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Peripheral Blood WT1 Expression Predicts Relapse in AML Patients Undergoing Allogeneic Stem Cell Transplantation

To evaluate if WT1 expression may predict relapse after allo-SCT, we analyzed WT1 levels on peripheral blood (PB) and bone marrow (BM) before and after allo-SCT in 24 AML patients with WT1 overexpression at diagnosis. Five copies of WT1/ABL × 10(4) from PB were identified as the threshold value that...

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Autores principales: Malagola, Michele, Skert, Cristina, Ruggeri, Giuseppina, Turra, Alessandro, Ribolla, Rossella, Cancelli, Valeria, Cattina, Federica, Alghisi, Elisa, Bernardi, Simona, Perucca, Simone, Di Palma, Andrea, Borlenghi, Erika, Pagani, Chiara, Rossi, Giuseppe, Caimi, Luigi, Russo, Domenico
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4150519/
https://www.ncbi.nlm.nih.gov/pubmed/25202702
http://dx.doi.org/10.1155/2014/123079
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author Malagola, Michele
Skert, Cristina
Ruggeri, Giuseppina
Turra, Alessandro
Ribolla, Rossella
Cancelli, Valeria
Cattina, Federica
Alghisi, Elisa
Bernardi, Simona
Perucca, Simone
Di Palma, Andrea
Borlenghi, Erika
Pagani, Chiara
Rossi, Giuseppe
Caimi, Luigi
Russo, Domenico
author_facet Malagola, Michele
Skert, Cristina
Ruggeri, Giuseppina
Turra, Alessandro
Ribolla, Rossella
Cancelli, Valeria
Cattina, Federica
Alghisi, Elisa
Bernardi, Simona
Perucca, Simone
Di Palma, Andrea
Borlenghi, Erika
Pagani, Chiara
Rossi, Giuseppe
Caimi, Luigi
Russo, Domenico
author_sort Malagola, Michele
collection PubMed
description To evaluate if WT1 expression may predict relapse after allo-SCT, we analyzed WT1 levels on peripheral blood (PB) and bone marrow (BM) before and after allo-SCT in 24 AML patients with WT1 overexpression at diagnosis. Five copies of WT1/ABL × 10(4) from PB were identified as the threshold value that correlated with relapse after allo-SCT. The same correlation was not identified when WT1 expression was assessed from bone marrow (BM). Eight out of 11 (73%) patients with a pre-allo-SCT PB-WT1 ≥ 5 and 4/13 (31%) patients with a pre-allo-SCT PB-WT1 < 5 relapsed, respectively (P = 0.04). The incidence of relapse was higher in patients with PB-WT1 ≥ 5 measured after allo-SCT, at the 3rd (56% versus 38%; P = 0.43) and at the 6th month (71% versus 20%; P = 0.03). Patients with pretransplant PB-WT1 < 5 had significantly better 2-year OS and LFS than patients with a PB-WT1 ≥ 5 (81% versus 0% and 63% versus 20%) (P = 0.02). Our data suggest the usefulness of WT1 monitoring from PB to predict the relapse in allotransplanted AML patients and to modulate the intensity of conditioning and/or the posttransplant immunosuppression in an attempt to reduce the posttransplant relapse risk.
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spelling pubmed-41505192014-09-08 Peripheral Blood WT1 Expression Predicts Relapse in AML Patients Undergoing Allogeneic Stem Cell Transplantation Malagola, Michele Skert, Cristina Ruggeri, Giuseppina Turra, Alessandro Ribolla, Rossella Cancelli, Valeria Cattina, Federica Alghisi, Elisa Bernardi, Simona Perucca, Simone Di Palma, Andrea Borlenghi, Erika Pagani, Chiara Rossi, Giuseppe Caimi, Luigi Russo, Domenico Biomed Res Int Research Article To evaluate if WT1 expression may predict relapse after allo-SCT, we analyzed WT1 levels on peripheral blood (PB) and bone marrow (BM) before and after allo-SCT in 24 AML patients with WT1 overexpression at diagnosis. Five copies of WT1/ABL × 10(4) from PB were identified as the threshold value that correlated with relapse after allo-SCT. The same correlation was not identified when WT1 expression was assessed from bone marrow (BM). Eight out of 11 (73%) patients with a pre-allo-SCT PB-WT1 ≥ 5 and 4/13 (31%) patients with a pre-allo-SCT PB-WT1 < 5 relapsed, respectively (P = 0.04). The incidence of relapse was higher in patients with PB-WT1 ≥ 5 measured after allo-SCT, at the 3rd (56% versus 38%; P = 0.43) and at the 6th month (71% versus 20%; P = 0.03). Patients with pretransplant PB-WT1 < 5 had significantly better 2-year OS and LFS than patients with a PB-WT1 ≥ 5 (81% versus 0% and 63% versus 20%) (P = 0.02). Our data suggest the usefulness of WT1 monitoring from PB to predict the relapse in allotransplanted AML patients and to modulate the intensity of conditioning and/or the posttransplant immunosuppression in an attempt to reduce the posttransplant relapse risk. Hindawi Publishing Corporation 2014 2014-08-17 /pmc/articles/PMC4150519/ /pubmed/25202702 http://dx.doi.org/10.1155/2014/123079 Text en Copyright © 2014 Michele Malagola et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Malagola, Michele
Skert, Cristina
Ruggeri, Giuseppina
Turra, Alessandro
Ribolla, Rossella
Cancelli, Valeria
Cattina, Federica
Alghisi, Elisa
Bernardi, Simona
Perucca, Simone
Di Palma, Andrea
Borlenghi, Erika
Pagani, Chiara
Rossi, Giuseppe
Caimi, Luigi
Russo, Domenico
Peripheral Blood WT1 Expression Predicts Relapse in AML Patients Undergoing Allogeneic Stem Cell Transplantation
title Peripheral Blood WT1 Expression Predicts Relapse in AML Patients Undergoing Allogeneic Stem Cell Transplantation
title_full Peripheral Blood WT1 Expression Predicts Relapse in AML Patients Undergoing Allogeneic Stem Cell Transplantation
title_fullStr Peripheral Blood WT1 Expression Predicts Relapse in AML Patients Undergoing Allogeneic Stem Cell Transplantation
title_full_unstemmed Peripheral Blood WT1 Expression Predicts Relapse in AML Patients Undergoing Allogeneic Stem Cell Transplantation
title_short Peripheral Blood WT1 Expression Predicts Relapse in AML Patients Undergoing Allogeneic Stem Cell Transplantation
title_sort peripheral blood wt1 expression predicts relapse in aml patients undergoing allogeneic stem cell transplantation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4150519/
https://www.ncbi.nlm.nih.gov/pubmed/25202702
http://dx.doi.org/10.1155/2014/123079
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