Innovative Trial Designs Are Practical Solutions for Improving the Treatment of Tuberculosis

被引:53
作者
Phillips, Patrick P. J. [2 ]
Gillespie, Stephen H. [3 ]
Boeree, Martin [4 ]
Heinrich, Norbert [1 ]
Aarnoutse, Rob [4 ]
McHugh, Tim [5 ]
Pletschette, Michel [1 ]
Lienhardt, Christian [6 ,7 ]
Hafner, Richard [8 ]
Mgone, Charles [9 ]
Zumla, Alimuddin [5 ]
Nunn, Andrew J. [2 ]
Hoelscher, Michael [1 ,10 ]
机构
[1] Univ Munich LMU, Div Infect Dis & Trop Med, Med Ctr, Munich, Germany
[2] MRC, Clin Trials Unit, London, England
[3] Univ St Andrews, Sch Med N Haugh, St Andrews, Fife, Scotland
[4] Radboud Univ Nijmegen, Med Ctr, Nijmegen, Netherlands
[5] UCL, Sch Med, London WC1E 6BT, England
[6] WHO, Stop TB Partnership, CH-1211 Geneva, Switzerland
[7] WHO, Stop TB Dept, CH-1211 Geneva, Switzerland
[8] NIAID, Div Aids, Bethesda, MD 20892 USA
[9] European & Dev Countries Clin Trials Partnership, The Hague, Netherlands
[10] Univ Munich LMU, German Ctr Infect Res, Munich, Germany
关键词
MYCOBACTERIUM-TUBERCULOSIS; CLINICAL-TRIALS; MESSENGER-RNA; PULMONARY TUBERCULOSIS; PHASE-II; MOXIFLOXACIN; SURROGATE; METHODOLOGY; BIOMARKER; CANCER;
D O I
10.1093/infdis/jis041
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A growing number of new drugs for the treatment of tuberculosis are in clinical development. Confirmatory phase 3 trials are expensive and time-consuming and the question of whether one particular drug combination can be used to treat tuberculosis is less important from a public health perspective than the question of which are the shortest, simplest, most effective, and safest regimens. While preclinical and phase 1 studies provide some guidance in the selection of combinations for clinical evaluation, a large number of combinations will require phase 2 testing to ensure that only the best regimens advance to phase 3. The multi-arm multi-stage trial design is an example of a treatment selection-adaptive design where multiple experimental arms are each simultaneously compared with a common control and interim analyses allow for poor performing arms to be dropped early. Such designs, if designed and implemented correctly, require fewer patients, can be completed in a shorter time frame, and answer more relevant questions without any loss in statistical validity or scientific integrity. There are, however, practical issues that must be considered in applying this in tuberculosis treatment trials. More innovative trials designs should be considered to speed drug and regimen development for the treatment of tuberculosis.
引用
收藏
页码:S250 / S257
页数:8
相关论文
共 23 条
[1]   Moxifloxacin versus ethambutol in the initial treatment of tuberculosis: a double-blind, randomised, controlled phase II trial [J].
Conde, Marcus B. ;
Efron, Anne ;
Laredo, Carla ;
Muzy De Souza, Gilvan R. ;
Graca, Nadja P. ;
Cezar, Michelle C. ;
Ram, Malathi ;
Chaudhary, Mohammad A. ;
Bishai, William R. ;
Kritski, Afranio L. ;
Chaisson, Richard E. .
LANCET, 2009, 373 (9670) :1183-1189
[2]   Use of nonlinear mixed-effects analysis for improved precision of early pharmacodynamic measures in tuberculosis treatment [J].
Davies, Geraint R. ;
Brindle, Richard ;
Khoo, Saye H. ;
Aarons, Leon J. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2006, 50 (09) :3154-3156
[3]   Measurement of sputum Mycobacterium tuberculosis messenger RNA as a surrogate for response to chemotherapy [J].
Desjardin, LE ;
Perkins, MD ;
Wolski, K ;
Haun, S ;
Teixeira, L ;
Chen, Y ;
Johnson, JL ;
Ellner, JJ ;
Dietze, R ;
Bates, J ;
Cave, MD ;
Eisenach, KD .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1999, 160 (01) :203-210
[4]   Substitution of Moxifloxacin for Isoniazid during Intensive Phase Treatment of Pulmonary Tuberculosis [J].
Dorman, Susan E. ;
Johnson, John L. ;
Goldberg, Stefan ;
Muzanye, Grace ;
Padayatchi, Nesri ;
Bozeman, Lorna ;
Heilig, Charles M. ;
Bernardo, John ;
Choudhri, Shurjeel ;
Grosset, Jacques H. ;
Guy, Elizabeth ;
Guyadeen, Priya ;
Leus, Maria Corazon ;
Maltas, Gina ;
Menzies, Dick ;
Nuermberger, Eric L. ;
Villarino, Margarita ;
Vernon, Andrew ;
Chaisson, Richard E. .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2009, 180 (03) :273-280
[5]  
Ellenberg S., 2002, DATA MONITORING COMM
[6]  
Gamboa F, 1997, INT J TUBERC LUNG D, V1, P542
[7]   Quantitative analysis of mRNA as a marker for viability of Mycobacterium tuberculosis [J].
Hellyer, TJ ;
DesJardin, LE ;
Hehman, GL ;
Cave, MD ;
Eisenach, KD .
JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (02) :290-295
[8]   Time to sputum culture conversion in multidrug-resistant tuberculosis: Predictors and relationship to treatment outcome [J].
Holtz, TH ;
Sternberg, M ;
Kammerer, S ;
Laserson, KF ;
Riekstina, V ;
Zarovska, E ;
Skripconoka, V ;
Wells, CD ;
Leimane, V .
ANNALS OF INTERNAL MEDICINE, 2006, 144 (09) :650-659
[9]   Molecular Bacterial Load Assay, a Culture-Free Biomarker for Rapid and Accurate Quantification of Sputum Mycobacterium tuberculosis Bacillary Load during Treatment [J].
Honeyborne, Isobella ;
McHugh, Timothy D. ;
Phillips, Patrick P. J. ;
Bannoo, Selina ;
Bateson, Anna ;
Carroll, Nora ;
Perrin, Felicity M. ;
Ronacher, Katharina ;
Wright, Laura ;
van Helden, Paul D. ;
Walzl, Gerhard ;
Gillespie, Stephen H. .
JOURNAL OF CLINICAL MICROBIOLOGY, 2011, 49 (11) :3905-3911
[10]  
Kosterink JGW, 2011, CURR PHARM DESIGN, V17, P2875, DOI 10.2174/138161211797470183