Real-world outcomes following ibrutinib dose reduction in patients with chronic lymphocytic leukemia/small lymphocytic lymphoma

被引:2
|
作者
Shadman, Mazyar [1 ]
Salkar, Monika [2 ]
Srivastava, Bhavini [2 ]
Karve, Sudeep [2 ]
Emond, Bruno [3 ]
Gogna, Priyanka [3 ]
Manceur, Ameur M. [3 ]
Lafeuille, Marie-Helene [3 ]
Rava, Andrew [4 ]
Sun, Haiyan [4 ]
Howarth, Amanda [4 ]
Tomicki, Samantha [4 ]
Agatep, Barnabie [5 ]
Jones, Barton [5 ]
Franceschini, Erin [2 ]
Saifan, Chadi [2 ]
Bacchus, Shaffee [2 ]
Roeker, Lindsey [6 ]
Stephens, Deborah M. [7 ]
机构
[1] Fred Hutchinson Canc Ctr, 1100 Fairview Ave N, Seattle, WA 98109 USA
[2] AbbVie, N Chicago, IL USA
[3] Anal Grp Inc, Montreal, PQ, Canada
[4] Genesis Res Grp, Hoboken, NJ USA
[5] Inovalon, Bowie, MD USA
[6] Mem Sloan Kettering Canc Ctr, New York, NY USA
[7] Univ N Carolina, Div Hematol, Chapel Hill, NC USA
基金
美国国家卫生研究院;
关键词
Chronic lymphocytic leukemia; ibrutinib; real-world evidence; dose reduction; DOSING PATTERNS; THERAPY; CLL;
D O I
10.1080/10428194.2024.2402814
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This study used real-world data from three separate United States (US) databases to evaluate dosing patterns and time to next treatment (TTNT) following the first-incident adverse event (AE) in patients with chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL) treated with first-line ibrutinib with and without dose reduction (DR). Median TTNT or death in patients with and without a DR following an AE in each database was as follows: Optum Clinformatics Data Mart (CDM): 59.5 and 30.6 months; ConcertAI: 27.1 and 18.0 months; and Medicare Fee-for-Service (FFS): 49.8 and 22.0 months, respectively. Median TTNT or death in patients with cardiac AEs, with and without a DR, was: Optum CDM: 44.4 and 22.9 months; ConcertAI: 29.9 and 18.3 months; and Medicare FFS: 49.6 and 14.0 months, respectively. Ibrutinib DR was associated with fewer outpatient visits and lower CLL/SLL-related medical costs. These findings suggest that utilizing ibrutinib DR may effectively manage tolerability without compromising clinical efficacy.
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页数:10
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