TY - JOUR
T1 - Current status and opportunities for therapeutic drug monitoring in the treatment of tuberculosis
AU - Zuur, Marlanka A.
AU - Bolhuis, Mathieu S.
AU - Anthony, Richard
AU - den Hertog, Alice
AU - van der Laan, Tridia
AU - Wilffert, Bob
AU - Lange, de, Wiel
AU - van Soolingen, Dick
AU - Alffenaar, Jan-Willem C.
PY - 2016/5
Y1 - 2016/5
N2 - Introduction: Tuberculosis remains a global health problem and pharmacokinetic variability has been postulated as one of the causes of treatment failure and acquired drug resistance. New developments enable implementation of therapeutic drug monitoring, a strategy to evaluate drug exposure in order to tailor the dose to the individual patient, in tuberculosis treatment.Areas covered: Literature on pharmacokinetics and pharmacodynamics of anti-tuberculosis drugs was explored to evaluate the effect of drug exposure in relation to drug susceptibility, toxicity and efficacy. New, down-sized strategies, like dried blood spot analysis and limited sampling strategies are reviewed. In addition, molecular resistance testing of Mycobacteria tuberculosis, combining a short turn-around time with relevant information on drug susceptibility of the causative pathogen was explored. Newly emerging host biomarkers provide information on the response to treatment.Expert opinion: Therapeutic drug monitoring can minimize toxicity and increase efficacy of tuberculosis treatment and prevent the development of resistance. Dried blood spot analysis and limited sampling strategies, can be combined to provide us with a more patient friendly approach. Furthermore, rapid information on drug susceptibility by molecular testing, and information from host biomarkers on the bacteriological response, can be used to further optimize tuberculosis treatment.
AB - Introduction: Tuberculosis remains a global health problem and pharmacokinetic variability has been postulated as one of the causes of treatment failure and acquired drug resistance. New developments enable implementation of therapeutic drug monitoring, a strategy to evaluate drug exposure in order to tailor the dose to the individual patient, in tuberculosis treatment.Areas covered: Literature on pharmacokinetics and pharmacodynamics of anti-tuberculosis drugs was explored to evaluate the effect of drug exposure in relation to drug susceptibility, toxicity and efficacy. New, down-sized strategies, like dried blood spot analysis and limited sampling strategies are reviewed. In addition, molecular resistance testing of Mycobacteria tuberculosis, combining a short turn-around time with relevant information on drug susceptibility of the causative pathogen was explored. Newly emerging host biomarkers provide information on the response to treatment.Expert opinion: Therapeutic drug monitoring can minimize toxicity and increase efficacy of tuberculosis treatment and prevent the development of resistance. Dried blood spot analysis and limited sampling strategies, can be combined to provide us with a more patient friendly approach. Furthermore, rapid information on drug susceptibility by molecular testing, and information from host biomarkers on the bacteriological response, can be used to further optimize tuberculosis treatment.
KW - Biomarkers
KW - dried blood spots
KW - drug susceptibility testing
KW - limited sampling
KW - molecular testing
KW - pharmacokinetics
KW - pharmacodynamics
KW - therapeutic drug monitoring
KW - tuberculosis treatment
KW - MULTIDRUG-RESISTANT TUBERCULOSIS
KW - DRIED BLOOD SPOTS
KW - LIMITED-SAMPLING STRATEGIES
KW - 1ST-LINE ANTITUBERCULOSIS DRUGS
KW - EARLY BACTERICIDAL ACTIVITY
KW - GENOTYPE MTBDRSL ASSAY
KW - MYCOBACTERIUM-TUBERCULOSIS
KW - PULMONARY TUBERCULOSIS
KW - PHARMACOKINETIC VARIABILITY
KW - CLINICAL-EVALUATION
U2 - 10.1517/17425255.2016.1162785
DO - 10.1517/17425255.2016.1162785
M3 - Review article
C2 - 26950189
SN - 1742-5255
VL - 12
SP - 509
EP - 521
JO - Expert Opinion on Drug Metabolism & Toxicology
JF - Expert Opinion on Drug Metabolism & Toxicology
IS - 5
ER -