← 返回

弥漫大 B 细胞淋巴瘤的免疫治疗

英文原题:Immune-based therapies in diffuse large B-cell lymphoma.

查看英文原题

Immune-based therapies in diffuse large B-cell lymphoma.

PubMed 2023/07/06(内容时间) Expert Opin Investig Drugs Q2 · IF 4.3(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

未来的治疗将尽量减少化疗暴露,并根据 underlying tumor biology 来选择,为无化疗方案的前景和改善 poor-risk 亚组的结局铺平道路。

研究思路结论见上方概要

弥漫性大B细胞淋巴瘤(DLBCL)是一种起源于B细胞的侵袭性、临床异质性恶性肿瘤,高达40%的患者在一线治疗后出现原发难治性疾病或复发。然而,过去5年中,基于新型免疫疗法(包括嵌合抗原受体(CAR)T细胞和抗体类药物)的DLBCL新药获批层出不穷。涵盖领域:本文总结了DLBCL治疗的最新进展,包括一线治疗以及复发/难治性背景(二线及以后)。在PubMed中对2000年至2023年3月期间与DLBCL免疫治疗途径相关的出版物进行了文献检索,并对文章进行了综述。检索词为immunotherapy、monoclonal antibodies、chimeric antigen receptor modified T-cell(CAR-T)和classification of DLBCL。选取了探索当前针对DLBCL的免疫疗法优势与弱点的相关临床试验和临床前研究。我们还探讨了DLBCL亚型生物学之间的内在差异以及内源性宿主免疫募集如何导致治疗疗效的差异。

展开英文摘要原文

INTRODUCTION: Diffuse large B-cell lymphoma (DLBCL) is an aggressive and clinically heterogeneous malignancy originating from B-cells with up to 40% of patients experiencing primary refractory disease or relapse after first-line treatment.

However, the past 5 years have seen a flurry of new drug approvals for DLBCL anchored upon new immune therapies, including chimeric antigen receptor (CAR) T-cells and antibody-based therapies. AREAS COVERED: This article summarizes recent advances in the treatment of DLBCL, including in the first line and relapsed and refractory setting (second-line and beyond).

A literature search was conducted for publications relevant to the immunotherapeutic approach to DLBCL from 2000 through March 2023 within PubMed and articles were reviewed. The search terms were immunotherapy, monoclonal antibodies, chimeric antigen receptor modified T-cell (CAR-T), and classification of DLBCL. Relevant clinical trials and pre-clinical studies exploring the strengths and weaknesses of current immune therapies against DLBCL were chosen.

We additionally explored how intrinsic differences amongst DLBCL subtype biology and endogenous host immune recruitment contribute to variable therapeutic efficacy. EXPERT OPINION: Future treatments will minimize chemotherapy exposure and be chosen by underlying tumor biology, paving the way for the promise of chemotherapeutic free regimens and improved outcomes for poor-risk subgroups.

论文信息

作者
McCurry D、Flowers CR、Bermack C
单位
Oncology Fellow, Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, USA.United States
期刊
Expert opinion on investigational drugs2023 Jan-Jun
原文标识
PubMed 37394970 · DOI 10.1080/13543784.2023.2230137