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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...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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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. |
format | Online Article Text |
id | pubmed-4150519 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
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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