Institute of Pediatric Hematology and Oncology, Hospices Civils de Lyon, Lyon, France.
Claude Bernard University - Lyon 1, Lyon, France.
Pediatr Blood Cancer. 2020 Jun;67(6):e28305. doi: 10.1002/pbc.28305. Epub 2020 Apr 19.
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.
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.
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.
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.
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。
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。
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。
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。