O'Neill Chloe, van de Donk Niels W C J
Amsterdam UMC, Vrije Universiteit Amsterdam Department of Hematology Amsterdam The Netherlands.
Cancer Center Amsterdam Cancer Biology and Immunology Amsterdam The Netherlands.
EJHaem. 2023 Jun 6;4(3):811-822. doi: 10.1002/jha2.729. eCollection 2023 Aug.
T-cell engaging bispecific antibodies (BsAbs) have substantial activity in heavily pretreated patients with multiple myeloma (MM). The overall response rate obtained with B-cell maturation antigen (BCMA)-targeting BsAbs is approximately 60%-70%, including a high proportion of patients achieving very good partial response or complete response. Comparable efficacy is seen with BsAbs targeting GPRC5D or FcRH5. Cytokine release syndrome is frequently observed with BsAb treatment, but mostly during the step-up doses and the first full dose. Early intervention with IL-6 receptor blocking antibodies (e.g., tocilizumab) prevents escalation to severe manifestations. Infections are also common during treatment and related to the extent of exposure to immune suppressive anti-MM agents, as well as development of hypogammaglobulinemia due to elimination of normal plasma cells, and probably because of T-cell exhaustion resulting from continuous BsAb-mediated T-cell activation. Adequate monitoring for infections and institution of infectious prophylaxis are essential. Patients treated with GPRC5D-targteing BsAbs often develop skin and nail disorders and loss of taste, which is likely related to GPRC5D expression in cells that produce hard keratin. Currently ongoing studies are aiming at further improving these results by evaluating BsAbs in combination with other drugs, such as immunomodulatory agents and anti-CD38 antibodies, as well as the application of BsAbs in earlier lines of therapy, including patients with newly diagnosed disease. We expect that the outcomes of patients with MM will further improve by the introduction of this novel type of T-cell immunotherapy.
T细胞接合双特异性抗体(BsAbs)在接受过大量预处理的多发性骨髓瘤(MM)患者中具有显著活性。使用靶向B细胞成熟抗原(BCMA)的BsAbs获得的总体缓解率约为60%-70%,其中很大一部分患者达到了非常好的部分缓解或完全缓解。靶向GPRC5D或FcRH5的BsAbs也显示出类似的疗效。使用BsAb治疗时经常观察到细胞因子释放综合征,但大多发生在剂量递增阶段和首次全剂量给药期间。早期使用IL-6受体阻断抗体(如托珠单抗)进行干预可防止病情升级为严重表现。治疗期间感染也很常见,这与接触免疫抑制性抗MM药物的程度有关,也与因正常浆细胞清除导致的低丙种球蛋白血症的发生有关,可能还与持续的BsAb介导的T细胞活化导致的T细胞耗竭有关。对感染进行充分监测并采取感染预防措施至关重要。接受靶向GPRC5D的BsAbs治疗的患者经常出现皮肤和指甲疾病以及味觉丧失,这可能与产生硬角蛋白的细胞中GPRC5D的表达有关。目前正在进行的研究旨在通过评估BsAbs与其他药物(如免疫调节剂和抗CD38抗体)联合使用,以及将BsAbs应用于更早的治疗线(包括新诊断疾病的患者)来进一步改善这些结果。我们预计,通过引入这种新型T细胞免疫疗法,MM患者的治疗结果将进一步改善。