Efficacy and safety of umeclidinium plus vilanterol versus tiotropium, vilanterol, or umeclidinium monotherapies over 24 weeks in patients with chronic obstructive pulmonary disease: results from two multicentre, blinded, randomised controlled trials
Summary Background Combination long-acting bronchodilator treatment might be more effective than long-acting bronchodilator monotherapy for the treatment of chronic obstructive pulmonary disease (COPD). We aimed to compare the efficacy and safety of umeclidinium (UMEC) plus vilanterol (VI) with tiot...
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| creator | Decramer, Marc, Dr Prof Anzueto, Antonio, Prof Kerwin, Edward, MD Kaelin, Thomas, DO Richard, Nathalie, MSc Crater, Glenn, MD Tabberer, Maggie, MSc Harris, Stephanie, BSc Church, Alison, MD |
| description | Summary Background Combination long-acting bronchodilator treatment might be more effective than long-acting bronchodilator monotherapy for the treatment of chronic obstructive pulmonary disease (COPD). We aimed to compare the efficacy and safety of umeclidinium (UMEC) plus vilanterol (VI) with tiotropium (TIO) monotherapy, UMEC monotherapy, or VI monotherapy in patients with moderate to very severe COPD. Methods In two multicentre, randomised, blinded, double-dummy, parallel-group, active-controlled trials, eligible patients (current or former smokers aged 40 years or older with an established clinical history of COPD) were randomly assigned in 1:1:1:1 ratio to UMEC 125 μg plus VI 25 μg, UMEC 62·5 μg plus VI 25 μg, TIO 18 μg, and either VI 25 μg (study 1) or UMEC 125 μg (study 2). All study drugs were used once daily for 24 weeks. TIO was delivered via the HandiHaler inhaler and all other active treatments were delivered via the ELLIPTA dry powder inhaler. Random assignment (by a validated computer-based system) was done by centre and was not stratified. All patients and physicians were masked to assigned treatment during the studies. The primary efficacy endpoint of both studies was trough forced expiratory volume in 1 s (FEV1 ) on day 169, which was analysed in the intention-to-treat population. Both studies are registered with ClinicalTrials.gov , numbers NCT01316900 (study 1) and NCT01316913 (study 2). Findings 1141 participants were recruited in study 1, and 1191 in study 2. For study 1, after exclusions, 208, 209, 214, and 212 patients were included in the intention-to-treat analyses for TIO monotherapy, VI monotherapy, UMEC 125 μg plus VI 25 μg, and UMEC 62·5 μg plus VI 25 μg, respectively. For study 2, 215, 222, 215, and 217 patients were included in the intention-to-treat analyses for TIO monotherapy, UMEC monotherapy, UMEC 125 μg plus VI 25 μg, and UMEC 62·5 μg plus VI 25 μg, respectively. In both studies, we noted improvements in trough FEV1 on day 169 for both doses of UMEC plus VI compared with TIO monotherapy (study 1, UMEC 125 μg plus VI 25 μg: 0·088 L [95% CI 0·036 to 0·140; p=0·0010]; study 1, UMEC 62·5 μg plus VI 25 μg: 0·090 L [0·039 to 0·141; p=0·0006]; study 2, UMEC 125 μg plus VI 25 μg: 0·074 L [0·025 to 0·123; p=0·0031]; study 2, UMEC 62·5 μg plus VI 25 μg: 0·060 L [0·010 to 0·109; nominal p=0·0182]). Both doses of UMEC plus VI also improved trough FEV1 compared with VI monotherapy (UMEC 125 μg plus VI 25 μg: 0·088 L [0·036 to 0·140 |
| doi_str_mv | 10.1016/S2213-2600(14)70065-7 |
| format | Article |
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We aimed to compare the efficacy and safety of umeclidinium (UMEC) plus vilanterol (VI) with tiotropium (TIO) monotherapy, UMEC monotherapy, or VI monotherapy in patients with moderate to very severe COPD. Methods In two multicentre, randomised, blinded, double-dummy, parallel-group, active-controlled trials, eligible patients (current or former smokers aged 40 years or older with an established clinical history of COPD) were randomly assigned in 1:1:1:1 ratio to UMEC 125 μg plus VI 25 μg, UMEC 62·5 μg plus VI 25 μg, TIO 18 μg, and either VI 25 μg (study 1) or UMEC 125 μg (study 2). All study drugs were used once daily for 24 weeks. TIO was delivered via the HandiHaler inhaler and all other active treatments were delivered via the ELLIPTA dry powder inhaler. Random assignment (by a validated computer-based system) was done by centre and was not stratified. All patients and physicians were masked to assigned treatment during the studies. The primary efficacy endpoint of both studies was trough forced expiratory volume in 1 s (FEV1 ) on day 169, which was analysed in the intention-to-treat population. Both studies are registered with ClinicalTrials.gov , numbers NCT01316900 (study 1) and NCT01316913 (study 2). Findings 1141 participants were recruited in study 1, and 1191 in study 2. For study 1, after exclusions, 208, 209, 214, and 212 patients were included in the intention-to-treat analyses for TIO monotherapy, VI monotherapy, UMEC 125 μg plus VI 25 μg, and UMEC 62·5 μg plus VI 25 μg, respectively. For study 2, 215, 222, 215, and 217 patients were included in the intention-to-treat analyses for TIO monotherapy, UMEC monotherapy, UMEC 125 μg plus VI 25 μg, and UMEC 62·5 μg plus VI 25 μg, respectively. In both studies, we noted improvements in trough FEV1 on day 169 for both doses of UMEC plus VI compared with TIO monotherapy (study 1, UMEC 125 μg plus VI 25 μg: 0·088 L [95% CI 0·036 to 0·140; p=0·0010]; study 1, UMEC 62·5 μg plus VI 25 μg: 0·090 L [0·039 to 0·141; p=0·0006]; study 2, UMEC 125 μg plus VI 25 μg: 0·074 L [0·025 to 0·123; p=0·0031]; study 2, UMEC 62·5 μg plus VI 25 μg: 0·060 L [0·010 to 0·109; nominal p=0·0182]). Both doses of UMEC plus VI also improved trough FEV1 compared with VI monotherapy (UMEC 125 μg plus VI 25 μg: 0·088 L [0·036 to 0·140; p=0·0010]; UMEC 62·5 μg plus VI 25 μg: 0·090 L [0·039 to 0·142; p=0·0006], but not compared with UMEC 125 μg monotherapy (UMEC 125 μg plus VI 25 μg: 0·037 L [−0·012 to 0·087; p=0·14]; UMEC 62·5 μg plus VI 25 μg: 0·022 L [−0·027 to 0·072; p=0·38]). All treatments produced improvements in dyspnoea and health-related quality of life; we noted no significant differences in symptoms, health status, or risk of exacerbation between UMEC plus VI and TIO. The most common on-treatment, severe-intensity adverse event in both studies was acute exacerbation of COPD (1–4 [<1–2%] patients across treatment groups in study 1 and 1–6 [<1–3%] patients in study 2). We recorded five to 15 (2–7%) on-treatment serious adverse events across treatment groups in study 1, and nine to 22 (4–10%) in study 2. We noted no substantial changes from baseline in vital signs, clinical laboratory findings, or electrocardiography findings in any of the treatment groups. Interpretation Combination treatment with once-daily UMEC plus VI improved lung function compared with VI monotherapy and TIO monotherapy in patients with COPD. Overall our results suggest that the combination of UMEC plus VI could be beneficial for the treatment of moderate to very severe COPD. Funding GlaxoSmithKline.</description><identifier>ISSN: 2213-2600</identifier><identifier>EISSN: 2213-2619</identifier><identifier>DOI: 10.1016/S2213-2600(14)70065-7</identifier><identifier>PMID: 24835833</identifier><language>eng</language><publisher>England</publisher><subject>Administration, Inhalation ; Aged ; Benzyl Alcohols - administration & dosage ; Bronchodilator Agents - administration & dosage ; Chlorobenzenes - administration & dosage ; Dose-Response Relationship, Drug ; Double-Blind Method ; Drug Combinations ; Female ; Follow-Up Studies ; Forced Expiratory Volume - drug effects ; Humans ; Male ; Middle Aged ; Pulmonary Disease, Chronic Obstructive - drug therapy ; Pulmonary Disease, Chronic Obstructive - physiopathology ; Pulmonary/Respiratory ; Quinuclidines - administration & dosage ; Scopolamine Derivatives - administration & dosage ; Time Factors ; Tiotropium Bromide ; Treatment Outcome</subject><ispartof>The lancet respiratory medicine, 2014-06, Vol.2 (6), p.472-486</ispartof><rights>Elsevier Ltd</rights><rights>2014 Elsevier Ltd</rights><rights>Copyright © 2014 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c420t-b76f40debfdb2a73b7cfb2c0fa5e569dd5c8bed36037fef58542ab59f5c841d03</citedby><cites>FETCH-LOGICAL-c420t-b76f40debfdb2a73b7cfb2c0fa5e569dd5c8bed36037fef58542ab59f5c841d03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24835833$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Decramer, Marc, Dr Prof</creatorcontrib><creatorcontrib>Anzueto, Antonio, Prof</creatorcontrib><creatorcontrib>Kerwin, Edward, MD</creatorcontrib><creatorcontrib>Kaelin, Thomas, DO</creatorcontrib><creatorcontrib>Richard, Nathalie, MSc</creatorcontrib><creatorcontrib>Crater, Glenn, MD</creatorcontrib><creatorcontrib>Tabberer, Maggie, MSc</creatorcontrib><creatorcontrib>Harris, Stephanie, BSc</creatorcontrib><creatorcontrib>Church, Alison, MD</creatorcontrib><title>Efficacy and safety of umeclidinium plus vilanterol versus tiotropium, vilanterol, or umeclidinium monotherapies over 24 weeks in patients with chronic obstructive pulmonary disease: results from two multicentre, blinded, randomised controlled trials</title><title>The lancet respiratory medicine</title><addtitle>Lancet Respir Med</addtitle><description>Summary Background Combination long-acting bronchodilator treatment might be more effective than long-acting bronchodilator monotherapy for the treatment of chronic obstructive pulmonary disease (COPD). We aimed to compare the efficacy and safety of umeclidinium (UMEC) plus vilanterol (VI) with tiotropium (TIO) monotherapy, UMEC monotherapy, or VI monotherapy in patients with moderate to very severe COPD. Methods In two multicentre, randomised, blinded, double-dummy, parallel-group, active-controlled trials, eligible patients (current or former smokers aged 40 years or older with an established clinical history of COPD) were randomly assigned in 1:1:1:1 ratio to UMEC 125 μg plus VI 25 μg, UMEC 62·5 μg plus VI 25 μg, TIO 18 μg, and either VI 25 μg (study 1) or UMEC 125 μg (study 2). All study drugs were used once daily for 24 weeks. TIO was delivered via the HandiHaler inhaler and all other active treatments were delivered via the ELLIPTA dry powder inhaler. Random assignment (by a validated computer-based system) was done by centre and was not stratified. All patients and physicians were masked to assigned treatment during the studies. The primary efficacy endpoint of both studies was trough forced expiratory volume in 1 s (FEV1 ) on day 169, which was analysed in the intention-to-treat population. Both studies are registered with ClinicalTrials.gov , numbers NCT01316900 (study 1) and NCT01316913 (study 2). Findings 1141 participants were recruited in study 1, and 1191 in study 2. For study 1, after exclusions, 208, 209, 214, and 212 patients were included in the intention-to-treat analyses for TIO monotherapy, VI monotherapy, UMEC 125 μg plus VI 25 μg, and UMEC 62·5 μg plus VI 25 μg, respectively. For study 2, 215, 222, 215, and 217 patients were included in the intention-to-treat analyses for TIO monotherapy, UMEC monotherapy, UMEC 125 μg plus VI 25 μg, and UMEC 62·5 μg plus VI 25 μg, respectively. In both studies, we noted improvements in trough FEV1 on day 169 for both doses of UMEC plus VI compared with TIO monotherapy (study 1, UMEC 125 μg plus VI 25 μg: 0·088 L [95% CI 0·036 to 0·140; p=0·0010]; study 1, UMEC 62·5 μg plus VI 25 μg: 0·090 L [0·039 to 0·141; p=0·0006]; study 2, UMEC 125 μg plus VI 25 μg: 0·074 L [0·025 to 0·123; p=0·0031]; study 2, UMEC 62·5 μg plus VI 25 μg: 0·060 L [0·010 to 0·109; nominal p=0·0182]). Both doses of UMEC plus VI also improved trough FEV1 compared with VI monotherapy (UMEC 125 μg plus VI 25 μg: 0·088 L [0·036 to 0·140; p=0·0010]; UMEC 62·5 μg plus VI 25 μg: 0·090 L [0·039 to 0·142; p=0·0006], but not compared with UMEC 125 μg monotherapy (UMEC 125 μg plus VI 25 μg: 0·037 L [−0·012 to 0·087; p=0·14]; UMEC 62·5 μg plus VI 25 μg: 0·022 L [−0·027 to 0·072; p=0·38]). All treatments produced improvements in dyspnoea and health-related quality of life; we noted no significant differences in symptoms, health status, or risk of exacerbation between UMEC plus VI and TIO. The most common on-treatment, severe-intensity adverse event in both studies was acute exacerbation of COPD (1–4 [<1–2%] patients across treatment groups in study 1 and 1–6 [<1–3%] patients in study 2). We recorded five to 15 (2–7%) on-treatment serious adverse events across treatment groups in study 1, and nine to 22 (4–10%) in study 2. We noted no substantial changes from baseline in vital signs, clinical laboratory findings, or electrocardiography findings in any of the treatment groups. Interpretation Combination treatment with once-daily UMEC plus VI improved lung function compared with VI monotherapy and TIO monotherapy in patients with COPD. Overall our results suggest that the combination of UMEC plus VI could be beneficial for the treatment of moderate to very severe COPD. Funding GlaxoSmithKline.</description><subject>Administration, Inhalation</subject><subject>Aged</subject><subject>Benzyl Alcohols - administration & dosage</subject><subject>Bronchodilator Agents - administration & dosage</subject><subject>Chlorobenzenes - administration & dosage</subject><subject>Dose-Response Relationship, Drug</subject><subject>Double-Blind Method</subject><subject>Drug Combinations</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Forced Expiratory Volume - drug effects</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Pulmonary Disease, Chronic Obstructive - drug therapy</subject><subject>Pulmonary Disease, Chronic Obstructive - physiopathology</subject><subject>Pulmonary/Respiratory</subject><subject>Quinuclidines - administration & dosage</subject><subject>Scopolamine Derivatives - administration & dosage</subject><subject>Time Factors</subject><subject>Tiotropium Bromide</subject><subject>Treatment Outcome</subject><issn>2213-2600</issn><issn>2213-2619</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUctuFDEQHCEQiUI-AdTHIO2CPZ7XcgChKDykSByAs-Wx21onnvFge3a1v86J3gcRcMGXtrurqt1dRfGcs1ec8eb117LkYlk2jF3x6mXLWFMv20fF-SnNV48f7oydFZcp3TE6XVeVrHpanJVVJ-pOiPPi5421Tiu9AzUaSMpi3kGwMA-ovTNudPMAk58TbJxXY8YYPGwwJspkF3IMEyEWf1QXEOLf9CGMIa8xqslhgkBsKCvYIt4ncCNMKjscc4Kty2vQ6xhGpyH0KcdZZ7dBmGZPGiruwLiEKuEbiJhmTxwbwwB5G2Cgp9OkE3EBvXejQbOASFOFgUgGdKBa8J6uOTrl07PiiaWAl6d4UXz_cPPt-tPy9svHz9fvb5eatpWXfdvYihnsrelL1Yq-1bYvNbOqxrpZGVPrrkcjGiZai7bu6qpUfb2ylK-4YeKiuDrqTjH8mDFlSR_S6GlhGOYkeS0qzgRjNUHrI1THkFJEK6foBhpccib3zsuD83Jvq-SVPDgvW-K9OLWY-wHNA-u3zwR4dwQgDbpxGGXStHSNxkXUWZrg_tvi7T8KZDAZpfw97jDdhTmOtEXJZSolO4rsNXh1UGjFLxwn2-8</recordid><startdate>20140601</startdate><enddate>20140601</enddate><creator>Decramer, Marc, Dr Prof</creator><creator>Anzueto, Antonio, Prof</creator><creator>Kerwin, Edward, MD</creator><creator>Kaelin, Thomas, DO</creator><creator>Richard, Nathalie, MSc</creator><creator>Crater, Glenn, MD</creator><creator>Tabberer, Maggie, MSc</creator><creator>Harris, Stephanie, BSc</creator><creator>Church, Alison, MD</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20140601</creationdate><title>Efficacy and safety of umeclidinium plus vilanterol versus tiotropium, vilanterol, or umeclidinium monotherapies over 24 weeks in patients with chronic obstructive pulmonary disease: results from two multicentre, blinded, randomised controlled trials</title><author>Decramer, Marc, Dr Prof ; Anzueto, Antonio, Prof ; Kerwin, Edward, MD ; Kaelin, Thomas, DO ; Richard, Nathalie, MSc ; Crater, Glenn, MD ; Tabberer, Maggie, MSc ; Harris, Stephanie, BSc ; Church, Alison, MD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c420t-b76f40debfdb2a73b7cfb2c0fa5e569dd5c8bed36037fef58542ab59f5c841d03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Administration, Inhalation</topic><topic>Aged</topic><topic>Benzyl Alcohols - administration & dosage</topic><topic>Bronchodilator Agents - administration & dosage</topic><topic>Chlorobenzenes - administration & dosage</topic><topic>Dose-Response Relationship, Drug</topic><topic>Double-Blind Method</topic><topic>Drug Combinations</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Forced Expiratory Volume - drug effects</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Pulmonary Disease, Chronic Obstructive - drug therapy</topic><topic>Pulmonary Disease, Chronic Obstructive - physiopathology</topic><topic>Pulmonary/Respiratory</topic><topic>Quinuclidines - administration & dosage</topic><topic>Scopolamine Derivatives - administration & dosage</topic><topic>Time Factors</topic><topic>Tiotropium Bromide</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Decramer, Marc, Dr Prof</creatorcontrib><creatorcontrib>Anzueto, Antonio, Prof</creatorcontrib><creatorcontrib>Kerwin, Edward, MD</creatorcontrib><creatorcontrib>Kaelin, Thomas, DO</creatorcontrib><creatorcontrib>Richard, Nathalie, MSc</creatorcontrib><creatorcontrib>Crater, Glenn, MD</creatorcontrib><creatorcontrib>Tabberer, Maggie, MSc</creatorcontrib><creatorcontrib>Harris, Stephanie, BSc</creatorcontrib><creatorcontrib>Church, Alison, MD</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The lancet respiratory medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Decramer, Marc, Dr Prof</au><au>Anzueto, Antonio, Prof</au><au>Kerwin, Edward, MD</au><au>Kaelin, Thomas, DO</au><au>Richard, Nathalie, MSc</au><au>Crater, Glenn, MD</au><au>Tabberer, Maggie, MSc</au><au>Harris, Stephanie, BSc</au><au>Church, Alison, MD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Efficacy and safety of umeclidinium plus vilanterol versus tiotropium, vilanterol, or umeclidinium monotherapies over 24 weeks in patients with chronic obstructive pulmonary disease: results from two multicentre, blinded, randomised controlled trials</atitle><jtitle>The lancet respiratory medicine</jtitle><addtitle>Lancet Respir Med</addtitle><date>2014-06-01</date><risdate>2014</risdate><volume>2</volume><issue>6</issue><spage>472</spage><epage>486</epage><pages>472-486</pages><issn>2213-2600</issn><eissn>2213-2619</eissn><abstract>Summary Background Combination long-acting bronchodilator treatment might be more effective than long-acting bronchodilator monotherapy for the treatment of chronic obstructive pulmonary disease (COPD). We aimed to compare the efficacy and safety of umeclidinium (UMEC) plus vilanterol (VI) with tiotropium (TIO) monotherapy, UMEC monotherapy, or VI monotherapy in patients with moderate to very severe COPD. Methods In two multicentre, randomised, blinded, double-dummy, parallel-group, active-controlled trials, eligible patients (current or former smokers aged 40 years or older with an established clinical history of COPD) were randomly assigned in 1:1:1:1 ratio to UMEC 125 μg plus VI 25 μg, UMEC 62·5 μg plus VI 25 μg, TIO 18 μg, and either VI 25 μg (study 1) or UMEC 125 μg (study 2). All study drugs were used once daily for 24 weeks. TIO was delivered via the HandiHaler inhaler and all other active treatments were delivered via the ELLIPTA dry powder inhaler. Random assignment (by a validated computer-based system) was done by centre and was not stratified. All patients and physicians were masked to assigned treatment during the studies. The primary efficacy endpoint of both studies was trough forced expiratory volume in 1 s (FEV1 ) on day 169, which was analysed in the intention-to-treat population. Both studies are registered with ClinicalTrials.gov , numbers NCT01316900 (study 1) and NCT01316913 (study 2). Findings 1141 participants were recruited in study 1, and 1191 in study 2. For study 1, after exclusions, 208, 209, 214, and 212 patients were included in the intention-to-treat analyses for TIO monotherapy, VI monotherapy, UMEC 125 μg plus VI 25 μg, and UMEC 62·5 μg plus VI 25 μg, respectively. For study 2, 215, 222, 215, and 217 patients were included in the intention-to-treat analyses for TIO monotherapy, UMEC monotherapy, UMEC 125 μg plus VI 25 μg, and UMEC 62·5 μg plus VI 25 μg, respectively. In both studies, we noted improvements in trough FEV1 on day 169 for both doses of UMEC plus VI compared with TIO monotherapy (study 1, UMEC 125 μg plus VI 25 μg: 0·088 L [95% CI 0·036 to 0·140; p=0·0010]; study 1, UMEC 62·5 μg plus VI 25 μg: 0·090 L [0·039 to 0·141; p=0·0006]; study 2, UMEC 125 μg plus VI 25 μg: 0·074 L [0·025 to 0·123; p=0·0031]; study 2, UMEC 62·5 μg plus VI 25 μg: 0·060 L [0·010 to 0·109; nominal p=0·0182]). Both doses of UMEC plus VI also improved trough FEV1 compared with VI monotherapy (UMEC 125 μg plus VI 25 μg: 0·088 L [0·036 to 0·140; p=0·0010]; UMEC 62·5 μg plus VI 25 μg: 0·090 L [0·039 to 0·142; p=0·0006], but not compared with UMEC 125 μg monotherapy (UMEC 125 μg plus VI 25 μg: 0·037 L [−0·012 to 0·087; p=0·14]; UMEC 62·5 μg plus VI 25 μg: 0·022 L [−0·027 to 0·072; p=0·38]). All treatments produced improvements in dyspnoea and health-related quality of life; we noted no significant differences in symptoms, health status, or risk of exacerbation between UMEC plus VI and TIO. The most common on-treatment, severe-intensity adverse event in both studies was acute exacerbation of COPD (1–4 [<1–2%] patients across treatment groups in study 1 and 1–6 [<1–3%] patients in study 2). We recorded five to 15 (2–7%) on-treatment serious adverse events across treatment groups in study 1, and nine to 22 (4–10%) in study 2. We noted no substantial changes from baseline in vital signs, clinical laboratory findings, or electrocardiography findings in any of the treatment groups. Interpretation Combination treatment with once-daily UMEC plus VI improved lung function compared with VI monotherapy and TIO monotherapy in patients with COPD. Overall our results suggest that the combination of UMEC plus VI could be beneficial for the treatment of moderate to very severe COPD. Funding GlaxoSmithKline.</abstract><cop>England</cop><pmid>24835833</pmid><doi>10.1016/S2213-2600(14)70065-7</doi><tpages>15</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 2213-2600 |
| ispartof | The lancet respiratory medicine, 2014-06, Vol.2 (6), p.472-486 |
| issn | 2213-2600 2213-2619 |
| language | eng |
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| source | MEDLINE; Alma/SFX Local Collection |
| subjects | Administration, Inhalation Aged Benzyl Alcohols - administration & dosage Bronchodilator Agents - administration & dosage Chlorobenzenes - administration & dosage Dose-Response Relationship, Drug Double-Blind Method Drug Combinations Female Follow-Up Studies Forced Expiratory Volume - drug effects Humans Male Middle Aged Pulmonary Disease, Chronic Obstructive - drug therapy Pulmonary Disease, Chronic Obstructive - physiopathology Pulmonary/Respiratory Quinuclidines - administration & dosage Scopolamine Derivatives - administration & dosage Time Factors Tiotropium Bromide Treatment Outcome |
| title | Efficacy and safety of umeclidinium plus vilanterol versus tiotropium, vilanterol, or umeclidinium monotherapies over 24 weeks in patients with chronic obstructive pulmonary disease: results from two multicentre, blinded, randomised controlled trials |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-30T22%3A51%3A41IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Efficacy%20and%20safety%20of%20umeclidinium%20plus%20vilanterol%20versus%20tiotropium,%20vilanterol,%20or%20umeclidinium%20monotherapies%20over%2024%20weeks%20in%20patients%20with%20chronic%20obstructive%20pulmonary%20disease:%20results%20from%20two%20multicentre,%20blinded,%20randomised%20controlled%20trials&rft.jtitle=The%20lancet%20respiratory%20medicine&rft.au=Decramer,%20Marc,%20Dr%20Prof&rft.date=2014-06-01&rft.volume=2&rft.issue=6&rft.spage=472&rft.epage=486&rft.pages=472-486&rft.issn=2213-2600&rft.eissn=2213-2619&rft_id=info:doi/10.1016/S2213-2600(14)70065-7&rft_dat=%3Cproquest_cross%3E1534103005%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1534103005&rft_id=info:pmid/24835833&rft_els_id=S2213260014700657&rfr_iscdi=true |