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. 2016 Feb 16;110(3):163–172. doi: 10.1093/trstmh/trv107

Table 1.

Recent evaluations of short (9 to 12-month) multidrug-resistant TB regimens

Site and date of report Regimen
No. patients Time to 95% treatment completion Treatment success, n (%)
Non-success, n (%)
Intensive Continuation Cure Completed Failure Death Default Relapsec
Bangladesh, 201024 4Km-Cfz-Gh--E-Hh-Z-Ptoa  5Gh-E-Z-Cfz 206 365 days 170 (82.5) 11 (5.3) 1 (0.5) 11 (5.3) 12 (5.8) 1 (0.5)
Bangladesh, 201425 4Km-Cfz-Gh--E-Hh-Z-Ptoa  5Gh-E-Z-Cfz 515b 363 days 418 (81.2) 17 (3.3) 7 (1.4) 29 (5.6) 40 (7.8) 4 (0.8)
Cameroon, 201526 4Km-Cfz-G-E-H-Z-Ptoa  8G-Cfz-Z-E-Pto 150 409 days 132 (88.0) 2 (1.3) 1 (0.7) 10 (6.7) 5 (3.3) 0

Numbers in front of drug combinations indicate planned months of therapy.

Cfz: clofazimine (50–100 mg); E: ethambutol (800–1200 mg); G: gatifloxacin (400 mg to all patients); Gh: gatifloxacin high dose (400–800 mg); H: isoniazid (300 mg to all patients); Hh: isoniazid high dose (300–600 mg); Km: kanamycin (500–1000 mg); Pto: prothionamide (500–1000 mg); Z: pyrazinamide (800–2000mg). Dose ranges indicate adjustment by weight.

a Intensive phase therapy extended until sputum smear conversion if not smear negative at 4 months.

b The second Bangladesh study represents a cumulative total of patients on the ‘Bangladesh’ regimen, so includes longer-term follow-up data on patients from the first study in addition to new data.

c Completion of 24 month follow-up to detect relapse amongst patients with treatment success was variable between these studies; 54% and 93%, respectively, in the Bangladesh studies and 75% in Cameroon.