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Relevance of treatment‐free remission recommendations in chronic phase chronic leukemia patients treated with frontline tyrosine kinase inhibitors

BACKGROUND: Tyrosine kinase inhibitors (TKI) can be safely discontinued in chronic phase chronic myeloid leukemia (CP‐CML) patients who had achieved a sustained deep molecular response. Based on the results of discontinuation trials, recommendations regarding patient selection for a treatment‐free r...

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Autores principales: Etienne, Gabriel, Faberes, Carole, Bauduer, Fréderic, Adiko, Didier, Lifermann, François, Dagada, Corinne, Lenoir, Caroline, Schmitt, Anna, Klein, Emilie, Fort, Marie‐Pierre, Bijou, Fontanet, Turcq, Beatrice, Robbesyn, Fanny, Durrieu, Françoise, Versmée, Laura, Madene, Samia, Moldovan, Marius, Katsahian, Sandrine, Charles‐Nelson, Anais, Lascaux, Axelle, Mahon, François‐Xavier, Dulucq, Stéphanie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8178499/
https://www.ncbi.nlm.nih.gov/pubmed/33988316
http://dx.doi.org/10.1002/cam4.3921
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author Etienne, Gabriel
Faberes, Carole
Bauduer, Fréderic
Adiko, Didier
Lifermann, François
Dagada, Corinne
Lenoir, Caroline
Schmitt, Anna
Klein, Emilie
Fort, Marie‐Pierre
Bijou, Fontanet
Turcq, Beatrice
Robbesyn, Fanny
Durrieu, Françoise
Versmée, Laura
Madene, Samia
Moldovan, Marius
Katsahian, Sandrine
Charles‐Nelson, Anais
Lascaux, Axelle
Mahon, François‐Xavier
Dulucq, Stéphanie
author_facet Etienne, Gabriel
Faberes, Carole
Bauduer, Fréderic
Adiko, Didier
Lifermann, François
Dagada, Corinne
Lenoir, Caroline
Schmitt, Anna
Klein, Emilie
Fort, Marie‐Pierre
Bijou, Fontanet
Turcq, Beatrice
Robbesyn, Fanny
Durrieu, Françoise
Versmée, Laura
Madene, Samia
Moldovan, Marius
Katsahian, Sandrine
Charles‐Nelson, Anais
Lascaux, Axelle
Mahon, François‐Xavier
Dulucq, Stéphanie
author_sort Etienne, Gabriel
collection PubMed
description BACKGROUND: Tyrosine kinase inhibitors (TKI) can be safely discontinued in chronic phase chronic myeloid leukemia (CP‐CML) patients who had achieved a sustained deep molecular response. Based on the results of discontinuation trials, recommendations regarding patient selection for a treatment‐free remission (TFR) attempt had been proposed. The aims of this study were to evaluate the rate of patients eligible for TKI discontinuation and molecular recurrence‐free survival (MRFS) after stop according to recommendations. METHODS: Over a 10‐year period, newly diagnosed CP‐CML patients and treated with first‐line TKI in the nine French participating centers were included. Eligibility to treatment discontinuation and MRFS were analyzed and compared according to selection criteria defined by recommendations and first‐line treatments. RESULTS: From January 2006 to December 2015, 398 patients were considered. Among them, 73% and 27% of patients received imatinib or either second or third generation tyrosine kinase inhibitors as frontline treatment, respectively. Considering the selection criteria defined by recommendations, up to 55% of the patients were selected as optimal candidates for treatment discontinuation. Overall 95/398 (24%) discontinued treatment. MRFS was 51.8% [95% CI 41.41–62.19] at 2 years and 43.8% [31.45–56.15] at 5 years. Patients receiving frontline second‐generation TKI and fulfilling the eligibility criteria suggested by recommendations had the lowest probability of molecular relapse after TKI stop when compare to others. CONCLUSION: One third of CP‐CML patients treated with TKI frontline fulfilled the selection criteria suggested by European LeukemiaNet TFR recommendations. Meeting selection criteria and second‐generation TKI frontline were associated with the highest MRFS.
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spelling pubmed-81784992021-06-15 Relevance of treatment‐free remission recommendations in chronic phase chronic leukemia patients treated with frontline tyrosine kinase inhibitors Etienne, Gabriel Faberes, Carole Bauduer, Fréderic Adiko, Didier Lifermann, François Dagada, Corinne Lenoir, Caroline Schmitt, Anna Klein, Emilie Fort, Marie‐Pierre Bijou, Fontanet Turcq, Beatrice Robbesyn, Fanny Durrieu, Françoise Versmée, Laura Madene, Samia Moldovan, Marius Katsahian, Sandrine Charles‐Nelson, Anais Lascaux, Axelle Mahon, François‐Xavier Dulucq, Stéphanie Cancer Med Clinical Cancer Research BACKGROUND: Tyrosine kinase inhibitors (TKI) can be safely discontinued in chronic phase chronic myeloid leukemia (CP‐CML) patients who had achieved a sustained deep molecular response. Based on the results of discontinuation trials, recommendations regarding patient selection for a treatment‐free remission (TFR) attempt had been proposed. The aims of this study were to evaluate the rate of patients eligible for TKI discontinuation and molecular recurrence‐free survival (MRFS) after stop according to recommendations. METHODS: Over a 10‐year period, newly diagnosed CP‐CML patients and treated with first‐line TKI in the nine French participating centers were included. Eligibility to treatment discontinuation and MRFS were analyzed and compared according to selection criteria defined by recommendations and first‐line treatments. RESULTS: From January 2006 to December 2015, 398 patients were considered. Among them, 73% and 27% of patients received imatinib or either second or third generation tyrosine kinase inhibitors as frontline treatment, respectively. Considering the selection criteria defined by recommendations, up to 55% of the patients were selected as optimal candidates for treatment discontinuation. Overall 95/398 (24%) discontinued treatment. MRFS was 51.8% [95% CI 41.41–62.19] at 2 years and 43.8% [31.45–56.15] at 5 years. Patients receiving frontline second‐generation TKI and fulfilling the eligibility criteria suggested by recommendations had the lowest probability of molecular relapse after TKI stop when compare to others. CONCLUSION: One third of CP‐CML patients treated with TKI frontline fulfilled the selection criteria suggested by European LeukemiaNet TFR recommendations. Meeting selection criteria and second‐generation TKI frontline were associated with the highest MRFS. John Wiley and Sons Inc. 2021-05-14 /pmc/articles/PMC8178499/ /pubmed/33988316 http://dx.doi.org/10.1002/cam4.3921 Text en © 2021 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Cancer Research
Etienne, Gabriel
Faberes, Carole
Bauduer, Fréderic
Adiko, Didier
Lifermann, François
Dagada, Corinne
Lenoir, Caroline
Schmitt, Anna
Klein, Emilie
Fort, Marie‐Pierre
Bijou, Fontanet
Turcq, Beatrice
Robbesyn, Fanny
Durrieu, Françoise
Versmée, Laura
Madene, Samia
Moldovan, Marius
Katsahian, Sandrine
Charles‐Nelson, Anais
Lascaux, Axelle
Mahon, François‐Xavier
Dulucq, Stéphanie
Relevance of treatment‐free remission recommendations in chronic phase chronic leukemia patients treated with frontline tyrosine kinase inhibitors
title Relevance of treatment‐free remission recommendations in chronic phase chronic leukemia patients treated with frontline tyrosine kinase inhibitors
title_full Relevance of treatment‐free remission recommendations in chronic phase chronic leukemia patients treated with frontline tyrosine kinase inhibitors
title_fullStr Relevance of treatment‐free remission recommendations in chronic phase chronic leukemia patients treated with frontline tyrosine kinase inhibitors
title_full_unstemmed Relevance of treatment‐free remission recommendations in chronic phase chronic leukemia patients treated with frontline tyrosine kinase inhibitors
title_short Relevance of treatment‐free remission recommendations in chronic phase chronic leukemia patients treated with frontline tyrosine kinase inhibitors
title_sort relevance of treatment‐free remission recommendations in chronic phase chronic leukemia patients treated with frontline tyrosine kinase inhibitors
topic Clinical Cancer Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8178499/
https://www.ncbi.nlm.nih.gov/pubmed/33988316
http://dx.doi.org/10.1002/cam4.3921
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