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在接受 Inotuzumab-Ozogamicin 治疗后,复发/难治性 B 淋巴细胞白血病成人患者中 CD22 表达缺失和 CD22 亚群扩增。

Loss of CD22 expression and expansion of a CD22 subpopulation in adults with relapsed/refractory B-lymphoblastic leukaemia after treatment with Inotuzumab-Ozogamicin.

机构信息

Department of Oncology, Haematology and Bone Marrow Transplantation With Section Pneumology, Hubertus Wald Tumorzentrum, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Department of Medicine A, Hematology and Oncology, University Hospital Münster, Münster, Germany.

出版信息

Ann Hematol. 2021 Nov;100(11):2727-2732. doi: 10.1007/s00277-021-04601-0. Epub 2021 Jul 31.

Abstract

Treatment options for relapsed or refractory B-lymphoblastic leukaemia (r/r B-ALL) are limited and the prognosis of these patients remains dismal, but novel immunotherapeutic options such as the anti-CD22 antibody-drug-conjugate Inotuzumab-Ozogamicin (InO) have improved outcomes in these patients. Flow cytometry is essential to assess antigen-expression prior to treatment initiation of antigen-directed immunotherapies. Here, we present flow cytometric and clinical data of three adult patients with r/r B-ALL who failed treatment with InO associated with reduced or lost antigen-expression. In addition, we present comparative data on two different diagnostic CD22-specific antibody clones that exhibit significant differences in staining intensities.

摘要

治疗复发或难治性 B 淋巴细胞白血病(r/r B-ALL)的选择有限,这些患者的预后仍然不容乐观,但新型免疫治疗选择,如抗 CD22 抗体药物偶联物 Inotuzumab-Ozogamicin(InO),已改善了这些患者的预后。在开始抗原导向的免疫治疗之前,流式细胞术对于评估抗原表达至关重要。在这里,我们介绍了 3 例成人 r/r B-ALL 患者的流式细胞术和临床数据,这些患者在接受 InO 治疗后出现抗原表达减少或丢失而治疗失败。此外,我们还介绍了两种不同的诊断性 CD22 特异性抗体克隆的比较数据,它们在染色强度上存在显著差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce03/8510963/525351557f04/277_2021_4601_Fig1_HTML.jpg

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