Zwaan Christian M, Reinhardt Dirk, Corbacioglu Selim, van Wering Elisabeth R, Bökkerink Jos P M, Tissing Wim J E, Samuelsson Ulf, Feingold Jay, Creutzig Ursula, Kaspers Gertjan J L
Department of Pediatric Hematology/Oncology, Vrije Universiteit University Medical Center, Amsterdam, The Netherlands.
Blood. 2003 May 15;101(10):3868-71. doi: 10.1182/blood-2002-07-1947. Epub 2003 Jan 23.
Gemtuzumab ozogamicin (GO; Mylotarg) was developed to treat CD33(+) acute myeloid leukemia (AML). To date, only studies in adults and preliminary data from a phase 1 study in children have been reported. We report data on 15 children with relapsed/refractory CD33(+) AML who were treated with GO monotherapy on compassionate use basis (4-9 mg/m(2) up to 3 courses). Eight children showed a reduction in bone marrow blasts to 5% or less, including 5 in complete remission without full platelet recovery (CRp). Three of the 5 children with CRp received transplants almost directly following the last GO course, without awaiting further platelet regeneration. Hence in these children no clear discrimination between complete remission (CR) and CRp could be made. In 6 of 8 responding patients further treatment was given consisting of stem cell transplantation (SCT). Two patients are still alive, currently 6 and 9 months after SCT. Hematologic toxicity was difficult to assess due to subsequent SCT or leukemia. Side effects, in one patient each included veno-occlusive disease, transient grade 3 hyperbilirubinemia, transient grade 3 transaminase elevation, and grade 3 hypotension during GO administration. No infections or mucositis occurred. This report demonstrates clinical efficacy of GO in a subset of relapsed/refractory pediatric CD33(+) AML patients and suggests that intensive postremission therapy after remission induction by GO may result in durable responses in some patients, although follow-up is still short. Further studies are needed to determine the efficacy and safety of GO in children with AML.
吉妥单抗奥唑米星(GO;商品名:麦罗塔)被开发用于治疗CD33(+)急性髓系白血病(AML)。迄今为止,仅报道了在成人中的研究以及一项儿童1期研究的初步数据。我们报告了15例复发/难治性CD33(+) AML儿童患者的数据,这些患者在同情用药的基础上接受了GO单药治疗(4 - 9 mg/m²,最多3个疗程)。8名儿童的骨髓原始细胞减少至5%或更低,其中5名达到完全缓解但血小板未完全恢复(CRp)。5名CRp儿童中有3名几乎在最后一个GO疗程后直接接受了移植,未等待血小板进一步恢复。因此,在这些儿童中无法明确区分完全缓解(CR)和CRp。在8名有反应的患者中,6名接受了包括干细胞移植(SCT)在内的进一步治疗。2名患者仍然存活,目前分别在SCT后6个月和9个月。由于随后的SCT或白血病,血液学毒性难以评估。副作用方面,在GO给药期间,分别有1名患者出现了静脉闭塞性疾病、短暂性3级高胆红素血症、短暂性3级转氨酶升高和3级低血压。未发生感染或黏膜炎。本报告证明了GO在一部分复发/难治性儿童CD33(+) AML患者中的临床疗效,并表明GO诱导缓解后进行强化缓解后治疗可能使部分患者产生持久反应,尽管随访时间仍然较短。需要进一步研究以确定GO在AML儿童患者中的疗效和安全性。