4.7 Article

Childhood asthma clusters and response to therapy in clinical trials

期刊

出版社

MOSBY-ELSEVIER
DOI: 10.1016/j.jaci.2013.09.002

关键词

Asthma; clustering; clinical trials; replication; pediatric; therapy response

资金

  1. Clinical and Translational Science Award (CTSA) program through the National Institutes of Health (NIH) National Center for Advancing Translational Sciences (NCATS) [UL1TR000427]
  2. National Heart, Lung, and Blood Institute (NHLBI) [F30HL112491, 5U10HL064287, 5U10HL064288, 5U10HL064295, 5U10HL064307, 5U10HL064305, 5U10HL064313]
  3. Washington University School of Medicine CTSA Infrastructure for Pediatric Research [5UL1RR02499204]
  4. Madison CTSA [1UL1RR025011]
  5. National Center for Research Resources [UL1RR025780]
  6. [M01 RR00036]
  7. [M01 RR00051]
  8. [5M01 RR00997]

向作者/读者索取更多资源

Background: Childhood asthma clusters, or subclasses, have been developed by computational methods without evaluation of clinical utility. Objective: To replicate and determine whether childhood asthma clusters previously identified computationally in the Severe Asthma Research Program (SARP) are associated with treatment responses in Childhood Asthma Research and Education (CARE) Network clinical trials. Methods: A cluster assignment model was determined by using SARP participant data. A total of 611 participants 6 to 18 years old from 3 CARE trials were assigned to SARP pediatric clusters. Primary and secondary outcomes were analyzed by cluster in each trial. Results: CARE participants were assigned to SARP clusters with high accuracy. Baseline characteristics were similar between SARP and CARE children of the same cluster. Treatment response in CARE trials was generally similar across clusters. However, with the caveat of a smaller sample size, children in the early-onset/severe-lung function cluster had best response with fluticasone/salmeterol (64% vs 23% 2.5x fluticasone and 13% fluticasone/montelukast in the Best ADd-on Therapy Giving Effective Responses trial; P=.011) and children in the early-onset/comorbidity cluster had the least clinical efficacy to treatments (eg, -0.076% change in FEV1 in the Characterizing Response to Leukotriene Receptor Antagonist and Inhaled Corticosteroid trial). Conclusions: In this study, we replicated SARP pediatric asthma clusters by using a separate, large clinical trials network. Early-onset/severe-lung function and early-onset/comorbidity clusters were associated with differential and limited response to therapy, respectively. Further prospective study of therapeutic response by cluster could provide new insights into childhood asthma treatment.

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