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吉妥珠单抗奥唑米星(抗CD33单克隆抗体,CMA-676,Mylotarg)在复发/难治性髓系白血病儿童中的疗效和耐受性

Efficacy and tolerability of gemtuzumab ozogamicin (anti-CD33 monoclonal antibody, CMA-676, Mylotarg) in children with relapsed/refractory myeloid leukemia.

作者信息

Brethon Benoit, Auvrignon Anne, Galambrun Claire, Yakouben Karima, Leblanc Thierry, Bertrand Yves, Leverger Guy, Baruchel André

机构信息

Unité de Pédiatrie à Orientation Hématologique, Hôpital Saint-Louis, Paris, France.

出版信息

BMC Cancer. 2006 Jun 28;6:172. doi: 10.1186/1471-2407-6-172.

Abstract

BACKGROUND

Gemtuzumab ozogamicin (GO) is a cytotoxic anti-CD33 monoclonal antibody that has given promising preliminary results in adult myeloid CD33+ AML. We conducted a retrospective multicenter study of 12 children treated with GO on a compassionate basis (median age 5.5 y). Three patients (2 MDS/AML, 1 JMML) were refractory to first-line treatment, 8 patients with de novo AML were in refractory first relapse, and one patient with de novo AML was in 2nd relapse after stem cell transplantation (SCT). CD33 expression exceeded 20% in all cases.

METHODS

GO was administered alone, at a unit dose of 3-9 mg/m2, once (3 patients), twice (3 patients), three (5 patients) or five times (1 patient). Mean follow-up was 128 days (8-585 d).

RESULTS

There were three complete responses (25%) leading to further curative treatment (SCT). Treatment failed in the other nine patients, and only one patient was alive at the end of follow-up. NCI-CTC grade III/IV adverse events comprised hematological toxicity (n = 12), hypertransaminasemia (n = 2), allergy and hyperbilirubinemia (1 case each). There was only one major adverse event (grade IV allergy). No case of sinusoidal obstruction syndrome occurred.

CONCLUSION

These results warrant a prospective trial of GO in a larger population of children with AML.

摘要

背景

吉妥单抗奥唑米星(GO)是一种细胞毒性抗CD33单克隆抗体,在成人髓系CD33+急性髓细胞白血病(AML)中已取得了有前景的初步结果。我们对12例接受GO同情用药治疗的儿童进行了一项回顾性多中心研究(中位年龄5.5岁)。3例患者(2例骨髓增生异常综合征/AML,1例幼年型粒单核细胞白血病)一线治疗无效,8例初发AML患者处于难治性首次复发状态,1例初发AML患者在干细胞移植(SCT)后处于第二次复发状态。所有病例中CD33表达均超过20%。

方法

单独给予GO,单位剂量为3-9mg/m2,给药1次(3例患者)、2次(3例患者)、3次(5例患者)或5次(1例患者)。平均随访时间为128天(8-585天)。

结果

有3例完全缓解(25%),从而得以进行进一步的根治性治疗(SCT)。其他9例患者治疗失败,随访结束时仅1例患者存活。美国国立癌症研究所通用毒性标准(NCI-CTC)III/IV级不良事件包括血液学毒性(n=12)、高转氨酶血症(n=2)、过敏和高胆红素血症(各1例)。仅发生1例严重不良事件(IV级过敏)。未发生肝窦阻塞综合征病例。

结论

这些结果表明有必要在更多的儿童AML患者中对GO进行前瞻性试验。

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本文引用的文献

1
Safety and efficacy of gemtuzumab ozogamicin in pediatric patients with advanced CD33+ acute myeloid leukemia.
Blood. 2005 Aug 15;106(4):1183-8. doi: 10.1182/blood-2004-10-3821. Epub 2005 May 10.
9
Hepatic sinusoidal obstruction after gemtuzumab ozogamicin (Mylotarg) therapy.
Blood. 2002 Apr 1;99(7):2310-4. doi: 10.1182/blood.v99.7.2310.

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