Treatment strategies for patients with diffuse large B-cell lymphoma

医学 美罗华 苯达莫司汀 来那度胺 肿瘤科 切碎 内科学 嵌合抗原受体 威尼斯人 淋巴瘤 布仑妥昔单抗维多汀 Blinatumoab公司 耐火材料(行星科学) 弥漫性大B细胞淋巴瘤 多发性骨髓瘤 白血病 免疫疗法 癌症 慢性淋巴细胞白血病 CD30 物理 天体生物学 淋巴细胞白血病
作者
Stefano Poletto,Mattia Novo,Luca Paruzzo,Pio Manlio Mirko Frascione,Umberto Vitolo
出处
期刊:Cancer Treatment Reviews [Elsevier]
卷期号:110: 102443-102443 被引量:135
标识
DOI:10.1016/j.ctrv.2022.102443
摘要

Highlights•The standard first line treatment in DLBCL is still represented by R-CHOP.•Several trials were designed trying to improve the frontline therapy outcome.•In R/R DLBCL new agents are expanding the landscape of the therapeutic options.•The introduction of these agents in the frontline setting is an encouraging strategy.•A tailored individualized strategy could be the real breakthrough for DLBCL treatment.AbstractDiffuse large B-cell lymphoma (DLBCL) is nowadays a curable disease with the frontline treatment R-CHOP, but 30–40% of patients are still unresponsive or relapse thereafter. In the recent era several upcoming new options are improving the therapeutic landscape for relapsed/refractory (R/R) DLBCL setting, first of all anti-CD19 chimeric antigen receptor T-cells (CAR-T) that already represent a standard of care as third-line therapy and are rapidly moving as second-line treatment for those who are refractory or early relapse after R-CHOP. Among these new therapies, the combinations polatuzumab plus rituximab and bendamustine, tafasitamab plus lenalidomide for transplant ineligible patients, and CD3xCD20 bispecific antibodies are the most relevant, but several other agents and strategies are on the way. On the other hand, in the last 20 years, several efforts have been spent in the attempt to ameliorate the outcome over R-CHOP for the frontline treatment of DLBCL shortening the interval between the cycles or intensifying treatment or adding novel drugs to R-CHOP without success, so far. Recent studies combining the anti-CD79b antibody-drug conjugate polatuzumab vedotin plus R-CHP and the anti-BCL2 agent venetoclax plus R-CHOP showed promising results. Preliminary data of new upcoming strategies characterized by a tailored therapy based on different molecular subtypes of DLBCL are encouraging, showing a benefit over the standard R-CHOP. In this manuscript, the literature data on the landscape of new therapies available and upcoming for both frontline and R/R settings of DLBCL will be critically reviewed.
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