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Treatment with idelalisib in patients with chronic lymphocytic leukemia – real world data from the registry of the German CLL Study Group
Idelalisib in combination with rituximab is an efficacious treatment for patients suffering from chronic lymphocytic leukemia (CLL) with known limitations due to toxicities. However, the benefit after prior Bruton tyrosine kinase inhibitor (BTKi) therapy remains unclear. For this analysis, 81 patien...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10567876/ https://www.ncbi.nlm.nih.gov/pubmed/37358640 http://dx.doi.org/10.1007/s00277-023-05314-2 |
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author | von Tresckow, Julia Heyl, Nikola Robrecht, Sandra Giza, Adam Aldaoud, Ali Schlag, Rudolf Klausmann, Martine Linde, Hartmut Stein, Wolfgang Schwarzer, Andreas Fischer, Kirsten Cramer, Paula Eichhorst, Barbara Hallek, Michael Fink, Anna Maria |
author_facet | von Tresckow, Julia Heyl, Nikola Robrecht, Sandra Giza, Adam Aldaoud, Ali Schlag, Rudolf Klausmann, Martine Linde, Hartmut Stein, Wolfgang Schwarzer, Andreas Fischer, Kirsten Cramer, Paula Eichhorst, Barbara Hallek, Michael Fink, Anna Maria |
author_sort | von Tresckow, Julia |
collection | PubMed |
description | Idelalisib in combination with rituximab is an efficacious treatment for patients suffering from chronic lymphocytic leukemia (CLL) with known limitations due to toxicities. However, the benefit after prior Bruton tyrosine kinase inhibitor (BTKi) therapy remains unclear. For this analysis, 81 patients included in a non-interventional registry study of the German CLL study group (registered at www.clinicaltrials.gov as # NCT02863692) meeting the predefined criteria of a confirmed diagnosis of CLL and being treated with idelalisib containing regimens outside clinical trials were considered. 11 patients were treatment naïve (13.6%) and 70 patients (86.4%) pretreated. Patients had median of one prior therapy line (range 0–11). Median treatment duration with idelalisib was 5.1 months (range 0–55.0 months). Of 58 patients with documented treatment outcome, 39 responded to idelalisib containing therapy (67.2%). Patients treated with the BTKi ibrutinib as last prior treatment prior to idelalisib responded in 71.4% compared to a response rate of 61.9% in patients without prior ibrutinib. Median event free survival (EFS) was 15.9 months with a 16 versus 14 months EFS in patients with ibrutinib as last prior treatment or not, respectively. Median overall survival was 46.6 months. In conclusion, treatment with idelalisib appears to have a valuable impact in patients being refractory to prior ibrutinib therapy even though there are limitations in our analysis due to the low number of patients included. |
format | Online Article Text |
id | pubmed-10567876 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-105678762023-10-13 Treatment with idelalisib in patients with chronic lymphocytic leukemia – real world data from the registry of the German CLL Study Group von Tresckow, Julia Heyl, Nikola Robrecht, Sandra Giza, Adam Aldaoud, Ali Schlag, Rudolf Klausmann, Martine Linde, Hartmut Stein, Wolfgang Schwarzer, Andreas Fischer, Kirsten Cramer, Paula Eichhorst, Barbara Hallek, Michael Fink, Anna Maria Ann Hematol Original Article Idelalisib in combination with rituximab is an efficacious treatment for patients suffering from chronic lymphocytic leukemia (CLL) with known limitations due to toxicities. However, the benefit after prior Bruton tyrosine kinase inhibitor (BTKi) therapy remains unclear. For this analysis, 81 patients included in a non-interventional registry study of the German CLL study group (registered at www.clinicaltrials.gov as # NCT02863692) meeting the predefined criteria of a confirmed diagnosis of CLL and being treated with idelalisib containing regimens outside clinical trials were considered. 11 patients were treatment naïve (13.6%) and 70 patients (86.4%) pretreated. Patients had median of one prior therapy line (range 0–11). Median treatment duration with idelalisib was 5.1 months (range 0–55.0 months). Of 58 patients with documented treatment outcome, 39 responded to idelalisib containing therapy (67.2%). Patients treated with the BTKi ibrutinib as last prior treatment prior to idelalisib responded in 71.4% compared to a response rate of 61.9% in patients without prior ibrutinib. Median event free survival (EFS) was 15.9 months with a 16 versus 14 months EFS in patients with ibrutinib as last prior treatment or not, respectively. Median overall survival was 46.6 months. In conclusion, treatment with idelalisib appears to have a valuable impact in patients being refractory to prior ibrutinib therapy even though there are limitations in our analysis due to the low number of patients included. Springer Berlin Heidelberg 2023-06-26 2023 /pmc/articles/PMC10567876/ /pubmed/37358640 http://dx.doi.org/10.1007/s00277-023-05314-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article von Tresckow, Julia Heyl, Nikola Robrecht, Sandra Giza, Adam Aldaoud, Ali Schlag, Rudolf Klausmann, Martine Linde, Hartmut Stein, Wolfgang Schwarzer, Andreas Fischer, Kirsten Cramer, Paula Eichhorst, Barbara Hallek, Michael Fink, Anna Maria Treatment with idelalisib in patients with chronic lymphocytic leukemia – real world data from the registry of the German CLL Study Group |
title | Treatment with idelalisib in patients with chronic lymphocytic leukemia – real world data from the registry of the German CLL Study Group |
title_full | Treatment with idelalisib in patients with chronic lymphocytic leukemia – real world data from the registry of the German CLL Study Group |
title_fullStr | Treatment with idelalisib in patients with chronic lymphocytic leukemia – real world data from the registry of the German CLL Study Group |
title_full_unstemmed | Treatment with idelalisib in patients with chronic lymphocytic leukemia – real world data from the registry of the German CLL Study Group |
title_short | Treatment with idelalisib in patients with chronic lymphocytic leukemia – real world data from the registry of the German CLL Study Group |
title_sort | treatment with idelalisib in patients with chronic lymphocytic leukemia – real world data from the registry of the german cll study group |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10567876/ https://www.ncbi.nlm.nih.gov/pubmed/37358640 http://dx.doi.org/10.1007/s00277-023-05314-2 |
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