Torabi Alireza, Love Jason, Hyun Teresa, Pham Angie, Gauthier Jordan, Hirayama Alexandre, Wu David, Naresh Kikkeri
Department of Laboratory Medicine and Pathology, University of Washington, Seattle 1959 NE Pacific Street, Box 357110, Seattle, WA, 98195, USA.
Department of Hematopathology, Fred Hutch Cancer Center, Seattle, WA, USA.
J Hematop. 2024 Dec;17(4):259-264. doi: 10.1007/s12308-024-00602-w. Epub 2024 Aug 26.
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.
靶向免疫疗法是治疗高危及难治性/复发性淋巴系统恶性肿瘤的一种很有前景的方法。尽管该策略在治疗非霍奇金B细胞淋巴瘤和浆细胞骨髓瘤方面已取得显著成功,但仍可能出现靶向抗原丢失导致的复发。极少数情况下,会发生多种谱系特异性标志物的完全丢失。我们在此描述2例B细胞肿瘤病例,并给出相关的免疫组织化学、细胞遗传学和分子学结果。在靶向CAR-T治疗后,这两例病例,一例侵袭性B细胞淋巴瘤和另一例浆细胞骨髓瘤,分别失去了B细胞和浆细胞抗原。靶向治疗后谱系特异性标志物的完全丢失是一种罕见事件,这使得复发肿瘤的诊断具有挑战性。在本文中,我们还回顾了文献并强调了靶向治疗后抗原丢失的可能机制。