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氟达拉滨、阿糖胞苷和分次吉妥珠单抗联合造血干细胞移植治疗儿童一线难治性急性髓系白血病:单中心经验。

Association of fludarabin, cytarabine, and fractioned gemtuzumab followed by hematopoietic stem cell transplantation for first-line refractory acute myeloid leukemia in children: A single-center experience.

机构信息

Institute of Pediatric Hematology and Oncology, Hospices Civils de Lyon, Lyon, France.

Claude Bernard University - Lyon 1, Lyon, France.

出版信息

Pediatr Blood Cancer. 2020 Jun;67(6):e28305. doi: 10.1002/pbc.28305. Epub 2020 Apr 19.

DOI:10.1002/pbc.28305
PMID:32307866
Abstract

CONTEXT

Acute myeloid leukemia (AML) is a rare disease in children, with only 50% to 60% event-free survival. Among patients with AML, 10% do not respond to first-line chemotherapy. There is no recommendation concerning second-line treatments. Gemtuzumab ozogamicin (GO) is a monoclonal antibody targeting CD33, linked to calicheamicin. We report the efficacy and tolerance of a salvage regimen of fludarabin, cytarabine, and GO (FLA-GO) in patients refractory to first-line treatment.

METHODS

Eight patients (median age 14.5 years), who had more than 2% minimal residual disease (MRD) by flow cytometry (MRD flow), received gemtuzumab 3 mg/m² on days 1, 4, 7, associated with cytarabine 2000 mg/m² and fludarabin 30 mg/m² on days 1 to 5.

RESULTS

Six patients achieved complete remission (CR) (blast count morphology ≤5 × 10 , CR-MRD flow <1 × 10 for four patients). Five patients received a second course. We observed 11 episodes of febrile neutropenia, including 6 septicemias without complication. There was no fungal infection or toxic death. Two patients received granulocyte colony stimulating factor. One patient had partial platelet recovery; one, prolonged pancytopenia. All patients received hematopoietic stem cell transplantation (HSCT). We observed five mild-to-severe sinusoidal obstruction syndromes during HSCT procedures, particularly in patients who did not receive defibrotide prophylaxis. At the date of last contact (median follow-up: 58 months; range: 22-78), six patients were in continuous CR with negative MRD. Two patients died of post-HSCT relapse.

CONCLUSION

FLA-GO is a good salvage regimen for pediatric refractory AML, with significant but acceptable toxicity. HSCT is mandatory to achieve sustained CR in these patients.

摘要

背景

急性髓系白血病(AML)在儿童中较为罕见,仅有 50%至 60%的无事件生存率。在 AML 患者中,有 10%对一线化疗无反应。目前尚无关于二线治疗的建议。吉妥珠单抗奥佐米星(GO)是一种靶向 CD33 的单克隆抗体,与加利车霉素相连。我们报告了在对一线治疗有抗药性的患者中使用氟达拉滨、阿糖胞苷和 GO(FLA-GO)进行挽救治疗的疗效和耐受性。

方法

8 名患者(中位年龄 14.5 岁),流式细胞术(MRD 流式)检测到超过 2%的微小残留病(MRD),在第 1、4、7 天接受吉妥珠单抗 3mg/m²,同时在第 1 至 5 天接受阿糖胞苷 2000mg/m²和氟达拉滨 30mg/m²。

结果

6 名患者达到完全缓解(CR)(形态学白血病计数≤5×10,4 名患者的 CR-MRD 流式<1×10)。5 名患者接受了第二个疗程。我们观察到 11 次发热性中性粒细胞减少症,其中 6 次为败血症且无并发症。无真菌感染或毒性死亡。两名患者接受了粒细胞集落刺激因子。一名患者血小板部分恢复;一名患者持续性全血细胞减少。所有患者均接受了造血干细胞移植(HSCT)。我们在 HSCT 过程中观察到 5 例轻至重度窦状隙阻塞综合征,特别是未接受地昔单抗预防的患者。在最后一次随访时(中位随访时间:58 个月;范围:22-78),6 名患者持续处于 CR 且 MRD 为阴性。两名患者因 HSCT 后复发而死亡。

结论

FLA-GO 是治疗儿科难治性 AML 的一种良好挽救方案,具有显著但可接受的毒性。为了使这些患者获得持续的 CR,HSCT 是必须的。

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