Flucytosine
|
| Systematic (IUPAC) name |
| 4-amino-5-fluoro-1,2-dihydropyrimidin-2-one |
| Clinical data |
| Trade names |
Ancobon |
| AHFS/Drugs.com |
monograph |
| MedlinePlus |
a601132 |
| Pregnancy cat. |
B3 (AU) C (US) |
| Legal status |
POM (UK) ℞-only (US) |
| Routes |
Oral, intravenous |
| Pharmacokinetic data |
| Bioavailability |
75 to 90% (oral) |
| Protein binding |
2.9 to 4% |
| Metabolism |
Minimal, in the GI tract |
| Half-life |
2.4 to 4.8 hours |
| Excretion |
Renal (90%) |
| Identifiers |
| CAS number |
2022-85-7 Y |
| ATC code |
D01AE21 J02AX01 |
| PubChem |
CID 3366 |
| DrugBank |
DB01099 |
| ChemSpider |
3249 Y |
| UNII |
D83282DT06 Y |
| KEGG |
D00323 Y |
| ChEBI |
CHEBI:5100 Y |
| ChEMBL |
CHEMBL1463 Y |
| Chemical data |
| Formula |
C4H4FN3O |
| Mol. mass |
129.093 g/mol |
|
|
InChI
-
InChI=1S/C4H4FN3O/c5-2-1-7-4(9)8-3(2)6/h1H,(H3,6,7,8,9) Y
Key:XRECTZIEBJDKEO-UHFFFAOYSA-N Y
|
Y (what is this?) (verify)
|
Flucytosine, or 5-fluorocytosine, a fluorinated pyrimidine analogue, is a synthetic antimycotic drug.
It is structurally related to the cytostatic fluorouracil and to floxuridine. It is available in oral and in some countries also in injectable form. A common brand name is Ancobon. Flucytosine was first synthesized in 1957 but its antifungal properties discovered in 1964. The drug is dispensed in capsules of 250 mg and 500 mg strength. The injectable form is diluted in 250 mL saline solution to contain 2.5 g total (10 mg/mL). The solution is physically incompatible with other drugs including amphotericin B.
|
Contents
- 1 Pharmacology
- 1.1 Mechanisms of action
- 1.2 Spectrum of susceptible fungi and resistance
- 1.3 Pharmacokinetic data
- 1.4 Human overdose
- 1.5 Human carcinogenity
- 2 Indications
- 3 Contraindications and cautions
- 4 Special Patient Groups
- 4.1 Pregnancy and lactation
- 4.2 Pediatric patients
- 5 Side effects
- 6 Interactions
- 7 Dosage
- 8 Use in immunocompromised patients
- 9 Veterinary uses
- 10 References
|
Pharmacology
Mechanisms of action
Two major mechanisms of action have been elucidated:
- One is that the drug is intrafungally converted into the cytostatic fluorouracil[1] that undergoes further steps of activation and finally interacts as 5-fluorouridinetriphosphate with RNA biosynthesis and disturbs the building of certain essential proteins.
- The other mechanism is the conversion into 5-fluorodeoxyuridinemonophosphate which inhibits fungal DNA synthesis.
Spectrum of susceptible fungi and resistance
Flucytosine is active in vitro as well as in vivo against some strains of Candida and Cryptococcus. Limited studies demonstrate that flucytosine may be of value against infections with Sporothrix, Aspergillus, Cladosporium, Exophila, and Phialophora. Resistance is quite commonly seen as well in treatment naive patients and under current treatment with flucytosine. In different strains of Candida resistance has been noted to occur in 1 to 50% of all specimens obtained from patients.
Pharmacokinetic data
Flucytosine is well absorbed (75 to 90%) from the gastrointestinal tract. Intake with meals slows the resorption, but does not decrease the amount resorbed. Following an oral dose of 2 grams peak serum levels are reached after approximately 6 hours. The time to peak level decreases with continued therapy. After 4 days peak levels are measured after 2 hours. The drug is eliminated renally. In normal patients flucytosine has reportedly a half-life of 2.5 to 6 hours. In patients with impaired renal function higher serum levels are seen and the drug tends to cumulate in these patients. The drug is mainly excreted unchanged in the urine (90% of an oral dose) and only traces are metabolized and excreted in the feces. Therapeutic serum levels range from 25 to 100 mcg/ml. Serum levels in excess of 100mcg are associated with a higher incidence of side-effects. Periodic measurements of serum levels are recommended for all patients and are a must in patients with renal damage.
Human overdose
Symptoms and their severities are unknown, because flucytosine is used under close medical supervision, but expected to be an excess of the usually encountered side effects on the bone marrow, gastrointestinal tract, liver and kidney function. Vigorous hydration and hemodialysis may be helpful to remove the drug from the body. Hemodialysis is particular useful in patients with impaired renal function.
Human carcinogenity
It is not known if flucytosine is a human carcinogen. The issue has been raised because traces of 5-fluorouracil, which is a known carcinogen, are found in the colon resulting from the metabolization of flucytosine.
Indications
Oral flucytosine is indicated for the treatment of serious infections caused by susceptible strains of Candida or Cryptococcus neoformans. It can also be used for the treatment of chromomycosis (chromoblastomycosis), if susceptible strains cause the infection. Flucytosine must not be used as a sole agent in life-threatening fungal infections due to relatively weak antifungal effects and fast development of resistance, but rather in combination with amphotericin B and/or azole antifungals such as fluconazole or itraconazole. Minor infections such as candidal cystitis may be treated with flucytosine alone. In some countries, treatment with slow intravenous infusions for no more than a week is also a therapeutic option, particular if the disease is life-threatening.
Contraindications and cautions
- All patients receiving flucytosine should be under strict medical supervision.
- Hematological, renal and liver function studies should be done frequently during therapy (initially daily, twice a week for the rest of treatment).
- Patients with preexisting bone marrow depression and liver impairment should be treated with caution.
- Concomitant treatment with brivudine is an absolute contraindication.
- Patients treated with drugs compromising bone marrow function (e.g. cytostatics) should be treated carefully. Blood cell counts should be taken very frequently.
- Patients with renal disease should receive flucytosine cautiously and in reduced doses. Guidelines for proper dosing exist. Serum level determinations are mandatory in these patients.
- Hypersensitivity to flucytosine is an absolute contraindication.
Special Patient Groups
Pregnancy and lactation
In animal models (rats), flucytosine has been found to be teratogenic. Sufficient human data does not exist. Pregnant women should be given flucytosine only if the potential benefits exceed the potential harm to the fetus.
It is not known if flucytosine is distributed in human breast milk. Given the potential risk to the child, the patient should not breastfeed during treatment with flucytosine.
Pediatric patients
The efficacy and safety in patients under 18 years of age has not been determined.
Side effects
- Antiproliferative actions on bone marrow and GI tissue: Due to the drug's preference to affect rapidly proliferating tissues, bone marrow depression (anemia, leukopenia, pancytopenia, or even rarely agranulocytosis) may occur. Aplastic anemia has also been seen. Bone marrow toxicity can be irreversible and may cause death, particular in immunocompromised patients. GI toxicity may be severe or rarely fatal and consists of anorexia, abdominal bloating, abdominal pain, diarrhea, dry mouth, duodenal ulcer, GI hemorrhage, nausea, vomiting, and ulcerative colitis.
- Liver function: Elevations of liver enzymes and bilirubin, hepatic dysfunction, jaundice and, in one patient, liver necrosis have all been seen. Some fatal cases have been reported, however the majority of cases was reversible.
- Renal function: Increased BUN and serum creatinine have been noted. Crystalluria (formation of crystals and excretion in the urine) and acute renal failure have also been seen.
- Adverse central nervous system effects are frequent and include confusion, hallucinations, psychosis, ataxia, hearing loss, headache, paresthesia, parkinsonism, peripheral neuropathy, vertigo and sedation.
- Skin reactions: Rash, pruritus, and photosensitivity have all been noticed. Toxic epidermal necrolysis (Lyell's syndrome) may also be encountered and may be life-threatening.
- Anaphylaxis: Sometimes cases of anaphylaxis consisting of diffuse erythema, pruritus, conjunctival injection, fever, abdominal pain, edema, hypotension and bronchospastic reactions are observed.
Interactions
For details see Contraindications and Cautions. Flucytosine may increase the toxicity of amphotericin B and vice versa, although the combination may be life-saving and should be used whenever indicated (e.g., cryptococcal meningitis). The cytostatic cytarabine inhibits the antimycotic activity of flucytosine.
Dosage
The recommended daily dose is 50 to 150 mg/kg of bodyweight orally, divided in four equal doses every six hours. If problems exist to swallow a complete single dose, the dose may be given in several partial amounts over 15 minutes. The dose for intravenous infusions is 50 mg/kg infused over 20 to 40 minutes every six hours. The duration of treatment depends on the clinical situation, but generally does not exceed seven days.
Use in immunocompromised patients
Serious fungal infections often occur in immunocompromised (e.g. HIV-infected) patients. These patients benefit from combination therapy including flucytosine, but the incidence of side-effects of a combination therapy, particular with amphotericin B, may be higher than in immunocompetent patients.
Veterinary uses
In some countries, such as Switzerland, flucytosine has been licensed to treat cats, dogs and birds (in most cases together with amphotericin B) for the same indications as in humans.
References
- ^ Vermes A, Guchelaar HJ, Dankert J (August 2000). "Flucytosine: a review of its pharmacology, clinical indications, pharmacokinetics, toxicity and drug interactions". J. Antimicrob. Chemother. 46 (2): 171–9. doi:10.1093/jac/46.2.171. PMID 10933638. http://jac.oxfordjournals.org/cgi/pmidlookup?view=long&pmid=10933638.
- AHFS Database online
- ClinPharm Wirkstoffliste (Switzerland, German information)
|
Antifungals (D01 and J02)
|
|
Wall/
membrane |
|
Ergosterol
inhibitors
|
Azoles
(lanosterol 14
alpha-demethylase inhibitors) |
|
Imidazoles
|
- topical: Bifonazole
- Butoconazole
- Clomidazole
- Clotrimazole#, Croconazole
- Econazole
- Fenticonazole
- Ketoconazole
- Isoconazole
- Miconazole#, Neticonazole
- Omoconazole
- Oxiconazole
- Sertaconazole
- Sulconazole
- Tioconazole
|
|
|
Triazoles
|
- topical: (Fluconazole#, Fosfluconazole
- Terconazole)
- systemic: (Fluconazole
- Hexaconazole
- Isavuconazole†, Itraconazole
- Posaconazole
- Voriconazole)
|
|
|
Thiazoles
|
topical: (Abafungin)
|
|
|
|
Polyene antimycotics
(ergosterol binding)
|
- topical: (Hamycin
- Natamycin
- Nystatin#)
systemic: (Amphotericin B#, Hamycin)
|
|
Allylamines
(squalene monooxygenase
inhibitors) |
- topical: (Amorolfine
- Butenafine
- Naftifine
- Terbinafine)
systemic: (Terbinafine)
|
|
|
|
β-glucan synthase
inhibitors
|
- echinocandins (Anidulafungin
- Caspofungin
- Micafungin)
|
|
|
| Intracellular |
|
Pyrimidine analogues/
Thymidylate synthase inhibitors
|
|
|
|
Mitotic inhibitors
|
|
|
|
| Others |
- Bromochlorosalicylanilide
- Methylrosaniline
- Tribromometacresol
- Undecylenic acid
- Polynoxylin
- Chlorophetanol
- Chlorphenesin
- Ticlatone
- Sulbentine
- Ethyl hydroxybenzoate
- Haloprogin
- Salicylic acid
- Selenium sulfide#
- Ciclopirox
- Amorolfine
- Dimazole
- Tolnaftate
- Tolciclate
- Sodium thiosulfate#
- Whitfield's ointment#
- Potassium iodide#
- Taurolidine
- Tea tree oil
- citronella oil
- lemon grass
- orange oil
- patchouli
- lemon myrtle
- PCP: Pentamidine
- Dapsone
- Atovaquone
|
|
- #WHO-EM
- ‡Withdrawn from market
- Clinical trials:
- †Phase III
- §Never to phase III
|
|
![carbonyl]-5- fluorocytosine of Formula IMA](https://1mg.info/0/4/t/1308.jpg)
