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Gain of 1q As a Prognostic Biomarker in Wilms Tumors (WTs) Treated With Preoperative Chemotherapy in the International Society of Paediatric Oncology (SIOP) WT 2001 Trial: A SIOP Renal Tumours Biology Consortium Study

PURPOSE: Wilms tumor (WT) is the most common pediatric renal tumor. Treatment planning under International Society of Paediatric Oncology (SIOP) protocols is based on staging and histologic assessment of response to preoperative chemotherapy. Despite high overall survival (OS), many relapses occur i...

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Autores principales: Chagtai, Tasnim, Zill, Christina, Dainese, Linda, Wegert, Jenny, Savola, Suvi, Popov, Sergey, Mifsud, William, Vujanić, Gordan, Sebire, Neil, Le Bouc, Yves, Ambros, Peter F., Kager, Leo, O'Sullivan, Maureen J., Blaise, Annick, Bergeron, Christophe, Mengelbier, Linda Holmquist, Gisselsson, David, Kool, Marcel, Tytgat, Godelieve A.M., van den Heuvel-Eibrink, Marry M., Graf, Norbert, van Tinteren, Harm, Coulomb, Aurore, Gessler, Manfred, Williams, Richard Dafydd, Pritchard-Jones, Kathy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Clinical Oncology 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5505170/
https://www.ncbi.nlm.nih.gov/pubmed/27432915
http://dx.doi.org/10.1200/JCO.2015.66.0001
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author Chagtai, Tasnim
Zill, Christina
Dainese, Linda
Wegert, Jenny
Savola, Suvi
Popov, Sergey
Mifsud, William
Vujanić, Gordan
Sebire, Neil
Le Bouc, Yves
Ambros, Peter F.
Kager, Leo
O'Sullivan, Maureen J.
Blaise, Annick
Bergeron, Christophe
Mengelbier, Linda Holmquist
Gisselsson, David
Kool, Marcel
Tytgat, Godelieve A.M.
van den Heuvel-Eibrink, Marry M.
Graf, Norbert
van Tinteren, Harm
Coulomb, Aurore
Gessler, Manfred
Williams, Richard Dafydd
Pritchard-Jones, Kathy
author_facet Chagtai, Tasnim
Zill, Christina
Dainese, Linda
Wegert, Jenny
Savola, Suvi
Popov, Sergey
Mifsud, William
Vujanić, Gordan
Sebire, Neil
Le Bouc, Yves
Ambros, Peter F.
Kager, Leo
O'Sullivan, Maureen J.
Blaise, Annick
Bergeron, Christophe
Mengelbier, Linda Holmquist
Gisselsson, David
Kool, Marcel
Tytgat, Godelieve A.M.
van den Heuvel-Eibrink, Marry M.
Graf, Norbert
van Tinteren, Harm
Coulomb, Aurore
Gessler, Manfred
Williams, Richard Dafydd
Pritchard-Jones, Kathy
author_sort Chagtai, Tasnim
collection PubMed
description PURPOSE: Wilms tumor (WT) is the most common pediatric renal tumor. Treatment planning under International Society of Paediatric Oncology (SIOP) protocols is based on staging and histologic assessment of response to preoperative chemotherapy. Despite high overall survival (OS), many relapses occur in patients without specific risk factors, and many successfully treated patients are exposed to treatments with significant risks of late effects. To investigate whether molecular biomarkers could improve risk stratification, we assessed 1q status and other potential copy number biomarkers in a large WT series. MATERIALS AND METHODS: WT nephrectomy samples from 586 SIOP WT 2001 patients were analyzed using a multiplex ligation-dependent probe amplification (MLPA) assay that measured the copy number of 1q and other regions of interest. RESULTS: One hundred sixty-seven (28%) of 586 WTs had 1q gain. Five-year event-free survival (EFS) was 75.0% in patients with 1q gain (95% CI, 68.5% to 82.0%) and 88.2% in patients without gain (95% CI, 85.0% to 91.4%). OS was 88.4% with gain (95% CI, 83.5% to 93.6%) and 94.4% without gain (95% CI, 92.1% to 96.7%). In univariable analysis, 1q gain was associated with poorer EFS (P < .001; hazard ratio, 2.33) and OS (P = .01; hazard ratio, 2.16). The association of 1q gain with poorer EFS retained significance in multivariable analysis adjusted for 1p and 16q loss, sex, stage, age, and histologic risk group. Gain of 1q remained associated with poorer EFS in tumor subsets limited to either intermediate-risk localized disease or nonanaplastic localized disease. Other notable aberrations associated with poorer EFS included MYCN gain and TP53 loss. CONCLUSION: Gain of 1q is a potentially valuable prognostic biomarker in WT, in addition to histologic response to preoperative chemotherapy and tumor stage.
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spelling pubmed-55051702017-07-20 Gain of 1q As a Prognostic Biomarker in Wilms Tumors (WTs) Treated With Preoperative Chemotherapy in the International Society of Paediatric Oncology (SIOP) WT 2001 Trial: A SIOP Renal Tumours Biology Consortium Study Chagtai, Tasnim Zill, Christina Dainese, Linda Wegert, Jenny Savola, Suvi Popov, Sergey Mifsud, William Vujanić, Gordan Sebire, Neil Le Bouc, Yves Ambros, Peter F. Kager, Leo O'Sullivan, Maureen J. Blaise, Annick Bergeron, Christophe Mengelbier, Linda Holmquist Gisselsson, David Kool, Marcel Tytgat, Godelieve A.M. van den Heuvel-Eibrink, Marry M. Graf, Norbert van Tinteren, Harm Coulomb, Aurore Gessler, Manfred Williams, Richard Dafydd Pritchard-Jones, Kathy J Clin Oncol ORIGINAL REPORTS PURPOSE: Wilms tumor (WT) is the most common pediatric renal tumor. Treatment planning under International Society of Paediatric Oncology (SIOP) protocols is based on staging and histologic assessment of response to preoperative chemotherapy. Despite high overall survival (OS), many relapses occur in patients without specific risk factors, and many successfully treated patients are exposed to treatments with significant risks of late effects. To investigate whether molecular biomarkers could improve risk stratification, we assessed 1q status and other potential copy number biomarkers in a large WT series. MATERIALS AND METHODS: WT nephrectomy samples from 586 SIOP WT 2001 patients were analyzed using a multiplex ligation-dependent probe amplification (MLPA) assay that measured the copy number of 1q and other regions of interest. RESULTS: One hundred sixty-seven (28%) of 586 WTs had 1q gain. Five-year event-free survival (EFS) was 75.0% in patients with 1q gain (95% CI, 68.5% to 82.0%) and 88.2% in patients without gain (95% CI, 85.0% to 91.4%). OS was 88.4% with gain (95% CI, 83.5% to 93.6%) and 94.4% without gain (95% CI, 92.1% to 96.7%). In univariable analysis, 1q gain was associated with poorer EFS (P < .001; hazard ratio, 2.33) and OS (P = .01; hazard ratio, 2.16). The association of 1q gain with poorer EFS retained significance in multivariable analysis adjusted for 1p and 16q loss, sex, stage, age, and histologic risk group. Gain of 1q remained associated with poorer EFS in tumor subsets limited to either intermediate-risk localized disease or nonanaplastic localized disease. Other notable aberrations associated with poorer EFS included MYCN gain and TP53 loss. CONCLUSION: Gain of 1q is a potentially valuable prognostic biomarker in WT, in addition to histologic response to preoperative chemotherapy and tumor stage. American Society of Clinical Oncology 2016-09-10 2016-07-18 /pmc/articles/PMC5505170/ /pubmed/27432915 http://dx.doi.org/10.1200/JCO.2015.66.0001 Text en © 2016 by American Society of Clinical Oncology http://creativecommons.org/licenses/by/4.0/ Licensed under the Creative Commons Attribution 4.0 License: http://creativecommons.org/licenses/by/4.0/
spellingShingle ORIGINAL REPORTS
Chagtai, Tasnim
Zill, Christina
Dainese, Linda
Wegert, Jenny
Savola, Suvi
Popov, Sergey
Mifsud, William
Vujanić, Gordan
Sebire, Neil
Le Bouc, Yves
Ambros, Peter F.
Kager, Leo
O'Sullivan, Maureen J.
Blaise, Annick
Bergeron, Christophe
Mengelbier, Linda Holmquist
Gisselsson, David
Kool, Marcel
Tytgat, Godelieve A.M.
van den Heuvel-Eibrink, Marry M.
Graf, Norbert
van Tinteren, Harm
Coulomb, Aurore
Gessler, Manfred
Williams, Richard Dafydd
Pritchard-Jones, Kathy
Gain of 1q As a Prognostic Biomarker in Wilms Tumors (WTs) Treated With Preoperative Chemotherapy in the International Society of Paediatric Oncology (SIOP) WT 2001 Trial: A SIOP Renal Tumours Biology Consortium Study
title Gain of 1q As a Prognostic Biomarker in Wilms Tumors (WTs) Treated With Preoperative Chemotherapy in the International Society of Paediatric Oncology (SIOP) WT 2001 Trial: A SIOP Renal Tumours Biology Consortium Study
title_full Gain of 1q As a Prognostic Biomarker in Wilms Tumors (WTs) Treated With Preoperative Chemotherapy in the International Society of Paediatric Oncology (SIOP) WT 2001 Trial: A SIOP Renal Tumours Biology Consortium Study
title_fullStr Gain of 1q As a Prognostic Biomarker in Wilms Tumors (WTs) Treated With Preoperative Chemotherapy in the International Society of Paediatric Oncology (SIOP) WT 2001 Trial: A SIOP Renal Tumours Biology Consortium Study
title_full_unstemmed Gain of 1q As a Prognostic Biomarker in Wilms Tumors (WTs) Treated With Preoperative Chemotherapy in the International Society of Paediatric Oncology (SIOP) WT 2001 Trial: A SIOP Renal Tumours Biology Consortium Study
title_short Gain of 1q As a Prognostic Biomarker in Wilms Tumors (WTs) Treated With Preoperative Chemotherapy in the International Society of Paediatric Oncology (SIOP) WT 2001 Trial: A SIOP Renal Tumours Biology Consortium Study
title_sort gain of 1q as a prognostic biomarker in wilms tumors (wts) treated with preoperative chemotherapy in the international society of paediatric oncology (siop) wt 2001 trial: a siop renal tumours biology consortium study
topic ORIGINAL REPORTS
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5505170/
https://www.ncbi.nlm.nih.gov/pubmed/27432915
http://dx.doi.org/10.1200/JCO.2015.66.0001
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