Berita Kesehatan
Jumat, 21 Jun 2019 13:46:02

Luis M. SeijoJoan B. SorianoGermán Peces-Barba

European Respiratory Journal 2019 53: 1900717; DOI: 10.1183/13993003.00717-2019

Abstract

New evidence regarding the protective effect of inhaled steroids in patients with COPD suggests that a controlled clinical trial is needed to investigate the potential benefit of inhaled steroids in preventing lung cancer in patients with COPD

Not long ago, chronic obstructive pulmonary disease (COPD) was considered a Cinderella, an unappealing disease lacking therapeutic options. It was also stigmatised as a consequence of the smoking habit that is a leading cause of COPD worldwide. However, as the Global Initiative for Chronic Obstructive Lung Disease (GOLD), and the joint American Thoracic Society/European Respiratory Society consensus documents suggest], COPD should be viewed as treatable and preventable, offering multiple opportunities for disease modification.

Inhalers developed for the treatment of asthma were tested empirically in COPD, long before a mechanistic rationale justified their use. Airway delivery was a common sense solution for a disease characterised by airway inflammation and bronchospasm. Inhaled corticosteroids (ICS) were an obvious therapeutic choice, especially in combination with long-acting bronchodilators (long-acting β-agonists (LABA)). Despite the growing evidence in favour of this strategy as a cornerstone of COPD treatment, the role of ICS continues to be controversial in current clinical practice.

The potential benefit of ICS in the prevention of lung cancer is a recurrent argument in this controversy, since smoking-induced inflammation also plays a role in lung carcinogenesis. The advent of combined long-acting bronchodilators and fears of ICS related long-term side-effects, have led to a questioning of the role of ICS in COPD. If lung cancer prevention is a collateral benefit of ICS treatment in COPD, current guidelines may be subject to change. Existing combinations of LABA and ICS are recommended for patients with asthma and COPD overlap, those with moderate or severe obstruction, and patients with frequent exacerbations. These COPD phenotypes benefit from a reduction in eosinophil counts, T-lymphocytes, neutrophils, and other biomarkers. However, it is unclear if the anti-inflammatory effect can be credited for a reduction in exacerbations or lung cancer incidence.

In this issue of the European Respiratory Journal, the study by Raymakers et al. contributes to a growing body of scientific evidence in favour of lung cancer chemoprevention with ICS. Raymakerset al. analysed a large population-based cohort of COPD patients and found that exposure to ICS in a sample of almost 40 000 individuals was associated with a 30% reduction in lung cancer risk (HR 0.70 (95% CI 0.61–0.80)). Their conclusion persisted after using five different time-dependent methods of quantifying exposure. The 2.5% incidence of lung cancer in the cohort identified from administrative data in British Columbia, Canada, during a mean follow-up of 5 years, matches that seen in other COPD population-based studies.

Keeping in mind that lung cancer is not only more common in patients with COPD, but is also more aggressive and lethal, COPD patients stand to benefit the most from ICS treatment. The limited evidence in favour of ICS chemoprevention for lung cancer comes from animal studies as well as population-based human studies. Prospective evidence, however, is scant and equivocal. Animal trials employing both fluticasone and budesonide seem to point to a protective effect. A sub-study of the COSMOS lung cancer screening trial randomised 200 patients to receive budesonide or placebo for 1 year; after 5 years of follow-up, non-solid and semi-solid nodules diminished in size in patients receiving steroids, despite no change in the incidence of lung cancer or the appearance of new solid nodules. That finding is remarkable given the small sample size and limited therapeutic exposure to ICS. Another study combining various trials of inhaled steroids in COPD concluded that ICS reduce all-cause mortality. In that study, ICS exposure was associated with a trend in favour of diminished cancer mortality. The beneficial effect appears to be dose-dependent, and perhaps more noticeable in women and former smokers. It has also been reported in asthmatic patients.

The current study is unique in implementing a 1-year latency period. This strategy is ingenious, since it avoids potential pitfalls related to the timing of ICS treatment. Ignoring the preclinical phase of lung cancer can otherwise lead to underestimating the potential benefit of ICS. One wonders if 12 months is long enough, since data from the NLST and PLCO trials suggest that the preclinical phase of lung cancer from resectable stage Ia to metastatic disease may last between 3 and 5 years. The authors partially address this limitation by performing a sensitivity analysis with a 2-year latency period, which also yielded statistically significant results.

Unfortunately, the lack of key variables, such as tobacco exposure, severity of the airway obstruction, a family history of lung cancer or the prevalence of radiological emphysema in the cohort, are obvious limitations of the study. In addition, some authors have found that lung cancer is more likely in patients with mild COPD, who might not benefit from the study's findings since they do not meet current indications for ICS treatment. Furthermore, since COPD is universally underdiagnosed, even in patients with lung cancer, the future of any chemopreventive role for ICS would depend on redoubling efforts to identify and treat COPD in the general population. In this respect, a diagnosis of COPD based on prescriptions can lead to major biases, including overlap with asthma and even overdiagnosis of COPD. Furthermore, previous population-based studies point to an even lower risk of lung cancer in patients with COPD treated with ICS. The reasons for this discrepancy may be methodological, but lead to the logical conclusion that a well-designed prospective randomised study controlled by placebo is needed. Such a study would allow head-to-head comparisons between placebo and ICS, controlling for COPD stage, smoking history, and potential biases such as the presence and severity of underlying emphysema. It would also clarify the role of ICS in men and women, and in former and active smokers, as well as dosing concerns. In our opinion, the study should include a screening arm capable of studying important surrogate end-points such as airway thickness, emphysema, and the evolution of pulmonary nodules, including ground-glass opacities, solid and semi-solid nodules detected by low dose computed tomography. Alternatively, a re-examination of data from recent clinical trials randomising patients with COPD to combination therapies with and without ICS might be a good start in order to build a case in favour of a larger multinational effort in this regard.

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