Daratumumab, Carfilzomib, Lenalidomide, and Dexamethasone With Minimal Residual Disease Response-Adapted Therapy in Newly Diagnosed Multiple Myeloma

被引:143
|
作者
Costa, Luciano J. [1 ,2 ]
Chhabra, Saurabh [3 ]
Medvedova, Eva [4 ]
Dholaria, Bhagirathbhai R. [5 ]
Schmidt, Timothy M. [6 ]
Godby, Kelly N. [1 ,2 ]
Silbermann, Rebecca [4 ]
Dhaka, Binod [3 ]
Bal, Susan [1 ,2 ]
Gid, Smith [1 ,2 ]
D'Souza, Anita [3 ]
Hall, Aric [6 ]
Hardwick, Pamela [2 ]
Omel, James
Cornell, Robert F. [5 ]
Had, Parameswaran [3 ]
Callander, Natalie S. [6 ]
机构
[1] Univ Alabama Birmingham, Div Hematol Oncol, Birmingham, AL 35294 USA
[2] Univ Alabama Birmingham, ONeal Comprehens Canc Ctr, Birmingham, AL 35294 USA
[3] Med Coll Wisconsin, Dept Med, Div Hematol Oncol, Milwaukee, WI 53226 USA
[4] Oregon Hlth & Sci Univ, Portland, OR 97201 USA
[5] Vanderbilt Univ, Med Ctr, Dept Med, Div Hematol & Oncol, Nashville, TN USA
[6] Univ Wisconsin, Madison, WI USA
关键词
STEM-CELL TRANSPLANTATION; GENE-EXPRESSION; MAINTENANCE; BORTEZOMIB; CONSENSUS; THALIDOMIDE;
D O I
10.1200/JCO.21.01935
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PURPOSE 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. METHODS 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(-5)). Patients with two consecutive MRD-negative assessments entered treatment-free MRD surveillance. RESULTS 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(-6), 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%). CONCLUSION 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.
引用
收藏
页码:2901 / +
页数:15
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