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Letter
Authors' response
  1. Kenneth R Chapman1,
  2. Neil C Barnes2,
  3. Andrew P Greening3,
  4. Paul W Jones4,
  5. Soren Pedersen5
  1. 1Asthma and Airway Centre, University Health Network, University of Toronto, Toronto, Canada
  2. 2Department of Respiratory Medicine, London Chest Hospital, London, UK
  3. 3Department of Pulmonary Disease, Respiratory Unit, Western General Hospital, Edinburgh, UK
  4. 4Division of Clinical Science, St George's, University of London, London, UK
  5. 5Pediatric Research Unit, Kolding Hospital, Kolding, Denmark

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We thank our colleagues who have forwarded questions and comments to the editors of Thorax, thereby engaging in a discussion of asthma strategy we believe to be long overdue. We must leave the editors of Thorax to respond to comments directed to their principles and policies, but suspect that our review was regarded by the editors and reviewers as a summary of single maintenance and reliever therapy (SMART) outcomes from a traditional yet unexplored perspective that might spark discussion in an important area. In doing so, we believe that the journal has behaved responsibly by encouraging scientific debate. The tenets of single maintenance and reliever therapy of asthma have represented a marked departure from contemporary asthma management perspectives. These include the following: (1) that a reactive and bronchodilator-driven strategy of asthma care is superior to the prevention of asthma symptoms and disability as long as a small aliquot of inhaled corticosteroid is inhaled at times of acute wheezing and breathlessness; (2) that comprehensive asthma control is no longer needed to evaluate asthma treatment and it is sufficient to measure the time between severe exacerbations; and (3) that rising sputum and biopsy markers of inflammation are of no concern in the choice of maintenance strategies. Until the present correspondence, the absence of discussion and debate concerning these proposals has puzzled us.

Dr Peters and Professor Jenkins have entitled their letter ‘Critical appraisal of Symbicort maintenance and reliever treatment misrepresents clinical evidence’.1 We had used the acronym SMART to represent ‘single maintenance and reliever therapy’ to engage in a broad discussion of asthma management principles and not a review of a specific pharmacotherapy; that will be the intended meaning of the acronym in this letter.2 Peters and Jenkins state that we have implied that fixed dose treatments ‘achieved target levels of control’ in reference to the review of control outcomes by Bateman and colleagues.3 We can find no mention of fixed dose treatment outcomes in this paragraph of our publication. Elsewhere in the review we have noted that the primary outcome for inhaled corticosteroids/long-acting β agonists (ICS/LABA) given in SMART fashion was superior to lower doses of ICS/LABA given in fixed dose fashion and also superior to fixed dose ICS monotherapy.

We thank Drs Peters, Yan, Reddel and Professor Jenkins1 4 for highlighting the second relevant Cochrane review.5 A thorough reading will reveal that, in the studies examined by Cates and Lasserson, the dosage of maintenance ICS was reduced during the run-in so that, under these conditions, exacerbations requiring oral steroids (but not hospitalisations) occurred less frequently when patients inhaled ICS/LABA rather than short-acting bronchodilator alone. This finding is consistent with our hypothesis that SMART may allow patients to self-treat exacerbations at home without seeking medical care, and begs the question whether it is better to prevent symptoms and exacerbations entirely by adequate amounts of maintenance anti-inflammatory therapy or to rescue patients once symptoms have occurred.

All correspondents appear concerned that, in the table, we displayed only the SMART control outcomes and not outcomes for the comparator limbs. We believe that this was appropriate as our aim was to examine the clinical usefulness of SMART in terms of the control parameters used widely to monitor asthma in the clinical setting. It was not our goal to analyse further the well-known superiority of ICS/LABA to ICS monotherapy or the superiority of higher doses of ICS/LABA to lower doses of ICS/LABA. Bowler and Serisier suggest that the poor control outcomes seen in these trials ‘reflects the severity of disease’ of participants.6 We respond that the failure of SMART therapy to control severe disease would hardly recommend its use in moderate or mild disease. Indeed, Cates and Lasserson's Cochrane review noted that no superiority was demonstrable with SMART in mild disease.5 We must add that it is probably more accurate to describe study participants as having severely uncontrolled disease at recruitment and not necessarily as having severe disease, given that optimal education, compliance and treatment may have controlled their disease.

Reddel and Yan4 suggest that our review of SMART results has been selective, a challenge that is difficult to address as we attempted to distil a large body of research literature, analysis and commentary into a review of acceptable length. In our review we acknowledged the well-known and often-emphasised primary outcome of SMART trials, but also attempted to discuss the much less frequently mentioned (and often concealed) effect of SMART therapy on asthma control. We have been chastised for highlighting this outcome and commenting on the dearth of discussion around control, but must note that Bateman and colleagues' manuscript estimating control (on a week-by-week rather than long-term basis) has only recently been published and was available to add to our review only at the galley proof stage of manuscript production.3 We did not wish to criticise the use of exacerbations as an end point in asthma trials but wished to point out that, by limiting the choice of primary end point to ‘time to severe exacerbation’ in all but one SMART trial (which used peak flow),7 the body of research has concealed the generally poor asthma control outcomes seen with this strategy. Although we referenced in our review the paper by Kuna and colleagues using double-dummy methodology,8 we suspect we are not alone in believing that blinding remains difficult and sometimes impossible when inquisitive and observant asthma patients are given bronchodilator-containing inhalers and placebo inhalers in a clinical trial setting. We are puzzled to be criticised for reference to older literature on electronic adherence devices9 and sought only to point out that electronic monitoring of relevant dry powder inhalers had long been available to explore the hypothesis that timing of medication use was somehow important to the mechanism of action of SMART. Reddel and Yan have mentioned numerous ‘errors’ in our review but provided only examples of our emphasis on control and compliance assessments hitherto overlooked in SMART research; we look forward to correcting any errors of fact they detect and report to us.

Finally, we wish to clarify further our thoughts concerning the measurement of inflammatory indices in SMART-treated patients. We agree with Peters and Jenkins that control outcomes were neither superior nor inferior for SMART compared with fixed dose treatment in the study by Pavord and colleagues,10 and would add that the study was neither adequately powered nor designed to examine this outcome. With respect to eosinophil counts being ‘in the range of control’, we are not sure that there is sufficient long-term literature using sputum eosinophil counts to declare with confidence that a particular level of airway eosinophilia is safe and acceptable in asthma. However, if one accepts that levels of <3% are tolerable, we note that it was only the mean sputum eosinophil count that was within this limit for SMART-treated patients and the rise in sputum eosinophils seen with SMART therapy probably increased the proportion of SMART-treated patients above the ‘acceptable’ limit. We find this increase as well as the doubling of biopsy eosinophil counts concerning.

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Footnotes

  • Competing interests In the past 3 years KRC has received compensation for consulting with Astra Zeneca, Boehringer-Ingelheim, CSL Behring, GlaxoSmithKline, Merck Frosst, Novartis, Nycomed, Pfizer, Roche, Schering Plough and Telacris; has undertaken research funded by AstraZeneca, Boehringer-Ingelheim, CSL Behring, Forest Labs, GlaxoSmithKline, Novartis, Parangenix, Roche and Talecris; and has participated in continuing medical education activities sponsored in whole or in part by AstraZeneca, Boehringer-Ingelheim, GlaxoSmithKline, MerckFrosst, Novartis, Nycomed, Pfizer and Talecris. NCB has lectured for or received consulting fees from GlaxoSmithKline, AstraZeneca, Altana, Merck Generics, Chiesi and TEVA and has received grant support from GlaxoSmithKline and AstraZeneca. APG has received lecture fees from AstraZeneca and GlaxoSmithKline in the past year. PWJ has received consultancy fees from GlaxoSmithKline, AstraZeneca, Almirall, Boehringer Ingelheim and Spiration; has received lecture fees from GlaxoSmithKline; and his institution will from his time as a consultant to Novartis. Within the past 3 years, SP has received compensation for consulting with Nycomed, GlaxoSmithKline, Neolab and AstraZeneca and has given lectures sponsored by Nycomed and GlaxoSmithKline. This manuscript was conceived, researched and written by the authors without assistance from employees of the pharmaceutical industry or their agents. No professional writers participated in the preparation of the manuscript.

  • Provenance and peer review Not commissioned; not externally peer reviewed.

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