Literature DB >> 34735756

Designing Clinical Trials in "Regular" COPD Versus Alpha-1 Antitrypsin Deficiency-Associated COPD: "More Alike Than Unalike?"

James K Stoller1.   

Abstract

Alpha-1 antitrypsin deficiency (AATD) predisposes to emphysema, liver disease, and panniculitis. This emphysema risk naturally invites a comparison between "regular" chronic obstructive pulmonary disease (COPD) (i.e., unrelated to AATD) and AATD-associated emphysema. Several features characterize both conditions. Both can be life-limiting and highly debilitating. Both are highly under-recognized. An important corollary of this comparison between "regular" COPD and AATD-associated COPD is whether both should be treated similarly and whether clinical trials to assess new therapies can be conducted similarly in both. Here, the distinctions between "regular" COPD and AATD-associated COPD are quite pronounced. Therapeutically, sparse available data suggest that lung volume reduction surgery confers less improvement in forced expiratory volume in 1 second (FEV1) in AATD and that such benefits are shorter-lived. Perhaps the most striking contrast between the 2 conditions is that clinical trial designs and conduct are necessarily very different. The relative scarcity of diagnosed individuals with AATD hampers recruitment to trials. Furthermore, primary outcome measures in trials of "regular" COPD must differ markedly from those of AATD-associated emphysema. Specifically, power calculations show that FEV1 and exacerbation frequency, which are amply represented as endpoints in large COPD trials, are infeasible in studies of AATD-associated emphysema. Rather, in the 3 available randomized controlled trials of intravenous augmentation therapy, the rate of emphysema progression based on serial computed tomography densitometry measurements has been the only feasible primary outcome measure. These considerations underscore the distinctive challenges and needs of conducting treatment trials in AATD-associated emphysema and emphasize that, with regard to clinical study design, the 2 conditions are "more unalike than alike." JCOPDF
© 2021.

Entities:  

Keywords:  alpha-1 antitrypsin deficiency; clinical trials; copd; endotype

Year:  2022        PMID: 34735756      PMCID: PMC8893971          DOI: 10.15326/jcopdf.2021.0261

Source DB:  PubMed          Journal:  Chronic Obstr Pulm Dis        ISSN: 2372-952X


  40 in total

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Journal:  Ther Adv Respir Dis       Date:  2010-07-26       Impact factor: 4.031

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Journal:  Am J Respir Crit Care Med       Date:  2007-09-13       Impact factor: 21.405

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Authors:  James K Stoller; Mark Brantly
Journal:  COPD       Date:  2013-03       Impact factor: 2.409

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Journal:  Lancet       Date:  2009-08-29       Impact factor: 79.321

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Journal:  Respir Med       Date:  2013-06-17       Impact factor: 3.415

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Authors:  Jan Stolk; Robert A Stockley; Berend C Stoel; Brendan G Cooper; Eeva Piitulainen; Niels Seersholm; Kenneth R Chapman; Jonathan G W Burdon; Marc Decramer; Raja T Abboud; Gregorius P M Mannes; Emiel F Wouters; Jeffrey E Garrett; Juan C Barros-Tizon; Erich W Russi; David A Lomas; William A MacNee; Alexis Rames
Journal:  Eur Respir J       Date:  2012-01-26       Impact factor: 16.671

9.  Reduced All-Cause Mortality in the ETHOS Trial of Budesonide/Glycopyrrolate/Formoterol for Chronic Obstructive Pulmonary Disease. A Randomized, Double-Blind, Multicenter, Parallel-Group Study.

Authors:  Fernando J Martinez; Klaus F Rabe; Gary T Ferguson; Jadwiga A Wedzicha; Dave Singh; Chen Wang; Kimberly Rossman; Earl St Rose; Roopa Trivedi; Shaila Ballal; Patrick Darken; Magnus Aurivillius; Colin Reisner; Paul Dorinsky
Journal:  Am J Respir Crit Care Med       Date:  2021-03-01       Impact factor: 21.405

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Authors:  Tomoko Nakanishi; Vincenzo Forgetta; Tomohiro Handa; Toyohiro Hirai; Vincent Mooser; G Mark Lathrop; William O C M Cookson; J Brent Richards
Journal:  Eur Respir J       Date:  2020-12-10       Impact factor: 16.671

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