TY - JOUR
T1 - The safety and efficacy of infliximab in moderate to severe chronic obstructive pulmonary disease
AU - Rennard, Stephen I.
AU - Fogarty, Charles
AU - Kelsen, Steven
AU - Long, William
AU - Ramsdell, Joe
AU - Allison, James
AU - Mahler, Donald
AU - Saadeh, Constantine
AU - Siler, Thomas
AU - Snell, Phillip
AU - Korenblat, Phillip
AU - Smith, William
AU - Kaye, Mitchell
AU - Mandel, Michael
AU - Andrews, Charles
AU - Prabhu, Rachakonda
AU - Donohue, James F.
AU - Watt, Rosemary
AU - Kim, Hung Lo
AU - Schlenker-Herceg, Rozsa
AU - Barnathan, Elliot S.
AU - Murray, John
PY - 2007/5/1
Y1 - 2007/5/1
N2 - Rationale: Chronic obstructive pulmonary disease (COPD) is a progressive, smoking-related, inflammatory lung disease in which tumor necrosis factor-α is overexpressed and has been suggested to play a pathogenic role. Objectives: To determine if infliximab, an anti-TNF-α antibody, results in clinical benefit and has an acceptable safety profile in patients with moderate to severe COPD. Methods: In a multicenter, randomized, double-blind, placebo-controlled, parallel-group, dose-finding study, subjects with moderate to severe COPD received infliximab (3 mg/kg [n = 78] or 5 mg/kg [n = 79]) or placebo (n = 77) at Weeks 0, 2, 6, 12, 18, and 24. Efficacy, health status, and safety were assessed through Week 44. Measurements and Main Results: Infliximab was generally well tolerated, but showed no treatment benefit as measured by the primary endpoint, Chronic Respiratory Questionnaire total score. Similarly, there was no change in secondary measures, including prebronchodilator FEV1, 6-min walk distance, SF-36 physical score, transition dyspnea index, or moderate-to-severe COPD exacerbations. Post hoc analysis revealed that subjects who were younger or cachectic showed improvement in the 6-min walk distance. Malignancies were diagnosed during the study in 9 of 157 infliximab-treated subjects versus 1 of 77 placebo-treated subjects. No opportunistic infections were observed, and there were no differences in the occurrence of antibiotic-requiring infections, although the incidence of pneumonia was higher in infliximab-treated subjects. No infection-related mortality was observed. Higher proportions of infliximab-treated subjects discontinued the study agent due to adverse events (20-27%) than did placebo-treated subjects (9%). Conclusions: Subjects with moderate to severe COPD did not benefit from treatment with infliximab. Although not statistically significant, more cases of cancer and pneumonia were observed in the infliximab-treated subjects. The impact of infliximab on malignancy risk in patients with COPD needs to be further elucidated.
AB - Rationale: Chronic obstructive pulmonary disease (COPD) is a progressive, smoking-related, inflammatory lung disease in which tumor necrosis factor-α is overexpressed and has been suggested to play a pathogenic role. Objectives: To determine if infliximab, an anti-TNF-α antibody, results in clinical benefit and has an acceptable safety profile in patients with moderate to severe COPD. Methods: In a multicenter, randomized, double-blind, placebo-controlled, parallel-group, dose-finding study, subjects with moderate to severe COPD received infliximab (3 mg/kg [n = 78] or 5 mg/kg [n = 79]) or placebo (n = 77) at Weeks 0, 2, 6, 12, 18, and 24. Efficacy, health status, and safety were assessed through Week 44. Measurements and Main Results: Infliximab was generally well tolerated, but showed no treatment benefit as measured by the primary endpoint, Chronic Respiratory Questionnaire total score. Similarly, there was no change in secondary measures, including prebronchodilator FEV1, 6-min walk distance, SF-36 physical score, transition dyspnea index, or moderate-to-severe COPD exacerbations. Post hoc analysis revealed that subjects who were younger or cachectic showed improvement in the 6-min walk distance. Malignancies were diagnosed during the study in 9 of 157 infliximab-treated subjects versus 1 of 77 placebo-treated subjects. No opportunistic infections were observed, and there were no differences in the occurrence of antibiotic-requiring infections, although the incidence of pneumonia was higher in infliximab-treated subjects. No infection-related mortality was observed. Higher proportions of infliximab-treated subjects discontinued the study agent due to adverse events (20-27%) than did placebo-treated subjects (9%). Conclusions: Subjects with moderate to severe COPD did not benefit from treatment with infliximab. Although not statistically significant, more cases of cancer and pneumonia were observed in the infliximab-treated subjects. The impact of infliximab on malignancy risk in patients with COPD needs to be further elucidated.
KW - Chronic obstructive pulmonary disease
KW - Infliximab
KW - Tumor necrosis factor-α
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U2 - 10.1164/rccm.200607-995OC
DO - 10.1164/rccm.200607-995OC
M3 - Article
C2 - 17290043
AN - SCOPUS:34247607712
SN - 1073-449X
VL - 175
SP - 926
EP - 934
JO - American Review of Respiratory Disease
JF - American Review of Respiratory Disease
IS - 9
ER -