Weekly carfilzomib, lenalidomide, and dexamethasone in relapsed or refractory multiple myeloma: A phase 1b study Journal Article


Authors: Biran, N.; Siegel, D.; Berdeja, J. G.; Raje, N.; Cornell, R. F.; Alsina, M.; Kovacsovics, T.; Fang, B.; Kimball, A. S.; Landgren, O.
Article Title: Weekly carfilzomib, lenalidomide, and dexamethasone in relapsed or refractory multiple myeloma: A phase 1b study
Abstract: Twice-weekly carfilzomib (27 mg/m2) with lenalidomide-dexamethasone (KRd) is a standard-of-care in relapsed or refractory multiple myeloma (RRMM). This phase 1b study evaluated KRd with once-weekly carfilzomib in RRMM. Patients received carfilzomib (30-minute infusion; 56 or 70mg/m2) on days 1, 8, and 15; lenalidomide 25 mg on days 1-21; and dexamethasone 40 mg on days 1, 8, 15, and 22 (day 22 omitted for cycles 9+) of 28-day cycles. Primary objective was safety/tolerability; efficacy was a secondary objective. Fifty-six RRMM patients enrolled: 22 during dose evaluation (56-mg/m2, n = 10; 70-mg/m2, n = 12) and 34 during dose expansion (all initiated dosing at 70 mg/m2). After 2 fatal adverse events (AEs) during 70-mg/m2 dose expansion, dosage reduction to 56 mg/m2 was permitted. Results are presented for carfilzomib 56-mg/m2 (n = 10) and 70-mg/m2 groups (dose evaluation/expansion; n = 46). Median carfilzomib dose was 53.2 mg/m2 (56-mg/m2 group) and 62.4 mg/m2 (70-mg/m2 group). Grade ≥3 AE rates were 70.0% (56 mg/m2) and 69.6% (70 mg/m2). Overall response rates were 90.0% (56 mg/m2) and 89.1% (70 mg/m2); ≥very good partial response rates were 50.0% (56 mg/m2) and 73.9% (70 mg/m2). Once-weekly KRd was active with acceptable toxicity in RRMM, supporting further evaluation of this regimen. © 2019 The Authors. American Journal of Hematology published by Wiley Periodicals, Inc.
Journal Title: American Journal of Hematology
Volume: 94
Issue: 7
ISSN: 0361-8609
Publisher: John Wiley & Sons, Inc.  
Date Published: 2019-07-01
Start Page: 794
End Page: 802
Language: English
DOI: 10.1002/ajh.25498
PUBMED: 31021005
PROVIDER: scopus
PMCID: PMC6593978
DOI/URL:
Notes: Source: Scopus
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  1. Carl Ola Landgren
    336 Landgren