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| ID | Type | Description | Link |
|---|---|---|---|
| NCI-2024-04798 | Registry Identifier | CTRP (Clinical Trial Reporting Program) | |
| 23-013283 | Other Identifier | Mayo Clinic Institutional Review Board |
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This study explores the potential value of a new blood test approach to detect measurable residual disease or early recurrence/progression in patients with cholangiocarcinoma.
PRIMARY OBJECTIVES:
I. To estimate the association of PUMA levels from peripheral blood with disease progression (radiographically or clinically) in patients that are candidates for curative surgical intervention of cholangiocarcinoma.
Ia. Pre- and post-neoadjuvant-treatment PUMA levels will be associated with treatment response to neoadjuvant therapy (short term progression).
Ib. Pre-surgical and post-surgical PUMA levels will be associated with progression free survival.
II. To estimate the association of PUMA levels from peripheral blood with postoperative survival in patients treated for cholangiocarcinoma.
OUTLINE: This is an observational study.
Patients undergo collection of blood samples and have their medical records reviewed on study. Patients also undergo collection of archived tissue samples on study.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Observational | Patients undergo collection of blood samples and have their medical records reviewed on study. Patients also undergo collection of archived tissue samples on study. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Non-Interventional Study | Other | Non-Interventional Study |
|
| Measure | Description | Time Frame |
|---|---|---|
| Associate of PUMA levels with short term progression | Proteins, mUtations, Methylated DNA, and Aneuploidy (PUMA) markers will be assessed pre- and post-treatment and will be associated with treatment response to therapy (short term progression; time to cholangiocarcinoma recurrence). | Up to 5 years |
| Associate of PUMA levels with progression free survival | Pre-surgical and post-surgical PUMA levels will be associated with progression free survival (time to death from cholangiocarcinoma). | Up to 5 years |
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Inclusion Criteria:
Exclusion Criteria:
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Patients with a clinical diagnosis of cholangiocarcinoma under evaluation for surgical intervention with intent to cure.
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| Name | Affiliation | Role |
|---|---|---|
| Nguyen H. Tran, MD | Mayo Clinic in Rochester | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Mayo Clinic in Rochester | Rochester | Minnesota | 55905 | United States |
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| Label | URL |
|---|---|
| Mayo Clinic Clinical Trials | View source |
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| ID | Term |
|---|---|
| D018281 | Cholangiocarcinoma |
| ID | Term |
|---|---|
| D000230 | Adenocarcinoma |
| D002277 | Carcinoma |
| D009375 | Neoplasms, Glandular and Epithelial |
| D009370 | Neoplasms by Histologic Type |
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Samples retained with permission of participant
| D009369 | Neoplasms |