incremental exercise test to volitional exhaustion on a bicycle ergometer
Time frame: From baseline until the end of12 weeks of supervised exercise. And after 12 weeks of no supervised exercise.
Changes in Muscle strength: Hand grip strength
Changes in hand grip strength, assessed using a dynamometer
Time frame: From baseline until the end of 12 weeks of supervised exercise. And after 12 weeks of no supervised exercise.
Changes in Functional performance: Habitual gait speed
Changes in habitual gait speed
Time frame: From baseline until the end of 12 weeks of supervised exercise. And after 12 weeks of no supervised exercise.
Changes in Functional performance: 30 seconds Sit-to-stand
Changes in the number of stands from sitting position that can be performed during 30 seconds
Time frame: From baseline until the end of 12 weeks of supervised exercise. And after 12 weeks of no supervised exercise.
Changes in Body composition and anthropometrics: Body mass
Changes in body mass
Time frame: From baseline until the end of 12 weeks of supervised exercise. And after 12 weeks of no supervised exercise.
Changes in Body composition and anthropometrics: Total lean mass
Changes in total lean mass assessed by dual energy x-ray absorptiometry (DXA)
Time frame: From baseline until the end of 12 weeks of supervised exercise. And after 12 weeks of no supervised exercise.
Changes in Body composition and anthropometrics: Total fat mass
Changes in total fat mass assessed by DXA
Time frame: From baseline until the end of 12 weeks of supervised exercise. And after 12 weeks of no supervised exercise.
Changes in Body composition and anthropometrics: Bone mineral density
Changes in bone mineral density assessed by DXA
Time frame: From baseline until the end of 12 weeks of supervised exercise. And after 12 weeks of no supervised exercise.
Changes in Blood biochemistry: C-reactive protein
Changes in resting C-reactive protein levels in blood
Time frame: From baseline until the end of 12 weeks of supervised exercise. And after 12 weeks of no supervised exercise.
Changes in Blood biochemistry: Insulin
Changes in resting insulin blood levels
Time frame: From baseline until the end of 12 weeks of supervised exercise. And after 12 weeks of no supervised exercise.
Changes in Blood biochemistry: Glucose
Changes in resting glucose blood levels
Time frame: From baseline until the end of 12 weeks of supervised exercise. And after 12 weeks of no supervised exercise.
Changes in Blood biochemistry: Triglycerides
Changes in resting triglycerides blood levels
Time frame: From baseline until the end of 12 weeks of supervised exercise. And after 12 weeks of no supervised exercise.
Changes in Blood biochemistry: LDL-Cholesterol
Changes in resting LDL-cholesterol blood levels
Time frame: From baseline until the end of 12 weeks of supervised exercise. And after 12 weeks of no supervised exercise.
Changes in Blood biochemistry: HDL-Cholesterol
Changes in resting HDL-cholesterol blood levels
Time frame: From baseline until the end of 12 weeks of supervised exercise. And after 12 weeks of no supervised exercise.
Changes in Blood biochemistry: Total Cholesterol
Changes in resting Cholesterol blood levels
Time frame: From baseline until the end of 12 weeks of supervised exercise. And after 12 weeks of no supervised exercise.
Changes in Blood biochemistry: HbA1c
Changes in resting HbA1c blood levels
Time frame: From baseline until the end of 12 weeks of supervised exercise. And after 12 weeks of no supervised exercise.
Changes in Blood biochemistry: total bilirubin
Changes in resting total bilirubin blood levels
Time frame: From baseline until the end of 12 weeks of supervised exercise. And after 12 weeks of no supervised exercise.
Changes in Blood biochemistry: Vitamin D (25-Hydroxy-Vitamin D(D3+D2))
Changes in resting Vitamin D (25-Hydroxy-Vitamin D(D3+D2)) blood levels
Time frame: From baseline until the end of 12 weeks of supervised exercise. And after 12 weeks of no supervised exercise.
Changes in Blood biochemistry: insulin growth factor 1 (IGF-1)
Changes in resting insulin growth factor 1 (IGF-1) blood levels
Time frame: From baseline until the end of 12 weeks of supervised exercise. And after 12 weeks of no supervised exercise.
Changes in Blood biochemistry: human growth hormone (HGH)
Changes in resting human growth hormone (HGH) blood levels
Time frame: From baseline until the end of 12 weeks of supervised exercise. And after 12 weeks of no supervised exercise.
Changes in Blood biochemistry: sex hormones (estrogen, progesterone and testosterone)
Changes in resting human sex hormones (estrogen, progesterone and testosterone)blood levels
Time frame: From baseline until the end of 12 weeks of supervised exercise. And after 12 weeks of no supervised exercise.
Changes in Cytokine levels in blood: Interleukin-6
Changes in resting Interleukin-6 blood levels
Time frame: From baseline until the end of 12 weeks of supervised exercise. And after 12 weeks of no supervised exercise.
Changes in Cytokine levels in blood: Tumor-necrosis-factor alpha (TNFalpha)
Changes in resting TNFalpha blood levels
Time frame: From baseline until the end of 12 weeks of supervised exercise. And after 12 weeks of no supervised exercise.
Changes in Patient-reported symptomatic adverse events
Patient-reported symptomatic adverse events, assessed using the using the Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE)
Time frame: From baseline until the end of 12 weeks of supervised exercise. And after 12 weeks of no supervised exercise.
Inflammatory markers in Bone marrow (BM) and peripheral blood
Changes in the inflammatory markers INF-γ, IL-1β, IL-2, IL-4, IL-6, IL-8, IL-10, IL-12p70, IL-13, TNF-α, adiponectin and leptin in bone marrow aspirate and peripheral blood
Time frame: From baseline until the end of 12 weeks of supervised exercise. And after 12 weeks of no supervised exercise.
Regulate the immune cell composition in the BM
Changes in immune cell composition in the BM measured by flow cytometry
Time frame: From baseline until the end of 12 weeks of supervised exercise. And after 12 weeks of no supervised exercise.
Change the variant allele frequency (VAF)
Changes in VAF detected with targeted next generation sequencing (NGS)
Time frame: From baseline until the end of 12 weeks of supervised exercise. And after 12 weeks of no supervised exercise.
Alter the composition of BMAT
Changes in BMAT composition
Time frame: From baseline until the end of 12 weeks of supervised exercise. And after 12 weeks of no supervised exercise.
Ifluence on the cytopenia(s)
Changes in blood cell counts (i.e., hemoglobin, white blood cell count, platelet count, absolute neutrophil count, lymphocyte count, basophil count, eosinophil count, monocyte count, reticulocyte count, peripheral blood blast count, red cell)
Time frame: From baseline until the end of 12 weeks of supervised exercise. And after 12 weeks of no supervised exercise.
Changes in Blood biochemistry: Lactate dehydrogenase (LDH)
Changes in resting Lactate dehydrogenase (LDH) blood levels
Time frame: From baseline until the end of 12 weeks of supervised exercise. And after 12 weeks of no supervised exercise.
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