In Vitro Quality Assessment of Myogenic Stem Cells in Multiple Patient Groups With Confirmed Skeletal Muscle Atrophy to Study Their Potential for Autologous Stem Cell Therapy
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 入组人数
- 7
- 试验地点
- 1
- 主要终点
- Number of mesoangioblasts ex vivo isolated from muscle biopsy
研究概览
简要总结
The goal of this clinical trial is to compare the quality of mesoangioblasts isolated from various patient groups suffering from muscle atrophy. This study includes cancer cachexia and muscle-impaired elderly and a control group of the same age.
The quality will be defined on these following outcomes:
- The number and distribution of the mesoangioblasts in a muscle biopsy to define if there are sufficient mesoangioblasts to start a culture.
- The proliferation capacity to define if we can culture them the numbers required for systemic treatment.
- The myogenic capacity to define if the mesoangioblasts are sufficiently capable to generate muscle fibres.
Participants will:
- Undergo a muscle biopsy (needle biopsy or rest material from surgery, ~50mg)
- Donate blood (~20 ml)
- Fill in SARC-F questionnaire (evaluate sarcopenia score)
- Fill in SQUASH questionnaire (evaluate physical activity of previous week) Researchers will compare groups (muscle-impaired elderly vs control; cancer cachexia vs control) to see if there is a difference regarding quality. These results will define the potential of autologous mesoangioblast therapy within these groups.
详细描述
No effective treatment is available for the loss of muscle tissue in non-genetic muscle diseases such as (cancer) cachexia and sarcopenia. Such a treatment would improve the quality of life, therapy success, and independency of these patients. The administration of healthy autologous muscle stem cells, called mesoangioblasts, that lead to muscle regeneration and increased muscle mass and function could be a novel therapeutic strategy to achieve this. A prerequisite is that the therapeutic potential of these mesoangioblasts is sufficient. Therefore, the main aim of this study is to assess this potential for mesoangioblasts of patients with lung cancer cachexia and with sarcopenia and determine the effect the cancer or age might have on the therapeutic potential.
This study is part of a larger project, called Generate Your Muscle (GYM), which aims to develop and commercially produce a stem cell therapy for recovery of muscle mass and strength in patients with genetic and non-genetic muscle disease and muscle breakdown. This will be achieved by administering large numbers of autologous mesoangioblasts (MABs) as an Advanced Therapy Medicinal Product (asCTMP) in the arteries, which will migrate to the damaged muscle, thereby restoring muscle mass and function. This strategy can only be successful for patients suffering from cachexia or sarcopenia, if these patients have enough mesoangioblasts, if these MABs can proliferate into the numbers requested for systemic treatment, if the energy capacity of the MABs is sufficient and if these mesoangioblasts still have a high myogenic potential. The aim of this study is to determine these parameters for patients with cancer cachexia or sarcopenia, as we know that they can be affected by the underlying condition. They will be compared to age-matched controls. If positive, the MABs will qualify as asCTMP for a clinical trial in a follow-up study.
研究设计
- 研究类型
- Observational
- 观察模型
- Case Control
- 时间视角
- Cross Sectional
入排标准
- 年龄范围
- 50 Years 至 80 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Lung cancer cachexia:
- •Diagnosed with NSCLC, stage III-IV
- •Diagnosed with cachexia (>5% unintentional body weight loss in past six months, >2% body weight loss with BMI <20, or skeletal muscle index for males <7.26 kg/m2; females <5.45 kg/m2)
- •Age 50-60 or 60-70
- •Written informed consent
- •Patient group: MIE
- •Scheduled for total hip, knee, or back surgery
- •Age 60-70 or 70-80 year
- •Written informed consent
- •Patients with scheduled knee-, hip-, and back surgery
- •Age 50-60, 60-70, and 70-80 year
- •Age and sex-matched to patient groups
- •Written informed consent
排除标准
- •No filled-in IC
- •Suffering from a muscular dystrophy or other disease known to affect muscle morphology or function
- •Have a weekly alcohol intake of ≥ 35 units (men) or ≥ 24 units (women)
- •Ongoing participation in other intervention clinical trials
- •Major surgery of the muscle within 4 weeks of the visit unrelated to the study
- •Patients unable and/or unwilling to comply with treatment and study instructions
- •Any other factor that in the opinion of the investigator excludes the patient from the study
研究组 & 干预措施
Muscle impaired elderly
Elderly scheduled for hip/knee/back surgery with III-IV ASA score, low grip strength and high scoring for sarcopenia
干预措施: In vitro analyse (Other)
Lung cancer cachexia
Non-small cell lung cancer patients stage III with reported cachexia
干预措施: In vitro analyse (Other)
Controls
Elderly scheduled for hip/knee/back surgery without any recorded muscle defects, I-II ASA score, average or high grip strength, low scoring for sarcopenia.
干预措施: In vitro analyse (Other)
结局指标
主要结局
Number of mesoangioblasts ex vivo isolated from muscle biopsy
时间窗: 1 day
The number of mesoangioblasts obtained from a muscle biopsy. Once cells reached \>80% confluency in a culture dish, FACS analysis will determine the amount of mesoangioblasts obtained.
Distribution of mesoangioblasts in a muscle biopsy
时间窗: 1 day
The number of mesoangioblasts in a muscle biopsy. Histochemistry will reveal the location of the pericyte-like mesoangioblasts surrounding the blood vessels when stained for pericyte marker NG2 proteoglycan.
Proliferation capacity of mesoangioblasts in vitro
时间窗: 1 day
The proliferation capacity to define whether we can culture them in the numbers required for systemic treatment. Doubling time will be assessed 3 separate instances with a hemocytometer. Population doubling level = 3.32 (log viable cells at harvest - log seeded cells)
Myogenic capacity of mesoangioblasts in vitro
时间窗: 1 day
The myogenic capacity to define if the mesoangioblasts are sufficiently capable to generate muscle fibres. Myogenic capacity is calculated as the number of nuclei in MF20-positive fibers divided by total number of nuclei per field.
次要结局
- Homing potential of mesoangioblasts in vitro(1 day)
- ATP production of mesoangioblasts in vitro(1 day)
- Difference in myogenic potential of mesoangioblasts and satellite cells in vitro(1 day)