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氟达拉滨-环磷酰胺-利妥昔单抗治疗慢性淋巴细胞白血病,重点关注靶向治疗时代前后的长期细胞减少症。

Fludarabine-Cyclophosphamide-Rituximab Treatment in Chronic Lymphocytic Leukemia, Focusing on Long Term Cytopenias Before and After the Era of Targeted Therapies.

机构信息

Division of Hematology, Department of Internal Medicine, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.

出版信息

Pathol Oncol Res. 2021 Apr 27;27:1609742. doi: 10.3389/pore.2021.1609742. eCollection 2021.

Abstract

The widespread application of fludarabine, cyclophosphamide, and rituximab combination is limited due to its toxicity, particularly the prolonged cytopenias. The study aimed to compare the prolonged cytopenias depending on fitness and report real-life data on dose reduction measures and efficacy. According to our database, 120 and 14 patients were treated with FCR between 2011 and 2015 and between 2016 and 2019. Out of the first cohort, 34 patients were treated in subsequent lines. The complete and partial remission rate after first-line treatment was 79%, 16% in the first cohort and 86%, 14% in the second cohort, respectively; and 47%, 35% after non first-line treatment. Based on today's standards, only 37.5% of the patients were fit for FCR. The frequency of persistent cytopenia was 14%, and it was significantly associated with fitness ( (1) = 6.001, = 0.014 for all patients). The small number of FCR treated patients after 2016 shows how the availability of targeted therapies, mostly ibrutinib, in later lines changed the first-line choice. Recently, it is recommended first-line for fit patients with mutated and no aberrations. With this narrow indication, a decrease in the frequency of persistent cytopenias is predicted.

摘要

氟达拉滨、环磷酰胺和利妥昔单抗联合广泛应用受到其毒性的限制,尤其是长期的细胞减少症。本研究旨在比较根据健康状况的长期细胞减少症,并报告关于剂量减少措施和疗效的真实数据。根据我们的数据库,2011 年至 2015 年和 2016 年至 2019 年期间分别有 120 名和 14 名患者接受了 FCR 治疗。在第一个队列中,34 名患者在后续线接受了治疗。一线治疗后的完全缓解率和部分缓解率分别为 79%、16%和第一队列中的 86%、14%;非一线治疗后的缓解率分别为 47%、35%。根据今天的标准,只有 37.5%的患者适合接受 FCR 治疗。持续性细胞减少症的频率为 14%,与健康状况显著相关((1) = 6.001,= 0.014 所有患者)。2016 年后接受 FCR 治疗的患者数量较少,表明靶向治疗(主要是伊布替尼)在后续线的可用性如何改变了一线选择。最近,对于有突变和无异常的适合患者,建议一线使用。有了这个狭窄的适应证,预计持续性细胞减少症的频率会降低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc6c/8262186/4b10059095db/pore-27-1609742-g001.jpg

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