New Strategies to Detect Cancers in Carriers of Mutations in RB1: Blood Tests Based on Tumor-educated Platelets, or Extracellular Vesicles.
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 378
- 试验地点
- 3
- 主要终点
- RNA expression on platelets and allelic DNA balance of EVs in the blood of adult RB1 mutation carriers (Rb-survivors) and retinoblastoma patients (children).
研究概览
简要总结
Rationale: Individuals with a cancer predisposition due to a mutation in the paradigm tumor suppressor gene RB1, have a high risk to develop the childhood cancer retinoblastoma (Rb). Biopsies are not possible in Rb, before treatment selection. Heritable Rb patients have also a high risk to develop other types of second primary, either childhood or adult, malignancies (SPMs), notably sarcomas and melanomas. Remarkably, SPMs are now the leading cause of death in heritable-Rb-survivors. Unfortunately, there are no well-developed regular surveillance protocols for SPMs in Rb survivors available right now. Recently, new non-invasive cancer test have been developed, based on either RNA-sequencing data from platelets (ThromboSeq), or on extracellular membrane vesicles (EVs) derived from tumor cells present in blood.
Objective:
- Determine the non-cancerous baseline in adult RB1-mutation carriers (heritable-Rb-survivors).
- Contribute to the biobanking of blood and cancerous tissues from RB1-mutation carriers with SPMs.
- The development of blood-based tests, either platelet or EV-based, for the detection of (the type of) tumors in RB1-mutation carriers.
Study design: Cross-sectional multicenter trial.
Study population:
- 40 Rb patients (children),
- 40 controls (children),
- 153 Rb survivors (adults),
- 153 controls (adults),
- 10 Rb survivors with SPM (children/adults).
Main study parameters/endpoints:
- Determine the non-cancerous baseline in adult RB1-mutation carriers (heritable-Rb-survivors).
- Contribute to the biobanking of blood and cancerous tissues from RB1-mutation carriers with SPMs.
Nature and extent of the burden and risks associated with participation, benefit and group relatedness:
Two blood samples totalling 10ml blood will be collected for every participant. Additionally, a short questionnaire has to be filled in concerning their and their family's cancer history. Blood draws will be done, when participants are already present in the hospital for other appointments, and thus no extra visits are required. For all children, blood will be collected through an already present IV, and so no extra venepuncture is required. Children have to be included because Rb is a tumor only present in this patient group.
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
- 0 Years 至 99 Years(Child, Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Adult (16 years and older):
- •Group 1: germline mutation RB
- •Group 2 (control): no germline mutation RB
- •Pediatric (until 6 years of age):
- •Group 1: somatic or germline mutation RB1 and retinoblastoma.
- •Group 2 (control): no mutation RB1.
排除标准
- •Adult (16 years and older):
- •Group 1: concomitant heritable (inherited) disorder other than caused by monoallelic mutation of RB
- •Group 2 (control): cancer or already known cancer predisposition syndrome.
- •Pediatric (until 6 years of age):
- •Group 1: concomitant heritable (inherited) disorder other than caused by monoallelic mutation of RB
- •Group 2: cancer or already known cancer predisposition syndrome.
结局指标
主要结局
RNA expression on platelets and allelic DNA balance of EVs in the blood of adult RB1 mutation carriers (Rb-survivors) and retinoblastoma patients (children).
时间窗: blood will be taken at study inclusion, patients will be followed throughout the study, max 3 years and 9 months.
blood analyses at time of inclusion to determine baseline
次要结局
- RNA expression on platelets, allelic DNA balance of EVs in blood and genomic analysis on tumor tissue of RB1-mutation carriers diagnosed with a second primary malignancy.(blood will be taken at study inclusion, patients will be followed throughout the study, max 3 years and 9 months. In case of second primary tumor a second sample will be taken.)
研究者
Armida W. M. Fabius
Principal Investigator
Amsterdam UMC, location VUmc
