Liu J, He H Y, Li L, Lu J, Qiang W T, Guo P, Hou N, Jiang H, Du J, Fu W J
Department of Hematology, Changzheng Hospital, the Second Military Medical University, Shanghai 200003, China.
Zhonghua Xue Ye Xue Za Zhi. 2021 Jan 14;42(1):27-32. doi: 10.3760/cma.j.issn.0253-2727.2021.01.006.
To investigate the efficacy and safety of daratumumab in relapsed and refractory multiple myeloma (RRMM) . The clinical characteristics, adverse reactions, efficacy, and prognosis of 46 patients with RRMM treated with daratumumab in Shanghai Changzheng Hospital from September 2017 to March 2020 were retrospectively analyzed. All patients were treated with daratumumab-based regimen: 8 in the Dd group, 35 in the DRd group, and 3 in the DVd group. With a median follow-up of 9.6 months, the overall response rate (ORR) was 75% [complete remission (CR) rate 18.2% ] among the 44 patients available for evaluation. The ORRs of patients resistant to bortezomib, lenalidomide, and both were 70.6% , 69.2% , and 63.6% , respectively. The CR rates of patients resistant to bortezomib, lenalidomide, and both were 17.6% , 11.5% , and 13.6% , respectively. No significant difference was observed in ORR and CR rates among the three groups. The ORRs of the DRd, DVd, and Dd groups were 85.3% , 66.7% , and 28.6% , respectively (=0.007) . The median PFS of 46 patients was 8.9 months, the median OS was not reached, and the 1-year OS rate was 74% . The median PFS and OS in the DRd group were longer than those in the Dd group (PFS: 14.4 months 2.0 months; OS: not reached 5.2 months) . After treatment with daratumumab, neutropenia is the most common hematological adverse reaction above grade 3. Non-hematological adverse reactions are mainly infusion-related adverse reactions and infections. Prognostic analysis showed that patients with extramedullary invasion had shorter PFS and OS compard with patients without extramedullary invasion (PFS: 5.7 14.4 months, =0.033; OS: 6.3 months not reached, =0.029) . The OS of patients with an ECOG score of 3-4 was significantly shorter than patients with an ECOG score of 1-2 (5.9 months not reached, =0.004) . Daratumumab-based regimens have good efficacy and safety in the treatment of RRMM.
探讨达雷妥尤单抗治疗复发难治性多发性骨髓瘤(RRMM)的疗效及安全性。回顾性分析2017年9月至2020年3月在上海长征医院接受达雷妥尤单抗治疗的46例RRMM患者的临床特征、不良反应、疗效及预后。所有患者均接受基于达雷妥尤单抗的方案治疗:Dd组8例,DRd组35例,DVd组3例。中位随访9.6个月,44例可评估患者的总缓解率(ORR)为75%[完全缓解(CR)率18.2%]。对硼替佐米、来那度胺耐药及两者均耐药患者的ORR分别为70.6%、69.2%和63.6%。对硼替佐米、来那度胺耐药及两者均耐药患者的CR率分别为17.6%、11.5%和13.6%。三组间ORR和CR率差异无统计学意义。DRd组、DVd组和Dd组的ORR分别为85.3%、66.7%和28.6%(P=0.007)。46例患者的中位无进展生存期(PFS)为8.9个月,中位总生存期(OS)未达到,1年OS率为74%。DRd组的中位PFS和OS长于Dd组(PFS:14.4个月对2.0个月;OS:未达到对5.2个月)。使用达雷妥尤单抗治疗后,3级以上最常见的血液学不良反应为中性粒细胞减少。非血液学不良反应主要为输液相关不良反应和感染。预后分析显示,髓外侵犯患者的PFS和OS短于无髓外侵犯患者(PFS:5.7个月对14.4个月,P=0.033;OS:6.3个月对未达到,P=0.029)。ECOG评分为3-4分患者的OS显著短于ECOG评分为1-2分的患者(5.9个月对未达到,P=0.004)。基于达雷妥尤单抗的方案治疗RRMM疗效和安全性良好。