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| Name | Class |
|---|---|
| National Pediatric Cancer Foundation | OTHER |
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To evaluate the ability of a multidisciplinary and multisite group, the Pediatric Evolutionary Tumor Board (pedsETB), to develop additional therapeutic strategies in patients without curative options or with suboptimal outcomes.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Participants Reviewed by ETB | Participants clinical history, available therapeutic options, and outcome expectations will be presented to the Evolutionary Tumor Board (ETB) along with images and pathology. Strategies and models will be presented regarding additional evolutionary ideas that can be applied. These ideas will be characterized (e.g. first strike-second strike, adaptive, novel sequential therapy, novel combination, novel dosing schedule, etc.). |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Peds Evolutionary Tumor Board (pedsETB) | Other | The pedsETB consists of evolutionary biologists, mathematicians, research scientists, statisticians, data scientists, radiologists, pathologists, oncologists (surgical, radiation, medical, and pediatric), and clinical trial coordinators. The pedsETB membership is inclusive of members from the participating institutions. The pedsETB will generate hypotheses, mathematical models, and experiments from the discussion towards further integration of evolutionary ideas towards therapeutic strategies for participants. The pedsETB will collect data through a chart review regarding adherence and results of ETB recommendation. |
| Measure | Description | Time Frame |
|---|---|---|
| The feasibility of the pedsETB developing therapeutic strategies | The investigators will measure the ability of a multidisciplinary group, the pedsETB, to develop additional therapeutic strategies in patients without curative options. The investigators plan to enroll 35 patients on the study. The primary objective will be successfully met if the pedsETB can develop an evolutionary based therapeutic strategy that differs from the oncologist's opinion prior to presentation for at least 80%, or 28 of these patients. | Baseline to up to 60 months from end of therapy |
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Inclusion Criteria:
The site investigator will make this determination based on their experience.
Exclusion Criteria:
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Participants who are patients at participating pedsETB sites.
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Jessica Crimella | Contact | 813-745-6250 | Jessica.Crimella@moffitt.org | |
| Jonathan Metts, MD | Contact |
| Name | Affiliation | Role |
|---|---|---|
| Jonathan Metts, MD | Moffitt Cancer Center | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Moffitt Cancer Center | Recruiting | Tampa | Florida | 33612 | United States |
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Peripheral blood collected at study enrollment and subsequently at designated time points:
Screening/Baseline/Enrollment, first post pedsETB Visit, and every 12 weeks (+/- 6 weeks) or upon changes in disease status, therapeutic intervention, and/or events of special interest at the discretion of the treating physician.
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| ID | Term |
|---|---|
| D009369 | Neoplasms |
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