Clinical Implications of New Drugs and Regimens for the Treatment of Drug-resistant Tuberculosis

1. Bedaquiline

Bedaquiline, a novel diarylquinoline compound that targets the proton pump of adenosine triphosphate (ATP) synthase in Mycobacterium tuberculosis (Mtb).17, 18 It has a potent anti-mycobacterial activity with a very low minimal inhibitory concentration (MIC) value of 0.003 mg/L against Mtb in vitro, although the MIC value (0.003-0.12 mg/L) varies according to the different bacterial subpopulations within drug susceptible and drug-resistant strains.19 The anti-mycobacterial activity is synergic in combination with primary TB drugs including isoniazid, rifampin, ethambutol, and pyrazinamide. It could also be synergic with new anti-TB drugs including SQ109,20 oxazolidinones (such as linezolid, sutezolid, AZD5847, and tedizolid) in combination with pretomanid which could improve the effectiveness of the regimen consisting of bedaquiline, pretomanid, and linezolid for XDR-TB (Nix-TB trial, ClinicalTrial.gov registration no. NCT02333799).21

In a phase IIa study of early bactericidal activity (EBA) for seven days in treatment-naïve sputum smear-positive pulmonary TB patients, the bactericidal activity was significant at a daily dose of 400 mg with a delayed onset of activity from day 4 to day 7 which were similar in magnitude of that of isoniazid and rifampin, but without the serious drug-related adverse reactions.22

In a phase IIb study for the efficacy and safety of bedaquiline in combination with a WHO-recommended background regimen for 8 weeks (C208 stage 1) and for 24 weeks (C208 stage 2), the bedaquiline group showed a significantly higher culture conversion rate compared to those in placebo group. The cure rate, defined by both WHO study protocols at 120 weeks, was also significantly higher in the bedaquiline group compared to those in placebo group (Table 1). Although drug-induced adverse reactions were no different in the two groups in both studies, more deaths were noticed in the bedaquiline group compared to the placebo group in the C208 stage 2 study (2 [2%] vs. 10 [13%], p=0.02). However, another study (C209) which enrolled patients with MDR-TB, including patients previously on second-line treatment and those with XDR-TB, in contrast to the preceding studies in which these patients were excluded, showed that the mortality rate in patients on treatment with bedaquiline was not higher (6.9%) than seen in previous study and the cure rate was sill comparable to previous study (72.2 % by study protocol definition and 61.0% by WHO definition). The study was limited in being a single arm and open-label one (Table 1).25 However, there still remain concerns about safety including a long half-life, hepatotoxicity, drug-induced QT prolongation, drug interactions with cytochrome P450 enzyme CYP3A4 inducers and about efficacies in patients with pre-XDR (MDR-TB with resistance against fluoroquinolone or second-line injectable drugs), XDR, HIV infected patients, patients younger than 18, and extrapulmonary TB.

TABLE 1
Sputum culture conversion rates and treatment outcomes in C208 stage 1, C208 stage 2, and C209 phase IIb studies for evaluation of the efficacy and safety of bedaquiline in patients with multi-drug resistant tuberculosis23, 24, 25

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In recent cohort studies, some of these safety and efficacy issues have been dealt with. Regarding efficacy, the culture conversion rate of the bedaquiline containing regimen was still high in patients with pre-XDR, XDR-TB and also HIV infected patients receiving antiretroviral therapy (ART).26, 27 Regarding safety, patients on bedaquiline in combination with various drugs including levofloxacin, clofazimine, and linezolid had no cardiac arrhythmia although there were corrected QT prolongations in the bedaquiline group. Regarding drug interactions in patients on ART, no serious adverse drug reactions including hepato- and renal-toxicity and cardiac arrhythmia were reported. These studies were limited because a small number of patients were used, with a short follow-up period. Therefore additional studies about these issues are still needed.

Resistance to this drug and cross resistance to clofazimine is another concern. Bedaquiline resistance is caused by mutations in atpE encoding a part of the F0 subunit of ATP synthase which is the target of the drug and rv0678.19, 28 Mutation in rv0678 causes transcriptional upregulation of mmpS5 and mmpL5 resulting in cross-resistance to clofazimine through the activation of MmpL proteins which are multisubstrate efflux pumps for which bedaquiline and clofazimine function as possible substrates.28 However, the clinical impact on drug resistance caused by this mutation and on the use of efflux pump inhibitors such as verapamil and protonophores, which may restore drug susceptibility, are yet to be determined.18, 29

Based on previous studies, bedaquiline is recommended for adult patients with pulmonary MDR-TB if the patients cannot have an effective regimen because of intolerance, resistance, or an unavailability of other TB drugs.30, 31, 32 Routine use of this drug for patients with MDR-TB is not recommended. Although there is no best regimen for this drug, it should be added to the WHO-recommended regimen. A close monitoring for adverse drug reactions of this drug and unexpected interactions with other drugs is also recommended.

2. Delamanid

Delamanid is a novel nitroimidazole compound which overcomes the mutagenicity of the drug and targets the mycobacterial cell wall by interrupting the synthesis of methoxy-mycolic and keto-mycolic acids.16, 33 It shows potent anti-mycobacterial activity with very low MICs ranging from 0.006 to 0.024 µg/mL in vitro to both drug-susceptible and drug-resistant Mtb strains which were 4-256 times lower than those of rifampin, isoniazid, ethambutol, streptomycin, CGI-17341, and pretomanid.33

In a phase IIa trial, a 14-day EBA study for evaluation of the anti-TB activity, pharmacokinetics, and toxicity of the drug with a dose of 100, 200, 300, or 400 mg delamanid taken once daily in patients with treatment-naïve smear-positive pulmonary TB showed a significant and continuous bactericidal activity.34 However, there was no dose-dependent bactericidal activity in this study: there was increasing bactericidal activity up to 300 mg daily, but it attenuated at 400 mg daily.34 The fall of the colony forming unit (CFU) of Mtb which is a method for measuring anti-TB activity in the EBA study reached significant levels on day 3 and then continued at a magnitude similar to the standard four drug regimen.34

In phase IIb, a randomized, placebo-controlled, multinational study in patients with pulmonary MDR-TB showed higher culture conversion rates on both Mycobacteria Growth Indicator Tube (MGIT) and solid medium in patients who received delamanid for 8 weeks in combination with WHO recommended optimized background regimen (OBR) than in patients on placebo in combination with OBR.35 A significant rapid culture conversion was also shown in both the MGIT system and solid medium in this study (Table 2).35, 36

TABLE 2
Sputum culture conversion rates and treatment outcomes in phase IIb studies (2 months of delamanid treatment for 204 study participants and 6-8 months of delamanid treatment for 208 and 116 study participants) in patients with multidrug-resistant tuberculosis35, 36

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A subsequent open-label extension trial showed that outcomes in patients with more than 6 months (6-8 months) of delamanid treatment were significantly higher than in patients with less than 2 months of delamanid or placebo.36 The mortality rate in patients with longer use of delamanid was significantly lower than in patients with shorter use of delamanid. However, in a subgroup analysis for patients with XDR-TB, there was no difference in favorable outcomes between the two groups (Table 2).36

Although two previous studies showed the efficacy of delamanid treatment in combination with OBR for 6 months, there remains safety concerns including QT prolongation especially in patients with hypoalbuminemia (<2.8 mg/dL) and efficacy concerns in the elderly, children, adolescents under 18 years, pregnant women, breast-feeding women, and patients with extrapulmonary TB.16

The recommended use of delamanid for treating TB is similar with that of bedaquiline.32, 37 Delamanid can strengthen the WHO-recommended MDR-TB regimen in patients who cannot have an effective regimen due to resistance, intolerance, and lack of availability of TB drugs. Although there is no data comparing the clinical efficacy and safety of delamanid and bedaquiline, delamanid might be more favorable in combination with CYP3A4 inducers because there is less interaction with this liver enzyme compared to bedaquiline.16 However, in patients with hypoalbuminemia, bedaquiline is favorable because delamanid causes QT prolongation in these patients.16

Current guidelines have not recommended combining bedaquiline and delamanid because there is no evidence regarding efficacy or safety risks including QT prolongation. However, this combination could be needed when an effective treatment regimen cannot be used due to drug resistance and intolerance to second-line TB drugs. Recently, two cases were reported which were both XDR-TB and extremely complicated.38, 39, 40, 41 Both cases showed favorable clinical, microbiological, and radiological response after six months of treatment. Regarding safety, one patient experienced a transient QT prolongation which resulted in a temporary discontinuation of bedaquiline, but the drug was restarted in addition to verapamil without a recurrence of QT prolongation.41 Although these two patients are not enough to make conclusions about combination of these two drugs, better data can be expected in clinical trials about this issue (ClinicalTrials.gov identifier NCT02583048 and NCT02754765).

3. Pretomanid

Pretomanid is a novel bicyclic nitroimidazole which has potent anti-mycobacterial activity against both drug-susceptible and -resistant Mtb with a low MIC ranging from 0.015 to 0.25 mg/mL, comparable to that of isoniazid.42 The mechanism of action of this drug is the disruption of the formation of mycolic acid, and bactericidal activity of this drug was shown in both replicating and hypoxic-static Mtb. In hypoxic conditions, the mechanism of anti-mycobacterial activity has been shown to be intracellular nitric oxide release.43 Based on the bactericidal and sterilizing activities of this drug in combination with moxifloxacin and pyrazinamide in a murine model, the efficacy of this regimen in patients with pulmonary TB was shown in a phase IIa 14-day EBA study and phase IIb multicenter, partly randomized clinical trial for 8 weeks of treatment.44, 45 In a phase IIa 14-day EBA study, this regimen showed comparable bactericidal activity compared to that of standard regimen and superior to those of other regimens including bedaquiline, bedaquiline-pyrazinamide, and bedaquiline-pretomanid.44 In a phase IIb study for 8 weeks of treatment, the bactericidal activity of this regimen measured by decreasing sputum colony counts during treatment period in patients with drug susceptible pulmonary TB were significantly higher than with a standard regimen.45 Moreover, in this trial, the bactericidal activity in patients with MDR-TB being treated with this regimen was comparable to that in patients with drug susceptible TB being treated with the standard regimen. Regarding safety, adverse drug reactions were not different among treatment groups with no events of QT prolongation of more than 500 ms. Although this regimen showed good efficacy and safety in previous studies, a phase III, open-label, partially randomized trial done by the TB alliance, a nonprofit product development partnership with a large portfolio of new TB drugs, for this regimen has been suspended at enrollment of participants (ClinicalTrials.gov identifier NCT02342886).

4. Sutezolid

Sutezolid (PNU-100480) is a novel oxazolidinone analogue. Linezolid is the first agent in this class with great efficacy against MDR-TB, although it has been used off-label, and serious adverse drug reactions including peripheral neuropathy, optic neuropathy, and myelosuppression limit the long term use of this drug. Sutezolid showed more potent anti-mycobacterial activity than linezolid against both drug-susceptible and drug-resistant strains of Mtb. In the murine TB model, this drug alone or in combination with first-line TB drugs and moxifloxacin showed better initial bactericidal activity and sterilizing activity than linezolid.46, 47 In phase I trials, this drug was safe and well tolerated at up to 1,500 mg in a single dose and up to 1,200 mg in combination for 14 or 28 days. In these trials, bactericidal activity measured by ex vivo whole-blood culture was maximized at the 600 mg, twice daily dose and augmented by pyrazinamide.48, 49 In phase IIa trials in patients with smear positive pulmonary TB, the dosages, the 600 mg, twice daily and 1,200 mg daily doses, were safe, well tolerated, and readily showed significant bactericidal activity in sputum and blood.50 Further studies for efficacy and safety about this drug and its combinations with other drugs are needed.