b细胞淋巴瘤即将到来的免疫治疗组合。

IF 4.1 Q2 IMMUNOLOGY
Immunotherapy advances Pub Date : 2021-02-09 eCollection Date: 2021-01-01 DOI:10.1093/immadv/ltab001
Patrick Greve, Friederike A G Meyer-Wentrup, Victor Peperzak, Marianne Boes
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引用次数: 3

摘要

在最初将b细胞淋巴瘤作为既定癌症治疗的辅助治疗后,免疫检查点抑制剂和其他免疫疗法现在被纳入成人和儿童患者的主流治疗方案。本文通过对2015-2020年注册的联合治疗试验的深入分析,概述了b细胞淋巴瘤联合治疗的现状。我们的分析为淋巴瘤治疗的快速发展提供了新的见解,这是由新的治疗武器库推动的。最后,我们展望了即将进行的临床试验,这些试验可能会使用系统的测试方法,将现有的化疗方案与新药物结合起来,以及免疫治疗和靶向治疗的新组合。未来的试验将以篮子或伞型试验的形式进行,以促进对针对肿瘤或相关免疫微环境中特定遗传变化的新药的评估。因此,淋巴瘤患者将受益于接受更有针对性的治疗,这种治疗基于化疗与靶向肿瘤生物学和免疫系统特定方面的新药物的协同作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Upcoming immunotherapeutic combinations for B-cell lymphoma.

Upcoming immunotherapeutic combinations for B-cell lymphoma.

Upcoming immunotherapeutic combinations for B-cell lymphoma.

Upcoming immunotherapeutic combinations for B-cell lymphoma.

After initial introduction for B-cell lymphomas as adjuvant therapies to established cancer treatments, immune checkpoint inhibitors and other immunotherapies are now integrated in mainstream regimens, both in adult and pediatric patients. We here provide an overview of the current status of combination therapies for B-cell lymphoma, by in-depth analysis of combination therapy trials registered between 2015-2020. Our analysis provides new insight into the rapid evolution in lymphoma treatment, as propelled by new additions to the treatment arsenal. We conclude with prospects on upcoming clinical trials which will likely use systematic testing approaches of more combinations of established chemotherapy regimens with new agents, as well as new combinations of immunotherapy and targeted therapy. Future trials will be set up as basket or umbrella-type trials to facilitate the evaluation of new drugs targeting specific genetic changes in the tumor or associated immune microenvironment. As such, lymphoma patients will benefit by receiving more tailored treatment that is based on synergistic effects of chemotherapy combined with new agents targeting specific aspects of tumor biology and the immune system.

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CiteScore
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