What happens to intolerant, relapsed or refractory chronic myeloid leukemia patients without access to clinical trials?

Objective: To assess clinical outcomes of intolerant, relapsed or refractory patients who could not be treated with new tyrosine kinase inhibitors or experimental therapies. Methods: A retrospective cohort of 90 chronic myeloid leukemia patients in all phases of the disease treated with imatinib mes...

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Main Authors: Guilherme Rasia Bosi, Laura Maria Fogliatto, Tito Emilio Vanelli Costa, Kamila Castro Grokoski, Mariana Pinto Pereira, Nathan Bugs, Marco Kalil, Christina Fraga, Liane Esteves Daudt, Lucia Mariano da Rocha Silla
Format: Article
Language:English
Published: Elsevier 2019-07-01
Series:Hematology, Transfusion and Cell Therapy
Online Access:http://www.sciencedirect.com/science/article/pii/S2531137919300288
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spelling doaj-35410a9a2b9f4a8887d3eaf9f18a140c2020-11-25T01:58:09ZengElsevierHematology, Transfusion and Cell Therapy2531-13792019-07-01413222228What happens to intolerant, relapsed or refractory chronic myeloid leukemia patients without access to clinical trials?Guilherme Rasia Bosi0Laura Maria Fogliatto1Tito Emilio Vanelli Costa2Kamila Castro Grokoski3Mariana Pinto Pereira4Nathan Bugs5Marco Kalil6Christina Fraga7Liane Esteves Daudt8Lucia Mariano da Rocha Silla9Corresponding author at: Serviço de Hematologia e Transplante de Medula Óssea do Hospital de Clínicas de Porto Alegre, R. Ramiro Barcelos, 2350 – Santa Cecilia, Porto Alegre CEP: 90035-007, RS, Brazil.; Universidade Federal do Rio Grande do Sul (UFRS), Porto Alegre, RS, BrazilUniversidade Federal do Rio Grande do Sul (UFRS), Porto Alegre, RS, BrazilUniversidade Federal do Rio Grande do Sul (UFRS), Porto Alegre, RS, BrazilUniversidade Federal do Rio Grande do Sul (UFRS), Porto Alegre, RS, BrazilUniversidade Federal do Rio Grande do Sul (UFRS), Porto Alegre, RS, BrazilUniversidade Federal do Rio Grande do Sul (UFRS), Porto Alegre, RS, BrazilUniversidade Federal do Rio Grande do Sul (UFRS), Porto Alegre, RS, BrazilUniversidade Federal do Rio Grande do Sul (UFRS), Porto Alegre, RS, BrazilUniversidade Federal do Rio Grande do Sul (UFRS), Porto Alegre, RS, BrazilUniversidade Federal do Rio Grande do Sul (UFRS), Porto Alegre, RS, BrazilObjective: To assess clinical outcomes of intolerant, relapsed or refractory patients who could not be treated with new tyrosine kinase inhibitors or experimental therapies. Methods: A retrospective cohort of 90 chronic myeloid leukemia patients in all phases of the disease treated with imatinib mesylate as their first TKI therapy, and with dasatinib or nilotinib as the next line of therapy. We evaluated clinical outcomes of these patients, with special focus on the group that needed more than two therapy lines. Results: Thirty-nine percent of patients were refractory or intolerant to imatinib. An 8-year overall survival rate of the patients who went through three or more lines of treatment was significantly lower, compared to those who were able to maintain imatinib as their first-line therapy (83% and 22%, respectively p < 0.01). Decreased overall survival was associated with advanced-phase disease (p < 0.01), failure to achieve major molecular response in first-line treatment (p < 0.01) and interruption of first-line treatment due to any reason (p = 0.023). Failure in achieving complete cytogenetic response and major molecular response and treatment interruption were associated with the progression to the third-line treatment. Conclusion: The critical outcome observed in relapsed, intolerant or refractory chronic phase CML patients reflects the unmet need for this group of patients without an alternative therapy, such as new drugs or experimental therapies in clinical trials. Broader access to newer treatment possibilities is a crucial asset to improve survival among CML patients, especially those refractory or intolerant to first-line therapies. Keywords: Chronic myeloid leukemia, Imatinib mesylate, Dasatinib, Nilotinib, Survival analysishttp://www.sciencedirect.com/science/article/pii/S2531137919300288
collection DOAJ
language English
format Article
sources DOAJ
author Guilherme Rasia Bosi
Laura Maria Fogliatto
Tito Emilio Vanelli Costa
Kamila Castro Grokoski
Mariana Pinto Pereira
Nathan Bugs
Marco Kalil
Christina Fraga
Liane Esteves Daudt
Lucia Mariano da Rocha Silla
spellingShingle Guilherme Rasia Bosi
Laura Maria Fogliatto
Tito Emilio Vanelli Costa
Kamila Castro Grokoski
Mariana Pinto Pereira
Nathan Bugs
Marco Kalil
Christina Fraga
Liane Esteves Daudt
Lucia Mariano da Rocha Silla
What happens to intolerant, relapsed or refractory chronic myeloid leukemia patients without access to clinical trials?
Hematology, Transfusion and Cell Therapy
author_facet Guilherme Rasia Bosi
Laura Maria Fogliatto
Tito Emilio Vanelli Costa
Kamila Castro Grokoski
Mariana Pinto Pereira
Nathan Bugs
Marco Kalil
Christina Fraga
Liane Esteves Daudt
Lucia Mariano da Rocha Silla
author_sort Guilherme Rasia Bosi
title What happens to intolerant, relapsed or refractory chronic myeloid leukemia patients without access to clinical trials?
title_short What happens to intolerant, relapsed or refractory chronic myeloid leukemia patients without access to clinical trials?
title_full What happens to intolerant, relapsed or refractory chronic myeloid leukemia patients without access to clinical trials?
title_fullStr What happens to intolerant, relapsed or refractory chronic myeloid leukemia patients without access to clinical trials?
title_full_unstemmed What happens to intolerant, relapsed or refractory chronic myeloid leukemia patients without access to clinical trials?
title_sort what happens to intolerant, relapsed or refractory chronic myeloid leukemia patients without access to clinical trials?
publisher Elsevier
series Hematology, Transfusion and Cell Therapy
issn 2531-1379
publishDate 2019-07-01
description Objective: To assess clinical outcomes of intolerant, relapsed or refractory patients who could not be treated with new tyrosine kinase inhibitors or experimental therapies. Methods: A retrospective cohort of 90 chronic myeloid leukemia patients in all phases of the disease treated with imatinib mesylate as their first TKI therapy, and with dasatinib or nilotinib as the next line of therapy. We evaluated clinical outcomes of these patients, with special focus on the group that needed more than two therapy lines. Results: Thirty-nine percent of patients were refractory or intolerant to imatinib. An 8-year overall survival rate of the patients who went through three or more lines of treatment was significantly lower, compared to those who were able to maintain imatinib as their first-line therapy (83% and 22%, respectively p < 0.01). Decreased overall survival was associated with advanced-phase disease (p < 0.01), failure to achieve major molecular response in first-line treatment (p < 0.01) and interruption of first-line treatment due to any reason (p = 0.023). Failure in achieving complete cytogenetic response and major molecular response and treatment interruption were associated with the progression to the third-line treatment. Conclusion: The critical outcome observed in relapsed, intolerant or refractory chronic phase CML patients reflects the unmet need for this group of patients without an alternative therapy, such as new drugs or experimental therapies in clinical trials. Broader access to newer treatment possibilities is a crucial asset to improve survival among CML patients, especially those refractory or intolerant to first-line therapies. Keywords: Chronic myeloid leukemia, Imatinib mesylate, Dasatinib, Nilotinib, Survival analysis
url http://www.sciencedirect.com/science/article/pii/S2531137919300288
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