对一名患有难治性急性白血病的儿童进行 PD-L1 和 CTLA-4 的检查点抑制。

International Journal of Hematologic Oncology Pub Date : 2019-01-16 eCollection Date: 2019-02-01 DOI:10.2217/ijh-2018-0009
Larisa Broglie, Jill Gershan, Michael J Burke
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引用次数: 0

摘要

多发性复发或难治性白血病患儿的生存率很低。研究发现,免疫检查点受体(如 PD-1、PD-L1 和 CTLA-4)的参与是导致治疗耐药的机制之一。对于成人癌症,PD-1(nivolumab)和 CTLA-4(ipilimumab)抑制剂已显示出良好的前景,反应率从 7% 到 40% 不等。使用急性髓性白血病细胞系进行的体外研究表明,急性髓性白血病胚泡可能同样利用 PD-1/PD-L1 轴来逃避抗癌免疫反应。我们报告了首例接受 nivolumab、ipilimumab 和 5-azacytidine 治疗的多发性复发/难治性白血病儿科患者,该患者能够耐受治疗并短暂改善症状。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Checkpoint inhibition of PD-L1 and CTLA-4 in a child with refractory acute leukemia.

Checkpoint inhibition of PD-L1 and CTLA-4 in a child with refractory acute leukemia.

Checkpoint inhibition of PD-L1 and CTLA-4 in a child with refractory acute leukemia.

Children with multiple relapsed or refractory leukemia have dismal survival. Research has identified engagement of immune checkpoint receptors (e.g., PD-1, PD-L1 and CTLA-4) as a mechanism for treatment resistance. For adult cancer, inhibitors of PD-1 (nivolumab) and CTLA-4 (ipilimumab) have shown promise with response rates ranging from 7 to 40%. In vitro studies using acute myeloid leukemia cell lines have shown that acute myeloid leukemia blasts may similarly utilize the PD-1/PD-L1 axis to evade an anticancer immune response. We report the first case of a pediatric patient with multiple relapsed/refractory leukemia treated with nivolumab, ipilimumab and 5-azacytidine who tolerated therapy with brief improvement of symptoms.

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自引率
0.00%
发文量
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审稿时长
13 weeks
期刊介绍: International Journal of Hematologic Oncology welcomes unsolicited article proposals. Email us today to discuss the suitability of your research and our options for authors, including Accelerated Publication. Find out more about publishing open access with us here.
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