6 Clinical Outcomes and Health-Care Resource Use Associated With Reslizumab Treatment in Adults With Severe Eosinophilic Asthma in Real-World Practice

被引:27
|
作者
Wechsler, Michael E. [1 ]
Peters, Stephen P. [2 ]
Hill, Tanisha D. [3 ]
Ariely, Rinat [3 ]
DePietro, Michael R. [3 ]
Driessen, Maurice T. [4 ]
Terasawa, Emi L. [5 ]
Thomason, Darren R. [5 ]
Panettieri, Reynold A., Jr. [6 ]
机构
[1] Natl Jewish Hlth, Denver, CO 80206 USA
[2] Wake Forest Sch Med, Winston Salem, NC 27101 USA
[3] Teva Branded Pharmaceut Prod R&D Inc, W Chester, PA USA
[4] Teva Pharmaceut Ind Ltd, Amsterdam, Netherlands
[5] Anal Grp Inc, New York, NY USA
[6] Rutgers State Univ, New Brunswick, NJ USA
关键词
asthma; eosinophilic lung disease; real-world study; respiratory care; PHENOTYPES; COSTS;
D O I
10.1016/j.chest.2020.11.060
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
BACKGROUND: Reslizumab, an anti-IL-5 monoclonal antibody, is indicated as add-on maintenance treatment for adults with severe eosinophilic asthma. RESEARCH QUESTION: What are the real-world outcomes associated with reslizumab use in patients with severe eosinophilic asthma in a US clinical practice? STUDY DESIGN AND METHODS: In this retrospective study, patient-level data from adults treated with reslizumab were obtained from center- and panel-based medical chart reviews. Eligible patients had available medical records and treatment history for >= 6 months before initiation of reslizumab treatment (index date) to >= 7 months after reslizumab initiation. The primary outcome was response to reslizumab treatment, based on clinical expert predefined definitions of response. Other outcomes included clinical asthma exacerbations (CAEs), use of maintenance oral corticosteroids (OCS), FEV1 percent predicted, Asthma Control Test (ACT) score, and health-care resource use (HRU). RESULTS: Medical charts were obtained for 215 patients. Most patients (58.6%) showed an excellent response, 16.3% showed a clinically meaningful response, 21.9% showed a partial response, and 3.3% were nonresponders or treatment failures. A significant reduction was observed in the proportion of patients experiencing a CAE in a 6-month period (from 86.0% to 40.5%; P < .001) and in the mean number of CAEs per patient (2.84 [SD, 2.41] vs 0.94 [SD, 1.86]) after reslizumab initiation. Improvements were observed in FEV1 percent predicted (65.1% [SD, 20.5%] vs 73.1% [SD, 23.1%]; P < .001) and in ACT scores (13.8 [SD, 4.2] vs 18.6 [SD, 4.0]; P<.001) before to after reslizumab initiation. Among patients usingmaintenanceOCS at baseline, more than half discontinued use of these by approximately 10 months after reslizumab initiation. Significant reductions in asthma-related HRU were observed after reslizumab initiation. INTERPRETATION: In clinical practice, reslizumab may have been initiated in response to heavy symptom burden and CAEs. Reslizumab was associated with improved clinical and patient-reported outcomes and significant reductions in asthma-related HRU.
引用
收藏
页码:1734 / 1746
页数:13
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