Assessing quality of life and survival in patients with rare cancers receiving targeted therapy
Official title: PRecision Oncology Evidence Development in Cancer Treatment - Clinical: PREDiCTc
Run by British Columbia Cancer Agency · NCT04814095 · Data updated 2026-11-12
This study is trying to see if targeted therapies can improve the quality of life and survival for people with advanced rare cancers.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 30 (estimated) |
| Sponsor | British Columbia Cancer Agency Academic / other |
| Drugs / interventions | immunotherapy |
| Locations | 1 site (Vancouver, British Columbia) |
| Status | Recruiting |
| Started | June 30, 2021 |
| Main results expected | May 1, 2028 |
| Study ends | May 1, 2028 |
| Registry record updated | October 19, 2026 |
| Trial ID | NCT04814095 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include adults aged 18 and older with incurable malignancies identified as having rare cancers or molecular aberrations currently receiving Health Canada approved targeted therapy that is not nationally funded.
✕Probably not a fit
Patients who are currently participating in other clinical trials or those unable to complete quality of life assessments may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This pilot clinical trial evaluates the real-world quality of life and survival outcomes for patients with advanced rare cancers or those harboring rare molecular aberrations who are treated with targeted therapies approved by Health Canada. The study aims to generate real-world evidence to support health technology assessments, which are crucial for funding decisions. By focusing on patients who may not have access to nationally funded treatments, the trial seeks to address the uncertainties surrounding the effectiveness and quality of life impacts of these therapies. Participants will undergo assessments of their quality of life and receive CT imaging as part of the intervention.
Why it matters
Potential benefit: If successful, this study could provide critical evidence to support funding and access to effective treatments for patients with rare cancers.
How similar studies have gone: While this approach is novel in its focus on rare cancers and real-world evidence, similar studies have shown promise in evaluating targeted therapies in other contexts.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Subject age greater than or equal to 18 years at the time of signature of informed consent. * Subjects with an incurable malignancy who have been identified to have a rare cancer or rare molecular aberration who is currently receiving Health Canada approved targeted therapy that is not nationally funded * ECOG 0-2 * Life expectancy of at least 12 weeks * Adequate hematologic and end organ function for drug treatment per the clinician's assessment * Asymptomatic or treated brain metastases permitted * Ability to give informed consent for the study procedures defined in this protocol. Exclusion Criteria: * Treatment with any approved or investigational agent or participation in another clinical trial with therapeutic intent within 14 days prior to enrollment. * Inability to complete quality of life questionnaires * Subjects who are felt by the treating clinician to be unfit to proceed with this protocol.
Where it's running
-
BC Cancer
Vancouver, British Columbia, Canada Recruiting
Study contacts
- Principal investigator: Cheryl Ho, MD — BC Cancer
- Study coordinator: Samantha Pollard, PhD
- Email: spollard@bccrc.ca
- Phone: 604-675-8000
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.