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IGHV mutational status and outcome for patients with chronic lymphocytic leukemia upon treatment: a Danish nationwide population-based study

Patients with chronic lymphocytic leukemia and unmutated immunoglobulin heavy-chain variable region gene (IGHV) have inferior survival from time of treatment in clinical studies. We assessed real-world outcomes based on mutational status and treatment regimen in a nationwide population-based cohort,...

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Autores principales: Rotbain, Emelie Curovic, Frederiksen, Henrik, Hjalgrim, Henrik, Rostgaard, Klaus, Egholm, Gudrun Jakubsdottir, Zahedi, Banafsheh, Poulsen, Christian Bjørn, Enggard, Lisbeth, da Cunha-Bang, Caspar, Niemann, Carsten Utoft
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ferrata Storti Foundation 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7271602/
https://www.ncbi.nlm.nih.gov/pubmed/31582540
http://dx.doi.org/10.3324/haematol.2019.220194
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author Rotbain, Emelie Curovic
Frederiksen, Henrik
Hjalgrim, Henrik
Rostgaard, Klaus
Egholm, Gudrun Jakubsdottir
Zahedi, Banafsheh
Poulsen, Christian Bjørn
Enggard, Lisbeth
da Cunha-Bang, Caspar
Niemann, Carsten Utoft
author_facet Rotbain, Emelie Curovic
Frederiksen, Henrik
Hjalgrim, Henrik
Rostgaard, Klaus
Egholm, Gudrun Jakubsdottir
Zahedi, Banafsheh
Poulsen, Christian Bjørn
Enggard, Lisbeth
da Cunha-Bang, Caspar
Niemann, Carsten Utoft
author_sort Rotbain, Emelie Curovic
collection PubMed
description Patients with chronic lymphocytic leukemia and unmutated immunoglobulin heavy-chain variable region gene (IGHV) have inferior survival from time of treatment in clinical studies. We assessed real-world outcomes based on mutational status and treatment regimen in a nationwide population-based cohort, comprising all 4,135 patients from the Danish chronic lymphocytic leukemia registry diagnosed between 2008 and 2017. In total, 850 patients with known mutational status received treatment: 42% of patients received intensive chemoimmunotherapy consisting of fludarabine, cyclophosphamide plus rituximab, or bendamustine plus rituximab; 27% received chlorambucil in combination with anti-CD20 antibodies or as monotherapy, and 31% received other, less common treatments. No difference in overall survival from time of first treatment according to mutational status was observed, while treatment-free survival from start of first treatment was inferior for patients with unmutated IGHV. The median treatment-free survival was 2.5 years for patients treated with chlorambucil plus anti-CD20, and 1 year for those who received chlorambucil monotherapy. The 3-year treatment-free survival rates for patients treated with fludarabine, cyclophosphamide plus rituximab, and bendamustine plus rituximab were 90% and 91% for those with mutated IGHV, and 76% and 53% for those with unmutated IGHV, respectively, and the 3-year overall survival rates were similar for the two regimens (86-88%). Thus, it appears that, in the real-world setting, patients progressing after intensive chemoimmunotherapy as first-line therapy can be rescued by subsequent treatment, without jeopardizing their long overall survival. Intensive chemoimmunotherapy remains a legitimate option alongside targeted agents, and part of a personalized treatment landscape in chronic lymphocytic leukemia, while improved supportive care and treatment options are warranted for unfit patients.
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spelling pubmed-72716022020-06-12 IGHV mutational status and outcome for patients with chronic lymphocytic leukemia upon treatment: a Danish nationwide population-based study Rotbain, Emelie Curovic Frederiksen, Henrik Hjalgrim, Henrik Rostgaard, Klaus Egholm, Gudrun Jakubsdottir Zahedi, Banafsheh Poulsen, Christian Bjørn Enggard, Lisbeth da Cunha-Bang, Caspar Niemann, Carsten Utoft Haematologica Articles Patients with chronic lymphocytic leukemia and unmutated immunoglobulin heavy-chain variable region gene (IGHV) have inferior survival from time of treatment in clinical studies. We assessed real-world outcomes based on mutational status and treatment regimen in a nationwide population-based cohort, comprising all 4,135 patients from the Danish chronic lymphocytic leukemia registry diagnosed between 2008 and 2017. In total, 850 patients with known mutational status received treatment: 42% of patients received intensive chemoimmunotherapy consisting of fludarabine, cyclophosphamide plus rituximab, or bendamustine plus rituximab; 27% received chlorambucil in combination with anti-CD20 antibodies or as monotherapy, and 31% received other, less common treatments. No difference in overall survival from time of first treatment according to mutational status was observed, while treatment-free survival from start of first treatment was inferior for patients with unmutated IGHV. The median treatment-free survival was 2.5 years for patients treated with chlorambucil plus anti-CD20, and 1 year for those who received chlorambucil monotherapy. The 3-year treatment-free survival rates for patients treated with fludarabine, cyclophosphamide plus rituximab, and bendamustine plus rituximab were 90% and 91% for those with mutated IGHV, and 76% and 53% for those with unmutated IGHV, respectively, and the 3-year overall survival rates were similar for the two regimens (86-88%). Thus, it appears that, in the real-world setting, patients progressing after intensive chemoimmunotherapy as first-line therapy can be rescued by subsequent treatment, without jeopardizing their long overall survival. Intensive chemoimmunotherapy remains a legitimate option alongside targeted agents, and part of a personalized treatment landscape in chronic lymphocytic leukemia, while improved supportive care and treatment options are warranted for unfit patients. Ferrata Storti Foundation 2020-06 /pmc/articles/PMC7271602/ /pubmed/31582540 http://dx.doi.org/10.3324/haematol.2019.220194 Text en Copyright© 2020 Ferrata Storti Foundation Material published in Haematologica is covered by copyright. All rights are reserved to the Ferrata Storti Foundation. Use of published material is allowed under the following terms and conditions: https://creativecommons.org/licenses/by-nc/4.0/legalcode. Copies of published material are allowed for personal or internal use. Sharing published material for non-commercial purposes is subject to the following conditions: https://creativecommons.org/licenses/by-nc/4.0/legalcode, sect. 3. Reproducing and sharing published material for commercial purposes is not allowed without permission in writing from the publisher.
spellingShingle Articles
Rotbain, Emelie Curovic
Frederiksen, Henrik
Hjalgrim, Henrik
Rostgaard, Klaus
Egholm, Gudrun Jakubsdottir
Zahedi, Banafsheh
Poulsen, Christian Bjørn
Enggard, Lisbeth
da Cunha-Bang, Caspar
Niemann, Carsten Utoft
IGHV mutational status and outcome for patients with chronic lymphocytic leukemia upon treatment: a Danish nationwide population-based study
title IGHV mutational status and outcome for patients with chronic lymphocytic leukemia upon treatment: a Danish nationwide population-based study
title_full IGHV mutational status and outcome for patients with chronic lymphocytic leukemia upon treatment: a Danish nationwide population-based study
title_fullStr IGHV mutational status and outcome for patients with chronic lymphocytic leukemia upon treatment: a Danish nationwide population-based study
title_full_unstemmed IGHV mutational status and outcome for patients with chronic lymphocytic leukemia upon treatment: a Danish nationwide population-based study
title_short IGHV mutational status and outcome for patients with chronic lymphocytic leukemia upon treatment: a Danish nationwide population-based study
title_sort ighv mutational status and outcome for patients with chronic lymphocytic leukemia upon treatment: a danish nationwide population-based study
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7271602/
https://www.ncbi.nlm.nih.gov/pubmed/31582540
http://dx.doi.org/10.3324/haematol.2019.220194
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