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Day 15 and Day 33 Minimal Residual Disease Assessment for Acute Lymphoblastic Leukemia Patients Treated According to the BFM ALL IC 2009 Protocol: Single-Center Experience of 133 Cases
Introduction: Childhood acute lymphoblastic leukemia (ALL) is a hematologic malignancy characterized by the acquisition of several genetic lesions in the lymphoid progenitors with subsequent proliferation advantage and lack of maturation. Along the years, it has been repeatedly shown that minimal re...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7338564/ https://www.ncbi.nlm.nih.gov/pubmed/32695667 http://dx.doi.org/10.3389/fonc.2020.00923 |
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author | Radu, Letitia-Elena Colita, Andrei Pasca, Sergiu Tomuleasa, Ciprian Popa, Codruta Serban, Catalin Gheorghe, Anca Serbanica, Andreea Jercan, Cristina Marcu, Andra Bica, Ana Teodorescu, Patric Constantinescu, Catalin Petrushev, Bobe Asan, Minodora Jardan, Cerasela Dragomir, Mihaela Tanase, Alina Colita, Anca |
author_facet | Radu, Letitia-Elena Colita, Andrei Pasca, Sergiu Tomuleasa, Ciprian Popa, Codruta Serban, Catalin Gheorghe, Anca Serbanica, Andreea Jercan, Cristina Marcu, Andra Bica, Ana Teodorescu, Patric Constantinescu, Catalin Petrushev, Bobe Asan, Minodora Jardan, Cerasela Dragomir, Mihaela Tanase, Alina Colita, Anca |
author_sort | Radu, Letitia-Elena |
collection | PubMed |
description | Introduction: Childhood acute lymphoblastic leukemia (ALL) is a hematologic malignancy characterized by the acquisition of several genetic lesions in the lymphoid progenitors with subsequent proliferation advantage and lack of maturation. Along the years, it has been repeatedly shown that minimal residual disease (MRD) plays an important role in prognosis and therapy choice. The aim of the current study was to determine the prognostic role of MRD in childhood ALL patients in conjunction with other relevant patient and disease characteristics, thus showing the real-life scenario of childhood ALL. Patients and Methods: The retrospective study includes childhood ALL patients that were treated according to the BFM ALL IC 2009 between January 2016 and December 2018 at the Fundeni Clinical Institute, Bucharest, Romania. Results: None of the variables significantly influenced the induction-related death in our study. None of the variables independently predicted relapse-free survival (RFS) with the highest tendency for statistical significance being represented by poor prednisone response. Non-relapse mortality (NRM) was independently predicted by age, prednisone response, and day 33 flow cytometry-MRD (FCM-MRD). Overall survival (OS) was independently predicted by prednisone response and day 33 FCM-MRD. Event-free survival (EFS) was independently predicted by age, prednisone response, and day 33 FCM-MRD. Conclusion : Prednisone response, day 15 FCM-MRD, day 33 FCM-MRD, and the risk group represent the most important factors that in the current study independently predict childhood ALL prognosis. |
format | Online Article Text |
id | pubmed-7338564 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73385642020-07-20 Day 15 and Day 33 Minimal Residual Disease Assessment for Acute Lymphoblastic Leukemia Patients Treated According to the BFM ALL IC 2009 Protocol: Single-Center Experience of 133 Cases Radu, Letitia-Elena Colita, Andrei Pasca, Sergiu Tomuleasa, Ciprian Popa, Codruta Serban, Catalin Gheorghe, Anca Serbanica, Andreea Jercan, Cristina Marcu, Andra Bica, Ana Teodorescu, Patric Constantinescu, Catalin Petrushev, Bobe Asan, Minodora Jardan, Cerasela Dragomir, Mihaela Tanase, Alina Colita, Anca Front Oncol Oncology Introduction: Childhood acute lymphoblastic leukemia (ALL) is a hematologic malignancy characterized by the acquisition of several genetic lesions in the lymphoid progenitors with subsequent proliferation advantage and lack of maturation. Along the years, it has been repeatedly shown that minimal residual disease (MRD) plays an important role in prognosis and therapy choice. The aim of the current study was to determine the prognostic role of MRD in childhood ALL patients in conjunction with other relevant patient and disease characteristics, thus showing the real-life scenario of childhood ALL. Patients and Methods: The retrospective study includes childhood ALL patients that were treated according to the BFM ALL IC 2009 between January 2016 and December 2018 at the Fundeni Clinical Institute, Bucharest, Romania. Results: None of the variables significantly influenced the induction-related death in our study. None of the variables independently predicted relapse-free survival (RFS) with the highest tendency for statistical significance being represented by poor prednisone response. Non-relapse mortality (NRM) was independently predicted by age, prednisone response, and day 33 flow cytometry-MRD (FCM-MRD). Overall survival (OS) was independently predicted by prednisone response and day 33 FCM-MRD. Event-free survival (EFS) was independently predicted by age, prednisone response, and day 33 FCM-MRD. Conclusion : Prednisone response, day 15 FCM-MRD, day 33 FCM-MRD, and the risk group represent the most important factors that in the current study independently predict childhood ALL prognosis. Frontiers Media S.A. 2020-06-30 /pmc/articles/PMC7338564/ /pubmed/32695667 http://dx.doi.org/10.3389/fonc.2020.00923 Text en Copyright © 2020 Radu, Colita, Pasca, Tomuleasa, Popa, Serban, Gheorghe, Serbanica, Jercan, Marcu, Bica, Teodorescu, Constantinescu, Petrushev, Asan, Jardan, Dragomir, Tanase and Colita. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Radu, Letitia-Elena Colita, Andrei Pasca, Sergiu Tomuleasa, Ciprian Popa, Codruta Serban, Catalin Gheorghe, Anca Serbanica, Andreea Jercan, Cristina Marcu, Andra Bica, Ana Teodorescu, Patric Constantinescu, Catalin Petrushev, Bobe Asan, Minodora Jardan, Cerasela Dragomir, Mihaela Tanase, Alina Colita, Anca Day 15 and Day 33 Minimal Residual Disease Assessment for Acute Lymphoblastic Leukemia Patients Treated According to the BFM ALL IC 2009 Protocol: Single-Center Experience of 133 Cases |
title | Day 15 and Day 33 Minimal Residual Disease Assessment for Acute Lymphoblastic Leukemia Patients Treated According to the BFM ALL IC 2009 Protocol: Single-Center Experience of 133 Cases |
title_full | Day 15 and Day 33 Minimal Residual Disease Assessment for Acute Lymphoblastic Leukemia Patients Treated According to the BFM ALL IC 2009 Protocol: Single-Center Experience of 133 Cases |
title_fullStr | Day 15 and Day 33 Minimal Residual Disease Assessment for Acute Lymphoblastic Leukemia Patients Treated According to the BFM ALL IC 2009 Protocol: Single-Center Experience of 133 Cases |
title_full_unstemmed | Day 15 and Day 33 Minimal Residual Disease Assessment for Acute Lymphoblastic Leukemia Patients Treated According to the BFM ALL IC 2009 Protocol: Single-Center Experience of 133 Cases |
title_short | Day 15 and Day 33 Minimal Residual Disease Assessment for Acute Lymphoblastic Leukemia Patients Treated According to the BFM ALL IC 2009 Protocol: Single-Center Experience of 133 Cases |
title_sort | day 15 and day 33 minimal residual disease assessment for acute lymphoblastic leukemia patients treated according to the bfm all ic 2009 protocol: single-center experience of 133 cases |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7338564/ https://www.ncbi.nlm.nih.gov/pubmed/32695667 http://dx.doi.org/10.3389/fonc.2020.00923 |
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