异基因造血干细胞移植后复发的慢性淋巴细胞白血病患者的Venetoclax治疗。

IF 5.1 2区 医学 Q1 HEMATOLOGY
Francesca Perutelli, Elia Boccellato, Maria Chiara Montalbano, Gioacchino Catania, Marina Deodato, Anna Maria Frustaci, Idanna Innocenti, Riccardo Moia, Francesca Maria Quaglia, Giulia Quaresmini, Paolo Rivela, Gianluca Gaidano, Mauro Krampera, Luca Laurenti, Alessandro Rambaldi, Benedetto Bruno, Candida Vitale, Marta Coscia
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引用次数: 0

摘要

同种异体造血干细胞移植(Allogeneic hematopoietic stem cell transplantation, alloHSCT)仍然是年轻和健康的具有高风险疾病特征的慢性淋巴细胞白血病(CLL)患者的一种选择。然而,同种异体移植患者通常被排除在临床试验之外,这使得关于同种异体造血干细胞移植后使用venetoclax的数据极为罕见。我们报告了来自意大利53个中心的7名在同种异体造血干细胞移植后接受venetoclax治疗的CLL患者的数据。这些患者在化疗免疫治疗(7/7)、依鲁替尼(5/7)和/或理想拉西布(1/7)失败后,于2006年至2021年间接受了同种异体造血干细胞移植。值得注意的是,3/7的患者在同种异体移植前已经接受了venetoclax为基础的治疗。同种异体造血干细胞移植后venetoclax治疗是安全的,不良事件与临床试验报告没有什么不同。重要的是,没有观察到对移植物抗宿主病(GvHD)病程的有意义的影响:4/7已经存在的慢性GvHD患者在venetoclax开始治疗后没有恶化,只有1例患者在venetoclax治疗期间发生了GvHD,这是按照标准临床实践进行管理的。在疗效方面,5/7的患者对venetoclax有临床反应,其中2例患者出现了无法检测到的微小残留疾病。据我们所知,这是在同种异体造血干细胞移植后使用venetoclax治疗CLL患者的最大系列报道。在这些经过大量预处理和高风险的患者中,先前的同种异体造血干细胞移植并没有影响venetoclax治疗的可行性,这种治疗缺乏意想不到的毒性,也不会加重GvHD。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Venetoclax therapy in chronic lymphocytic leukaemia patients relapsed after allogeneic haematopoietic stem cell transplantation.

Allogeneic hematopoietic stem cell transplantation (alloHSCT) remains an option for young and fit chronic lymphocytic leukaemia (CLL) patients with high-risk disease features. However, allotransplanted patients are generally excluded from clinical trials, making data regarding the use of venetoclax after alloHSCT extremely rare. We report data from 7 CLL patients who received venetoclax after alloHSCT among 53 Italian centers. These patients underwent alloHSCT between 2006 and 2021 after failing chemoimmunotherapy (7/7), ibrutinib (5/7) and/or idelalisib (1/7). Of note, 3/7 patients had already received venetoclax-based therapy before alloHSCT. Post-allo HSCT venetoclax treatment resulted safe, with adverse events not different from what reported in clinical trials. Importantly, no meaningful impact on graft versus host disease (GvHD) course was observed: 4/7 patients with pre-existing chronic GvHD had no exacerbation after venetoclax start, and only one patient developed GvHD during venetoclax therapy, that was managed as per standard clinical practice. Concerning efficacy, 5/7 patients presented a clinical response to venetoclax, with two patients achieving an undetectable minimal residual disease. To our knowledge, this is the largest reported series of CLL patients treated with venetoclax after alloHSCT. In these heavily pretreated and high-risk patients, previous alloHSCT did not compromise the feasibility of venetoclax therapy, that lacked unexpected toxicities and did not exacerbate GvHD.

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来源期刊
CiteScore
8.60
自引率
4.60%
发文量
565
审稿时长
1 months
期刊介绍: The British Journal of Haematology publishes original research papers in clinical, laboratory and experimental haematology. The Journal also features annotations, reviews, short reports, images in haematology and Letters to the Editor.
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