Patient-derived organoids as a platform for modeling a patient’s response to chemoradiotherapy in esophageal cancer

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作者
Tatiana A. Karakasheva
Joel T. Gabre
Uma M. Sachdeva
Ricardo Cruz-Acuña
Eric W. Lin
Maureen DeMarshall
Gary W. Falk
Gregory G. Ginsberg
Zhaohai Yang
Michele M. Kim
Eric S. Diffenderfer
Jason R. Pitarresi
Jinyang Li
Amanda B. Muir
Kathryn E. Hamilton
Hiroshi Nakagawa
Adam J. Bass
Anil K. Rustgi
机构
[1] University of Pennsylvania,Division of Gastroenterology, Department of Medicine, Perelman School of Medicine
[2] Children’s Hospital of Philadelphia,Gastrointestinal Epithelium Modeling Program, Division of Gastroenterology, Hepatology and Nutrition
[3] Massachusetts General Hospital,Division of Thoracic Surgery
[4] University of Pennsylvania,Department of Pathology and Laboratory Medicine, Perelman School of Medicine
[5] Columbia University Irving Medical Center,Division of Digestive and Liver Diseases, Department of Medicine and Herbert Irving Comprehensive Cancer Research Center
[6] University of Pennsylvania,Department of Radiation Oncology, Perelman School of Medicine
[7] Harvard Medical School,Dana
[8] Broad Institute,Farber Cancer Institute
[9] Columbia University Irving Medical Center,Herbert Irving Comprehensive Cancer Research Center
[10] Massachusetts General Hospital,undefined
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摘要
3D patient-derived organoids (PDOs) have been utilized to evaluate potential therapies for patients with different cancers. However, the use of PDOs created from treatment-naive patient biopsies for prediction of clinical outcomes in patients with esophageal cancer has not yet been reported. Herein we describe a pilot prospective observational study with the goal of determining whether esophageal cancer PDOs created from treatment naive patients can model or predict clinical outcomes. Endoscopic biopsies of treatment-naive patients at a single tertiary care center were used to generate esophageal cancer PDOs, which were treated with standard-of-care chemotherapy, gamma-irradiation, and newer non-standard approaches, such as proton beam therapy or two small molecule inhibitors. Clinical outcomes of patients following neoadjuvant treatment were compared to their in vitro PDO responses, demonstrating the PDO’s ability to mirror clinical response, suggesting the value of PDOs in prediction of clinical response to new therapeutic approaches. Future prospective clinical trials should test the use of pre-treatment PDOs to identify specific, targeted therapies for individual patients with esophageal adenocarcinoma.
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