The Landscape of Checkpoint Inhibition in the Management of Hematological Malignancies

Shukaib Arslan, A. Herrera, M. A. Malki
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Abstract

The programmed-death 1 (PD-1) and cytotoxic T-lymphocyte associated protein 4 (CTLA-4) pathways are inhibitory immune checkpoints involved in the escape of cancer cells from the immune system. Inhibition of these immune checkpoints can lead to the induction of body’s immune response to these cancer cells. To activate the immune system against the tumor cells, various monoclonal antibodies targeting these pathways have been developed. Many of such antibodies have been approved for therapy in solid tumor malignancies and now some hematological malignancies. Here, we review the available data regarding the response to PD-1 and CTLA-4 pathway blockade in hematological malignancies including Hodgin lymphoma, non-Hodgkin lymhoma, multiple myeloma and myeloid neoplasms as well as before and after hematopoietic cell transplantation. We also discuss the specific concerns and differences related to their use in hematological malignancies (HMs) as compared to solid tumors.
检查点抑制在血液系统恶性肿瘤治疗中的前景
程序性死亡1 (PD-1)和细胞毒性t淋巴细胞相关蛋白4 (CTLA-4)途径是参与癌细胞逃离免疫系统的抑制免疫检查点。抑制这些免疫检查点可以诱导机体对这些癌细胞的免疫反应。为了激活针对肿瘤细胞的免疫系统,各种针对这些途径的单克隆抗体已经被开发出来。许多这样的抗体已被批准用于治疗实体瘤恶性肿瘤和现在的一些血液系统恶性肿瘤。在这里,我们回顾了PD-1和CTLA-4通路阻断在血液恶性肿瘤(包括霍奇金淋巴瘤、非霍奇金淋巴瘤、多发性骨髓瘤和髓系肿瘤)以及造血细胞移植前后的反应的现有数据。我们还讨论了与实体瘤相比,它们在血液恶性肿瘤(HMs)中使用的具体问题和差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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