Reinhardt D, Diekamp S, Fleischhack G, Corbacioglu C, Jürgens H, Dworzak M, Kaspers G, Creutzig U, Zwaan C M
Children's Hospital, Department of Pediatric Hematology/Oncology, University of Münster, Germany.
Onkologie. 2004 Jun;27(3):269-72. doi: 10.1159/000075606.
Gemtuzumab ozogamicin (GO) is an immunoconjugate consisting of the CD33 antibody and calicheamicin, a potent cytotoxic agent. Developed for targeted treatment of CD33-positive AML, studies in adults showed its efficacy in relapsed and refractory AML.
We report 12 children with multiple relapsed or refractory AML receiving GO as compassionate use. 11 children had initially been treated according to the AML-BFM 93 or 98 protocol, 1 girl received relapse treatment (liposomal daunorubicin/FLAG) due to secondary AML. After relapse, 10 children received an intensive relapse therapy (AML-BFM 97 or international AML-Relapse Study 2001/01). 2 of them had been transplanted in first or second CR before GO therapy.
5 of 12 children responded to treatment with blast reduction to below 5%, but no child achieved CR after GO. Time until reoccurrence of blasts in almost all children with GO response was 3-8 months. In 5 children stem cell transplantation (SCT) was performed after GO therapy. 4 of them suffered from further progression of AML, 1 boy is in second remission with a follow-up of 8 months. 2 children had severe side effects. An anaphylactic reaction with severe hypotension was managed by catecholamine support and intensive care. In 1 girl, who relapsed after SCT in first remission, a veno-occlusive disease of the liver occurred, but could be treated successfully with defibrotide.
GO therapy can induce blast reduction in children who have no further conventional treatment options. Frequency and severity of adverse events are limited, and therapy seems to be feasible for children with a sufficient general condition. Controlled studies are necessary to learn more about efficacy and side effects, especially implications for further therapy.
吉妥珠单抗奥唑米星(GO)是一种免疫偶联物,由CD33抗体和强力细胞毒性药物卡奇霉素组成。它被开发用于靶向治疗CD33阳性急性髓系白血病(AML),成人研究显示其对复发和难治性AML有效。
我们报告了12例多次复发或难治性AML儿童接受GO作为同情用药的情况。11名儿童最初按照AML-BFM 93或98方案进行治疗,1名女孩因继发性AML接受了复发治疗(脂质体柔红霉素/FLAG)。复发后,10名儿童接受了强化复发治疗(AML-BFM 97或国际AML复发研究2001/01)。其中2人在GO治疗前已在首次或第二次完全缓解(CR)时进行了移植。
12名儿童中有5名对治疗有反应,原始细胞减少至5%以下,但没有儿童在GO治疗后达到CR。几乎所有有GO反应的儿童原始细胞再次出现的时间为3 - 8个月。5名儿童在GO治疗后进行了干细胞移植(SCT)。其中4人AML进一步进展,1名男孩处于第二次缓解期,随访8个月。2名儿童出现严重副作用。一次伴有严重低血压的过敏反应通过儿茶酚胺支持和重症监护进行处理。在1名首次缓解期进行SCT后复发的女孩中,发生了肝静脉闭塞病,但用去纤苷成功治疗。
GO治疗可使没有进一步常规治疗选择的儿童原始细胞减少。不良事件的频率和严重程度有限,对于一般状况良好的儿童,该治疗似乎是可行的。需要进行对照研究以更多了解疗效和副作用,特别是对进一步治疗的影响。