The safety and efficacy of infliximab in moderate to severe chronic obstructive pulmonary disease

被引:312
作者
Rennard, Stephen I.
Fogarty, Charles
Kelsen, Steven
Long, William
Ramsdell, Joe
Allison, James
Mahler, Donald
Saadeh, Constantine
Siler, Thomas
Snell, Phillip
Korenblat, Phillip
Smith, William
Kaye, Mitchell
Mandel, Michael
Andrews, Charles
Prabhu, Rachakonda
Donohue, James F.
Watt, Rosemary
Lo, Kim Hung
Schlenker-Herceg, Rozsa
Barnathan, Elliot S.
Murray, John
机构
[1] Univ Nebraska, Med Ctr, Omaha, NE 68198 USA
[2] Spartanburg Pharmaceut Res, Spartanburg, SC USA
[3] Temple Univ, Med Ctr, Philadelphia, PA 19122 USA
[4] Neem Res Grp, Charlotte, NC USA
[5] Univ Calif San Diego, Clin Trials Ctr, San Diego, CA 92103 USA
[6] Neem Res Grp, Columbia, SC USA
[7] Dartmouth Hitchcock Med Ctr, Lebanon, NH 03766 USA
[8] Amarillo Ctr Clin Res Ltd, Amarillo, TX USA
[9] Midw Chest Consultants PC, St Charles, MO USA
[10] Mt View Clin Res Inc, Greer, SC USA
[11] Clin Res Ctr LLC, St Louis, MO USA
[12] New Orleans Ctr Clin Res, New Orleans, LA USA
[13] Minnesota Lung Ctr, Minneapolis, MN USA
[14] Pulm Res Associates LLC, Larchmont, NY USA
[15] Lung Diagnost Ltd, San Antonio, TX USA
[16] Red Rock Res Ctr, Las Vegas, NV USA
[17] Univ N Carolina, Chapel Hill, NC USA
[18] Centocor Res & Dev Inc, Malvern, PA USA
[19] Vanderbilt Univ, Med Ctr, Nashville, TN USA
关键词
chronic obstructive pulmonary disease; infliximab; tumor necrosis factor-alpha;
D O I
10.1164/rccm.200607-995OC
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Rationale: Chronic obstructive pulmonary disease (COPD) is a progressive, smoking-related, inflammatoiy lung disease in which tumor necrosis factor-at is overexpressed and has been suggested to play a pathogenic role. Objectives: To determine if infliximab, an anti-TINF-alpha 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 prebron-chodilator 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 place bo-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.
引用
收藏
页码:926 / 934
页数:9
相关论文
共 37 条
[1]   Granulocyte inflammatory markers and airway infection during acute exacerbation of chronic obstructive pulmonary disease [J].
Aaron, SD ;
Angel, JB ;
Lunau, M ;
Wright, K ;
Fex, C ;
Le Saux, N ;
Dales, RE .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2001, 163 (02) :349-355
[2]   Tumor necrosis factor-α in the pathogenesis and treatment of cancer [J].
Anderson, GM ;
Nakada, MT ;
DeWitte, M .
CURRENT OPINION IN PHARMACOLOGY, 2004, 4 (04) :314-320
[4]   Tumor necrosis factor or tumor promoting factor? [J].
Balkwill, F .
CYTOKINE & GROWTH FACTOR REVIEWS, 2002, 13 (02) :135-141
[5]   COPD: current therapeutic interventions and future approaches [J].
Barnes, PJ ;
Stockley, RA .
EUROPEAN RESPIRATORY JOURNAL, 2005, 25 (06) :1084-1106
[6]  
Beers MN., 2000, MERCK MANUAL GERIATR
[7]   Randomized, double-blind, placebo-controlled, pilot trial of infliximab, a chimeric monoclonal antibody to tumor necrosis factor-α, in patients with moderate-to-severe heart failure -: Results of the Anti-TNF Therapy Against Congestive Heart Failure (ATTACH) trial [J].
Chung, ES ;
Packer, M ;
Lo, KH ;
Fasanmade, AA ;
Willerson, JT .
CIRCULATION, 2003, 107 (25) :3133-3140
[8]   Tumor necrosis factor-α drives 70% of cigarette smoke-induced emphysema in the mouse [J].
Churg, A ;
Wang, RD ;
Tai, H ;
Wang, XS ;
Xie, CS ;
Wright, JL .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2004, 170 (05) :492-498
[9]   ATS statement: Guidelines for the six-minute walk test [J].
Crapo, RO ;
Casaburi, R ;
Coates, AL ;
Enright, PL ;
MacIntyre, NR ;
McKay, RT ;
Johnson, D ;
Wanger, JS ;
Zeballos, RJ ;
Bittner, V ;
Mottram, C .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2002, 166 (01) :111-117
[10]   Elevated TNF-alpha production by peripheral blood monocytes of weight-losing COPD patients [J].
deGodoy, I ;
Donahoe, M ;
Calhoun, WJ ;
Mancino, J ;
Rogers, RM .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1996, 153 (02) :633-637