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Keeping phase III tuberculosis trials relevant: Adapting to a rapidly changing landscape

Authors :
Christian Lienhardt
Patrick P. J. Phillips
Carole D. Mitnick
James D. Neaton
Andrew J. Nunn
Payam Nahid
UCSF Center for Tuberculosis [San Francisco, CA, États-Unis]
University of California [San Francisco] (UC San Francisco)
University of California (UC)-University of California (UC)
Harvard Medical School [Boston] (HMS)
School of Public Health [Minneapolis, MN, États-Unis]
University of Minnesota [Twin Cities] (UMN)
University of Minnesota System-University of Minnesota System
Recherches Translationnelles sur le VIH et les maladies infectieuses endémiques et émergentes (TransVIHMI)
Institut de Recherche pour le Développement (IRD)-Université de Yaoundé I-Université Cheikh Anta Diop [Dakar, Sénégal] (UCAD)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Montpellier (UM)
Université de Montpellier (UM)
Institut de Recherche pour le Développement (IRD [France-Sud])
Medical Research Council Clinical Trials Unit (MRC CTU)
University College of London [London] (UCL)
University of California [San Francisco] (UCSF)
University of California-University of California
Recherches Translationnelles sur le VIH et les maladies infectieuses endémiques er émergentes (TransVIHMI)
Université Cheikh Anta Diop [Dakar, Sénégal] (UCAD)-Institut de Recherche pour le Développement (IRD)-Université de Yaoundé I-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Montpellier (UM)-Université Montpellier 1 (UM1)
Bodescot, Myriam
Source :
PLoS medicine, 16(3):e1002767, PLoS Medicine, PLoS Medicine, 2019, 16 (3), pp.e1002767. ⟨10.1371/journal.pmed.1002767⟩, PLoS medicine, vol 16, iss 3, PLoS Medicine, Vol 16, Iss 3, p e1002767 (2019), PLoS Medicine, Public Library of Science, 2019, 16 (3), pp.e1002767. ⟨10.1371/journal.pmed.1002767⟩
Publication Year :
2019

Abstract

SUMMARY POINTS: (*) The landscape of tuberculosis (TB) treatment has evolved considerably over the last 10 years, necessitating careful consideration of various trial design aspects to ensure that TB phase III trials are still impactful at trial completion, often more than 4–5 years after initial design. (*) The choice of control is guided by the specific trial objectives, weighing the relative merits of internal validity and external generalizability alongside randomization in making the correct inference. A particular challenge occurs when international or national guidelines change during the trial. (*) Improved execution and relevance of noninferiority trials for TB require greater emphasis on study quality, especially maximizing treatment adherence and minimizing missing outcome data; preferred use of intention-to-treat rather than per-protocol analyses; more careful justification of the margin of noninferiority; and consideration of recent innovations such as a Bayesian approach to noninferiority. (*) Many adaptive trial designs are well suited to optimization of TB treatment. A thorough understanding of type I error rates and biases in treatment effect estimates is critical for regulatory approval and consideration in establishing World Health Organization (WHO) guidelines. (*) Treatment stratification is an area of limited experience for TB trials, and trialists must learn from well-established methodology in other disease areas. (*) Explanatory trials are important for evaluating the efficacy of an intervention under close to ideal conditions. However, no single trial can address all relevant questions about a given therapeutic intervention at one time, and pragmatic trials will be essential for public health and policy decision-making purposes. (*) TB treatment trials today should favor bold and creative approaches that can produce high-quality evidence for effective, patient-centered care made accessible to all 10 million new TB patients, including the half-million with drug-resistant TB (DR-TB), each year.

Details

Language :
English
ISSN :
15491277 and 15491676
Database :
OpenAIRE
Journal :
PLoS medicine, 16(3):e1002767, PLoS Medicine, PLoS Medicine, 2019, 16 (3), pp.e1002767. ⟨10.1371/journal.pmed.1002767⟩, PLoS medicine, vol 16, iss 3, PLoS Medicine, Vol 16, Iss 3, p e1002767 (2019), PLoS Medicine, Public Library of Science, 2019, 16 (3), pp.e1002767. ⟨10.1371/journal.pmed.1002767⟩
Accession number :
edsair.doi.dedup.....39480946ab37b602d93da442cf5976a7
Full Text :
https://doi.org/10.1371/journal.pmed.1002767⟩