Division of Hematology/Oncology, University of Alabama at Birmingham, Birmingham, AL.
O'Neal Comprehensive Cancer Center at University of Alabama at Birmingham, Birmingham, AL.
J Clin Oncol. 2022 Sep 1;40(25):2901-2912. doi: 10.1200/JCO.21.01935. Epub 2021 Dec 13.
The MASTER trial combined daratumumab, carfilzomib, lenalidomide, and dexamethasone (Dara-KRd) in newly diagnosed multiple myeloma (NDMM), using minimal residual disease (MRD) by next-generation sequencing (NGS) to inform the use and duration of Dara-KRd post-autologous hematopoietic cell transplantation (AHCT) and treatment cessation in patients with two consecutive MRD-negative assessments.
This multicenter, single-arm, phase II trial enrolled patients with NDMM with planed enrichment for high-risk cytogenetic abnormalities (HRCAs). Patients received Dara-KRd induction, AHCT, and Dara-KRd consolidation, according to MRD status. MRD was evaluated by NGS at the end of induction, post-AHCT, and every four cycles (maximum of eight cycles) of consolidation. Primary end point was achievement of MRD negativity (< 10). Patients with two consecutive MRD-negative assessments entered treatment-free MRD surveillance.
Among 123 participants, 43% had none, 37% had 1, and 20% had 2+ HRCA. Median age was 60 years (range, 36-79 years), and 96% had MRD trackable by NGS. Median follow-up was 25.1 months. Overall, 80% of patients reached MRD negativity (78%, 82%, and 79% for patients with 0, 1, and 2+ HRCA, respectively), 66% reached MRD < 10, and 71% reached two consecutive MRD-negative assessments during therapy, entering treatment-free surveillance. Two-year progression-free survival was 87% (91%, 97%, and 58% for patients with 0, 1, and 2+ HRCA, respectively). Cumulative incidence of MRD resurgence or progression 12 months after cessation of therapy was 4%, 0%, and 27% for patients with 0, 1, or 2+ HRCA, respectively. Most common serious adverse events were pneumonia (6%) and venous thromboembolism (3%).
Dara-KRd, AHCT, and MRD response-adapted consolidation leads to high rate of MRD negativity in NDMM. For patients with 0 or 1 HRCA, this strategy creates the opportunity of MRD surveillance as an alternative to indefinite maintenance.
MASTER 试验联合达雷妥尤单抗、卡非佐米、来那度胺和地塞米松(Dara-KRd)治疗新诊断多发性骨髓瘤(NDMM),通过下一代测序(NGS)检测微小残留病灶(MRD)来指导 Dara-KRd 在自体造血细胞移植(AHCT)后的使用和持续时间,并在连续两次 MRD 阴性评估的患者中停止治疗。
这项多中心、单臂、二期临床试验招募了计划进行高危细胞遗传学异常(HRCAs)富集的 NDMM 患者。患者接受 Dara-KRd 诱导、AHCT 和 Dara-KRd 巩固治疗,根据 MRD 状态而定。MRD 通过 NGS 在诱导结束时、AHCT 后和巩固治疗的每四个周期(最多 8 个周期)进行评估。主要终点是达到 MRD 阴性(<10)。连续两次 MRD 阴性评估的患者进入无治疗 MRD 监测。
在 123 名参与者中,43%的患者无 HRCA,37%的患者有 1 个 HRCA,20%的患者有 2 个或更多 HRCA。中位年龄为 60 岁(范围为 36-79 岁),96%的患者可通过 NGS 进行 MRD 检测。中位随访时间为 25.1 个月。总体而言,80%的患者达到了 MRD 阴性(0、1 和 2+HRCA 的患者分别为 80%、82%和 79%),66%的患者达到了 MRD<10,71%的患者在治疗期间达到了连续两次 MRD 阴性评估,进入了无治疗监测。两年无进展生存率为 87%(0、1 和 2+HRCA 的患者分别为 91%、97%和 58%)。治疗停止后 12 个月时,MRD 复发或进展的累积发生率分别为 4%、0%和 27%,对于 0、1 或 2+HRCA 的患者分别为 0%、0%和 27%。最常见的严重不良事件是肺炎(6%)和静脉血栓栓塞(3%)。
Dara-KRd、AHCT 和基于 MRD 反应的巩固治疗可使 NDMM 患者达到高比例的 MRD 阴性。对于 0 或 1 HRCA 的患者,该策略为 MRD 监测提供了机会,可作为无限期维持治疗的替代方案。