Intensified tuberculosis treatment to reduce the mortality of HIV-infected and uninfected patients with tuberculosis meningitis (INTENSE-TBM): study protocol for a phase III randomized controlled trial
Thomas Maitre,
Maryline Bonnet,
Alexandra Calmy,
Mihaja Raberahona,
Rivonirina Andry Rakotoarivelo,
Niaina Rakotosamimanana,
Juan Ambrosioni,
José M. Miró,
Pierre Debeaudrap,
Conrad Muzoora,
Angharad Davis,
Graeme Meintjes,
Sean Wasserman,
Robert Wilkinson,
Serge Eholié,
Frédéric Ello Nogbou,
Maria-Camilla Calvo-Cortes,
Corine Chazallon,
Vanessa Machault,
Xavier Anglaret,
Fabrice Bonnet
Affiliations
Thomas Maitre
Sorbonne Université, INSERM U1135, Cimi-Paris, Department of Pneumology and Thoracic oncology, Reference Centre for Rare Lung Diseases, APHP Tenon Hospital
Maryline Bonnet
Université Montpellier, IRD, INSERM, TransVIHMI
Alexandra Calmy
Division of Infectious Diseases, HIV-AIDS Unit, Geneva University Hospitals
Mihaja Raberahona
Centre d’Infectiologie Charles Mérieux (CICM)
Rivonirina Andry Rakotoarivelo
Centre d’Infectiologie Charles Mérieux (CICM)
Niaina Rakotosamimanana
Mycobacteria Unit, Institut Pasteur de Madagascar
Juan Ambrosioni
HIV Unit, Infectious Diseases Service, Hospital Clínic-IDIBAPS, University of Barcelona
José M. Miró
HIV Unit, Infectious Diseases Service, Hospital Clínic-IDIBAPS, University of Barcelona
Pierre Debeaudrap
CEPED, Institut de Recherche pour le Développement, Université Paris Descartes, INSERM 1244
Conrad Muzoora
Department of Internal Medicine, Mbarara University of Science and Technology
Angharad Davis
The Francis Crick Institute
Graeme Meintjes
Wellcome Centre for Infectious Diseases Research in Africa (CIDRI-Africa), Institute of Infectious Disease and Molecular Medicine, University of Cape Town
Sean Wasserman
Wellcome Centre for Infectious Diseases Research in Africa (CIDRI-Africa), Institute of Infectious Disease and Molecular Medicine, University of Cape Town
Robert Wilkinson
The Francis Crick Institute
Serge Eholié
Centre Hospitalier Universitaire (CHU) Treichville
Frédéric Ello Nogbou
Programme ANRS Coopération Côte d’Ivoire (PAC-CI)
Maria-Camilla Calvo-Cortes
Inserm – ANRS|MIE (Emerging Infectious Diseases)
Corine Chazallon
University of Bordeaux, National Institute for Health and Medical Research (INSERM) UMR 1219, Research Institute for Sustainable Development (IRD) EMR 271, Bordeaux Population Health Centre
Vanessa Machault
University of Bordeaux, National Institute for Health and Medical Research (INSERM) UMR 1219, Research Institute for Sustainable Development (IRD) EMR 271, Bordeaux Population Health Centre
Xavier Anglaret
University of Bordeaux, National Institute for Health and Medical Research (INSERM) UMR 1219, Research Institute for Sustainable Development (IRD) EMR 271, Bordeaux Population Health Centre
Fabrice Bonnet
University of Bordeaux, National Institute for Health and Medical Research (INSERM) UMR 1219, Research Institute for Sustainable Development (IRD) EMR 271, Bordeaux Population Health Centre
Abstract Background Tuberculous meningitis (TBM) is the most lethal and disabling form of tuberculosis (TB), particularly in sub-Saharan Africa. Current anti-TB treatment is poorly effective since TBM mortality reaches 40% in HIV-negative patients and up to 70% in HIV-co-infected patients. To reduce TBM-induced morbidity and mortality, the INTENSE-TBM trial evaluates two interventions in both HIV-infected and uninfected patients: an anti-TB treatment intensification using oral high-dose rifampicin (35 mg/kg daily) and linezolid (1200 mg daily and then 600 mg daily) during the first 8 weeks of the anti-TB treatment and the use of adjunctive aspirin (200 mg daily). Methods This is a randomized controlled, phase III, multicenter, 2 × 2 factorial plan superiority trial. The trial has four arms, combining the two experimental treatments (intensified TBM regimen and aspirin) with the two reference treatments (WHO standard TB treatment and placebo), and is open-label for anti-TB treatment and double-blind placebo-controlled for aspirin treatment. This trial is conducted in adults or adolescents of age ≥15 years with TBM defined as “definite,” “probable,” or “possible” using Tuberculosis Meningitis International Research Consortium criteria, in four African countries: Ivory Coast, Madagascar, Uganda, and South Africa. The primary outcome is all-cause death between inclusion and week 40. Discussion The INTENSE-TBM trial represents a key opportunity to enhance TBM treatment with widely available existing drugs notably in high-incidence settings of both TB and HIV. The trial design is pragmatic and the results will permit early and effective applications in TBM patient care, in both HIV and TB high-incidence countries. Trial registration ClinicalTrials.gov NCT04145258. Registered on October 30, 2019.