Farmaci antifunginei

1] DermatophytesMicrosporum, Epidermophyton e Trichophyton

2] Candida3] Aspergillus4] Cryptococcus5] Rhizopus...

Funghi patogeni per l‘uomo

Un fungo è un organismo appartenente alla famiglia degli eucarioti quali la famiglia dei lieviti, muffe ed i caratteristici funghi edili e tossici

Microsporum canis

Candida albicans

Infezioni cutanee da funghi

Trichophyton mentagrophytes

Microsporum canis (Tinea capitis)

Tinea corporis

Tinea faciei Tinea cruris

Candidiosi, Stomatite, Mughetto Intertrigine da candida (ascelle)

Candidiosi da pannolino

Oncimicosi

POLIENIAmphotericina B, Nistatina

AZOLIImidazoles:

Ketoconazolo..Triazoles: Fluconazolo,

itraconazolo, voriconazolo, posaconazolo, ravuconazolo

ALLILAMMINETerbinafina, butenafina

MORFOLINEAmorolfine

PIRIMIDINE FLUORINATEFlucitosina

Farmaci antifunginei suddivisi per classi

ECHINOCANDINECaspofungin, anidulafungin, micafungin

PEPTIDE-NUCLEOSIDENikkomicina Z

DERIVATI TETRAIDROFURANICISordarine,

azasordarine ALTRI

Griseofulvina

Farmaci antifunginei suddivisi per classi

Nature Reviews Drug Discovery | AOP, published online 20 August 2010; doi:10.1038/nrd3074

1] Agenti che interferiscono con l ‘ integrita’della membrana

Amphotericina B, Nistatina

2] Inibitori della sintesi dell ‘ ergosterolo

Azoli, allilamine, morfoline

3] Inibitori degli acidi nucleiciFlucitosina

4] AntimitoticiGriseofulvina

5] Inibitori della sintesi del glucano

Echinocandine

6] Inibitori della sintesi della chitina

Nikkomicina

MECCANISMO DI AZIONE

7] Inibitori della sintesi proteica

Sordarine, azasordarine

Generic Name Brand Namenaftifine Naftin

Generic Name Brand Name

clotrimazole  

econazole Spectazole

ketoconazole Nizoral

oxiconazole Oxistat

sertaconazole Ertaczo

sulconazole Exelderm

Generic Name Brand Name

butenafine Mentax

ciclopirox Loprox

clotrimazole-betamethasone Lotrisone

Topical allylamines

Topical azoles

Other topical antifungals

AMFOTERICINA B genera dei pori nella membrana

Usi terapeutici :

- Leishemaniosi mucocutanea americana- Aspergillosi invasiva- Blastomicosi- Candidiosi ( E’ presente per il 60% nei pazienti affetti da HIV e in più dell’80% in sogggetti con AIDS.)- Meningite criptococcica in pazienti con HIV- Criptococcosi polmonare- Infezioni funginee del SNC

Effetti collaterali generali :

Perdita di peso corporeoDiarrea, indigestione, perdita dell’appetito, nausea, vomitoFebbre, mal di testa

Effetti collaterali gravi :

Aritmia cardiaca, ipotensione tromboflebitiIpocaliemiaAnafilassiNefrotossicitàconvulsioni

Effetti collaterali Amfotericina B

In addition to infusion-related adverse effects, Amphotericin B ( AmB) may be associated with considerable cumulative toxicity like cardiotoxicity, neurotoxicity and, most notably, nephrotoxicity (60–80% of patients), the latter manifesting in tubular injury and a poorly understood renal vasoconstriction. Although AmB’s nephrotoxic effects are to a certain extent preventable (e.g. by sodium supplementation) and reversible, they represent the main dose-limiting determinants. Fortunately, all approved lipid-based formulations were shown to significant ly reduce t he likelihood of severe azotaemia compared to conventional D-AmB, even in patients treated concomitantly with other nephrotoxic drugs. Thus, in many hospitals, conventional D-AmB, despite its lower cost, is largely abandoned as a therapeutic agent against IA . Despite its unfavourable safety profile, AmB still represents the best proven and most important therapeutic option in salvage situations and in the management of breakthrough infections.

Ketoconazolo

TERB

Lo Squalene è il precursore di tutte le famiglie di steroidi

Il ketoconazolo può essere micostatico o fungicida a seconda delle dosi. Inibisce la sintesi dell’ergosterolo che porta come risultato il danno della membrana cellulare con fuoriscita degli elementi intracellulari necessari per la vita del fungo. Inibisce la sintesi dei trigliceridi e dei fosfolipidi dei funghi.

Il fluconazolo è un inibitore del CYP450 umano particolarmente degli isoenzimi CYP2C9 e CYP3A4.

Meccanismo di azione

Classification of triazoles

First generation of triazoles• Fluconazole• Itraconazole

Second generation of triazoles• Voriconazole • Posaconazole • Ravuconazole

Fluconazole: Fluconazole is an oral and parenteral agent. It readily penetrates into tissues due to its low lipophilic nature and limited protein binding; it is approximately 90% bioavailable. Concentrations in urine are several fold greater than in blood (10- to 20-fold greater) (11,12). Rare, but serious, hepatotoxicity may be associated with fluconazole. Drug interactions are possible because fluconazole is an inducer of cytochrome P450 isoenzymes. Clinical use in paediatrics: Fluconazole, the azole that is most widely used in paediatrics, is often used in the treatment of Candida and cryptococcal infections. It is more active against Candida albicans compared with other candidial strains (eg, Candida parapsilosis, Candida glabrata, Candida krusei and Candida tropicalis).

Voriconazole (VRC) is a triazole antifungal agent, which demonstrated good activity against Aspergillus strains, even when resistant to AmB and itraconazole (ITC). As is the case for all triazole antifungal agents, VRC inhibits the fungal enzyme 14 alfa-lanosterol demethylase, which catalyses a key step in the membrane synthesis, namely the conversion of lanosterol to ergosterol.

Voriconazole

Although all the antifungals have some hepatotoxic potential, the imidazoles seem to have a higher incidence; therefore, it is important to determine liver status before prescribing. Of greater concern is the large list of interactions mostly related to cytochrome P450 metabolism, a very long list of prominent drugs, including the statins.

TRIAZOLI

Inibizione deglienzimi coinvolti nellasintesi di ergosteroloda parte dei farmaciAntifunginei azolici, morfolinici e allilaminici.

Meccanismo di resistenza dei funghi agli azoli

1) Alterazione della 14 alfa demetilasi

2) Sovraespressione della lanosterolo demetilasi

3) Alterazione dei sistemi di efflusso

4) Cambiamento della composizione degli steroli di

membranadella cellula funginea

FLUCITOSINA(5-fluorocitosina)

Flucitosinacytosine deaminase

5 fluorouracile

5 fluorouracile 5-fluorodeo5-fluorodeossissiuridinuridinaa monomonoffososffatatoo

InInibizione sintesi DNAibizione sintesi DNA

5 fluorouracileUracil fosforibosil trasferasi

Acido 5 fluoro uridilico

Acido 5 fluoro uridilicoFosforilazione

5-fluoro-UTP5-fluoro-UTP

Incorporato nella sintesi dell‘RNA con risultato di inibizione della sintesi proteica

EchinocandineCaspofungina

Inibizione della sintesi del glucano componente della membrana cellulare

caspofungin, micafungin and anidulafungin

Echinocandina B

Caspofungina Viene somministrata per via endovenosa

MECHANISM OF ACTION AND IN VITRO ACTIVITY

In common with other echinocandins, micafungin inhibits the synthesis of 1,3-b-D-glucan, a major component of fungal cell wall, in a non-competitive, concentration-dependent manner. Micafungin has potent and fungicidal activity against a wide range of Candida spp. in vitro, including fluconazole-resistant Candida spp. and multidrug-resistant Candida spp. residing in biofilms .

Micafungin has poor oral bioavailability and is only available for intravenous administration. The compound is extensively (>99%) bound to plasma proteins, metabolized by the liver, and excretion predominantly occurs via the fecal route.

Meccanismo di resistenza alle echinocandine

Nel gene FKS1 è codificato l’enzima glucano sintasi mentre nel gene GNS1 è codificato un enzima che prende parte alla sintesi (estensione) degli acidi grassi.

Mutazioni genetiche di laboratorio hanno messo in evidenza che la mutazione di questi enzimi porta alla comparsa di resistenza alle echinocandine

Chitin is made by chitin synthases requiring specific microvesicles, the chitosomes, for intracellular transport. Fungi contain several chitin synthases, some of which may be essential at a certain stage. This phenomenon is important to take into account for drug design. The most widely studied chitin synthase inhibitors are polyoxins and nikkomycins that probably bind to the catalytic site of chitin synthases.

La Chitina è un polimero della N-acetilglucosamina, costituente principale della membrana cellulare dei funghi

La Nikkomicina è un inibitore della sintesi della chitina

Sir,Until the last decade, antifungal therapy was based mostly on drugs acting on the fungal membrane, such as amphotericin B and azoles, and the rationale for the use of combination therapy remained questionable.1 Thus, the only drug combination of two antifungals with two modes of activity used clinically, primarily in cryptococcosis, was amphotericin B and 5-fluorocytosine.2 The introduction of echinocandins, which act on the fungal cell wall by inhibiting glucan synthesis, opened the approach to explore different drug combinations, such as echinocandins and polyenes, or echinocandins and azoles,3,4 for various mycoses. Nikkomycin Z inhibits chitin synthesis, by acting as a competitive analogue of chitin synthase substrate UDP-N-acetylglucosamine.3 Since chitin is found in most fungal cell walls, inhibition of its synthesis may be considered as a potentialmeans for antifungal therapy.

Voriconazole is a triazole antifungal agent and is a second generation synthetic derivative of fuconazole; it is effective against yeast and lamentous fungi. The primary mode of action of voriconazole is the inhibition of cytochrome P-450- mediated 14-α-lanosterol demethylation, an essential step in fungal ergosterol biosynthesis and the resulting ergosterol depletion causes fungal cell wall destruction.

J Dtsch Dermatol Ges. 2011 Apr;9(4):274-6. doi: 10.1111/j.1610-0387.2010.07563.x. Epub 2010 Nov 3.

Severe phototoxicity associated with long-term voriconazole treatment.Vöhringer S, Schrum J, Ott H, Höger PH.Department of Pediatric Dermatology, Catholic Children's Hospital Wilhelmstift, Hamburg, Germany.Abstract

Voriconazole is a second-generation triazole antifungal approved for the treatment of invasive fungal infections, particularly with Aspergillus, Candida, Fusarium, and Scedosporium spp. Frequently reported adverse effects of voriconazole include visual disturbance (21 %), elevated liver enzymes (15.6 %) and rashes (7 %), which are largely attributable to drug-induced photosensitivity. We report a case of serious phototoxicity in a 8 year old boy who underwent chemotherapy for AML. He received voriconazole for the treatment and subsequent re-infection prophylaxis after pulmonary aspergillosis. One year after the start of therapy he developed blistering eruptions on his face after minimal sunlight exposure. Recent reports about the development of squamous cell carcinoma and melanoma, respectively, in children during and after oral therapy withvoriconazole seem to warrant systematic follow-up investigations of all voriconazole-treated patients.

Expert Rev Pharmacoecon Outcomes Res. 2010 Dec;10(6):623-36.Pharmacoeconomics of voriconazole in the management of invasive fungal infections.Al-Badriyeh D, Heng SC, Neoh CF, Slavin M, Stewart K, Kong DC.College of Pharmacy, Qatar University, Doha, Qatar.AbstractThe incidence of invasive fungal infection has risen in recent years with the introduction of more intensive chemotherapy regimens and the advent of stem cell and solid-organ transplants. In patients undergoing chemotherapy, mortality rates ranging from 50 to 90% have been associated with documented invasive fungal infection. Voriconazole is a second-generation triazole, which is a synthesized derivative of fluconazole. It was first approved for marketing in the USA in 2002.Voriconazole has excellent bioavailability and is available in oral and intravenous dosage form. It has extended-spectrum antifungal activity whereby it is highly effective against a variety of fungal organisms, including Candida, Fusarium, Paecilomyces and Scedosporium species, but it is especially known for its activity against the Aspergillu s species.Voriconazole has become widely used for three types of treatment strategies (i.e., targeted, empirical and prophylactic). However, voriconazole is a high-cost antifungal agent and, therefore, its effectiveness should be scrutinized, taking into consideration its cost in relation to the costs of other comparable antifungal agents. This article summarizes the 18 identified peer-reviewed publications on the pharmacoeconomics of voriconazole in the English literature, up to March 2010, and provides a view on its future role in therapy. Comparisons with existing antifungals are provided when possible to illustrate the potential role of voriconazole in a clinical setting. The studies took place in a variety of countries and were all retrospective in nature, with the majority suggesting that voriconazole is a more cost-effective option for antifungal treatment. Of the 18 evaluations, 11 were related to the economic impact of voriconazole against invasive aspergillosis only. Economic data to guide the use of voriconazole as prophylaxis or empirical therapy as well as targeted therapy against invasive candidiasis remain limited.

Major information on the best therapeutic strategies forcryptococcal meningoencephalitis derives from therapeutic trialsinvolving HIV-positive [1,2,3] or HIV-negative patients [4].According to the current Infectious Diseases Society of America(IDSA) guidelines, the treatment should depend on anatomic siteand host’s immunological status. Induction therapy using acombination of amphotericin B (AMB, 0.7–1 mg/kg/d) andflucytosine (5FC, 100 mg/kg/d) for 2 weeks followed by aconsolidation phase of 10 weeks by fluconazole (FCZ, 400 mg/d)should be prescribed for central nervous system infection (CNS) inboth HIV-positive and -negative patients, based mostly on dataextrapolated from trials in HIV-infected patients [5] and retrospectivestudies onHIV-negative patients [6,7].

Conclusion: Our results support the conclusion that induction therapy with AMB+5FC for at least 14 daysshould be prescribed rather than any other induction treatments in all patients with high fungal burden at baselineregardless of their HIV serostatus and of the presence of proven meningoencephalitis.

Objectives: Invasive fungal infections are a major cause of mortality among patients at risk. Treatmentguidelines vary on optimal treatment strategies. We aimed to determine the effects of different antifungaltherapies on global response rates, mortality and safety.Methods: We searched independently and in duplicate 10 electronic databases from inception to May2009. We selected any randomized trial assessing established antifungal therapies for confirmed cases ofinvasive candidiasis among predominantly adult populations. We performed a meta-analysis and thenconducted a Bayesian mixed treatment comparison to differentiate treatment effectiveness. Sensitivityanalyses included dosage forms of amphotericin B and fluconazole compared to other azoles.Results: Our analysis included 11 studies enrolling a total of 965 patients. For our primary analysis ofglobal response rates, we pooled 7 trials comparing azoles to amphotericin B, Relative Risk [RR] 0.87 (95%Confidence Interval [CI], 0.78–0.96, P = 0.007, I2 = 43%, P = 0.09. We also pooled 2 trials of echinocandinsversus amphotericin B and found a pooled RR of 1.10 (95% CI, 0.99–1.23, P = 0.08). One study comparedanidulafungin to fluconazole and yielded a RR of 1.26 (95% CI, 1.06–1.51) in favor of anidulafungin. Wepooled 7 trials assessing azoles versus amphotericin B for all-cause mortality, resulting in a pooled RR of0.88 (95% CI, 0.74–1.05, P = 0.17, I2 = 0%, P = 0.96). Echinocandins versus amphotericin B (2 trials) for all causemortality resulted in a pooled RR of 1.01 (95% CI, 0.84–1.20, P = 0.93). Anidulafungin versusfluconazole resulted in a RR of 0.73 (95% CI, 0.48–1.10, P = 0.34). Our mixed treatment comparisonanalysis found similar within-class effects across all interventions. Adverse event profiles differed, withamphotericin B exhibiting larger adverse event effects.Conclusion: Treatment options appear to offer preferential effects on response rates and mortality .When mycologic data are available, therapy should be tailored.

Invasive candidiasis has emerged as an important nosocomial infection, especially in critically ill patients.We review the epidemiology of invasive candidiasis with an emphasis on data from Taiwan. An increasing incidence of candidemia became apparent from 1980 to the end of the 1990s, followed by relative stability.Crude mortality rates of patients with candidemia were in the range of 35% to 60%. Candida albicans remains the predominant cause of invasive candidiasis in Taiwan and accounts for more than 50% of all cases. Candida tropicalis, Candida glabrata and Candida parapsilosis are the three most common nonalbicans Candida species that cause invasive candidiasis. The above four Candida species account for more than 90% of invasive candidiasis in Taiwan. Overall, invasive Candida isolates have remained highly susceptible to fluconazole (> 90% susceptibility) over the past two decades. However, periodic surveillance is needed to monitor antifungal resistance because reduced fluconazole susceptibility in non-albicansCandida is not an uncommon trend. Voriconazole and echinocandins continue to exhibit excellent in vitro activity against invasive Candida isolates. [J Formos Med Assoc 2009;108(6):443–451]

Topical polyene or azole antifungal agents are effective in most cases. Drug choice is dictated by several factors, including the patient’s medical history, oral symptoms and predicted compliance with application method. Some common regimes are given below.Nystatin oral suspension (100 000 units ⁄mL – 1 mL topically), or nystatin pastilles (100 000 IU) four times daily for 7 to 14 days should resolve most local candidal infections. Note that some studies indicate nystatin to be ineffective for Candidal lesions in cancer patients.

http://infection.thelancet.com Vol 6 April 2006