跳至主要内容
临床试验/NCT05403177
NCT05403177招募中不适用

Marathon of Hope Cancer Centres Network Study for Ontario (MOHCCN-O)

University Health Network, Toronto6 个研究点 分布在 1 个国家目标入组 500 人开始时间: 2022年6月23日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
500
试验地点
6
主要终点
Number of patients included in a pan-Canadian cohort with comprehensive clinical and genomic data

研究概览

简要总结

The Marathon of Hope Cancer Centres Network (MOHCCN) is a national network of cancer centres that pursue collaborative cancer research in precision medicine (an emerging approach for disease treatment and prevention that considers individual variability in DNA, environment and lifestyle) to accelerate the discovery of innovations and improve the health outcomes for cancer patients

详细描述

The purpose of this study is to use evolving technologies such as genomics and artificial intelligence to study cancer so that the right treatment can be given to the right patient, at the right time. Approximately 15,000 participants will take part in the greater MOHCCN study across Canada in the first 5 years, and ultimately the goal is to enroll up to 100,000 over next 10 years.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with histological and/or cytological confirmation of blood or solid tumor malignancies. For tumour types where pre-surgical biopsy is not routinely performed to confirm a pathologic diagnosis of cancer, patients may consent to this protocol, but eligibility must be confirmed after pathology is finalized demonstrating presence of malignancy
  • All patients must be able to satisfy the required minimum data elements for the 15k gold standard cohort through:
  • Already existing data that satisfies the minimal requirements of a gold standard case (refer to Table 1)
  • Have sufficient biospecimens (tumor and/or blood samples) available for more comprehensive molecular and immunophenotypic characterization
  • Patients who do not satisfy the required minimum data elements but would like to participate, maybe requested to donate blood and undergo a fresh biopsy if the archived Formalin-fixed paraffin-embedded (FFPE) samples are not available, or in cases where a fresh tumor biopsy is deemed necessary for molecular profiling.
  • Participating patients must agree to share their anonymized clinical and genomic data

排除标准

  • 未提供

结局指标

主要结局

Number of patients included in a pan-Canadian cohort with comprehensive clinical and genomic data

时间窗: 5 years

Consolidate and annotate data from patients included in a pan-Canadian cohort

次要结局

  • Development of standard practices to create a unique shareable dataset of molecular, imaging, clinical and health outcome information on Canadian cancer cases(5 years)
  • Clinical effectiveness and cost-effectiveness of precision cancer medicine to advance clinical implementation and reimbursement decisions(5 years)
  • Development and collection of patient-reported outcomes to enhance patient-centeredness in precision cancer medicine(5 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (6)

Loading locations...

相似试验