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在嵌合抗原受体(CAR)时代,针对弥漫性大B细胞淋巴瘤的CD19靶点:其他运输方式。

Targeting CD19 for diffuse large B cell lymphoma in the era of CARs: Other modes of transportation.

作者信息

Sermer David, Elavalakanar Pavania, Abramson Jeremy S, Palomba M Lia, Salles Gilles, Arnason Jon

机构信息

Beth Israel Deaconess Medical Center, Boston, MA, USA; Harvard Medical School, Boston, MA, USA.

Beth Israel Deaconess Medical Center, Boston, MA, USA.

出版信息

Blood Rev. 2023 Jan;57:101002. doi: 10.1016/j.blre.2022.101002. Epub 2022 Aug 17.

Abstract

CD19 is nearly ubiquitously expressed on B-lymphocytes and in B-cell malignancies. Although CD19-directed CAR T cells have greatly improved outcomes in B-cell malignancies, there are significant limitations with this therapy. CD19 can also be effectively targeted by other drug classes, such as monoclonal antibodies, antibody-drug conjugates, and bispecific T cell engagers or antibodies. However, the optimal patient selection and sequencing of these novel therapies has not yet been established. In this review, we discuss the utilization of CD19 as a target for the treatment of DLBCL, focusing on tafasitamab, loncastuximab tesirine, and blinatumomab. We provide a comprehensive review of the pivotal clinical trials, discussing the strength and limitations of the data for each agent. We explore the emerging evidence that CD19 expression is retained following exposure to these agents and that patients can be successfully re-challenged with anti-CD19 therapies of a different drug class upon disease relapse post-CAR T cells. Finally, we discuss how these drugs potentially fit into the most current treatment paradigm for DLBCL.

摘要

CD19在B淋巴细胞和B细胞恶性肿瘤中几乎普遍表达。尽管靶向CD19的嵌合抗原受体(CAR)T细胞极大地改善了B细胞恶性肿瘤的治疗结果,但这种疗法存在重大局限性。CD19也可被其他药物类别有效靶向,如单克隆抗体、抗体药物偶联物以及双特异性T细胞衔接器或抗体。然而,这些新型疗法的最佳患者选择和治疗顺序尚未确定。在本综述中,我们讨论了将CD19用作治疗弥漫性大B细胞淋巴瘤(DLBCL)靶点的应用,重点关注塔法西他单抗、朗卡司他单抗替西瑞林和博纳吐单抗。我们对关键临床试验进行了全面综述,讨论了每种药物数据的优势和局限性。我们探讨了新出现的证据,即暴露于这些药物后CD19表达仍得以保留,并且在CAR T细胞治疗后疾病复发时,患者可以成功接受不同药物类别的抗CD19疗法再次治疗。最后,我们讨论了这些药物如何可能融入DLBCL的最新治疗模式。

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