Department of Leukemia, University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Department of Leukemia, University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Best Pract Res Clin Haematol. 2020 Dec;33(4):101226. doi: 10.1016/j.beha.2020.101226. Epub 2020 Nov 18.
The recent development of monoclonal antibodies targeting CD19, CD20, and CD22 has significantly improved long-term survival in patients with acute lymphoblastic leukemia (ALL), both in the frontline and relapsed and refractory setting. The incorporation of CD20 monoclonal antibodies (e.g. rituximab) has improved cure rates from 35% to 50% in those with precursor B-cell ALL and from 40 to 80% in those with Burkitt leukemia. More novel antibodies, such as drug conjugates antibodies (e.g. inotuzumab ozogamicin) and bispecific T-cell engagers (e.g. blinatumomab), have shown significant promise in improving outcomes in the relapsed and refractory setting and are currently being studied in the frontline setting, with hopes to further improve long-term outcomes. In this chapter, we will review the role of monoclonal antibodies and how the incorporation of these agents has revolutionized and changed the treatment management of ALL in the frontline setting.
针对 CD19、CD20 和 CD22 的单克隆抗体的最新发展,显著提高了急性淋巴细胞白血病(ALL)患者的长期生存率,无论是在一线还是复发和难治性疾病环境中。在前体 B 细胞 ALL 患者中,将 CD20 单克隆抗体(如利妥昔单抗)纳入治疗方案,使治愈率从 35%提高到 50%,在伯基特白血病患者中,从 40%提高到 80%。更新型的抗体,如药物偶联抗体(如奥加妥珠单抗)和双特异性 T 细胞衔接器(如blinatumomab),在改善复发和难治性疾病环境中的疗效方面显示出了显著的前景,目前正在一线疾病环境中进行研究,有望进一步提高长期疗效。在这一章中,我们将回顾单克隆抗体的作用,以及这些药物的应用如何彻底改变和改变 ALL 的一线治疗管理。