Abstract 2815: Patient derived orthotopic xenograft (PDOX) model developed from needle biopsy specimen replicated clinical outcomes in advanced pancreatic cancer
Introduction: A patient-derived xenograft (PDX) as a preclinical model can reflect the pathological and molecular features and drug responsibility of a patient’s tumor. PDXs have been generated by subcutaneously implanting surgically resected tumor fragments into immunodeficient mice. Unfortunately,...
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Veröffentlicht in: | Cancer research (Chicago, Ill.) Ill.), 2017-07, Vol.77 (13_Supplement), p.2815-2815 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Introduction:
A patient-derived xenograft (PDX) as a preclinical model can reflect the pathological and molecular features and drug responsibility of a patient’s tumor. PDXs have been generated by subcutaneously implanting surgically resected tumor fragments into immunodeficient mice. Unfortunately, 80 % of pancreatic cancer patients is unresectable and they show highly aggressive and metastatic tumors. In most cases, diagnoses are confirmed histologically and diagnosed through endoscopic ultrasonography-guided/fine-needle aspiration (EUS/FNA) or percutaneous liver biopsy. However, they are not suitable for subcutaneous implantation into mice due to their threadlike shape and very small size. Therefore, the lack of patient-derived model system in pancreatic cancer is in desperate need of new strategy to cover unresectable patients as well as resectable. Here, we pioneered the development of a unresectable patient-derived orthotopic xenograft (PDOX) model satisfied with short period and high success rate, and made the best use of them as the test model for drug response.
Methods and Results:
PDOX models were established with a technique of direct surgical orthotopic implantation into the pancreatic tail of Athymic nude mice. PDOX models using fine needle biopsy had a higher success rate of engraftment, nearly 40% (17 cases among 44 cases) in patients with a time to progression of |
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ISSN: | 0008-5472 1538-7445 |
DOI: | 10.1158/1538-7445.AM2017-2815 |