Treatment with idelalisib in patients with chronic lymphocytic leukemia - real world data from the registry of the German CLL Study Group

被引:5
|
作者
von Tresckow, Julia [1 ]
Heyl, Nikola [2 ,3 ,4 ]
Robrecht, Sandra [2 ,3 ,4 ]
Giza, Adam [2 ,3 ,4 ]
Aldaoud, Ali [5 ]
Schlag, Rudolf [6 ]
Klausmann, Martine [7 ]
Linde, Hartmut [8 ]
Stein, Wolfgang [9 ]
Schwarzer, Andreas [10 ]
Fischer, Kirsten [2 ,3 ,4 ]
Cramer, Paula [2 ,3 ,4 ]
Eichhorst, Barbara [2 ,3 ,4 ]
Hallek, Michael [2 ,3 ,4 ]
Fink, Anna Maria [2 ,3 ,4 ]
机构
[1] Univ Duisburg Essen, Univ Hosp Essen, West German Canc Ctr, Clin Hematol & Stem Cell Transplantat, Hufelandstr 55, D-45147 Essen, Germany
[2] Univ Cologne, Dept Internal Med 1, Cologne, Germany
[3] Univ Cologne, Fac Med, Ctr Integrated Oncol Aachen, Cologne, Germany
[4] Univ Cologne, Univ Hosp Cologne, Cologne, Germany
[5] Praxis Hamatol & Onkol, Leipzig, Germany
[6] Hamatol Onkol Schwerpunktpraxis, Wurzburg, Germany
[7] Gemeinschaftspraxis, Aschaffenburg, Germany
[8] MVZ Blut & Krebserkrankungen, Potsdam, Germany
[9] Klinikum Frankfurt Oder, Frankfurt, Germany
[10] Onkopraxis Probstheida, Leipzig, Germany
关键词
Idelalisib; Chronic lymphocytic leukemia; Real-world-data; RITUXIMAB; IBRUTINIB;
D O I
10.1007/s00277-023-05314-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 na & iuml;ve (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.
引用
收藏
页码:3083 / 3090
页数:8
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