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Biliary tract cancer patient-derived xenografts: Surgeon impact on individualized medicine

BACKGROUND & AIMS: Biliary tract tumors are uncommon but highly aggressive malignancies with poor survival outcomes. Due to their low incidence, research into effective therapeutics has been limited. Novel research platforms for pre-clinical studies are desperately needed. We sought to develop a...

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Autores principales: Leiting, Jennifer L., Murphy, Stephen J., Bergquist, John R., Hernandez, Matthew C., Ivanics, Tommy, Abdelrahman, Amro M., Yang, Lin, Lynch, Isaac, Smadbeck, James B., Cleary, Sean P., Nagorney, David M., Torbenson, Michael S., Graham, Rondell P., Roberts, Lewis R., Gores, Gregory J., Smoot, Rory L., Truty, Mark J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7066236/
https://www.ncbi.nlm.nih.gov/pubmed/32181445
http://dx.doi.org/10.1016/j.jhepr.2020.100068
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author Leiting, Jennifer L.
Murphy, Stephen J.
Bergquist, John R.
Hernandez, Matthew C.
Ivanics, Tommy
Abdelrahman, Amro M.
Yang, Lin
Lynch, Isaac
Smadbeck, James B.
Cleary, Sean P.
Nagorney, David M.
Torbenson, Michael S.
Graham, Rondell P.
Roberts, Lewis R.
Gores, Gregory J.
Smoot, Rory L.
Truty, Mark J.
author_facet Leiting, Jennifer L.
Murphy, Stephen J.
Bergquist, John R.
Hernandez, Matthew C.
Ivanics, Tommy
Abdelrahman, Amro M.
Yang, Lin
Lynch, Isaac
Smadbeck, James B.
Cleary, Sean P.
Nagorney, David M.
Torbenson, Michael S.
Graham, Rondell P.
Roberts, Lewis R.
Gores, Gregory J.
Smoot, Rory L.
Truty, Mark J.
author_sort Leiting, Jennifer L.
collection PubMed
description BACKGROUND & AIMS: Biliary tract tumors are uncommon but highly aggressive malignancies with poor survival outcomes. Due to their low incidence, research into effective therapeutics has been limited. Novel research platforms for pre-clinical studies are desperately needed. We sought to develop a patient-derived biliary tract cancer xenograft catalog. METHODS: With appropriate consent and approval, surplus malignant tissues were obtained from surgical resection or radiographic biopsy and implanted into immunocompromised mice. Mice were monitored for xenograft growth. Established xenografts were verified by a hepatobiliary pathologist. Xenograft characteristics were correlated with original patient/tumor characteristics and oncologic outcomes. A subset of xenografts were then genomically characterized using Mate Pair sequencing (MPseq). RESULTS: Between October 2013 and January 2018, 87 patients with histologically confirmed biliary tract carcinomas were enrolled. Of the 87 patients, 47 validated PDX models were successfully generated. The majority of the PDX models were created from surgical resection specimens (n = 44, 94%), which were more likely to successfully engraft when compared to radiologic biopsies (p = 0.03). Histologic recapitulation of original patient tumor morphology was observed in all xenografts. Successful engraftment was an independent predictor for worse recurrence-free survival. MPseq showed genetically diverse tumors with frequent alterations of CDKN2A, SMAD4, NRG1, TP53. Sequencing also identified worse survival in patients with tumors containing tetraploid genomes. CONCLUSIONS: This is the largest series of biliary tract cancer xenografts reported to date. Histologic and genomic analysis of patient-derived xenografts demonstrates accurate recapitulation of original tumor morphology with direct correlations to patient outcomes. Successful development of biliary cancer tumografts is feasible and may be used to direct subsequent therapy in high recurrence risk patients. LAY SUMMARY: Patient biliary tract tumors grown in immunocompromised mice are an invaluable resource in the treatment of biliary tract cancers. They can be used to guide individualized cancer treatment in high-risk patients.
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spelling pubmed-70662362020-03-16 Biliary tract cancer patient-derived xenografts: Surgeon impact on individualized medicine Leiting, Jennifer L. Murphy, Stephen J. Bergquist, John R. Hernandez, Matthew C. Ivanics, Tommy Abdelrahman, Amro M. Yang, Lin Lynch, Isaac Smadbeck, James B. Cleary, Sean P. Nagorney, David M. Torbenson, Michael S. Graham, Rondell P. Roberts, Lewis R. Gores, Gregory J. Smoot, Rory L. Truty, Mark J. JHEP Rep Research Article BACKGROUND & AIMS: Biliary tract tumors are uncommon but highly aggressive malignancies with poor survival outcomes. Due to their low incidence, research into effective therapeutics has been limited. Novel research platforms for pre-clinical studies are desperately needed. We sought to develop a patient-derived biliary tract cancer xenograft catalog. METHODS: With appropriate consent and approval, surplus malignant tissues were obtained from surgical resection or radiographic biopsy and implanted into immunocompromised mice. Mice were monitored for xenograft growth. Established xenografts were verified by a hepatobiliary pathologist. Xenograft characteristics were correlated with original patient/tumor characteristics and oncologic outcomes. A subset of xenografts were then genomically characterized using Mate Pair sequencing (MPseq). RESULTS: Between October 2013 and January 2018, 87 patients with histologically confirmed biliary tract carcinomas were enrolled. Of the 87 patients, 47 validated PDX models were successfully generated. The majority of the PDX models were created from surgical resection specimens (n = 44, 94%), which were more likely to successfully engraft when compared to radiologic biopsies (p = 0.03). Histologic recapitulation of original patient tumor morphology was observed in all xenografts. Successful engraftment was an independent predictor for worse recurrence-free survival. MPseq showed genetically diverse tumors with frequent alterations of CDKN2A, SMAD4, NRG1, TP53. Sequencing also identified worse survival in patients with tumors containing tetraploid genomes. CONCLUSIONS: This is the largest series of biliary tract cancer xenografts reported to date. Histologic and genomic analysis of patient-derived xenografts demonstrates accurate recapitulation of original tumor morphology with direct correlations to patient outcomes. Successful development of biliary cancer tumografts is feasible and may be used to direct subsequent therapy in high recurrence risk patients. LAY SUMMARY: Patient biliary tract tumors grown in immunocompromised mice are an invaluable resource in the treatment of biliary tract cancers. They can be used to guide individualized cancer treatment in high-risk patients. Elsevier 2020-01-16 /pmc/articles/PMC7066236/ /pubmed/32181445 http://dx.doi.org/10.1016/j.jhepr.2020.100068 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Leiting, Jennifer L.
Murphy, Stephen J.
Bergquist, John R.
Hernandez, Matthew C.
Ivanics, Tommy
Abdelrahman, Amro M.
Yang, Lin
Lynch, Isaac
Smadbeck, James B.
Cleary, Sean P.
Nagorney, David M.
Torbenson, Michael S.
Graham, Rondell P.
Roberts, Lewis R.
Gores, Gregory J.
Smoot, Rory L.
Truty, Mark J.
Biliary tract cancer patient-derived xenografts: Surgeon impact on individualized medicine
title Biliary tract cancer patient-derived xenografts: Surgeon impact on individualized medicine
title_full Biliary tract cancer patient-derived xenografts: Surgeon impact on individualized medicine
title_fullStr Biliary tract cancer patient-derived xenografts: Surgeon impact on individualized medicine
title_full_unstemmed Biliary tract cancer patient-derived xenografts: Surgeon impact on individualized medicine
title_short Biliary tract cancer patient-derived xenografts: Surgeon impact on individualized medicine
title_sort biliary tract cancer patient-derived xenografts: surgeon impact on individualized medicine
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7066236/
https://www.ncbi.nlm.nih.gov/pubmed/32181445
http://dx.doi.org/10.1016/j.jhepr.2020.100068
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