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吉妥珠单抗奥唑米星巩固治疗对急性髓系白血病造血干细胞动员的影响:20例患者分析

Impact of gemtuzumab ozogamicin consolidation on hematopoietic stem cells (HSCs) mobilization in AML: analysis of 20 patients.

作者信息

Perrone Salvatore, Capria Saveria, Bernardi Massimo, Marchesi Francesco, Ortu La Barbera Elettra, Trisolini Silvia Maria, Minotti Clara, Shafii Bafti Mahnaz, Scerpa Maria Cristina, Mulé Antonino, Ciceri Fabio, Martelli Maurizio, Cimino Giuseppe

机构信息

Hematology, Polo Universitario Pontino, "Sapienza", Via A. Canova S.M. Goretti Hospital, 04100, Latina, Italy.

Haematology, Department of Translational and Precision Medicine, Sapienza University of Rome, Rome, Italy.

出版信息

Ann Hematol. 2023 Apr;102(4):769-775. doi: 10.1007/s00277-023-05129-1. Epub 2023 Feb 16.

Abstract

Gemtuzumab ozogamicin (GO), is an anti-CD33 monoclonal antibody, approved for AML CD33 + , those patients with low and intermediate-risk who obtain a complete response may also be candidated for consolidation with autologous stem cell transplantation (ASCT). However, there are scant data on the mobilization of hemopoietic stem cells (HSC) after fractionated GO. We retrospectively studied data from five Italian centers and identified 20 patients (median age 54 years, range 29-69, 15 female, 15 NPM1) that attempted HSC mobilization after fractionated doses of GO + "7 + 3" regimen and 1-2 cycles of consolidation (GO + HDAC + daunorubicin). After chemotherapy and standard G-CSF, 11/20 patients (55%) reached the threshold of 20 CD34 + /µL, and HSC were successfully harvested, while 9 patients (45%) failed. The median day of apheresis was Day + 26 from the start of chemotherapy (range 22-39 days). In good mobilizer patients, the median circulating CD34 + cells were 35.9 cells/µL and the median CD34 + harvested were 4.65 × 10/kg of patients' body weight. With a median follow-up of 12.7 months, at 24 months from the first diagnosis, 93.3% of all 20 patients were alive and the median overall survival was 25 months. The 2-year RFS rate from the timepoint of the first CR was 72.6%, while the median RFS was not reached. However, only five patients underwent ASCT and achieved full engraftment.In conclusion, in our cohort of patients, the addition of GO reduced HSC mobilization and harvesting, which was reached in about 55% of patients. Nevertheless, further studies are warranted to evaluate the effects of fractionated doses of GO on HSC mobilization and ASCT outcomes.

摘要

吉妥珠单抗奥唑米星(GO)是一种抗CD33单克隆抗体,被批准用于治疗急性髓系白血病(AML)CD33阳性患者,那些获得完全缓解的低危和中危患者也可能适合接受自体干细胞移植(ASCT)巩固治疗。然而,关于分次使用GO后造血干细胞(HSC)动员的数据很少。我们回顾性研究了来自五个意大利中心的数据,确定了20例患者(中位年龄54岁,范围29 - 69岁,15名女性,15名NPM1阳性),这些患者在接受分次剂量的GO + “7 + 3”方案及1 - 2个周期巩固治疗(GO + 组蛋白去乙酰化酶抑制剂 + 柔红霉素)后尝试进行HSC动员。化疗和标准粒细胞集落刺激因子(G - CSF)治疗后,20例患者中有11例(55%)达到了每微升20个CD34 + 细胞的阈值,HSC成功采集,而9例患者(45%)失败。采集的中位时间是化疗开始后的第26天(范围22 - 39天)。在动员效果良好的患者中,循环CD34 + 细胞的中位数量为每微升35.9个,采集的CD34 + 细胞中位数量为每千克患者体重4.65×10个。中位随访12.7个月,在首次诊断后的24个月时,20例患者中有93.3%存活,中位总生存期为25个月。从首次完全缓解时间点开始计算的2年无复发生存率为72.6%,而中位无复发生存期未达到。然而,只有5例患者接受了ASCT并实现了完全植入。总之,在我们的患者队列中,添加GO降低了HSC的动员和采集成功率,约55%的患者达到了采集标准。尽管如此,仍需要进一步研究来评估分次剂量的GO对HSC动员和ASCT结果的影响。

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