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1 Second-line Anti-TB drugs Session 5

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Second-line Anti-TB drugsSession 5

USAID TB CARE II PROJECT

The five drug groups

• Group 1: First-line oral drugs

• Group 2: Injectables

• Group 3: Fluoroquinolones

• Group 4: Other second-line drugs

• Group 5: Possible reinforcing drugs (drugs with unclear efficacy)

An MDR-TB treatment regimen requires the use of at least four active medications against TB (but often involves five)

USAID TB CARE II PROJECT

Kanamycin (Km)

GROUP 2 — INJECTABLE• Aminoglycoside

• Interferes with protein synthesis through disruption of ribosome

Dose: 1 g IM/IV (15-20 mg/kg)

Side effects:• Nephrotoxicity

• Ototoxicity

• Electrolyte wasting

Adjust dose for renal failure

USAID TB CARE II PROJECT

Amikacin (Amk)

GROUP 2 — INJECTABLE• Aminoglycoside

• Highly similar to kanamycin (can be essentially considered the same drug)

Dose: 1 g IM/IV (15-20 mg/kg) daily

Side effects: • Same as kanamycin; renal failure

and ototoxicity

High cross-resistance with kanamycin

Adjust dose in renal failure (same as kanamycin)

USAID TB CARE II PROJECT

Capreomycin (Cm)

GROUP 2 — INJECTABLE• Polypeptide

• Structurally and functionally similar to aminoglycosides

Dose: 1 g IM/IV (15-20 mg/kg) daily

Side effects • same as Km/Amk

Some cross-resistance with Km/Amk

Adjust dose for renal failure

USAID TB CARE II PROJECT

Ofloxacin (Ofx)

GROUP 3 — FLUOROQUINOLONE

• Inhibits DNA-gyrase

Dose: 800 mg daily

Side effects• Generally well-tolerated

• GI upset, rash, CNS disturbance

Avoid antacids around time of ingestion (reduces absorption)

Near complete cross-resistance with other fluoroquinolones

USAID TB CARE II PROJECT

Levofloxacin (Lfx)

GROUP 3 — FLUOROQUINOLONE

Dose: 750 mg daily for <50 kg (1000 mg daily for > 75kg)• A higher dose for tuberculosis is

used than for other infections

Side effects• Generally well-tolerated

• GI upset, rash, CNS disturbance

Adjust dose in renal failure

USAID TB CARE II PROJECT

Moxifloxacin (Mfx)

GROUP 3 — FLUOROQUINOLONE

• May be more active than earlier generation quinolones

Dose: 400 mg daily

Near complete cross-resistance with other fluoroquinolones• Moxifloxacin may have limited

efficacy against some strains resistant to ofloxacin

No dose adjustment in renal failure• Hepatically cleared

USAID TB CARE II PROJECT

Ethionamide (Eto)

GROUP 4 — OTHER SECOND LINE DRUGS

• Derivative of isonicotinic acid (same family as isoniazid)

Dose: 500-1000 mg daily in divided doses

Side effects• GI upset, hypothyroidism,

peripheral neuropathy

Partial cross-resistance with isoniazid, complete with prothionamide

Hepatically excreted

Co-administer vitamin B6

USAID TB CARE II PROJECT

Prothionamide (Pto)

GROUP 4 — OTHER SECOND LINE DRUGS

• Structurally similar to ethionamide

Dose: 500-1000 mg daily in divided doses

Overall side effect profile similar to ethionamide• Slightly less GI side effects

Complete cross-resistance with ethionamide

USAID TB CARE II PROJECT

Cycloserine (Cs)

GROUP 4 — OTHER SECOND LINE DRUGS

• Alanine analogue

• Interferes with cell-wall proteoglycan synthesis

Dose: 500-1000 mg daily in divided doses

Side effects:• Seizures, psychosis, depression,

irritability, headache

Renally excreted

Effective CNS penetration

Co-administer B6

USAID TB CARE II PROJECT

Terizidone (Trd)

GROUP 4 — OTHER SECOND LINE DRUGS

• Structure is composed of two connected molecules of cycloserine

• Commonly used in South Africa in place of cycloserine

Dose: 500-1000 mg daily in divided doses

Possibly less side effects than cycloserine

Not yet recommended by the WHO• There is less information on terizidone

than cycloserine and no direct studies comparing the two

USAID TB CARE II PROJECT

Para-aminosalicylic acid (PAS)

GROUP 4 — OTHER SECOND LINE DRUGS

• Various formulations; delayed-release microcapsules (PASER) best tolerated

Dose of PASER is 4 g (1 sachet) twice daily

Side effects• GI upset, hypothyroidism

• Hepatitis, electrolyte abnormalities

Hepatic metabolism, renal excretion

Administer with acidic food or drink

USAID TB CARE II PROJECT

Group 5: Possible reinforcing agents

Minimal clinical data to support use in MDR-TB therapy.

Should only be used in cases of extreme drug resistance (XDR-TB):

• Amoxicillin/clavulanic acid

• Clofazamine

• Linezolid

• High dose isoniazid

• Imipenem

USAID TB CARE II PROJECT

Amoxicillin-clavulanic acid (AMX-CLV)

GROUP 5• Beta-lactam antibiotic with beta-

lactamase inhibitor

Dose• 1000/250 mg twice daily or

• 875/125mg twice daily

Side effects• GI upset, rash

Contraindicated: Penicillin allergy

USAID TB CARE II PROJECT

Clofazimine (CFZ)

GROUP 5• Substituted iminophenazine

Usual adult dose is 100 mg daily

Side effects• Bronzing of skin

• Malabsorption

• Abdominal pain (can be severe)

USAID TB CARE II PROJECT

Linezolid (LZD)

GROUP 5• Oxazolidinone: inhibits protein

synthesis, interacting with ribosomal RNA

Dosing • Coated tablets: 400 and 600 mg• Intravenous solution: 2 mg/ml;

100, 200, or 300 mg bags• Usual dose: 600 mg twice daily. • Some case series have successfully

used daily half dosing (600 mg once daily) to decrease toxicity and maintain efficacy, however neuropathic reactions seem to be related to duration of therapy rather than dose.

USAID TB CARE II PROJECT

Linezolid (LZD) (Continued)

Side effects

• Generally well tolerated for treatment courses ≤28 days.

• Common: diarrhea, nausea, headache, insomnia, and rash.

• More serious:

– myelosuppression (generally reversible with discontinuation of the drug)

– optic neuropathy (usually resolved over time with drug discontinuation)

– peripheral neuropathy (possibly irreversible).

• Rare: hypertension, lactic acidosis, pancreatitis

USAID TB CARE II PROJECT

Linezolid (LZD) (Continued)

Monitoring • CBC weekly during the initial period, then monthly, and then as

needed based on symptoms.• There is little clinical experience with prolonged use.• Visual function should be monitored in all patients taking linezolid

for extended periods (≥3 months) and in all patients reporting new visual symptoms regardless of length of therapy.

Alerting symptoms:• Black, tarry stools or severe diarrhea• Unusual bleeding or bruising• Extreme tiredness or weakness• Numbness, tingling, or burning pain in your hands, arms, legs, or

feet• Change in visual acuity, vision blurring, or visual field defect • Headache, nausea, or vomiting

USAID TB CARE II PROJECT

High-dose isoniazid (H)

GROUP 5 (AT HIGH DOSES)

Dosing• 16 to 18 mg/kg per day, typically

600 mg to 1200 mg per week

• Some clinicians give it three times a week instead of daily at the 16 to 18 mg/kg dosing

USAID TB CARE II PROJECT

Imipenem/Cilastin

GROUP 5—BETA-LACTAM/CARBAPENEM

In vitro activity—very limited clinical experience

Dosing• Adults: 1000 mg IV every 12 hours

• In children, meropenem preferred: 20-40 mg/kg/dose IV every 8 hours up to 2 grams per day (high rates of seizures were seen in children treated with imipenem for TB meningitis

Side effects• Diarrhea, nausea, vomiting

• Seizure noted in CNS infections

USAID TB CARE II PROJECT

Global TB drug pipeline

USAID TB CARE II PROJECT

Weight-based dosing

Second-line anti-TB drugs are usually dosed based on weight according to the next three slides.

If a patient gains weight during the treatment they move up a weight band and the dosage of drugs should be adjusted accordingly.

Example: A patient who starts treatment at 45 kg will be started on 500 mg of ethionamide. Once the patient’s weight increases above 50 kg the dose should be adjusted to 750 mg per day.

USAID TB CARE II PROJECT

Cross-resistance

Aminoglycosides

• Minimal cross resistance between SM and other aminoglycosides

• KM and AM have almost complete cross resistance

• Cross resistance between CM and KM and/or AM has been documented

Fluoroquinolones

• Mutations that confer resistance to one fluoroquinolone will confer some degree of resistance to all, but the clinical significance of this is unclear (e.g. moxifloxacin may have limited efficacy against some strains resistant to ofloxacin).