Karsten Imke E, Shumilov Evgenii, Schmitz Norbert, Lenz Georg
Department of Medicine A, Hematology, Oncology, and Pneumology, University Hospital Muenster, Muenster, Germany.
Br J Haematol. 2024 Dec;205(6):2163-2174. doi: 10.1111/bjh.19860. Epub 2024 Oct 28.
Diffuse large B-cell lymphoma (DLBCL) is the most common aggressive lymphoma, accounting for ~40% of all cases in adults. Whilst approximately two-thirds of DLBCL patients can be cured by first-line therapy, one-third of patients are primary refractory or relapse after an initial response (r/r DLBCL). Recent advances in the treatment of DLBCL have been achieved by a plethora of novel drugs, such as monoclonal antibodies, antibody-drug conjugates (ADC), bi-specific T-cell engagers (BITEs), and CD-19 directed chimeric antigen receptor (CAR)-T-cell therapies. The increasing number of therapeutic options significantly improved the outcome of patients; however, the therapeutic algorithm has become increasingly complex. In this review, we provide an overview of novel therapies for DLBCL patients and potential treatment sequencing from first to second, third, and later lines.
弥漫性大B细胞淋巴瘤(DLBCL)是最常见的侵袭性淋巴瘤,约占成人淋巴瘤病例的40%。虽然约三分之二的DLBCL患者可通过一线治疗治愈,但三分之一的患者为原发性难治性或在初始缓解后复发(复发/难治性DLBCL)。DLBCL治疗的最新进展得益于大量新型药物,如单克隆抗体、抗体药物偶联物(ADC)、双特异性T细胞衔接器(BITE)以及靶向CD-19的嵌合抗原受体(CAR)-T细胞疗法。治疗选择的增加显著改善了患者的预后;然而,治疗方案已变得日益复杂。在本综述中,我们概述了DLBCL患者的新型疗法以及从一线到二线、三线及后续治疗的潜在治疗顺序。