Interest in paromomycin for the treatment of visceral leishmaniasis (kala-azar)

Abstract

Introduction

Leishmaniasis is an important parasitic infection of the blood. It is classified as a protozoan disease, and it is caused by Leishmania spp. Leishmaniasis is found in many countries throughout the world, and it is classified as an important vector-borne infection. The transmission of disease is via a vector: in this case, the bite of a fly. Leishmaniasis transmission can be from an infected human or animal (especially a canine) to another human.1–3 There are two important groups of problematic sand flies: genus Phlebotomus in undeveloped countries, and genus Lutzomyia in more developed areas.1–5 As a result of the nature of vector-borne diseases, vector control is the focus of disease control.6 It is estimated that more than 1 million new cases of leishmaniasis occur each year.7 At present, leishmaniasis is classified as an important neglected tropical disease.8 The disease is highly prevalent in many poor and developing countries. In addition, the extension of the disease into new settings has been reported for the past two decades.8,9 Hence, leishmaniasis is currently a disease of global concern. Another important problem involving the control of leishmaniasis is the difficulty of treating this disease. The problem of drug resistance has emerged in many endemic areas. In recent years, some new drugs have been introduced to fight drug-resistant leishmaniasis. The aim of this article is to provide a critical review of the treatment of visceral leishmaniasis with the new drug paromomycin. This article will discuss several specific aspects of the drug, including both its benefits and its side effects.

Clinical aspects of visceral leishmaniasis

Leishmaniasis is an important vector-borne disease, and it is classified as one of the most important tropical fly-borne infections. This disease can cause two types of clinical manifestations: cutaneous forms10–12 and visceral forms.13–15 The reticuloendothelial system, the spleen, and the liver are the main parts of the body that are affected by visceral leishmaniasis.13–15 In approximately 10% of cases, some additional bone marrow involvement can be observed.1,2 The disease can be both chronic and deadly. Patients usually experience a delay before diagnosis and treatment. Visceral leishmaniasis is common in immunocompromised hosts; thus, it is a focused disease that is currently under surveillance for immunocompromised patients.16 With regard to the epidemiology of visceral leishmanaisis, the endemic areas include the Middle East and South Asia.13–15 Visceral leishmaniasis was previously limited to these endemic areas. However, the emergence of the disease in new settings has been continuously reported for several years.8,9 The migration of disease is an important issue in modern travel medicine.

The diagnosis of visceral leishmaniasis can be difficult, and it is often delayed. In endemic areas, most diagnoses are usually derived from the microscopic examination of tissue smears.14 Better serology and molecular methods are usually not available as a result of resource limitation.14 The management of visceral leishmaniasis still requires good diagnostic and therapeutic approaches. Continuous research and development regarding the treatment of visceral leishmaniasis is needed. At present, the treatment for visceral leishmaniasis requires long courses of medication and parenteral administration.13 The cost of treatment is considered quite expensive in resource-limited settings.13 There is no doubt that medication and medical care are the two main factors that affect the cost-effectiveness ranking of the selection of new treatment.17 Nevertheless, research and development regarding the treatment of visceral leishmaniasis has led to many improvements.18 It is hoped that the use of these new drugs will lead to the complete elimination of visceral leismaniasis.19 In addition, active case-finding and vector-control strategies should not be overlooked; these activities remain very significant for the successful control of visceral leishmaniasis.20

Why do we need a new drug for the treatment of visceral leishmaniasis?

Visceral leishmaniasis is classified as a treatable disease. Early diagnosis and treatment are important to the successful management of patients. With regard to treatment, medical therapy with the use of an antileishmanial drug is the key approach. Antileishmanial drugs have been used for the treatment of visceral leishmaniasis for a long time. However, as time passes, problems with old drugs are detected, and new drugs are needed (Table 1). The classical treatment, which is based on a pentavalent antimony complex, involves frequent drug resistance.13,14 There are many problems with the current treatment of visceral leishmaniasis treatment. These problems lead to poor outcomes of the treatment in general. However, the main concern is the drug treatment.

Problems with drug treatment are common in settings where disease incidence is high. For example, in India, where visceral leishmaniasis is highly prevalent, the problem of drug resistance is common.14 The first classical drug, antimony, is already useless as a result of drug resistance, and has not been used since the 1970s.21 A report by Olliaro et al concluded that “unresponsiveness to antimony has developed steadily in the past to such an extent that antimony must now be replaced, despite attempts to stop its progression by increasing dose and duration of therapy.”22

The second-line drugs pentamidine and amphotericin B remain effective, but their use is limited as a result of toxicity and availability.13,14 Both pentamidine and amphotericin B are more effective for getting rid of the parasites than the classical pentavalent antimony complex. As compared with amphotericin B, pentamidine is easier to use, it has fewer side effects, and it is not light sensitive; hence, it is more widely used. However, the problem of drug resistance is also observed with pentamidine. The failure rate of pentamidine use has been reported to be as high as 33% in India; this has led to the conclusion that this drug is not particularly useful, and the increasing or doubling of the dose is routinely required.23 A combination of drugs is also used for the treatment of leishmaniasis; however, its effectiveness has not been confirmed.24–26 In addition, newer drugs (eg, new lipid formulations of amphotericin B, the new oral drug miltefosine) have been licensed for a few years, but the main problem with these is their cost.13,14 A similar situation is also observed with the use of sodium stibogluconate therapy.27 With all of this information in mind, there is no doubt that new drugs for visceral leishmaniasis treatment are required.

A new drug for the treatment of leishmaniasis: paromomycin

Paromomycin is an antibiotic drug that was introduced for the treatment of visceral leishmaniasis in 2006. It is classified as a new aminoglycoside antibiotic. Paromomycin originated from the bacterial pathogen Streptomyces rimosus var. paromomycinus. It is considered a broad-spectrum antibiotic, and it is also used for the treatment of parasitic infestation.28 With regard to pharmaceutical information,29–33 paromomycin is an aminoglycoside antibiotic. It was first discovered during the 1950s, and it exists as paromomycin sulfate. It is a white and amorphous product. Paromomycin is stable and water soluble. It has been reported that paromomycin can bear heat up to 120°C for 24 hours. However, if it is exposed to heat of 130°C, degradation can be seen, and it loses a third of its biological activity.34 The chemical composition of paromomycin sulfate is 0–2, 6-diamino-2, 6-dideoxy-β-L-idopyranosyl-(1→3)-0-β-D-ribofuranosyl-(1→5)-0-[2-amino-2-deoxy-α-D-glucopyranosyl-(1→4)]-2-deoxystreptamine sulfate salt. The molecular formula is C23H45 N5O14 xH2SO4, and the molecular weight is equal to 615.64. The classical available form of paromomycin in medical marketing is the paromomycin sulfate capsule, and the brand name is Humatin^® (Caraco Pharmaceutical Laboratories, Ltd, Detroit, MI). The paromomycin capsule is for oral intake, and each one contains 250 mg. The newer form of paromomycin, the injection form, was successfully pharmaceutically produced. It is mainly given as an intramuscular injection. This form is widely used for systemic infection. An ointment form has also been prepared for the treatment of local skin infections.35 Finally, the inhalation form of paromomycin has recently been produced, and it is also indicated for the treatment of some systemic infections (eg, cryptosporidiosis).36 The indications for the usage of each form of paromomycin are different (Table 2).

With regard to pharmacokinetics and pharmacodynamics, both the in vitro and in vivo antibacterial actions of paromomycin are high. The drug is as highly effective as neomycin. However, the classical oral form poses the problem of absorption. After oral administration, almost all of the drug cannot be effectively absorbed, and nearly all of the drug is recoverable from the stool; hence, it is useful for the treatment of intestinal infection. With long-term, high-dose treatment, there is also no systematic absorption of oral paromomycin.37 Paromomycin is considered active against several Gram-negative and Gram-positive bacteria, and it is also active against some protozoa and cestodes. At first, paromomycin was indicated for intestinal amebiasis,38–40 and its usage was later expanded for many other infections, including visceral leishmaniasis. Although paromomycin is considered a broad-spectrum antibiotic, it does not affect the pattern of useful intestinal microflora. Iwaki et al reported that, “after administration was discontinued, reduced bowel flora was returned to the normal range within a few days.”41 For the injection form of the drug, the pharmacokinetics study revealed that the peak concentration of paromomycin can be derived 2 hours after administration, and the drug is completely eliminated within 24 hours.42 The elevation of blood urea and blood urea nitrogen can be observed after an intramuscular injection dose of 90 mg/kg.43 The inhibition of protein synthesis by binding to 16S ribosomal RNA is the main drug action.43 Fourmy et al reported that paromomycin binding resulted in a local conformational change in the A site of 16S ribosomal RNA.44 The detected changes at the N1 positions of A1492 and A1493 on the minor groove side of the A-site RNA implied a mechanism of action that occurred during translation.44 In conclusion, the main action of paromomycin is the inhibition of translation.44,45

It is generally recommended that paromomycin be used for the treatment or prevention of infections that are proven to be caused by a susceptible pathogen. This reduces the chance of the development of drug-resistant bacteria, and it maintains the effectiveness of the drug. Paromomycin is contraindicated for those patients with a history of previous hypersensitivity reactions (eg, drug allergy) and intestinal obstruction (for the oral form). Cross reactivity to neomycin can be seen, and this is an important precaution to remember when using paromomycin.46 The standard dosage for oral paromomycin is 25 to 35 mg per kilogram of body weight daily. The administration of the drug should be done in three divided doses with meals, and the use of the drug should be continuous for 5 to 10 days. Some adverse reactions or side effects of paromomycin can be seen; the important ones include nausea, abdominal cramps, and diarrhea. The chance of developing a side effect significantly increases in any patients who receive a dose of more than 3 g per day.

Recently, advancements in pharmacology have allowed for the development of a newer modified version of paromomycin. The so-called “paromomycin-loaded albumin microsphere” has been in use for a few years. The preparation of paromomycin-loaded albumin microspheres (ie, <5 μm) helps to better target macrophages for treatment. This is useful for the treatment of leishmaniasis.47 Khan et al reported that “pharmacokinetic studies demonstrated nearly 80% reduction in C_(max) of paromomycin when administered as paromomycin-loaded albumin microsphere, compared to other formulations at equivalent dose.”43 In addition, it has been observed that there are no symptoms of toxicity with the use of paromomycin-loaded albumin microspheres at the level that was reported to be toxic for classical paromomycin.43 According to a clinical trial by Thakur et al, it has been confirmed that injectable paromomycin is effective and safe for the treatment of patients with visceral leishmaniasis.48

Efficacy of paromomycin in the treatment of leishmaniasis

Paromomycin, which was introduced in 2006, can be thought of as a new candidate for the treatment of leishmaniasis.49–51 Sundar and Chakravarty stated that “paromomycin, with its excellent efficacy, low cost, shorter duration of administration and good safety profile, has the potential to be used as a first-line drug.”52 Indeed, based on the nature of broadspectrum antibiotics as previously described, paromomycin is useful for the treatment of many infections. For the treatment of leishmaniasis, paromomycin is one of two new recommended drugs, in addition to miltefosine, which was introduced in 2002.53

For visceral leishmaniasis, a paromomycin intramuscular injection can be effectively used. It can also be effective for patients with resistance to other drugs, including sitamaquine.54 There are many recent trials, in both animals and humans, that have looked at the treatment of visceral leishmaniasis with paromomycin. The pioneering study of the effects of paromomycin on visceral leishmaniasis in rats was reported by Buffet et al.55 In this study, a good efficacy of paromomycin was observed; this study was the origin for the further development of this drug for visceral leishmaniasis treatment. A continuous study by Williams et al in a rat model also confirmed the antileishmanial activity of the drug both in vitro and in vivo.56 The effectiveness of the widely used injection regimen has also been confirmed for humans.48 Chunge et al studied several regimens for the treatment of visceral leishmaniasis and concluded that “treatment with aminosidine [paromomycin] alone was the cheapest and safest regime.”57 A 21-day course of 20 mg per kilogram of body weight per day should be used as first-line treatment for visceral leishmaniasis.58–61 A reduction of liver and spleen size can be observed an average of 2 years after treatment, and the weight gain seen among patients taking this drug is a sign of a good response.61 Generally, the complete disappearance of the parasite can be seen 6 to 7 months after drug administration.62 The efficacy of paromomycin is equal to that of amphotericin B. It has also been noted that paromomycin is not inferior to amphotericin B.63 The severe adverse effects, especially nephrotoxicity and fever, are significantly lower in patients who are receiving paromomycin as compared with those who are receiving amphotericin B.63 Nevertheless, some adverse effects (eg, the elevation of liver enzymes, pain at the infection site) are more common among patients who are receiving paromomycin.63,64 In addition, dermal leishmaniasis after visceral leishmaniasis has also been reported as a cutaneous manifestation after treatment.65

It should be noted that paromomycin is considered cost-effective from a pharmacoeconomic perspective. On the basis of a recent assessment from India, it has been reported that “paromomycin is the cheapest option ($7450 to treat 1000 patients).”66 This is equal to “US$2 for paromomycin in an outpatient setting.”67 Nevertheless, paromomycin monotherapy poses a risk for the development of drug resistance.68 Therefore, the use of combination therapy is recommended for the management of visceral leishmaniasis that is aiming at successful control. Banerjee et al concluded that, “once the elimination target of one case per 10,000 population has been reached, combination therapies involving miltefosine and paromomycin can be introduced to ensure long-term availability of several drugs for visceral leishmaniasis and to protect against resistance.”69

As noted previously, newer, modified paromomycin given via the liposome technique is also available for the treatment of visceral lesihmaniasis.68 Paromomycin-associated stearylamine-bearing liposome is the best example of this.70

Future trends in the use of paromomycin for the treatment of visceral leishmaniasis

There can be no doubt that paromomycin will be used worldwide for the treatment of visceral leishmaniasis as a result of its good effectiveness. However, the problem of drug resistance will continue to grow if there is no control of appropriate, rational usage. The continuum for the development of a new generation of paromomycin involves the hope for a better and safer drug for the management of visceral leishmaniasis.

Conclusion

Paromomycin is an old antibiotic that has been newly approved for use in the treatment of leishmaniasis. The use of paromomycin treatment has been confirmed for its efficacy and safety in the management of patients with visceral leishmaniasis. This drug is inexpensive, and it has been accepted as a first-line alternative drug in the setting of resistance to classical antileishmanial drugs.

Footnotes

References