Table 1.
New pharmacotherapies in COPD management
Agency approval | Indication GOLD grade | Efficacy
|
Safety and adverse effects | General remarks | ||||
---|---|---|---|---|---|---|---|---|
FEV1 improvement | Exercise | Exacerbations | Health status and symptoms | |||||
New LAMA monotherapy | ||||||||
Aclidinium | US, EU | GOLD B, C, D | ++ | ++ | ++ | ++ | Bronchospasm, nasopharingitis (6%), headache (5%), dry mouth (<2%) | Faster onset of action to tiotropium, better nighttime FEV1, BID dosing |
Glycopyrronium | EU | GOLD B, C, D | +++ | ++ | ++ | ++ | Antimuscarinic and cardiac side effects similar to placebo | Rapid onset, very good safety profile |
Umeclidinium | US, EU | GOLD B, C, D | ++ | ++,• | ++,• | ++,• | Minimal antimuscarinic side effects | Combined with vilanterol |
New LABA monotherapy | ||||||||
Indacaterol | US, EU | GOLD B, C, D | +++ | ++ | ++ | ++ | Cough (6.5%), headache (5.1%), nausea (2.4%) | Improved cardiovascular safety profile and lung function compared to salmeterol |
Vilanterol | US, EU | GOLD B, C, D | ++ | ++,• | ++,• | ++ | Nasopharingitis (10%), headache (9%), dry mouth (< 10%) | |
Olodaterol | US | GOLD B, C, D | ++ | ++ | − | ++ | Nasopharyngitis (11%), dizziness (>2%), rash (>2%), arthralgia (>2%) | |
Abediterol | − | +++ | Better lung function impact in comparison to indacaterol | |||||
New LAMA-LABA combination therapy | ||||||||
Umeclidinium and vilanterol | US, EU | GOLD C, D | +++ | ++ | ++ | No increase in adverse events compared to placebo | First LAMA-LABA approved by the US FDA for maintenance treatment | |
Glycopyrronium and indacaterol | EU | GOLD C, D | +++ | +++ | +++ | No increase in adverse events compared to tiotropium or glycopyrronium alone | Significantly better FEV1 and SGRQ compared to tiotropium and glycopyrronium alone | |
Tiotropium and olodaterol | − | GOLD C, D | +++ | + | +++ | No significant difference in adverse events compared to monocomponents | Significant improvement in SGRQ score was only seen in the 5/5 μg dosing | |
Aclidinium and formoterol | EU | GOLD C, D | +++ | − | −/++ | Nasopharingitis (7.8%), headache (7.5%) | Significant improvement in FEV1 1-hour postdosing compared to monocomponents | |
Glycopyrrolate and formoterol | GOLD C, D | +++ | Improvement in FEV1 from 0 hours to 12 hours versus monotherapy with glycopyrrolate, formoterol, or tiotropium | |||||
New LABA-ICS combination therapies | ||||||||
Vilanterol and fluticasone | US, EU | GOLD C, D | + | +++ | Compared to vilanterol alone, FDC leads to an increased risk of pneumonia | Once-daily FDC of LABA-ICS | ||
Indacaterol and mometasone | − | GOLD C, D | ++ | |||||
Formoterol and ciclesonide | − | GOLD C, D | ++ | ++ | Oral candidiasis was the most common adverse event | Noninferiority comparison to combined fluticasone propionate/salmeterol in asthma | ||
Formoterol and fluticasone | EU, Japan | GOLD C, D | +++ | Approved for asthma, but in Phase III clinical trials for moderate to severe COPD | More rapid bronchodilator effect than fluticasone propionate/salmeterol | |||
Triple LABA-LAMA-ICS therapy | − | GOLD C, D | ++ | − | ++ | No significant difference in adverse events compared to dual or monocomponents | A 40% reduction in mortality compared with ICS/LABA in a retrospective analysis | |
Dual muscarinic antagonist-β2-agonists | − | ++a | Transient hypokalemic effect in 3/41 patients receiving additional high-dose salbutamol | GSK961081 has demonstrated effective bronchoprotection in early trials | ||||
Oral medications | ||||||||
Roflumilast | US, EU | GOLD C, D | ++a | ++ | − | Weight loss, nausea, diarrhea, and psychiatric symptoms | Recommended use only in advanced COPD as an add-on therapy | |
Azithromycin | US, EU | GOLD C, D | ++ | QT interval prolongation, ototoxicity, and drug-drug interactions | Careful risk-benefit assessment given the side-effect profile | |||
Moxifloxacin | US, EU | GOLD C, D | ++ | −/++ | Significant Gl side effects compared to the placebo group | Intermittent pulsed therapy with 5 days of moxifloxacin every 8 weeks for six courses | ||
Simvastatin | US, EU | GOLD C, D | − | − | No significant difference in fatal or nonfatal adverse events | No significant difference in exacerbations in one randomized, placebo-controlled trial |
Notes: −No improvement in the published literature; +nonsignificant improvement; ++significantly improved compared to placebo; +++significantly improved to other drugs of the same class;
in combination therapy;
improved FEV1 from baseline.
Abbreviations: GOLD, Global Initiative for Chronic Obstructive Lung Disease; LAMA, long-acting muscarinic antagonist; US, United States; EU, European Union; BID, twice daily; LABA, long-acting β-2 sympathomimetic agonist; FDA, Food and Drug Administration; FEV1, forced expiratory volume in I second; SGRQ, St George’s Respiratory Questionnaire; ICS, inhaled corticosteroid; FDC, fixed-dose combination; Gl, gastrointestinal.