Galanina Natalie, Kline Justin, Bishop Michael R
Department of Hematology/Oncology, UC San Diego Moores Cancer Center, La Jolla, California, USA.
Section of Hematology/Oncology, University of Chicago, Chicago, IL, USA.
Ther Adv Hematol. 2017 Feb;8(2):81-90. doi: 10.1177/2040620716673787. Epub 2017 Jan 22.
Following the successful application of immune checkpoint blockade therapy (CBT) in refractory solid tumors, it has recently gained momentum as a promising modality in the treatment of relapsed lymphoma. This significant therapeutic advance stems from decades of research that elucidated the role of immune regulation pathways and the mechanisms by which tumors can engage these critical pathways to escape immune detection. To date, two main pathways, the cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) and programmed death 1 (PD-1), have emerged as key targets of CBT demonstrating unprecedented activity particularly in heavily pretreated relapsed/refractory Hodgkin lymphoma and some forms of non-Hodgkin disease. Herein we provide a brief discussion of checkpoint blockade in the context of lymphoma biology with a specific focus on novel checkpoint inhibitors and their therapeutic activity. We discuss current clinical trials and the landscape of CBT to underscore both the remarkable progress and foreseeable limitations of this novel treatment strategy. In particular, we build upon state-of-the-art knowledge and clinical insights gained from the early trials to review potential approaches to how CBT may be integrated with other treatment modalities, including chemoimmunotherapy to improve patient outcomes in the future. Finally, as the role of CBT evolves to potentially become a cornerstone of therapy in refractory/relapsed lymphoma, we briefly emphasize the importance of predictive biomarkers in an effort to select appropriate patients who are most likely to derive benefit from CBT.
随着免疫检查点阻断疗法(CBT)在难治性实体瘤治疗中的成功应用,它最近作为一种有前景的治疗方式在复发性淋巴瘤治疗中获得了发展势头。这一重大治疗进展源于数十年的研究,这些研究阐明了免疫调节通路的作用以及肿瘤能够利用这些关键通路逃避免疫检测的机制。迄今为止,两条主要通路,即细胞毒性T淋巴细胞相关蛋白4(CTLA - 4)和程序性死亡1(PD - 1),已成为CBT的关键靶点,显示出前所未有的活性,特别是在经过大量预处理的复发性/难治性霍奇金淋巴瘤和某些形式的非霍奇金病中。在此,我们在淋巴瘤生物学背景下简要讨论检查点阻断,特别关注新型检查点抑制剂及其治疗活性。我们讨论当前的临床试验和CBT的情况,以强调这种新型治疗策略的显著进展和可预见的局限性。特别是,我们基于早期试验获得的最新知识和临床见解,回顾CBT如何与其他治疗方式(包括化学免疫疗法)相结合以改善未来患者预后的潜在方法。最后,随着CBT的作用逐渐发展成为难治性/复发性淋巴瘤治疗的基石,我们简要强调预测性生物标志物的重要性,以便选择最有可能从CBT中获益的合适患者。