Qureshi Zaheer, Jamil Abdur, Altaf Faryal, Siddique Rimsha, Ahmed Faizan
School of Medicine, Quinnipiac University, Bridgeport, CT, USA.
Department of Medicine, Samaritan Medical Centre Watertown, Watertown, NY, USA.
Ann Hematol. 2024 Dec;103(12):4901-4912. doi: 10.1007/s00277-024-06078-z. Epub 2024 Nov 8.
To synthesize the evidence on the efficacy and safety of teclistamab in treating relapsed/refractory multiple myeloma (RRMM). A systematic search for records published from inception until June 2024 was conducted on PubMed, Web of Science, EMBASE, and Google Scholar databases. Five studies with 661 RRMM patients were included in the analysis. The pooled results showed that teclistamab led to an overall response rate (ORR) of 62.8% (95% Confidence Interval (CI): 58.6-66.8), a ≥ very good partial response or better (VGPR) of 52.1% (95% CI: 46.8-57.3), and a ≥ complete response or better (CR) of 29.5% (95% CI: 21.9-38.4). When the ORR was assessed in different subgroups, we found that patients with extramedullary disease (EMD) had considerably lower ORR than those without EMD (45% vs. 71%, p < 0.0001). The ORR was significantly lower in patients with prior (B-cell maturation antigen) BCMA-directed therapy (OR: 2.24, p = 0.002) and those with stage III disease (OR: 3.69, p = 0.0001). However, the subgroup analyses showed no considerable difference in the ORR between patients with high or standard-risk cytogenetics (OR: 1.05 p = 0.82) and those with penta-drug or triple-class-refractory disease (OR: 0.97 p = 0.89). Regarding the safety of teclistamab, the pooled results showed that the incidence of grade ≥ 3 adverse events was high (90.7%). However, grade ≥ 3 cytokine release syndrome (CRS) and neurotoxic events were low (1.5% and 2.2%, respectively). RRMM patients treated with teclistamab display good response rates.
综合有关替西妥单抗治疗复发/难治性多发性骨髓瘤(RRMM)疗效和安全性的证据。对PubMed、科学网、EMBASE和谷歌学术数据库进行了系统检索,以查找从数据库创建至2024年6月发表的记录。分析纳入了五项研究,共661例RRMM患者。汇总结果显示,替西妥单抗导致的总缓解率(ORR)为62.8%(95%置信区间(CI):58.6 - 66.8),≥非常好的部分缓解或更好(VGPR)为52.1%(95%CI:46.8 - 57.3),≥完全缓解或更好(CR)为29.5%(95%CI:21.9 - 38.4)。在不同亚组中评估ORR时,我们发现有髓外疾病(EMD)的患者ORR显著低于无EMD的患者(45%对71%,p < 0.0001)。接受过既往(B细胞成熟抗原)BCMA定向治疗的患者ORR显著更低(OR:2.24,p = 0.002),III期疾病患者也是如此(OR:3.69,p = 0.0001)。然而,亚组分析显示,高风险或标准风险细胞遗传学患者与五药难治或三类难治性疾病患者之间的ORR无显著差异(OR:1.05,p = 0.82)。关于替西妥单抗的安全性,汇总结果显示≥3级不良事件的发生率很高(90.7%)。然而,≥3级细胞因子释放综合征(CRS)和神经毒性事件的发生率较低(分别为1.5%和2.2%)。接受替西妥单抗治疗RRMM患者显示出良好的缓解率。