Azacitidine (Vidaza®) in Pediatric Patients with Relapsed Advanced MDS and JMML: Results of a Phase I/II Study by the ITCC Consortium and the EWOG-MDS Group (Study ITCC-015).

IF 3.4 3区 医学 Q1 PEDIATRICS
Pediatric Drugs Pub Date : 2023-11-01 Epub Date: 2023-09-11 DOI:10.1007/s40272-023-00588-5
Alba Rubio-San-Simón, Natasha K A van Eijkelenburg, Raoull Hoogendijk, Henrik Hasle, Charlotte M Niemeyer, Michael N Dworzak, Marco Zecca, Marta Lopez-Yurda, Julie M Janssen, Alwin D R Huitema, Marry M van den Heuvel-Eibrink, Eric J Laille, Harm van Tinteren, Christian M Zwaan
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引用次数: 0

Abstract

Background: Advanced myelodysplastic syndrome (MDS) and juvenile myelomonocytic leukemia (JMML) are rare hematological malignancies in children. A second allograft is recommended if a relapse occurs after hematopoietic stem cell transplantation, but the outcome is poor.

Objective: We conducted a phase I/II multicenter study to evaluate the safety, pharmacokinetics, and activity of azacitidine in children with relapsed MDS/JMML prior to the second hematopoietic stem cell transplantation.

Methods: Patients enrolled from June 2013 to March 2019 received azacitidine intravenously/subcutaneously once daily on days 1-7 of a 28-day cycle. The MDS and JMML cohorts followed a two-stage design separately, with a safety run-in for JMML. Response and safety data were used to evaluate efficacy and establish the recommended dose. Pharmacokinetics was also analyzed. The study closed prematurely because of low recruitment.

Results: Six patients with MDS and four patients with JMML received a median of three and five cycles, respectively. Azacitidine 75 mg/m2 was well tolerated and plasma concentration-time profiles were similar to observed in adults. The most prevalent grade 3-4 adverse event was myelotoxicity. No responses were seen in patients with MDS, but 83% achieved stable disease; four patients underwent an allotransplant. Overall response rate in the JMML cohort was 75% (two complete responses; one partial response) and all responders underwent hematopoietic stem cell transplantation. One-year overall survival was 67% (95% confidence interval 38-100) in MDS and 50% (95% confidence interval 19-100) in JMML.

Conclusions: Azacitidine 75 mg/m2 prior to a second hematopoietic stem cell transplantation is safe in children with relapsed MDS/JMML. Although the long-term advantage remains to be assessed, this study suggests that azacitidine is an efficacious option for relapsed JMML.

Clinical trial registration: EudraCT 2010-022235-10.

Abstract Image

阿扎胞苷(Vidaza®)治疗复发性晚期MDS和JMML儿科患者:ITCC联盟和eogg -MDS组(研究ITCC-015)的I/II期研究结果
背景:晚期骨髓增生异常综合征(MDS)和青少年骨髓单核细胞白血病(JMML)是罕见的儿童血液系统恶性肿瘤。如果造血干细胞移植后复发,建议进行第二次同种异体移植,但效果不佳。目的:我们进行了一项I/II期多中心研究,以评估阿扎胞苷在复发性MDS/JMML儿童第二次造血干细胞移植前的安全性、药代动力学和活性。方法:2013年6月至2019年3月入选的患者在28天周期的第1-7天每天静脉注射/皮下注射一次阿扎胞苷。MDS和JMML队列分别遵循两阶段设计,并为JMML进行安全磨合。疗效和安全性数据用于评估疗效并确定推荐剂量。还分析了药物动力学。由于招募人数少,该研究提前结束。结果:6名MDS患者和4名JMML患者分别接受了三个和五个周期的中位数。阿扎胞苷75mg/m2耐受性良好,血浆浓度-时间曲线与成人相似。最常见的3-4级不良事件是骨髓毒性。MDS患者没有反应,但83%的患者病情稳定;4名患者接受了同种异体移植。JMML队列的总应答率为75%(两次完全应答;一次部分应答),所有应答者均接受了造血干细胞移植。MDS的一年总生存率为67%(95%可信区间38-100),JMML的一年总体生存率为50%(95%置信区间19-100)。结论:第二次造血干细胞移植前75 mg/m2的阿扎胞苷对复发性MDS/JMML的儿童是安全的。尽管长期优势仍有待评估,但本研究表明,阿扎胞苷是治疗复发性JMML的有效选择。临床试验注册:EudraCT 2010-022235-10。
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来源期刊
Pediatric Drugs
Pediatric Drugs PEDIATRICS-PHARMACOLOGY & PHARMACY
CiteScore
7.20
自引率
0.00%
发文量
54
审稿时长
>12 weeks
期刊介绍: Pediatric Drugs promotes the optimization and advancement of all aspects of pharmacotherapy for healthcare professionals interested in pediatric drug therapy (including vaccines). The program of review and original research articles provides healthcare decision makers with clinically applicable knowledge on issues relevant to drug therapy in all areas of neonatology and the care of children and adolescents. The Journal includes: -overviews of contentious or emerging issues. -comprehensive narrative reviews of topics relating to the effective and safe management of drug therapy through all stages of pediatric development. -practical reviews covering optimum drug management of specific clinical situations. -systematic reviews that collate empirical evidence to answer a specific research question, using explicit, systematic methods as outlined by the PRISMA statement. -Adis Drug Reviews of the properties and place in therapy of both newer and established drugs in the pediatric population. -original research articles reporting the results of well-designed studies with a strong link to clinical practice, such as clinical pharmacodynamic and pharmacokinetic studies, clinical trials, meta-analyses, outcomes research, and pharmacoeconomic and pharmacoepidemiological studies. Additional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in Pediatric Drugs may be accompanied by plain language summaries to assist readers who have some knowledge of, but not in-depth expertise in, the area to understand important medical advances.
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