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Towards personalized induction therapy for esophageal adenocarcinoma: organoids derived from endoscopic biopsy recapitulate the pre-treatment tumor
by
Derouet, Mathieu F.
, Kalimuthu, Sangeetha
, Darling, Gail E.
, Allen, Jonathan
, Ng, Christine
, Tsao, Ming-Sound
, Yeung, Jonathan C.
, Radulovich, Nikolina
, Wilson, Gavin W.
in
631/67/1504/1477
/ 631/67/70
/ Adenocarcinoma - drug therapy
/ Adult
/ Aged
/ Aged, 80 and over
/ Barrett Esophagus - drug therapy
/ Chemotherapy
/ Esophageal cancer
/ Esophageal Neoplasms - drug therapy
/ Female
/ Filamentation
/ Histology
/ Humanities and Social Sciences
/ Humans
/ Induction Chemotherapy - methods
/ Induction therapy
/ Lasers
/ Male
/ Middle Aged
/ multidisciplinary
/ Organoids - cytology
/ Precision Medicine - methods
/ Science
/ Science (multidisciplinary)
/ Surgery
/ Tumors
2020
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Towards personalized induction therapy for esophageal adenocarcinoma: organoids derived from endoscopic biopsy recapitulate the pre-treatment tumor
by
Derouet, Mathieu F.
, Kalimuthu, Sangeetha
, Darling, Gail E.
, Allen, Jonathan
, Ng, Christine
, Tsao, Ming-Sound
, Yeung, Jonathan C.
, Radulovich, Nikolina
, Wilson, Gavin W.
in
631/67/1504/1477
/ 631/67/70
/ Adenocarcinoma - drug therapy
/ Adult
/ Aged
/ Aged, 80 and over
/ Barrett Esophagus - drug therapy
/ Chemotherapy
/ Esophageal cancer
/ Esophageal Neoplasms - drug therapy
/ Female
/ Filamentation
/ Histology
/ Humanities and Social Sciences
/ Humans
/ Induction Chemotherapy - methods
/ Induction therapy
/ Lasers
/ Male
/ Middle Aged
/ multidisciplinary
/ Organoids - cytology
/ Precision Medicine - methods
/ Science
/ Science (multidisciplinary)
/ Surgery
/ Tumors
2020
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Towards personalized induction therapy for esophageal adenocarcinoma: organoids derived from endoscopic biopsy recapitulate the pre-treatment tumor
by
Derouet, Mathieu F.
, Kalimuthu, Sangeetha
, Darling, Gail E.
, Allen, Jonathan
, Ng, Christine
, Tsao, Ming-Sound
, Yeung, Jonathan C.
, Radulovich, Nikolina
, Wilson, Gavin W.
in
631/67/1504/1477
/ 631/67/70
/ Adenocarcinoma - drug therapy
/ Adult
/ Aged
/ Aged, 80 and over
/ Barrett Esophagus - drug therapy
/ Chemotherapy
/ Esophageal cancer
/ Esophageal Neoplasms - drug therapy
/ Female
/ Filamentation
/ Histology
/ Humanities and Social Sciences
/ Humans
/ Induction Chemotherapy - methods
/ Induction therapy
/ Lasers
/ Male
/ Middle Aged
/ multidisciplinary
/ Organoids - cytology
/ Precision Medicine - methods
/ Science
/ Science (multidisciplinary)
/ Surgery
/ Tumors
2020
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Towards personalized induction therapy for esophageal adenocarcinoma: organoids derived from endoscopic biopsy recapitulate the pre-treatment tumor
Journal Article
Towards personalized induction therapy for esophageal adenocarcinoma: organoids derived from endoscopic biopsy recapitulate the pre-treatment tumor
2020
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Overview
Esophageal adenocarcinoma has few known recurrent mutations and therefore robust, reliable and reproducible patient-specific models are needed for personalized treatment. Patient-derived organoid culture is a strategy that may allow for the personalized study of esophageal adenocarcinoma and the development of personalized induction therapy. We therefore developed a protocol to establish EAC organoids from endoscopic biopsies of naïve esophageal adenocarcinomas. Histologic characterization and molecular characterization of organoids by whole exome sequencing demonstrated recapitulation of the tumors’ histology and genomic (~ 60% SNV overlap) characteristics. Drug testing using clinically appropriate chemotherapeutics and targeted therapeutics showed an overlap between the patient’s tumor response and the corresponding organoids’ response. Furthermore, we identified Barrett’s esophagus epithelium as a potential source of organoid culture contamination. In conclusion, organoids can be robustly cultured from endoscopic biopsies of esophageal adenocarcinoma and recapitulate the originating tumor. This model demonstrates promise as a tool to better personalize therapy for esophageal adenocarcinoma patients.
Publisher
Nature Publishing Group UK,Nature Publishing Group
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