Complete loss of lineage defining antigens in two cases of B-cell malignancies following CAR-T therapy.

IF 0.6 4区 医学 Q4 HEMATOLOGY
Alireza Torabi, Jason Love, Teresa Hyun, Angie Pham, Jordan Gauthier, Alexandre Hirayama, David Wu, Kikkeri Naresh
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引用次数: 0

Abstract

Targeted immunotherapy is a promising approach in treating high-risk and refractory/relapsed lymphoid malignancies. Although this strategy has shown a significant success in treating non-Hodgkin B-cell lymphomas and plasma cell myeloma, relapse with loss of targeted antigen can occur. Rarely, complete loss of multiple lineage specific markers can happen. We are describing 2 cases of B-cell neoplasms along with contributing immunohistochemistry, cytogenetic, and molecular results. Post-targeted CAR-T therapy, both cases, one aggressive B-cell lymphoma and the other plasma cell myeloma, lost B-cell, and plasma cell antigens, respectively. Complete loss of lineage specific markers post-targeted therapy is a rare event that makes the diagnosis of the relapsed neoplasm challenging. In this article, we also reviewed the literature and highlighted possible mechanisms of antigen loss following targeted therapy.

Abstract Image

两例 B 细胞恶性肿瘤患者在接受 CAR-T 疗法后完全丧失了血统定义抗原。
靶向免疫疗法是治疗高危和难治/复发淋巴恶性肿瘤的一种很有前景的方法。虽然这一策略在治疗非霍奇金 B 细胞淋巴瘤和浆细胞骨髓瘤方面取得了巨大成功,但仍有可能因靶向抗原丢失而复发。在极少数情况下,可能会出现多个系特异性标志物完全丧失的情况。我们将介绍 2 例 B 细胞肿瘤病例以及相关的免疫组化、细胞遗传学和分子结果。这两个病例(一个是侵袭性 B 细胞淋巴瘤,另一个是浆细胞骨髓瘤)在接受 CAR-T 靶向治疗后分别丧失了 B 细胞和浆细胞抗原。靶向治疗后系特异性标志物的完全丧失是一种罕见的情况,这使得复发肿瘤的诊断具有挑战性。在本文中,我们还回顾了相关文献,并强调了靶向治疗后抗原丢失的可能机制。
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来源期刊
Journal of Hematopathology
Journal of Hematopathology HEMATOLOGYPATHOLOGY-PATHOLOGY
CiteScore
0.80
自引率
0.00%
发文量
45
期刊介绍: The Journal of Hematopathology aims at providing pathologists with a special interest in hematopathology with all the information needed to perform modern pathology in evaluating lymphoid tissues and bone marrow. To this end the journal publishes reviews, editorials, comments, original papers, guidelines and protocols, papers on ancillary techniques, and occasional case reports in the fields of the pathology, molecular biology, and clinical features of diseases of the hematopoietic system. The journal is the unique reference point for all pathologists with an interest in hematopathology. Molecular biologists involved in the expanding field of molecular diagnostics and research on lymphomas and leukemia benefit from the journal, too. Furthermore, the journal is of major interest for hematologists dealing with patients suffering from lymphomas, leukemias, and other diseases. The journal is unique in its true international character. Especially in the field of hematopathology it is clear that there are huge geographical variations in incidence of diseases. This is not only locally relevant, but due to globalization, relevant for all those involved in the management of patients.
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