Carfilzomib prescribing patterns and outcomes for relapsed or refractory multiple myeloma: a real-world analysis

被引:1
作者
Dong, Sharlene [1 ]
Banerjee, Rahul [2 ]
Khan, Adeel M. [1 ]
Wang, Mengru [3 ]
Wang, Xiaoliang [3 ]
Afghahi, Anosheh [3 ]
Afrough, Aimaz [1 ]
Janakiram, Murali [4 ]
Wang, Bo [5 ]
Cowan, Andrew J. [2 ]
Sperling, Adam S. [6 ]
Anderson Jr, Larry D. [1 ]
Rajkumar, S. Vincent [7 ]
Kaur, Gurbakhash [1 ,8 ]
机构
[1] UT Southwestern Med Ctr, Harold C Simmons Comprehens Canc Ctr, Dallas, TX 75390 USA
[2] Fred Hutchinson Canc Ctr, Seattle, WA USA
[3] Flatiron Hlth Inc, New York, NY USA
[4] City Hope Natl Med Ctr, Canc Ctr, Duarte, CA USA
[5] Willamette Valley Canc Inst, Eugene, OR USA
[6] Dana Farber Canc Inst, Boston, MA USA
[7] Mayo Clin, Rochester, MN USA
[8] Mt Sinai Sch Med, New York, NY 10029 USA
关键词
SINGLE-AGENT CARFILZOMIB; OPEN-LABEL; IRREVERSIBLE INHIBITOR; PHASE-II; DEXAMETHASONE; BORTEZOMIB; CRITERIA;
D O I
10.1038/s41408-025-01256-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Despite the widespread use of carfilzomib (K) in relapsed/refractory multiple myeloma (RRMM), there is no consensus on optimal K dose in milligrams per square meter (mg/m2) or dosing schedule. We assessed three modern K prescribing patterns in RRMM using a large United States electronic health record-derived database. Our final cohort (n = 486) included 136 patients (28.0%) who received K 56 mg/m2 once weekly (K56-1x), 86 (17.7%) who received 56 mg/m2 twice weekly (K56-2x), and 264 (54.3%) who received 70 mg/m2 once weekly (K70-1x). Between 2016 and 2023, once-weekly dosing became more common: K70-1x proportions changed from 21.1% in 2016 to 50.6% in 2023, K56-1x from 15.8% to 37.0%, and K56-2x from 63.2% to 12.3%. Median progression-free survival was 13.0 months [95% confidence interval (CI) 11.2-20.7] for K56-1x, 13.2 months (95% CI 9.0-28.1 months) for K56-2x, and 10.9 months (95% CI 9.9-15.3 months) for K70-1x; these differences were not statistically significant (log-rank p = 0.46). Rates of heart failure was comparable (<5% in all cohorts). In summary, our findings do not support improved outcomes with twice-weekly carfilzomib in RRMM. K56-1x may provide the best balance of efficacy, safety, and avoidance of time toxicity from frequent infusions.
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页数:9
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