Giulio Cassanello, Alejandro Luna de Abia, Lorenzo Falchi
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引用次数: 0
Abstract
Immunotherapy has shaped the treatment approach to diffuse large B-cell lymphoma (DLBCL), with rituximab leading to remarkable improvements in outcomes for both relapsed and treatment-naïve patients. Recently, groundbreaking immunotherapies like chimeric antigen receptor T-cells have entered the treatment arena for relapsed/refractory (R/R) DLBCL and gained regulatory approval in several countries. The concept of harnessing a patient's own T-cells to combat cancer has been further explored through the development of bispecific antibodies (BsAbs), a class of engineered antibody products designed to simultaneously target two different antigens. These novel drugs have demonstrated impressive single-agent activity and manageable toxicity in patients with heavily pretreated B-cell non-Hodgkin lymphoma. In this review, we provide an up-to-date overview of recently completed or ongoing BsAbs trials in patients with R/R DLBCL, including single-agent results, emerging combination data, and novel constructs.
免疫疗法塑造了弥漫大B细胞淋巴瘤(DLBCL)的治疗方法,利妥昔单抗使复发和治疗无效患者的疗效都得到了显著改善。最近,嵌合抗原受体 T 细胞等突破性免疫疗法也进入了复发/难治性(R/R)DLBCL 的治疗领域,并在多个国家获得了监管部门的批准。通过开发双特异性抗体(BsAbs),人们进一步探索了利用患者自身 T 细胞抗击癌症的概念。这些新型药物已在接受过大量预处理的 B 细胞非霍奇金淋巴瘤患者身上显示出令人印象深刻的单药活性和可控毒性。在这篇综述中,我们将概述最近完成或正在进行的针对 R/R DLBCL 患者的 BsAbs 试验的最新情况,包括单药结果、新出现的联合用药数据和新型构建物。
期刊介绍:
OncoImmunology is a dynamic, high-profile, open access journal that comprehensively covers tumor immunology and immunotherapy.
As cancer immunotherapy advances, OncoImmunology is committed to publishing top-tier research encompassing all facets of basic and applied tumor immunology.
The journal covers a wide range of topics, including:
-Basic and translational studies in immunology of both solid and hematological malignancies
-Inflammation, innate and acquired immune responses against cancer
-Mechanisms of cancer immunoediting and immune evasion
-Modern immunotherapies, including immunomodulators, immune checkpoint inhibitors, T-cell, NK-cell, and macrophage engagers, and CAR T cells
-Immunological effects of conventional anticancer therapies.