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Prospective Validation of an Ex Vivo, Patient-Derived 3D Spheroid Model for Response Predictions in Newly Diagnosed Ovarian Cancer

Although 70–80% of newly diagnosed ovarian cancer patients respond to first-line therapy, almost all relapse and five-year survival remains below 50%. One strategy to increase five-year survival is prolonging time to relapse by improving first-line therapy response. However, no biomarker today can a...

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Autores principales: Shuford, Stephen, Wilhelm, Christine, Rayner, Melissa, Elrod, Ashley, Millard, Melissa, Mattingly, Christina, Lotstein, Alina, Smith, Ashley M., Guo, Qi Jin, O’Donnell, Lauren, Elder, Jeffrey, Puls, Larry, Weroha, S. John, Hou, Xiaonan, Zanfagnin, Valentina, Nick, Alpa, Stany, Michael P., Maxwell, G. Larry, Conrads, Thomas, Sood, Anil K., Orr, David, Holmes, Lillia M., Gevaert, Matthew, Crosswell, Howland E., DesRochers, Teresa M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6671958/
https://www.ncbi.nlm.nih.gov/pubmed/31371750
http://dx.doi.org/10.1038/s41598-019-47578-7
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author Shuford, Stephen
Wilhelm, Christine
Rayner, Melissa
Elrod, Ashley
Millard, Melissa
Mattingly, Christina
Lotstein, Alina
Smith, Ashley M.
Guo, Qi Jin
O’Donnell, Lauren
Elder, Jeffrey
Puls, Larry
Weroha, S. John
Hou, Xiaonan
Zanfagnin, Valentina
Nick, Alpa
Stany, Michael P.
Maxwell, G. Larry
Conrads, Thomas
Sood, Anil K.
Orr, David
Holmes, Lillia M.
Gevaert, Matthew
Crosswell, Howland E.
DesRochers, Teresa M.
author_facet Shuford, Stephen
Wilhelm, Christine
Rayner, Melissa
Elrod, Ashley
Millard, Melissa
Mattingly, Christina
Lotstein, Alina
Smith, Ashley M.
Guo, Qi Jin
O’Donnell, Lauren
Elder, Jeffrey
Puls, Larry
Weroha, S. John
Hou, Xiaonan
Zanfagnin, Valentina
Nick, Alpa
Stany, Michael P.
Maxwell, G. Larry
Conrads, Thomas
Sood, Anil K.
Orr, David
Holmes, Lillia M.
Gevaert, Matthew
Crosswell, Howland E.
DesRochers, Teresa M.
author_sort Shuford, Stephen
collection PubMed
description Although 70–80% of newly diagnosed ovarian cancer patients respond to first-line therapy, almost all relapse and five-year survival remains below 50%. One strategy to increase five-year survival is prolonging time to relapse by improving first-line therapy response. However, no biomarker today can accurately predict individual response to therapy. In this study, we present analytical and prospective clinical validation of a new test that utilizes primary patient tissue in 3D cell culture to make patient-specific response predictions prior to initiation of treatment in the clinic. Test results were generated within seven days of tissue receipt from newly diagnosed ovarian cancer patients obtained at standard surgical debulking or laparoscopic biopsy. Patients were followed for clinical response to chemotherapy. In a study population of 44, the 32 test-predicted Responders had a clinical response rate of 100% across both adjuvant and neoadjuvant treated populations with an overall prediction accuracy of 89% (39 of 44, p < 0.0001). The test also functioned as a prognostic readout with test-predicted Responders having a significantly increased progression-free survival compared to test-predicted Non-Responders, p = 0.01. This correlative accuracy establishes the test’s potential to benefit ovarian cancer patients through accurate prediction of patient-specific response before treatment.
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spelling pubmed-66719582019-08-07 Prospective Validation of an Ex Vivo, Patient-Derived 3D Spheroid Model for Response Predictions in Newly Diagnosed Ovarian Cancer Shuford, Stephen Wilhelm, Christine Rayner, Melissa Elrod, Ashley Millard, Melissa Mattingly, Christina Lotstein, Alina Smith, Ashley M. Guo, Qi Jin O’Donnell, Lauren Elder, Jeffrey Puls, Larry Weroha, S. John Hou, Xiaonan Zanfagnin, Valentina Nick, Alpa Stany, Michael P. Maxwell, G. Larry Conrads, Thomas Sood, Anil K. Orr, David Holmes, Lillia M. Gevaert, Matthew Crosswell, Howland E. DesRochers, Teresa M. Sci Rep Article Although 70–80% of newly diagnosed ovarian cancer patients respond to first-line therapy, almost all relapse and five-year survival remains below 50%. One strategy to increase five-year survival is prolonging time to relapse by improving first-line therapy response. However, no biomarker today can accurately predict individual response to therapy. In this study, we present analytical and prospective clinical validation of a new test that utilizes primary patient tissue in 3D cell culture to make patient-specific response predictions prior to initiation of treatment in the clinic. Test results were generated within seven days of tissue receipt from newly diagnosed ovarian cancer patients obtained at standard surgical debulking or laparoscopic biopsy. Patients were followed for clinical response to chemotherapy. In a study population of 44, the 32 test-predicted Responders had a clinical response rate of 100% across both adjuvant and neoadjuvant treated populations with an overall prediction accuracy of 89% (39 of 44, p < 0.0001). The test also functioned as a prognostic readout with test-predicted Responders having a significantly increased progression-free survival compared to test-predicted Non-Responders, p = 0.01. This correlative accuracy establishes the test’s potential to benefit ovarian cancer patients through accurate prediction of patient-specific response before treatment. Nature Publishing Group UK 2019-08-01 /pmc/articles/PMC6671958/ /pubmed/31371750 http://dx.doi.org/10.1038/s41598-019-47578-7 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Shuford, Stephen
Wilhelm, Christine
Rayner, Melissa
Elrod, Ashley
Millard, Melissa
Mattingly, Christina
Lotstein, Alina
Smith, Ashley M.
Guo, Qi Jin
O’Donnell, Lauren
Elder, Jeffrey
Puls, Larry
Weroha, S. John
Hou, Xiaonan
Zanfagnin, Valentina
Nick, Alpa
Stany, Michael P.
Maxwell, G. Larry
Conrads, Thomas
Sood, Anil K.
Orr, David
Holmes, Lillia M.
Gevaert, Matthew
Crosswell, Howland E.
DesRochers, Teresa M.
Prospective Validation of an Ex Vivo, Patient-Derived 3D Spheroid Model for Response Predictions in Newly Diagnosed Ovarian Cancer
title Prospective Validation of an Ex Vivo, Patient-Derived 3D Spheroid Model for Response Predictions in Newly Diagnosed Ovarian Cancer
title_full Prospective Validation of an Ex Vivo, Patient-Derived 3D Spheroid Model for Response Predictions in Newly Diagnosed Ovarian Cancer
title_fullStr Prospective Validation of an Ex Vivo, Patient-Derived 3D Spheroid Model for Response Predictions in Newly Diagnosed Ovarian Cancer
title_full_unstemmed Prospective Validation of an Ex Vivo, Patient-Derived 3D Spheroid Model for Response Predictions in Newly Diagnosed Ovarian Cancer
title_short Prospective Validation of an Ex Vivo, Patient-Derived 3D Spheroid Model for Response Predictions in Newly Diagnosed Ovarian Cancer
title_sort prospective validation of an ex vivo, patient-derived 3d spheroid model for response predictions in newly diagnosed ovarian cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6671958/
https://www.ncbi.nlm.nih.gov/pubmed/31371750
http://dx.doi.org/10.1038/s41598-019-47578-7
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