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依地鲁赛布治疗慢性淋巴细胞白血病患者——来自德国慢性淋巴细胞白血病研究组注册登记处的真实世界数据。

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

作者信息

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

机构信息

Clinic for Hematology and Stem Cell Transplantation, West German Cancer Center, University Hospital Essen, University of Duisburg-Essen, Hufelandstr. 55, 45147, Essen, Germany.

Department I for Internal Medicine and Centre of Integrated Oncology Aachen, Bonn, Cologne, Duesseldorf, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.

出版信息

Ann Hematol. 2023 Nov;102(11):3083-3090. doi: 10.1007/s00277-023-05314-2. Epub 2023 Jun 26.

Abstract

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.

摘要

idelalisib联合利妥昔单抗是治疗慢性淋巴细胞白血病(CLL)患者的一种有效疗法,但已知存在因毒性导致的局限性。然而,在先前接受布鲁顿酪氨酸激酶抑制剂(BTKi)治疗后的获益仍不明确。对于本分析,纳入了德国CLL研究组一项非干预性注册研究(在www.clinicaltrials.gov上注册为#NCT02863692)的81例患者,这些患者符合CLL确诊的预定义标准,并在临床试验之外接受含idelalisib方案治疗。11例患者未接受过治疗(13.6%),70例患者(86.4%)接受过预处理。患者既往治疗线数的中位数为1(范围0 - 11)。idelalisib的中位治疗持续时间为5.1个月(范围0 - 55.0个月)。在58例有记录治疗结果的患者中,39例对含idelalisib的治疗有反应(67.2%)。在idelalisib之前最后一次接受BTKi依鲁替尼治疗的患者中,反应率为71.4%,而未接受过依鲁替尼治疗的患者反应率为6 .19%。中位无事件生存期(EFS)为15.9个月,最后一次接受依鲁替尼治疗的患者与未接受依鲁替尼治疗的患者的EFS分别为16个月和14个月。中位总生存期为46.6个月。总之,尽管由于纳入患者数量较少,我们的分析存在局限性,但idelalisib治疗似乎对先前依鲁替尼治疗难治的患者有重要影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/751c/10567876/092620138001/277_2023_5314_Fig1_HTML.jpg

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