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不适合 CAR-T 细胞治疗患者的复发/难治性大 B 细胞淋巴瘤管理

英文原题:Management of relapsed or refractory large B-cell lymphoma in patients ineligible for CAR-T cell therapy.

查看英文原题

Management of relapsed or refractory large B-cell lymphoma in patients ineligible for CAR-T cell therapy.

PubMed 2022/03/15(内容时间) Expert Rev Hematol Q2 · IF 2.8(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

研究概要

应对这一情景将揭示新的挑战,包括确定这些治疗的理想顺序、最有效的组合,以及寻找一致的预测因素以帮助选择适合的 LBCL 患者人群。目前,针对 CAR-T 不合格患者这一新的且具有挑战性的群体,支持性临床研究必须继续作为一个主要焦点,与 CAR-T 细胞治疗的进展相辅相成。

研究思路结论见上方概要

CAR-T(CAR-T)疗法已经彻底改变了复发/难治性大B细胞淋巴瘤(LBCL)的治疗。然而,被排除在外或无法获得CAR-T 的患者对临床医生而言仍是一项挑战,且通常预后极差。这一类患者的治疗格局正在不断演变:过去2-3年间,已有新药获批,可单用或联合使用,同时新型治疗模式正在研究中。涵盖领域:此后,我们综述了当前可用的治疗策略:传统化疗、抗体药物偶联物ADC(主要为polatuzumab和loncastuxumab)、双特异性抗体(CD19/CD3及重点关注新型CD20/CD3抗体)、免疫调节药物(涵盖tafasitamab和来那度胺、检查点抑制剂主要用于PMBL)、小分子药物(selinexor、BTK和PI3K抑制剂)以及放疗的作用。

展开英文摘要原文

INTRODUCTION: Chimeric antigen receptor T (CAR-T) therapy has revolutionized the treatment of relapsed/refractory large B-cell lymphoma (LBCL).

However, patients who are excluded or have no access to CAR-T represent a challenge for clinicians and have generally a dismal outcome. The landscape for this category of patients is constantly evolving: new agents have been approved in the last 2-3 years, alone or in combination, and novel treatment modalities are under investigation. AREAS COVERED: Thereafter, we reviewed the currently available therapeutic strategies: conventional chemotherapy, antibody-drug conjugate ADC (mainly polatuzumab and loncastuxumab), bispecific antibodies (CD19/CD3 and focus on novel CD20/CD3 Abs), immunomodulatory drugs (covering tafasitamab and lenalidomide, checkpoint inhibitors mainly in PMBL), small molecules (selinexor, BTK, and PI3K inhibitors), and the role of radiotherapy.

EXPERT OPINION: Navigating this scenario will uncover new challenges, including identifying an ideal sequence for these therapies, the most effective combinations, and search for consistent predictive factors to help selecting the appropriate population of LBCL patients. At present, supporting clinical research for CAR-T ineligible patients, a new and challenging group, must remain a major focus that is complementary to advances in CAR T-cell therapy.

论文信息

作者
Perrone S、Lopedote P、Levis M、Di Rocco A、Smith SD
第一作者单位
Hematology, Polo Universitario Pontino, S.M. Goretti Hospital, Latina, Italy.Italy
通讯作者单位
Division of Medical Oncology, Department of Internal Medicine, University of Washington, Seattle.United States
期刊
Expert review of hematology2022 Mar
原文标识
PubMed 35184664 · DOI 10.1080/17474086.2022.2044778