Houston Methodist Baytown Hospital, Baytown, TX.
Am J Health Syst Pharm. 2019 Oct 30;76(22):1825-1834. doi: 10.1093/ajhp/zxz202.
This article summarizes current targeted therapies that have received regulatory approval for the treatment of B- and T-cell lymphomas.
Over the last 20 years, new drug therapies for lymphomas of B cells and T cells have expanded considerably. Targeted therapies for B-cell lymphomas include: (1) monoclonal antibodies directed at the CD20 lymphocyte antigen, examples of which are rituximab, ofatumumab, and obinutuzumab; (2) gene transfer therapy, an example of which is chimeric antigen receptor-modified T-cell (CAR-T) therapy directed at the CD19 antigen expressed on the cell surface of both immature and mature B cells; and (3) small-molecule inhibitors (ibrutinib, acalabrutinib, copanlisib, duvelisib, and idelalisib) that target the B-cell receptor signaling pathway. Of note, brentuximab vedotin is an antibody-drug conjugate that targets CD30, another lymphocyte antigen expressed on the cell surface of both Hodgkin lymphoma (a variant of B-cell lymphoma) and some T-cell lymphomas. Although aberrant epigenetic signaling pathways are present in both B- and T-cell lymphomas, epigenetic inhibitors (examples include belinostat, vorinostat, and romidepsin) are currently approved by the Food and Drug Administration for T-cell lymphomas only. In addition, therapies that target the tumor microenvironment have been developed. Examples include mogamulizumab, bortezomib, lenalidomide, nivolumab, and pembrolizumab. In summary, the efficacy of these agents has led to the development of supportive care to mitigate adverse effects, due to the presence of on- or off-target toxicities.
The therapeutic landscape of lymphomas has continued to evolve. In turn, the efficacy of these agents has led to the development of supportive care to mitigate adverse effects, due to the presence of on- or off-target toxicities. Further opportunities are warranted to identify patients who are most likely to achieve durable response and reduce the risk of disease progression. Ongoing trials with current and investigational agents may further elucidate their place in therapy and therapeutic benefits.
本文总结了目前已获得监管部门批准用于治疗 B 细胞和 T 细胞淋巴瘤的靶向治疗方法。
在过去的 20 年中,B 细胞和 T 细胞淋巴瘤的新药治疗方法有了显著的扩展。B 细胞淋巴瘤的靶向治疗方法包括:(1)针对 CD20 淋巴细胞抗原的单克隆抗体,例如利妥昔单抗、奥法妥珠单抗和奥滨尤妥珠单抗;(2)基因转移治疗,例如针对幼稚和成熟 B 细胞表面表达的 CD19 抗原的嵌合抗原受体修饰 T 细胞(CAR-T)治疗;(3)小分子抑制剂(伊布替尼、阿卡替尼、copanlisib、duvelisib 和idelalisib),它们靶向 B 细胞受体信号通路。值得注意的是,brentuximab vedotin 是一种针对 CD30 的抗体药物偶联物,CD30 是另一种淋巴细胞抗原,存在于霍奇金淋巴瘤(B 细胞淋巴瘤的一种变体)和一些 T 细胞淋巴瘤的细胞表面。尽管 B 细胞和 T 细胞淋巴瘤中都存在异常的表观遗传信号通路,但目前只有食品和药物管理局批准了用于 T 细胞淋巴瘤的表观遗传抑制剂(例如 belinostat、vorinostat 和 romidepsin)。此外,还开发了针对肿瘤微环境的治疗方法。例如 mogamulizumab、硼替佐米、来那度胺、nivolumab 和 pembrolizumab。总之,这些药物的疗效导致了支持性治疗的发展,以减轻由于存在靶内或靶外毒性而产生的不良反应。
淋巴瘤的治疗格局不断发展。反过来,这些药物的疗效导致了支持性治疗的发展,以减轻由于存在靶内或靶外毒性而产生的不良反应。有必要进一步寻找最有可能获得持久缓解并降低疾病进展风险的患者。目前正在进行的针对现有和研究性药物的临床试验可能会进一步阐明它们在治疗中的地位和治疗益处。