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Prediction of outcomes by early treatment responses in childhood T-cell acute lymphoblastic leukemia: a retrospective study in China

BACKGROUND: Early treatment responses are important prognostic factors in childhood T-cell acute lymphoblastic leukemia (T-ALL) patients. The predictive values of early treatment responses in Chinese childhood T-ALL patients were still unknown. METHODS: From January 2003 to December 2012, 74 consecu...

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Autores principales: Wei, Wei, Chen, Xiaojuan, Zou, Yao, Chang, Lixian, An, Wenbin, Wan, Yang, Liu, Tianfeng, Yang, Wenyu, Chen, Yumei, Guo, Ye, Zhu, Xiaofan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4502910/
https://www.ncbi.nlm.nih.gov/pubmed/26174476
http://dx.doi.org/10.1186/s12887-015-0390-z
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author Wei, Wei
Chen, Xiaojuan
Zou, Yao
Chang, Lixian
An, Wenbin
Wan, Yang
Liu, Tianfeng
Yang, Wenyu
Chen, Yumei
Guo, Ye
Zhu, Xiaofan
author_facet Wei, Wei
Chen, Xiaojuan
Zou, Yao
Chang, Lixian
An, Wenbin
Wan, Yang
Liu, Tianfeng
Yang, Wenyu
Chen, Yumei
Guo, Ye
Zhu, Xiaofan
author_sort Wei, Wei
collection PubMed
description BACKGROUND: Early treatment responses are important prognostic factors in childhood T-cell acute lymphoblastic leukemia (T-ALL) patients. The predictive values of early treatment responses in Chinese childhood T-ALL patients were still unknown. METHODS: From January 2003 to December 2012, 74 consecutive patients aged ≤15 years with newly diagnosed T-ALL were treated with BCH-2003 protocol or CCLG-2008 protocol in the Department of Pediatric, Institute of Hematology and Blood Diseases Hospital in China. Predictive values of early treatment responses, including prednisone response, bone marrow morphology at day 15 and day 33 during induction chemotherapy, and minimal residual disease (MRD) monitored by flow cytometry after induction therapy (time point 1, TP1) and before consolidation therapy (time point 2, TP2), were analyzed. RESULTS: The 5-year event free survival (EFS) and overall survival (OS) rates for these patients were 62.5 % (SE, 6.4) and 62.7 % (SE, 6.6), respectively. Prednisone poor responder was strongly associated with increased chance of induction failure (14.8 %) and decreased survival rate (5 year EFS rate, 51.1 % (SE, 10.5)). Patients with ≥25 % blast cells in bone marrow at day 15 were more likely to have an inferior outcome. 93.2 % of the T-ALL patients achieved complete remission at day 33 while patients with resistant disease all died of disease progression. MRD ≥10(−2) at TP1 or MRD ≥10(−3) at TP2 was significantly related to dismal prognosis. Risk groups classified by MRD at two time points could stratify patients into different groups: 29.0 % of the patients were MRD standard risk (MRD < 10(−4) at both time points) with 3-year EFS rate of 100 %, 29.0 % were MRD high risk (MRD ≥10(−2) at TP1 or MRD ≥10(−2) at TP2) with 3-year EFS rate of 55.6 % (SE, 16.6) , and the rest of patients were defined as MRD intermediate risk with 3-year EFS rate of 85.7 % (SE, 13.2). CONCLUSION: Our study demonstrated that MRD was the most powerful predictor of treatment outcome in childhood T-ALL patients and conventional morphological assessments of treatment response still played important roles in predicting treatment outcome and tailoring treatment intensity especially in countries with inadequate skills or financial resources for MRD monitoring. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12887-015-0390-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-45029102015-07-16 Prediction of outcomes by early treatment responses in childhood T-cell acute lymphoblastic leukemia: a retrospective study in China Wei, Wei Chen, Xiaojuan Zou, Yao Chang, Lixian An, Wenbin Wan, Yang Liu, Tianfeng Yang, Wenyu Chen, Yumei Guo, Ye Zhu, Xiaofan BMC Pediatr Research Article BACKGROUND: Early treatment responses are important prognostic factors in childhood T-cell acute lymphoblastic leukemia (T-ALL) patients. The predictive values of early treatment responses in Chinese childhood T-ALL patients were still unknown. METHODS: From January 2003 to December 2012, 74 consecutive patients aged ≤15 years with newly diagnosed T-ALL were treated with BCH-2003 protocol or CCLG-2008 protocol in the Department of Pediatric, Institute of Hematology and Blood Diseases Hospital in China. Predictive values of early treatment responses, including prednisone response, bone marrow morphology at day 15 and day 33 during induction chemotherapy, and minimal residual disease (MRD) monitored by flow cytometry after induction therapy (time point 1, TP1) and before consolidation therapy (time point 2, TP2), were analyzed. RESULTS: The 5-year event free survival (EFS) and overall survival (OS) rates for these patients were 62.5 % (SE, 6.4) and 62.7 % (SE, 6.6), respectively. Prednisone poor responder was strongly associated with increased chance of induction failure (14.8 %) and decreased survival rate (5 year EFS rate, 51.1 % (SE, 10.5)). Patients with ≥25 % blast cells in bone marrow at day 15 were more likely to have an inferior outcome. 93.2 % of the T-ALL patients achieved complete remission at day 33 while patients with resistant disease all died of disease progression. MRD ≥10(−2) at TP1 or MRD ≥10(−3) at TP2 was significantly related to dismal prognosis. Risk groups classified by MRD at two time points could stratify patients into different groups: 29.0 % of the patients were MRD standard risk (MRD < 10(−4) at both time points) with 3-year EFS rate of 100 %, 29.0 % were MRD high risk (MRD ≥10(−2) at TP1 or MRD ≥10(−2) at TP2) with 3-year EFS rate of 55.6 % (SE, 16.6) , and the rest of patients were defined as MRD intermediate risk with 3-year EFS rate of 85.7 % (SE, 13.2). CONCLUSION: Our study demonstrated that MRD was the most powerful predictor of treatment outcome in childhood T-ALL patients and conventional morphological assessments of treatment response still played important roles in predicting treatment outcome and tailoring treatment intensity especially in countries with inadequate skills or financial resources for MRD monitoring. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12887-015-0390-z) contains supplementary material, which is available to authorized users. BioMed Central 2015-07-15 /pmc/articles/PMC4502910/ /pubmed/26174476 http://dx.doi.org/10.1186/s12887-015-0390-z Text en © Wei et al. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Wei, Wei
Chen, Xiaojuan
Zou, Yao
Chang, Lixian
An, Wenbin
Wan, Yang
Liu, Tianfeng
Yang, Wenyu
Chen, Yumei
Guo, Ye
Zhu, Xiaofan
Prediction of outcomes by early treatment responses in childhood T-cell acute lymphoblastic leukemia: a retrospective study in China
title Prediction of outcomes by early treatment responses in childhood T-cell acute lymphoblastic leukemia: a retrospective study in China
title_full Prediction of outcomes by early treatment responses in childhood T-cell acute lymphoblastic leukemia: a retrospective study in China
title_fullStr Prediction of outcomes by early treatment responses in childhood T-cell acute lymphoblastic leukemia: a retrospective study in China
title_full_unstemmed Prediction of outcomes by early treatment responses in childhood T-cell acute lymphoblastic leukemia: a retrospective study in China
title_short Prediction of outcomes by early treatment responses in childhood T-cell acute lymphoblastic leukemia: a retrospective study in China
title_sort prediction of outcomes by early treatment responses in childhood t-cell acute lymphoblastic leukemia: a retrospective study in china
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4502910/
https://www.ncbi.nlm.nih.gov/pubmed/26174476
http://dx.doi.org/10.1186/s12887-015-0390-z
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