Piccini Matteo, Pilerci Sofia, Merlini Marta, Grieco Pietro, Scappini Barbara, Bencini Sara, Peruzzi Benedetta, Caporale Roberto, Signori Leonardo, Pancani Fabiana, Vannucchi Alessandro Maria, Gianfaldoni Giacomo
SOD Ematologia, Università degli Studi di Firenze e Azienda Ospedaliera Universitaria Careggi, 50139 Firenze, Italy.
Scuola di Specializzazione in Ematologia, Università degli Studi di Firenze, 50139 Firenze, Italy.
J Clin Med. 2021 Apr 14;10(8):1684. doi: 10.3390/jcm10081684.
Relapsed/refractory (R/R) acute myeloid leukemia (AML) is a largely unmet medical need, owing to the lack of standardized, effective treatment approaches, resulting in an overall dismal outcome. The only curative option for R/R AML patients is allogeneic hematopoietic stem cell transplantation (HSCT) which is only applicable in a fraction of patients due to the scarce efficacy and high toxicity of salvage regimens. Recently, a number of targeted agents with relatively favorable toxicity profiles have been explored in clinical trials for R/R AML patients. The Bcl-2 inhibitor venetoclax, in combination with hypomethylating agents or low dose cytarabine, has produced impressive results for newly diagnosed AML, while its role in R/R disease is not well defined yet. We retrospectively analyzed the clinical outcomes of 47 R/R AML patients treated with venetoclax-based regimens between March 2018 and December 2020 at our institution. Overall, we report a composite complete response rate of 55% with an overall acceptable toxicity profile. Outcomes were particularly favorable for NPM1 mutated patients, unlike for FLT3-ITD positive patients irrespective of NPM1 status. For patients treated with intention to transplant, the procedure could be finally performed in 54%. These findings suggest a role for venetoclax-based regimens in R/R AML patients and support the design of prospective studies.
复发/难治性(R/R)急性髓系白血病(AML)在很大程度上存在未满足的医疗需求,这是由于缺乏标准化的有效治疗方法,导致总体预后不佳。R/R AML患者唯一的治愈选择是异基因造血干细胞移植(HSCT),但由于挽救方案疗效不佳且毒性高,该方法仅适用于一小部分患者。最近,一些毒性相对较好的靶向药物已在R/R AML患者的临床试验中进行探索。Bcl-2抑制剂维奈克拉与去甲基化药物或低剂量阿糖胞苷联合使用,对新诊断的AML产生了令人印象深刻的结果,但其在R/R疾病中的作用尚未明确。我们回顾性分析了2018年3月至2020年12月在我院接受维奈克拉方案治疗的47例R/R AML患者的临床结局。总体而言,我们报告的综合完全缓解率为55%,毒性总体可接受。NPM1突变患者的结局特别好,而FLT3-ITD阳性患者的结局则不然,无论其NPM1状态如何。对于有意进行移植治疗的患者,最终有54%的患者能够进行移植手术。这些发现表明维奈克拉方案在R/R AML患者中具有一定作用,并支持开展前瞻性研究的设计。