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The feasibility of PETHEMA ALL-96 regimen on treatment of patients with acute lymphoid leukemia
BACKGROUND: Asparaginase-based treatment regimen for acute lymphocytic leukemia (ALL) is considered as feasible, but there is still a lack of data. In this study, considering the results of other regimen that were not optimum in previous studies. Here, we aimed to investigate the feasibility of PETH...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10199372/ https://www.ncbi.nlm.nih.gov/pubmed/37213449 http://dx.doi.org/10.4103/jrms.jrms_4_22 |
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author | Ashrafi, Farzaneh Sadeghi, Alireza Derakhshandeh, Ali Oghab, Padideh |
author_facet | Ashrafi, Farzaneh Sadeghi, Alireza Derakhshandeh, Ali Oghab, Padideh |
author_sort | Ashrafi, Farzaneh |
collection | PubMed |
description | BACKGROUND: Asparaginase-based treatment regimen for acute lymphocytic leukemia (ALL) is considered as feasible, but there is still a lack of data. In this study, considering the results of other regimen that were not optimum in previous studies. Here, we aimed to investigate the feasibility of PETHEMA ALL-96 treatment regimen. MATERIALS AND METHODS: This is a retrospective feasibility study that was performed in 2019–2021 on 13 patients diagnosed with B-cell ALL. Patients were treated by PETHEMA ALL-96 regimen during induction, consolidation, reinduction, and maintenance phases. Patients were followed for 2 years after initiation of PETHEMA ALL-96 regimen for disease-free survival (DFS) and overall survival (OS) of all patients were evaluated after 2 years. RESULTS: Data of 11 patients were analyzed. Within 28 days after treatments, all patients (100%) had no blasts in the bone marrow that was considered as complete remission (CR). The CR rate was 100% within 6 months and 12 months and 81.8% within 2 years after the treatments. Evaluation of OS, CR, and DFS regarding 6, 12, and 24 months showed 100% for all items after 6 and 12 months. After 24 months, the CR was 90.9%, the OS was 81.8% and the DFS was 90.9%. None of the patients died during the induction phase and during the 12 months study. No side effects were observed. CONCLUSION: The PETHEMA ALL-96 had high feasibility and survival rates with no side effects during the study course. It is believed that PETHEMA ALL-96 regimen has beneficial outcomes in young patients with ALL. |
format | Online Article Text |
id | pubmed-10199372 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-101993722023-05-21 The feasibility of PETHEMA ALL-96 regimen on treatment of patients with acute lymphoid leukemia Ashrafi, Farzaneh Sadeghi, Alireza Derakhshandeh, Ali Oghab, Padideh J Res Med Sci Original Article BACKGROUND: Asparaginase-based treatment regimen for acute lymphocytic leukemia (ALL) is considered as feasible, but there is still a lack of data. In this study, considering the results of other regimen that were not optimum in previous studies. Here, we aimed to investigate the feasibility of PETHEMA ALL-96 treatment regimen. MATERIALS AND METHODS: This is a retrospective feasibility study that was performed in 2019–2021 on 13 patients diagnosed with B-cell ALL. Patients were treated by PETHEMA ALL-96 regimen during induction, consolidation, reinduction, and maintenance phases. Patients were followed for 2 years after initiation of PETHEMA ALL-96 regimen for disease-free survival (DFS) and overall survival (OS) of all patients were evaluated after 2 years. RESULTS: Data of 11 patients were analyzed. Within 28 days after treatments, all patients (100%) had no blasts in the bone marrow that was considered as complete remission (CR). The CR rate was 100% within 6 months and 12 months and 81.8% within 2 years after the treatments. Evaluation of OS, CR, and DFS regarding 6, 12, and 24 months showed 100% for all items after 6 and 12 months. After 24 months, the CR was 90.9%, the OS was 81.8% and the DFS was 90.9%. None of the patients died during the induction phase and during the 12 months study. No side effects were observed. CONCLUSION: The PETHEMA ALL-96 had high feasibility and survival rates with no side effects during the study course. It is believed that PETHEMA ALL-96 regimen has beneficial outcomes in young patients with ALL. Wolters Kluwer - Medknow 2023-04-20 /pmc/articles/PMC10199372/ /pubmed/37213449 http://dx.doi.org/10.4103/jrms.jrms_4_22 Text en Copyright: © 2023 Journal of Research in Medical Sciences https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Ashrafi, Farzaneh Sadeghi, Alireza Derakhshandeh, Ali Oghab, Padideh The feasibility of PETHEMA ALL-96 regimen on treatment of patients with acute lymphoid leukemia |
title | The feasibility of PETHEMA ALL-96 regimen on treatment of patients with acute lymphoid leukemia |
title_full | The feasibility of PETHEMA ALL-96 regimen on treatment of patients with acute lymphoid leukemia |
title_fullStr | The feasibility of PETHEMA ALL-96 regimen on treatment of patients with acute lymphoid leukemia |
title_full_unstemmed | The feasibility of PETHEMA ALL-96 regimen on treatment of patients with acute lymphoid leukemia |
title_short | The feasibility of PETHEMA ALL-96 regimen on treatment of patients with acute lymphoid leukemia |
title_sort | feasibility of pethema all-96 regimen on treatment of patients with acute lymphoid leukemia |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10199372/ https://www.ncbi.nlm.nih.gov/pubmed/37213449 http://dx.doi.org/10.4103/jrms.jrms_4_22 |
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