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Dasatinib vs. imatinib in patients with chronic myeloid leukemia in chronic phase (CML-CP) who have not achieved an optimal response to 3 months of imatinib therapy: the DASCERN randomized study
Early molecular response is associated with improved probability of deep molecular response and superior survival in patients with CML-CP. However, ~1 in 3 patients on first-line imatinib do not achieve this threshold. The phase 2b DASCERN trial (NCT01593254) assessed the outcome of early switch to...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7387297/ https://www.ncbi.nlm.nih.gov/pubmed/32265500 http://dx.doi.org/10.1038/s41375-020-0805-1 |
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author | Cortes, Jorge E. Jiang, Qian Wang, Jianxiang Weng, Jianyu Zhu, Huanling Liu, Xiaoli Hochhaus, Andreas Kim, Dong-Wook Radich, Jerald Savona, Michael Martin-Regueira, Patricia Sy, Oumar Gurnani, Renuka Saglio, Giuseppe |
author_facet | Cortes, Jorge E. Jiang, Qian Wang, Jianxiang Weng, Jianyu Zhu, Huanling Liu, Xiaoli Hochhaus, Andreas Kim, Dong-Wook Radich, Jerald Savona, Michael Martin-Regueira, Patricia Sy, Oumar Gurnani, Renuka Saglio, Giuseppe |
author_sort | Cortes, Jorge E. |
collection | PubMed |
description | Early molecular response is associated with improved probability of deep molecular response and superior survival in patients with CML-CP. However, ~1 in 3 patients on first-line imatinib do not achieve this threshold. The phase 2b DASCERN trial (NCT01593254) assessed the outcome of early switch to dasatinib in patients with suboptimal response to first-line imatinib. Adult patients with CML-CP were randomized (2:1) to receive 100 mg dasatinib (n = 174) or continue imatinib at ≥400 mg (n = 86). The primary endpoint was the rate of major molecular response (MMR) at 12 months, which was 29% (dasatinib) and 13% (imatinib; P = 0.005). After ≥2 years of follow-up, 45 patients (52%) randomized to continue imatinib had crossed over to dasatinib. Considering treatment crossover, the 2-year cumulative MMR rate was 64% with dasatinib and 41% with imatinib (66% and 67%, respectively by intent-to-treat). Adverse events were consistent with the established safety profiles of both drugs. The results of this first prospective study support early monitoring of patients treated with first-line imatinib, and suggest that switching to dasatinib in cases of suboptimal response may offer clinical benefit. Further follow-up is needed to assess the long-term clinical benefit of early switching. |
format | Online Article Text |
id | pubmed-7387297 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73872972020-08-11 Dasatinib vs. imatinib in patients with chronic myeloid leukemia in chronic phase (CML-CP) who have not achieved an optimal response to 3 months of imatinib therapy: the DASCERN randomized study Cortes, Jorge E. Jiang, Qian Wang, Jianxiang Weng, Jianyu Zhu, Huanling Liu, Xiaoli Hochhaus, Andreas Kim, Dong-Wook Radich, Jerald Savona, Michael Martin-Regueira, Patricia Sy, Oumar Gurnani, Renuka Saglio, Giuseppe Leukemia Article Early molecular response is associated with improved probability of deep molecular response and superior survival in patients with CML-CP. However, ~1 in 3 patients on first-line imatinib do not achieve this threshold. The phase 2b DASCERN trial (NCT01593254) assessed the outcome of early switch to dasatinib in patients with suboptimal response to first-line imatinib. Adult patients with CML-CP were randomized (2:1) to receive 100 mg dasatinib (n = 174) or continue imatinib at ≥400 mg (n = 86). The primary endpoint was the rate of major molecular response (MMR) at 12 months, which was 29% (dasatinib) and 13% (imatinib; P = 0.005). After ≥2 years of follow-up, 45 patients (52%) randomized to continue imatinib had crossed over to dasatinib. Considering treatment crossover, the 2-year cumulative MMR rate was 64% with dasatinib and 41% with imatinib (66% and 67%, respectively by intent-to-treat). Adverse events were consistent with the established safety profiles of both drugs. The results of this first prospective study support early monitoring of patients treated with first-line imatinib, and suggest that switching to dasatinib in cases of suboptimal response may offer clinical benefit. Further follow-up is needed to assess the long-term clinical benefit of early switching. Nature Publishing Group UK 2020-04-07 2020 /pmc/articles/PMC7387297/ /pubmed/32265500 http://dx.doi.org/10.1038/s41375-020-0805-1 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Cortes, Jorge E. Jiang, Qian Wang, Jianxiang Weng, Jianyu Zhu, Huanling Liu, Xiaoli Hochhaus, Andreas Kim, Dong-Wook Radich, Jerald Savona, Michael Martin-Regueira, Patricia Sy, Oumar Gurnani, Renuka Saglio, Giuseppe Dasatinib vs. imatinib in patients with chronic myeloid leukemia in chronic phase (CML-CP) who have not achieved an optimal response to 3 months of imatinib therapy: the DASCERN randomized study |
title | Dasatinib vs. imatinib in patients with chronic myeloid leukemia in chronic phase (CML-CP) who have not achieved an optimal response to 3 months of imatinib therapy: the DASCERN randomized study |
title_full | Dasatinib vs. imatinib in patients with chronic myeloid leukemia in chronic phase (CML-CP) who have not achieved an optimal response to 3 months of imatinib therapy: the DASCERN randomized study |
title_fullStr | Dasatinib vs. imatinib in patients with chronic myeloid leukemia in chronic phase (CML-CP) who have not achieved an optimal response to 3 months of imatinib therapy: the DASCERN randomized study |
title_full_unstemmed | Dasatinib vs. imatinib in patients with chronic myeloid leukemia in chronic phase (CML-CP) who have not achieved an optimal response to 3 months of imatinib therapy: the DASCERN randomized study |
title_short | Dasatinib vs. imatinib in patients with chronic myeloid leukemia in chronic phase (CML-CP) who have not achieved an optimal response to 3 months of imatinib therapy: the DASCERN randomized study |
title_sort | dasatinib vs. imatinib in patients with chronic myeloid leukemia in chronic phase (cml-cp) who have not achieved an optimal response to 3 months of imatinib therapy: the dascern randomized study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7387297/ https://www.ncbi.nlm.nih.gov/pubmed/32265500 http://dx.doi.org/10.1038/s41375-020-0805-1 |
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