Dabrowska-Iwanicka Anna, Nowakowski Grzegorz S
Department of Lymphoid Malignancies, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Division of Hematology, Mayo Clinic, Rochester, MN.
Blood. 2024 Dec 19;144(25):2573-2582. doi: 10.1182/blood.2023020779.
Diffuse large B-cell lymphoma (DLBCL), not otherwise specified, is the most common subtype of large B-cell lymphoma, with differences in prognosis reflecting heterogeneity in the pathological, molecular, and clinical features. Current treatment standard is based on multiagent chemotherapy, including anthracycline and monoclonal anti-CD20 antibody, which leads to cure in 60% of patients. Recent years have brought new insights into lymphoma biology and have helped refine the risk groups. The results of these studies inspired the design of new clinical trials with targeted therapies and response-adapted strategies and allowed to identify groups of patients potentially benefiting from new agents. This review summarizes recent progress in identifying high-risk patients with DLBCL using clinical and biological prognostic factors assessed at diagnosis and during treatment in the front-line setting, as well as new treatment strategies with the application of targeted agents and immunotherapy, including response-adapted strategies.
弥漫性大B细胞淋巴瘤(DLBCL),未另行规定的,是大B细胞淋巴瘤最常见的亚型,其预后差异反映了病理、分子和临床特征的异质性。目前的治疗标准基于多药化疗,包括蒽环类药物和单克隆抗CD20抗体,可使60%的患者治愈。近年来,对淋巴瘤生物学有了新的认识,并有助于完善风险分组。这些研究结果激发了针对靶向治疗和反应适应性策略的新临床试验设计,并有助于识别可能从新药物中获益的患者群体。本综述总结了在一线治疗中,利用诊断时和治疗期间评估的临床和生物学预后因素识别高危DLBCL患者的最新进展,以及应用靶向药物和免疫疗法的新治疗策略,包括反应适应性策略。
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