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Targeted therapy with a selective BCL-2 inhibitor in older patients with acute myeloid leukemia
BACKGROUND: Older patients with acute myeloid leukemia are particularly difficult to treat, as they have a high risk of comorbidities, poor performance status and less tolerability to chemotherapy, as well as a more aggressive disease biology, responsible for the resistance to treatment. There is a...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Hematologia e Hemoterapia
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6517609/ https://www.ncbi.nlm.nih.gov/pubmed/31084767 http://dx.doi.org/10.1016/j.htct.2018.09.001 |
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author | Campos, Elisabete do Vale Pinto, Ricardo |
author_facet | Campos, Elisabete do Vale Pinto, Ricardo |
author_sort | Campos, Elisabete do Vale |
collection | PubMed |
description | BACKGROUND: Older patients with acute myeloid leukemia are particularly difficult to treat, as they have a high risk of comorbidities, poor performance status and less tolerability to chemotherapy, as well as a more aggressive disease biology, responsible for the resistance to treatment. There is a need to explore novel therapeutic agents that are more effective and tolerable. Venetoclax, a BCL-2 inhibitor is a promising agent, as BCL-2 overexpression is present in 84% of acute myeloid leukemia patients at diagnosis and 95% of patients at relapse and has been associated with leukemia cell survival, chemotherapy resistance and poor prognosis. OBJECTIVE: To review the available data about venetoclax in acute myeloid leukemia and how it can influence the treatment in older patients. METHODS: Using the Pubmed database, we selected 29 articles published within the last 15 years, considering preclinical and clinical trials and review studies that combined venetoclax with acute myeloid leukemia. RESULTS: Venetoclax has demonstrated promising results in preclinical and clinical trials, especially in patients with poor prognosis and the IDH mutation, with an excellent side-effect profile. However, resistance seems to develop rapidly with venetoclax monotherapy, because of antiapoptotic escape mechanisms. CONCLUSIONS: While the results with the use of venetoclax seem encouraging, it is not likely that targeting a single pathway will result in long-term disease control. The solution includes the use of combined therapy to block resistance mechanisms and enhance apoptosis, by reducing MCL-1, increasing BIM or inhibiting the complex IV in the mitochondria. |
format | Online Article Text |
id | pubmed-6517609 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Sociedade Brasileira de Hematologia e Hemoterapia |
record_format | MEDLINE/PubMed |
spelling | pubmed-65176092019-05-23 Targeted therapy with a selective BCL-2 inhibitor in older patients with acute myeloid leukemia Campos, Elisabete do Vale Pinto, Ricardo Hematol Transfus Cell Ther Review Article BACKGROUND: Older patients with acute myeloid leukemia are particularly difficult to treat, as they have a high risk of comorbidities, poor performance status and less tolerability to chemotherapy, as well as a more aggressive disease biology, responsible for the resistance to treatment. There is a need to explore novel therapeutic agents that are more effective and tolerable. Venetoclax, a BCL-2 inhibitor is a promising agent, as BCL-2 overexpression is present in 84% of acute myeloid leukemia patients at diagnosis and 95% of patients at relapse and has been associated with leukemia cell survival, chemotherapy resistance and poor prognosis. OBJECTIVE: To review the available data about venetoclax in acute myeloid leukemia and how it can influence the treatment in older patients. METHODS: Using the Pubmed database, we selected 29 articles published within the last 15 years, considering preclinical and clinical trials and review studies that combined venetoclax with acute myeloid leukemia. RESULTS: Venetoclax has demonstrated promising results in preclinical and clinical trials, especially in patients with poor prognosis and the IDH mutation, with an excellent side-effect profile. However, resistance seems to develop rapidly with venetoclax monotherapy, because of antiapoptotic escape mechanisms. CONCLUSIONS: While the results with the use of venetoclax seem encouraging, it is not likely that targeting a single pathway will result in long-term disease control. The solution includes the use of combined therapy to block resistance mechanisms and enhance apoptosis, by reducing MCL-1, increasing BIM or inhibiting the complex IV in the mitochondria. Sociedade Brasileira de Hematologia e Hemoterapia 2019 2018-12-29 /pmc/articles/PMC6517609/ /pubmed/31084767 http://dx.doi.org/10.1016/j.htct.2018.09.001 Text en © 2018 Associação Brasileira de Hematologia, Hemoterapia e Terapia Celular. Published by Elsevier Editora Ltda. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Review Article Campos, Elisabete do Vale Pinto, Ricardo Targeted therapy with a selective BCL-2 inhibitor in older patients with acute myeloid leukemia |
title | Targeted therapy with a selective BCL-2 inhibitor in older patients with acute myeloid leukemia |
title_full | Targeted therapy with a selective BCL-2 inhibitor in older patients with acute myeloid leukemia |
title_fullStr | Targeted therapy with a selective BCL-2 inhibitor in older patients with acute myeloid leukemia |
title_full_unstemmed | Targeted therapy with a selective BCL-2 inhibitor in older patients with acute myeloid leukemia |
title_short | Targeted therapy with a selective BCL-2 inhibitor in older patients with acute myeloid leukemia |
title_sort | targeted therapy with a selective bcl-2 inhibitor in older patients with acute myeloid leukemia |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6517609/ https://www.ncbi.nlm.nih.gov/pubmed/31084767 http://dx.doi.org/10.1016/j.htct.2018.09.001 |
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