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

Author:

Costa Luciano J.12ORCID,Chhabra Saurabh3ORCID,Medvedova Eva4ORCID,Dholaria Bhagirathbhai R.5ORCID,Schmidt Timothy M.6ORCID,Godby Kelly N.12,Silbermann Rebecca4ORCID,Dhakal Binod3ORCID,Bal Susan12ORCID,Giri Smith12ORCID,D'Souza Anita3ORCID,Hall Aric6ORCID,Hardwick Pamela2,Omel James7,Cornell Robert F.5ORCID,Hari Parameswaran3ORCID,Callander Natalie S.6ORCID

Affiliation:

1. Division of Hematology/Oncology, University of Alabama at Birmingham, Birmingham, AL

2. O'Neal Comprehensive Cancer Center at University of Alabama at Birmingham, Birmingham, AL

3. Division of Hematology/Oncology, Department of Medicine, Medical College of Wisconsin, Milwaukee, WI

4. Oregon Health & Science University, Portland, OR

5. Department of Medicine, Division of Hematology and Oncology, Vanderbilt University Medical Center, Nashville, TN

6. University of Wisconsin, Madison, WI

7. Independent Patient Advocate, Omaha, NE

Abstract

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.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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