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Analysis of hereditary angioedema attacks requiring a second dose of ecallantide
被引:11
|作者:
Li, H. Henry
[1
]
Campion, Marilyn
Craig, Timothy J.
[2
]
Soteres, Daniel F.
[3
]
Riedl, Marc
[4
]
Lumry, William R.
[5
]
MacGinnitie, Andrew J.
[6
]
Shea, Elizabeth P.
[7
]
Bernstein, Jonathan A.
[8
]
机构:
[1] Inst Asthma & Allergy, Wheaton, MD 20902 USA
[2] Penn State Univ, Hershey, PA USA
[3] Asthma & Allergy Associates PC, Colorado Springs, CO USA
[4] Univ Calif Los Angeles, David Geffen Sch Med, Los Angeles, CA 90095 USA
[5] AARA Res Ctr, Dallas, TX USA
[6] Boston Childrens Hosp, Boston, MA USA
[7] Dyax Corp, Burlington, MA USA
[8] Univ Cincinnati, Cincinnati, OH USA
关键词:
C1 INHIBITOR CONCENTRATE;
DOUBLE-BLIND;
RECEPTOR ANTAGONIST;
ICATIBANT;
MANAGEMENT;
SYMPTOMS;
EFFICACY;
TRIAL;
D O I:
10.1016/j.anai.2012.12.004
中图分类号:
R392 [医学免疫学];
学科分类号:
100102 ;
摘要:
Background: Effective treatment of acute attacks is critical in managing hereditary angioedema (HAE). Ecallantide, a plasma kallikrein inhibitor, is approved for the treatment of HAE attacks. Occasionally, a second dose is needed when treating attacks of HAE. Objective: To evaluate the characteristics of HAE attacks requiring a second dose (dose B) of ecallantide. Methods: Data from all ecallantide clinical trials (EDEMA2, EDEMA4, and DX-88/19) that allowed an open-label dose B were included in this analysis. Patient and attack characteristics potentially predictive of dose B after ecallantide were analyzed by logistic regression. A multivariate model was built using a backward selection process, incorporating variables from the univariate model with P <.20 and removing factors with the highest P value until only significant (P <.05) factors remained. Results: The analysis included 732 ecallantide-treated HAE attacks in 179 patients. Dose B was required in 88 attacks (12.0%), most (80.5%) for incomplete response. By attack location, 31 of 325 abdominal attacks (9.5%), 17 of 158 laryngeal attacks (10.8%), and 40 of 242 peripheral attacks (16.5%) required dose B. On the basis of the univariate analysis, baseline severity (odds ratio = 1.33, P =.15) and peripheral attack (odds ratio = 1.80, P =.01) were identified as potential predictive factors; abdominal attacks had an inverse correlation (odds ratio = 0.64, P =.055). However, the multivariate analysis identified only peripheral attacks as statistically significantly correlated (P <.05) with dose B requirement. Conclusion: A single, 30-mg dose of ecallantide was effective for most HAE attacks (88.0%). Patients with peripheral attacks of HAE were more likely to require a second dose of ecallantide after 4 hours. Trial Registration: clinicaltrials.gov Identifiers: not applicable for EDEMA2 (trial was conducted before registration requirements were implemented), NCT00457015 for EDEMA4, and NCT00456508 for DX-88/19. (C) 2013 American College of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.
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页码:168 / 172
页数:5
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