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A Study of Pancreatic Cancer in Xenografts From Liver Metastases

A Feasibility Study Of Developing Murine Primary Xenografts From Biopsies Of Liver Metastases In Patients With Advanced Pancreatic Cancer

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01774643
Enrollment
31
Registered
2013-01-24
Start date
2013-01-31
Completion date
2022-11-30
Last updated
2023-01-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Blood Samples, Liver Metastases, Pancreatic Cancer, Tumor Tissue Biopsy

Keywords

Pancreatic cancer, Liver metastases, Tumor tissue biopsy, Blood samples, Xenografts, Murine, Genomic profiling, Circulating biomarkers

Brief summary

This is a feasibility study to perform image-guided liver biopsies in 25 patients who have pancreatic cancer with liver metastasis (cancer in the pancreas that has spread to the liver). This will contribute with samples for the bio-bank (bank of tumors) and develop xenografts (human tumors growing in mice) for further analysis of genes.

Detailed description

This study might bring a better understanding of the metastatic pancreatic cancer and evaluate the differences between the metastatic and the primary pancreatic cancer (the type that does not have metastasis).

Interventions

None listed

Sponsors

University Health Network, Toronto
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Minimum age of 18 years old * Pancreatic cancer with liver metastasis * No contraindication to image-guided biopsy of liver metastasis, including uncontrolled bleeding diathesis, uncontrolled malignant pain, inability to lie supine etc) and no significant hepatic dysfunction. * Provide written informed consent * ECOG 0,1 or 2

Exclusion criteria

* Inability to lie supine for more than 30 minutes * ECOG 3 or more * Serious medical risk factors involving any of the major organ systems or including uncontrolled bleeding diathesis, uncontrolled malignant pain, inability to lie supine etc) and no significant hepatic dysfunction.

Design outcomes

Primary

MeasureTime frameDescription
Number of patients with adverse events due to biopsiesup to 2 yearsMonitoring adverse events during trial related to biopsies
Number of successful xenograftsup to 2 yearsdetermine the take rate or success of establishing xenografts
Number of similarities and differences between original patient tumor sample with xenograft sampleup to 2 yearscomplete histological and molecular comparison of original patient sample with murine xenograft
Engraftment rate compared to clinical data (response to treatment, disease-free survival, overall survival)up to date of death from any causedetermine the correlation between engraftment rate and clinical data (response to treatment, disease-free survival, overall survival).

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026