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

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity Health Network, Toronto

About this trial

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

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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

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.

Disqualifiers

None

Trial population

Any cancer patient

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

500 Participants
are grouped into 1 trial group
Group A: MOHCCN-O

Trial outcomes

Primary outcomes

1

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

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

Time frame
5 years

Secondary outcomes

1

Development of standard practices to create a unique shareable dataset of molecular, imaging, clinical and health outcome information on Canadian cancer cases

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

Time frame
5 years
2

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

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

Time frame
5 years
3

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

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

Time frame
5 years

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

University Health Network, Toronto

Lead sponsor

Princess Margaret Hospital, Canada

Collaborator

Ontario Institute for Cancer Research

Collaborator

Terry Fox Research Institute

Collaborator

Queen's University, Kingston, Ontario

Collaborator

Ottawa Hospital Research Institute

Collaborator

Kingston Health Sciences Centre

Collaborator

Windsor Regional Hospital

Collaborator

University of Windsor

Collaborator

London Health Sciences Centre

Collaborator

London Health Sciences Centre Research Institute

Collaborator