Pharmacotyping of Pancreatic Patient-derived Organoids
Pharmacotyping of Patient-derived Pancreatic Cancer Organoids From Endoscopic Ultrasound-guided Biopsy as a Tool for Predicting Oncological Response
1 other identifier
observational
88
1 country
1
Brief Summary
EUS-FNB samples will be used for organoid cultures, which will be co-cultured with cancer associated fibroblasts derived from the surrounding stroma of the lesion. The organoid cultures will be used for pharmacotyping using relevant chemotherapeutic agents used in the clinic, and the organoid's response compared with the patient's response.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Jul 2021
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 1, 2021
CompletedFirst Submitted
Initial submission to the registry
October 14, 2021
CompletedFirst Posted
Study publicly available on registry
January 19, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 30, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
August 31, 2025
CompletedOctober 3, 2024
October 1, 2024
4.2 years
October 14, 2021
October 2, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Measurement of organoid's response to therapy
Response of patient derived organoids to standard chemotherapeutic agents used for treatment of patients with pancreatic cancer
Organoid co-cultures will be established and pharmacotyped in a timeframe of 2-4 weeks.
Validation of patient's response to therapy
Computed tomography (CT) scan of the thorax and abdomen are performed at baseline (within 28 days prior to first study drug administration) to assess efficacy of the drugs in patients.
3 months follow up
Comparison between organoid's and patient's response
The response measured in the pharmacoscreen of organoids will be compared with the patient's response
4 months
Interventions
No intervention
Eligibility Criteria
Patients with histopathological confirmation of pancreatic ductal adenocarcimona, ineligible for surgery, planned to start standard first line treatment
You may qualify if:
- Signed informed consent
- Histopathological confirmation of PDAC and planned standard first-line treatment prior to entering this study OR Patients suspected of primary locally advanced, non-metastatic PDAC based on cross-sectional imaging undergoing diagnostic standard of care (SOC) EUS-FNB procedure
- Age \> 18 years and older
- Life expectancy greater than 3 months
- ECOG/WHO Performance Status (PS) 0-1
- Patients must have normal organ and marrow function as defined below:
- White blood cell count (WBC) ≥ 3 x 10⁹/L
- Platelet count ≥ 100 x 10⁹/L
- Serum bilirubin ≤1.5 x upper limit of normal (ULN) (patients with Gilbert's Syndrome must have a total bilirubin ≤ 50 mmol/L)
- PP ≥ 40 or INR ≤ 1.5
- Serum creatinine ≤ 1.5 x ULN or CrCl ≥ 40 mL/min (using the Cockcroft-Gault formula)
You may not qualify if:
- Contraindications for nurse administered propofol sedation (NAPS)
- Contraindications for EUS-FNB procedure
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Herlev Hospitallead
- Rigshospitalet, Denmarkcollaborator
Study Sites (1)
Endoscopy Unit, Herlev Hospital
Herlev, Copenhagen, 2730, Denmark
Related Publications (13)
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PMID: 25557080BACKGROUNDTiriac H, Bucobo JC, Tzimas D, Grewel S, Lacomb JF, Rowehl LM, Nagula S, Wu M, Kim J, Sasson A, Vignesh S, Martello L, Munoz-Sagastibelza M, Somma J, Tuveson DA, Li E, Buscaglia JM. Successful creation of pancreatic cancer organoids by means of EUS-guided fine-needle biopsy sampling for personalized cancer treatment. Gastrointest Endosc. 2018 Jun;87(6):1474-1480. doi: 10.1016/j.gie.2017.12.032. Epub 2018 Jan 9.
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PMID: 20491528RESULT
Biospecimen
organoid cultures will be derived from endoscopic ultrasound-guided fine needle biopsies
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Pia H Klausen, PhD
Rigshospitalet, Denmark
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
October 14, 2021
First Posted
January 19, 2022
Study Start
July 1, 2021
Primary Completion
August 30, 2025
Study Completion
August 31, 2025
Last Updated
October 3, 2024
Record last verified: 2024-10
Data Sharing
- IPD Sharing
- Will not share