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

Recruiting
Conditions
Kidney Cancer
Pancreas Cancer
Leukemia
Solid Tumor
Colorectal Cancer
Breast Cancer
Head and Neck Cancer
Lung Cancer
Prostate Cancer
Melanoma
Registration Number
NCT05403177
Lead Sponsor
University Health Network, Toronto
Brief Summary

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

Detailed Description

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.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
500
Inclusion Criteria
  1. 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

  2. All patients must be able to satisfy the required minimum data elements for the 15k gold standard cohort through:

    1. Already existing data that satisfies the minimal requirements of a gold standard case (refer to Table 1)
    2. Have sufficient biospecimens (tumor and/or blood samples) available for more comprehensive molecular and immunophenotypic characterization
  3. 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.

  4. Participating patients must agree to share their anonymized clinical and genomic data

Exclusion Criteria

None.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Number of patients included in a pan-Canadian cohort with comprehensive clinical and genomic data5 years

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

Secondary Outcome Measures
NameTimeMethod
Development of standard practices to create a unique shareable dataset of molecular, imaging, clinical and health outcome information on Canadian cancer cases5 years

Improve the cancer research paradigm by bringing teams or researchers together and leverage valuable information genomic and clinical data from Canadian cancer cases.

Clinical effectiveness and cost-effectiveness of precision cancer medicine to advance clinical implementation and reimbursement decisions5 years

Health technology assessment tools will be used to evaluate the real-world value of precision medicine

Development and collection of patient-reported outcomes to enhance patient-centeredness in precision cancer medicine5 years

Health technology assessment tools will be used to evaluate the real-world value of precision medicine

Trial Locations

Locations (3)

Kingston Health Sciences Centre

🇨🇦

Kingston, Ontario, Canada

Ottawa Health Research Institute

🇨🇦

Ottawa, Ontario, Canada

Princess Margaret Cancer Centre

🇨🇦

Toronto, Ontario, Canada

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