http://orcid.org/0000-0001-9154-8327
Figures
Abstract
Background
We investigated the relationship of treatment regimens for visceral leishmaniasis (VL) with post-kala-azar dermal leishmaniasis (PKDL) and visceral leishmaniasis relapse (VLR) development.
Methods
Study subjects included cohorts of patients cured of VL since treatment with monotherapy by sodium stibogluconate (SSG), miltefosine (MF), paromomycin intramuscular injection (PMIM), liposomal amphotericin B [AmBisome (AMB)] in a single dose (SDAMB) and in multidose (MDAMB), and combination therapies by AMB+PMIM, AMB+MF, and PMIM+MF. Follow up period was 4 years after treatment. Cohorts were prospective except SSG (retrospective) and MF (partially retrospective). We compared incidence proportion and rate in 100-person-4year of PKDL and VLR by treatment regimens using univariate and multivariate analysis.
Findings
974 of 984 enrolled participants completed the study. Overall incidence proportion for PKDL and VLR was 12.3% (95% CI, 10.4%–14.5%) and 7.0% (95% CI, 5.6%–8.8%) respectively. The incidence rate (95% CI) of PKDL and VLR was 14.0 (8.6–22.7) and 7.6 (4.1–14.7) accordingly. SSG cohort had the lowest incidence rate of PKDL at 3.0 (1.3–7.3) and VLR at 1.8 (0.6–5.6), followed by MDAMB at 8.2 (4.3–15.7) for PKDL and at 2.7 (0.9–8.4) for VLR.
Interpretation
Development of PKDL and VLR is related with treatment regimens for VL. SSG and MDAMB resulted in less incidence of PKDL and VLR compared to other treatment regimens. MDAMB should be considered for VL as a first step for prevention of PKDL and VLR since SSG is highly toxic and not recommended for VL.
Author summary
Post-kala-azar Dermal Leishmaniasis (PKDL), a sequale of visceral leishmaniasis (VL), and reappearance VL (visceral leishmaniasis relapse, VLR) are intra-epidemic reservoirs of VL and threats control of VL in long run. Currently there is no strategy for prevention of PKDL and VLR. If a relationship between treatment for VL and development of PKDL and VLR is there, and then selection of proper treatment regimen for VL should prevent PKDL and VLR. So far no study has been carried out to investigate the relationship between treatment regimens for VL and development of PKDL and VLR. The study demonstrated that multi-dose liposomal amphotericin B (AmBisome) defined as MDAMB herein for VL results in least PKDL and VLR among all existing and recommended by WHO treatment regimens for VL. We recommend adaptation of MDAMB in the national visceral leishmaniasis elimination program for VL cases management during subsequent phases of the national program when VL burden is low and hospitalization of VL patients for 3-5-days is now feasible.
Citation: Mondal D, Kumar A, Sharma A, Ahmed MM, Hasnain MG, Alim A, et al. (2019) Relationship between treatment regimens for visceral leishmaniasis and development of post-kala-azar dermal leishmaniasis and visceral leishmaniasis relapse: A cohort study from Bangladesh. PLoS Negl Trop Dis 13(8): e0007653. https://doi.org/10.1371/journal.pntd.0007653
Editor: Jesus G. Valenzuela, National Institute of Allergy and Infectious Diseases, UNITED STATES
Received: April 17, 2019; Accepted: July 23, 2019; Published: August 15, 2019
Copyright: © 2019 Mondal et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are available within the manuscript and its Supporting Information files.
Funding: This study was funded by the Bill & Melinda Gates Foundation. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Visceral leishmaniasis (VL) or kala-azar has been a public health problem in Bangladesh over the centuries [1]. About 150,000 people have suffered from VL since 1994 in Bangaldesh [2]. Victims of VL are the poorest of the poor living in the rural areas of the country. The epidemiology of VL in Bangladesh, India, and Nepal is similar. In these three countries, the protozoan parasite Leishmania donovani (LD) is the only causative agent of VL, humans are the only reservoir, and the female Phlebotomas argentipes sandfly is the only vector. In 2005, these three countries signed a memorandum of understanding to eliminate VL as a public health problem by 2015, targeting to keep VL incidence less than 1 per 10 000 people at upazila (sub-district), block and district levels in Bangladesh, India and Nepal respectively [3]. However, the target was not achieved in 2015. Current WHO Road Map aims to eliminate Neglected Tropical Diseases including VL by 2020 [4]. Bangladesh and Nepal achieved the target in 2016 and 2013 respectively.
VL peaks periodically in the Indian subcontinent; this is known as the natural trend of VL [5]. It is believed that during inter-epidemic periods, cases of post-kala-azar dermal leishmaniasis (PKDL) fuel the transmission of LD in endemic communities. PKDL is a sequel of infection by LD parasite; it develops mostly among patients who have been treated for VL [6–7]. PKDL also may develop among individuals with asymptomatic infection with the parasite [7]. Hypopigmented macular, papular, and nodular or combined skin lesion are the key clinical features of PKDL [6]. Skin lesions usually do not itch and have intact skin sensitivity. Patients with PKDL are clinically healthy and usually do not seek medical care unless they are stigmatized by their lesions. Patients with PKDL harbor the parasite in their skin for years and are infective to sandflies [8–9]. In this way, they continue transmission of LD in the community and threaten VL control in long run. Failure to control PKDL, therefore, is a substantial challenge to the success of the South-East Asia Region Kala-azar Elimination Programme (KAEP) [10].
Visceral leishmaniasis relapse (VLR) is defined as the reappearance of VL after complete cure at 6 months after treatment. VLR patients have higher concentration of the parasite in their peripheral blood compared to that of new VL patients, are infective to sandflies, sustain transmission of the infection, and threaten VL control [9, 11]. Therefore, VLR also present challenges for controlling VL in the long run. To date, there are no preventive strategies against PKDL and VLR development.
Sodium stibogluconate (SSG) for 6 months or miltefosine (MF) for 84 days are current treatment options for PKDL [10]. Both drugs are toxic, and serious adverse events associated with them are common [6, 12]. Further, efficacy with either treatment does not exceed 90% and relapse after treatment with MF also has been reported [10]. Therefore, a strategy to prevent PKDL is urgently needed. Incomplete treatment for VL has been shown as a risk factor for PKDL in Nepal [13]. A study in India found that VL patients living in areas with high arsenic exposure are more prone to develop PKDL [14]. Immune gene polymorphism has been associated with the development of PKDL in Sudan [15]. An association between SSG treatment for VL and PKDL development has been speculated [16]. However, subsequent reports showed that PKDL also developed after treatment of VL with MF, paromomycin intramuscular injection (PMIM), and liposomal amphotericin B [AmBisome (AMB)] [17–19]. To date, there has been no study of the relationship between treatment for VL and development of PKDL and VLR.
SSG was the only drug for treatment of VL for more than 70 years. Later, MF, PMIM, and AMB either in monotherapy or in combination of any two drugs were introduced for treatment of VL [20–23]. In this study, we aim to investigate the relationship of PKDL and VLR development to VL treatment among cured VL patients treated with different treatment regimens.
Methods
Study site, design, population, enrolment, and follow-up of study subjects
The study site was Mymensingh, the most VL-endemic district in Bangladesh. This was a cohort study which included cured VL patients treated with different treatment regimens for new VL (please see below). Duration of the study was October, 2014 to December, 2018. Study participants were enrolled after a study initiation meeting, investigator training, and training of field staff in diagnosis of suspected PKDL and VLR. Using clinical trial logs and hospital records (only for MF cohort), study participants were actively searched and identified at their current places of residence. They were invited to participate in the study to complete four years of follow-up, as well as provide information regarding VLR and PKDL (if any) since treatment for VL. Trained field research assistants followed up study subjects through home visits every 3 months until completion of the 4-year follow-up period. The study physician referred suspected PKDL/VLR cases to the study clinic, Surya Kanta Kala-azar Research Centre, for medical examination, confirmation, and management.
Study cohort types and sample size
SSG cohort.
200 new VL patients were treated in the trial “A Pilot Study for Capacity Building for a Multi-centre, Randomized Trial for Treatment of Kala-Azar in Bangladesh,” which was conducted from July 2007 to January 2009 in the Community Based Medical College Hospital, Mymensingh [NCT01240473]. Patients received SSG at a dose of 20 mg/kilogram body weight/day as a single intramuscular injection for 28 days. SSG cohort included 168 cured patients from this trial. This was a completely retrospective cohort; more than 4 years had passed since all participants in this cohort were treated for VL.
MF cohort.
The National Kala-azar Elimination Programme of Bangladesh (NKEP) used oral MF (Impavido) monotherapy for treatment of new VL from 2009 to mid 2013. MF cohort included 150 cured VL patients who had been diagnosed and treated with MF monotherapy, following the NKEP case management guideline, in the Muktagacha Upazila Health Complex in Mymensingh from April 2010 to July 2013 [24]. Adult patients and children aged 12 years and weighing ≥25 kg received 50 mg MF cap twice/day for 28 days. Children less than 12 years old with body weight <25 kg received oral MF at a dose of 2.5 mg/kilogram/day for 28 days. 60/150 subjects in this cohort had retrospective follow-up; the rest had prospective follow-up.
PMIM cohort.
The trial titled “Effectiveness study of Paromomycin IM Injection (PMIM) for the treatment of visceral leishmaniasis (VL) in Bangladesh” was a phase IIIb, open-label, multicenter, single-arm trial where 120 new VL patients were treated with PMIM at a dose of 11 mg/kilogram/day for 21 days (NCT01328457) from February 2011 to June 2012 [23]. PMIM cohort had 105 subjects.
SDAMB cohort.
300 VL patients received treatment with liposomal amphotericin B [AmBisome (AMB)] under an open-label, single-arm trial of a feasibility study (CTRN12612000367842) in the Muktagacha Upazila Health Complex from February 2012 to February 2013 [20]. AMB was applied in a single intravenous infusion at a dose of 10 mg/kilogram body weight for at least 3 hours. SDAMB cohort had 126 subjects.
MDAMB and combination (AMB+PMIM, PMIM+MF, and AMB+MF) cohorts: The study “Safety and efficacy of short course combination regimens with AmBisome, miltefosine and paromomycin for the treatment of visceral leishmaniasis (VL) in Bangladesh” was conducted in the upazila health complexes of Mymensingh from August 2010 to April 2014 (NCT01122771). The study used and compared four treatment regimens for VL [22]. The treatment regimens (and number of patients) were:
- AMB at a dose of 5 mg/kilogram/day on days 1, 3, and 5 (N = 159). For the present study, we assigned 126 cured patients from this regimen to the MDAMB cohort.
- Combination of single intravenous infusion of AMB at a dose of 5mg/kilogram followed by PMIM at 11 mg/kilogram body weight/day (AMB+PMIM) for 10 days (N = 159). AMB+PMIM cohort had 126 cured patients for the current study.
- Combination of single intravenous infusion of AMB at a dose of 5 mg/kilogram on day 1 followed by oral MF (AMB+MF) at above mentioned dosage/day for 7 days (N = 142). We enrolled 126 cured patients from this treatment regimen in the AMB+MF cohort of the present study.
- Combination of PMIM for 10 days and oral MF (PMIM+MF) for 7 days in above mentioned doses (N = 142). We enrolled 126 cured patients from this treatment in the PMIM+MF cohort of the present study.
Case definitions
A suspected PKDL patient was a person with history of kala-azar and skin lesions; a probable PKDL case was a suspected PKDL case with positive rK39 test; and a confirmed PKDL case was a probable PKDL case with LD parasite documented either by slit skin examination, culture, or polymerase chain reaction. Probable and confirmed PKDL cases were eligible for treatment following the national guideline for kala-azar [24].
A suspected case of VLR was a case of cured VL with fever for more than 2 weeks and splenomegaly. A confirmed case of VLR was a suspected case of VLR with LD bodies in spleen aspirates documented by microscopy/LD DNA in spleen aspirates or peripheral blood buffy coat.
Statistical analysis
A standard data management plan has been developed by the experts at Clinical data management centre, Christian Medical College (CMC), Vellore, India. Oracle Clinical (OC) version 4.6.6 was used to design web-based dual data entry system following the annotated Case Report Form (CRF) of this study. External monitors checked and approved all CRFs before data entry. Data management team at CMC further scrutinized dual entered data and generated data clarification forms which were clarified by the data management and field team in icddr,b. Following data quality control checks, the data management team at CMC provided a final clean data set for analysis. We used Chi-square test for comparing proportions of various socio-demographic variables of the study participant between different cohorts. Comparison of mean/median between cohorts was done by parametric or non-parametric test where applicable. We calculated both the incidence proportion and rate (100-person-4years) of PKDL and VLR. Finally we performed a Cox-proportional hazard model using SSG cohort with least incidence of PKDL and VLR as reference to investigate the independent risk factor(s) for development of PKDL and VLR. Data were analysis using STATA 13.
Ethics statement
The icddr,b Ethical Review Committee, Western Institutional Review Board (WIRB), and PATH Research Ethics Committee approved the study. Informed voluntary written consent from adults and assent from children between 11 and 17 years old were obtained for their participation. In cases of study participants who were less than 11 years old, consent from a parent/legal guardian was also obtained.
Results
Study population characteristics
974/984 enrolled subjects completed the study, indicating 1% lost to follow-up (Table 1).
Study cohorts differed significantly in terms of age groups, sex, education level, monthly expenditure, family size, house type, ownership of cattle and bed-nets, and bed-net use (Table 2).
These variables were taken as covariates for multivariate analysis later.
Burden, risk factor, and trend for PKDL
121/984 developed PKDL (mean, 95% CI, 12.3%, 10.4%–14.5%) with a median time 2.6 years (IQR, 1.84–3.12). The incidence proportion (mean, 95% CI) with PKDL was lowest in the SSG (3.0%, 1.2%–7.0%), followed by the MDAMB (8.0%, 4.2%–14.7%), MF (9.3%, 5.6%–15.2%), AMB+PMIM (10.7%, 6.1%–18.1%), SDAMB (15.9%, 10.4%–23.5%), AMB+MF (16.2%, 10.2%–24.7%), PMIM (19.1%, 12.5%–27.9%), and PMIM+MF (22.9%, 15.7%–32.0%) (Table 3). The SSG differed significantly from all other cohorts, except the MDAMB cohort.
All 984 participants contributed 1 370 628 days of observation, with a mean of 1393 days (95% CI, 13 80–1406) when cohorts were looked for PKDL development. The average incidence rate (100-person-4years) of PKDL was 14.0 (8.6–22.7). SSG cohort had lowest incidence rate (3.0, 1.3–7.3), followed by the MDAMB (8.2, 4.3–15.7), MF (9.7, 5.7–16.4), AMB+PMIM (11.3, 6.4–19.9), SDAMB (16.9, 10.9–26.2), AMB+MF (17.1, 10.6–27.5), PMIM (20.1, 13.0–31.2), and PMIM+MF (25.3, 16.9–37.7) (Table 3). Incidence rate of PKDL of SSG and MDAMB cohorts did not differ significantly.
Assuming SSG cohort as a reference we analyzed Cox Proportional Hazard Ratio for other cohorts for development of PKDL (Table 4). The average (95% CI) hazard ratio adjusted for confounders for development of PKDL was 2.7 (0.9–8.1), 3.4 (1.2–9.5), 3.5 (1.2–10.0), 5.8 (2.1–15.8), 6.0 (2.2–16.4), 6.2 (2.3–16.7), and 8.0 (3.0–21.1) for MDAMB, MF, AMB+PMIM, SDAMB, AMB+MF, PMIM, and PMIM+MF, respectively (Table 4). The MDAMB’s hazard ratio did not differ statistically significantly with the reference cohort. However, hazard ratio of all other cohorts was statistically significant (Table 4). We did not find any covariates as a statistically significant factor for PKDL development (Table 4). Further, when compared existing treatment regimens excluding SSG and using MDAMB as a reference, all treatment regimens had higher hazard ratio for PKDL which was statistically significant for AMB+MF, PMIM and PMIM+MF (Table 5), borderline significant for SDAMB and statistically insignificant MF and AMB+PMIM (Table 5).
The average trend for development of PKDL peaked at year 3 since treatment for VL (Fig 1). Interestingly, when stratified by cohorts, the PMIM, AMB+MF, and MDAMB cohorts showed upward trends for PKDL development (Fig 1).
Burden, risk factor, and trend for VLR
Of the 984 participants, 69 had VLR with a median time 1.05 years (IQR, 0.77–1.53) for 1 364 974 person-days of observation (mean 95% CI, 1387, 1371–1404) (Table 6).
Overall incidence proportion of VLR was 7% (95% CI, 7.0%, 5.6%–8.8%). The SSG cohort had lowest incidence proportion (mean, 95% CI) for VLR (1.8%, 0.6%–5.5%), followed by the MDAMB (2.7%, 0.8%–8.0%), AMB+PMIM (3.6%, 1.3%–9.3%), PMIM+MF (4.8%, 2.0%–11.1%), AMB+MF (6.7%, 3.2%–13.5%), SDAMB (7.9%, 4.3%–14.2%), PMIM (14.3%, 8.7%–22.5%), and MF arms (14.7%, 9.8%–21.4%).
The overall incidence rate (100-person-4years) of VLR was 7.6 (95% CI, 4.1–14.7). SSG cohort had lowest VLR incidence rate (rate, 95%CI) (1.8, 0.6–5.6), followed by the MDAMB (2.7, 0.9–8.4), AMB+PMIM (3.7, 1.4–9.8), PMIM+MF (5.0, 2.1–12.0) AMB+MF (7.0, 3.3–14.7), SDAMB (8.4, 4.5–15.6), PMIM (16.0, 9.6–26.5), and MF (16.3, 10.7–24.7) cohorts (Table 6). The Cox proportional hazard ratio (mean, 95% CI) for VLR incidence adjusted for covariates considering the SSG arm as reference, was lowest for the MDAMB arm (1.3, 0.3–6.3), followed by the AMB+PMIM (1.9, 0.4–8.7), PMIM+MF (2.2, 0.5–9.2), AMB+MF (3.5, 0.9–13.5), SDAMB (3.5, 1.0–13.0), MF (7.5, 2.2–25.6), and PMIM (7.7, 2.2–27.1) cohorts (Table 7). The hazard ratio of the MDAMB, AMB+PMIM, PMIM+MF, AMB+MF, and SDAMB arms for VLR was higher but statistically insignificant, but the higher hazard ratio of the MF and PMIM arms was statistically significant (Table 7). None of the covariates had any significant association with VLR development. Using MDAMB as a reference we found higher but statistically insignificant hazard ration for VLR of AMB+PMIM, PMIM+MF, AMB+MF and SDAMB whereas hazard ration for VLR of MF and PMIM was six times higher and statistically significant (Table 8). The overall trend of VLR peaked at 1 year and then declined thereafter. The VLR trend had a similar pattern for all study arms (Fig 2).
Discussion
Key findings of the current study are: there was a significant relationship between the treatment regimens for VL and the development of PKDL and VLR; and the socio-demographic factors investigated in this study did not have any relationship with PKDL nor with VLR development. The study is unique and included all treatment regimens so far for VL.
SSG was the only treatment for VL for a century. It became less efficacious over time due to parasite resistance to SSG. Further, the World Health Organization (WHO) Expert Committee on the Control of Leishmaniases (WHOECCL) does not recommend SSG for VL due to its long treatment duration and severe toxicity [25]. Though SSG for VL was protective against PKDL and VLR, we do not recommend this treatment for VL due to its severe toxicity. The SSG cohort, however, served as reference—as a cohort with the lowest burden of PKDL and VLR and facilitated comparison of PKDL and VLR by other treatment regimens. In our study, SSG resulted in 3.0% (95% CI, 1.3–7.3) incidence of PKDL. A study in Nepal reported a little higher incidence of PKDL after SSG treatment for VL at 5.4%. It also found incomplete treatment for VL as a risk factor for PKDL.13 The difference between the two studies can be explained by the difference in study designs and populations. In our study, all patients had complete treatment with SSG; this was not case in the Nepalese study. A population-based study in Bangladesh found a cumulative incidence of PKDL of 17% for 5 years [7]. The study had 1002 VL patients treated with SSG, MF, and AMB. The study did not stratify PKDL incidence by treatment regimens.
MF monotherapy was introduced in the KAEP after successful completion of phase III and phase IV studies [26–27]. Decreased efficacy of MF; high rate of treatment incompliance; adverse reactions, including renal toxicity and hepatotoxicity; and the availability more safe and effective drug (AMB), led the WHOECCL not to recommend MF monotherapy for treatment of VL.25 The highest rate of VLR after MF monotherapy in this study (16.3%), further justify the recommendation of the WHOECCL [25].
PMIM monotherapy was developed by the One World Health for treatment of VL [23]. We observed very high rates of PKDL (20%) and VLR (16%) with this treatment for VL. Our observation supports the WHOECCL, which did not recommend PMIM monotherapy for VL [25].
Availability of AMB, a highly safe and effective drug for treatment of VL, changes the scenario for VL case management. Currently, this is the drug of choice for VL case management in the KAEP. AMB is expensive; the national programs of Bangladesh, India, and Nepal get it as a donation from the developer Gilead Sciences, Inc. through WHO.
The KAEP has three phases: the attack phase, consolidation phase, and maintenance phase [24]. During the attack phase, the VL case burden was 21 times higher than the VL elimination target [28]. Bangladesh and Nepal completed the attack phase and achieved the target. AMB in a single intravenous infusion at a dose of 10 mg/kilogram body weight is the first treatment option for VL in Bangladesh. This treatment regimen was particularly suitable in the attack phase due to its high safety and efficacy for VL, 100% compliance, and 1 to 2 days of patient hospitalization. During the attack phase of the NKEP when VL burden was very high, SDAMB was the most suitable VL treatment option. However, our study highlighted a concern about its continuation during the consolidation and maintenance phases of the program, as it resulted in a very high incidence of PKDL (17%) and VLR (8.4%).
Combination therapy with AMB+MF, AMB+PMIM, and PMIM+MF was introduced for treatment of VL by the Drugs for Neglected Diseases initiative. Present study provides important findings for the first time that PKDL and VLR also develop after different combination therapies for VL. The AMB+MF and PMIM+MF combinations resulted in a very high incidence of PKDL, 17% and 25% respectively. The combination of AMB+PMIM gave better results; the rate of PKDL and VLR was 11.3% and 3.7% respectively. Among the combination regimens, AMB+PMIM had the least incidence of PKDL and VLR. It is interesting that combination therapies showed different patterns in terms of PKDL and VLR development.
The MDAMB treatment regimen for VL had the lowest incidence of PKDL and VLR compared to all other treatment regimens except SSG. MDAMB resulted in 8.2% PKDL and 2.7% VLR for 4 years. The less incidence of PKDL by MDAMB compared to that by SDAMB could be explained by the findings from a recent experimental study. The study found that the skin pharmacokinetics of AmBisome was different when AmBisome was given as a single dose and as a multidose for treatment of murine cutaneous leishmaniasis [29]. AmBisome when it was given in a multidose it resulted in a better accumulation of the drug in the skin, more reduction in skin parasite load and skin lesion size [29]. A study in India reported even less incidence of PKDL after treatment of VL with MDAMB at a dose of 20 mg/kilogram body weight. Our MDAMB cohort received 15 mg/kilogram body weight of AMB for treatment of their VL. The study in India had PKDL cases who passively reported to the health facility. Therefore, there may have been under-reporting; this could be another reason for the lower PKDL incidence in that study [30].
All cohorts showed a similar trend for VLR: VLR peaked in the first year after treatment. However, PKDL development peaked in the third year after treatment for VL, but this was not the case when results were stratified by treatment regimens. The PKDL trend continued upward with MDAMB, PMIM, and AMB+MF. This necessitates follow-up of cured VL patients for at least 3 years by the NKEP for early detection of PKDL and VLR cases. This also demands longer observation MDAMB, PMIM, and AMB+MF cohorts to find the moment of a downward trend.
Our study has some limitations. The entire SSG and partial MF arms were retrospective cohorts, whereas all other arms were prospective cohorts. The SSG and MF arms were conducted when the VL burden was comparatively higher in the country. Since PKDL and VLR are consequences of VL, it would bias study results if the study aimed to survey the PKDL/VLR burden in the community. Our study aimed to investigate the PKDL/VLR incidence only in cured VL patients; therefore, results are free from biases related to time. Another limitation of the study is that the mean days of observation differed in the arms due to different sample sizes. Therefore, a cohort with higher mean days of observation should have a higher incidence of PKDL/VLR. Interestingly, the SSG arm had the highest mean days of observation and the least incidence of PKDL and VLR. The treatment regimen therefore dictated the incidence of PKDL and VLR. The study had been carried out using cured VL patients of the clinical trials in Bangladesh. So, external validity of the study is yet to be established and its results may not be generalizable for other countries.
In summary, SSG and MDAMB for VL had least incidences of PKDL and VLR. MDAMB had least hazard ratio for PKDL development compare to other treatment regimens. Since SSG is no more recommended for VL, MDAMB should be the choice for VL in the consolidation and maintenance phases of the NKEP in Bangladesh until better molecules than AMB are found. Therefore, we highly recommend MDAMB for treatment of VL for NKEP in Bangladesh during its consolidation and maintenance phases.
Acknowledgments
We express our gratitude to Dr. Raj Shankar Ghosh and Dr. Philippe Desjeux for their kind advice and guidance during the inception phase of the study.
References
- 1. Bern C, Chowdhury R. The epidemiology of visceral leishmaniasis in Bangladesh: prospects for improved control. Indian J Med Res 2006; 123 (3): 275–88. pmid:16778310
- 2. Chowdhury R, Mondal D, Chowdhury V, Faria S, Alvar J, Nabi SG et al. How far are we from visceral leishmaniasis elimination in Bangladesh? An assessment of epidemiological surveillance data. PLoS Negl Trop Dis 2014; 8 (8): e3020. pmid:25144317
- 3.
World Health Organization (WHO) Regional Office for South-East Asia (SEARO). Regional strategic framework for elimination of kala-azar from the South-East Asia region (2005–2015). New Delhi: WHO SEARO; 2005. http://apps.searo.who.int/pds_docs/b0211.pdf (accessed March, 24, 2019).
- 4.
World Health Organization (WHO). Accelerating work to overcome the global impact of neglected tropical diseases: a roadmap for implementation. Geneva: WHO; 2012: pp. 1–37. https://www.who.int/neglected_diseases/NTD_RoadMap_2012_Fullversion.pdf (accessed March, 24, 2019).
- 5. Singh OP, Hasker E, Boelaert M, Sundar S. Elimination of visceral leishmaniasis on the Indian subcontinent. Lancet Infect Dis 2016; 16:e304–9. pmid:27692643
- 6. Zijlstra EE, Musa AM, Khalil EAG, el-Hassan IM, el-Hassan AM. Post-kala-azar dermal leishmaniasis. Lancet Infect Dis 2003; 3 (2): 87–98. pmid:12560194
- 7. Islam S, Kenah E, Bhuiyan MA, Rahman KM, Goodhew B, Ghalib CM, et al. Clinical and immunological aspects of post-kala-azar dermal leishmaniasis in Bangladesh. Am J Trop Med Hyg 2013; 89 (2): 345–53. pmid:23817330
- 8. Molina R, Ghosh D, Carrillo E, Monnerat S, Bern C, Mondal D et al. Infectivity of post-kala-azar dermal leishmaniasis patients to sand flies: revisiting a proof of concept in the context of the kala-azar elimination program in the Indian subcontinent. Clin Infect Dis 2017; 65 (1): 150–3. pmid:28520851
- 9. Mondal D, Bern C, Ghosh D, Rashid M, Molina R, Chowdhury R et al. Quantifying the infectiousness of post-kala-azar dermal leishmaniasis towards sandflies. Clin Infect Dis 2018. pmid:30357373
- 10. Zijlstra EE, Alves F, Rijal S, Arana B, Alvar J. Post-kala-azar dermal leishmaniasis in the Indian subcontinent: a threat to the South-East Asia Region Kala-azar Elimination Programme. PLoS Negl Trop Dis 2017; 11 (11): e0005877. pmid:29145397
- 11. Hossain F, Ghosh P, Khan MAA, Duthie MS, Vallur AC, Picone A et al. Real-time PCR in detection and quantitation of Leishmania donovani for the diagnosis of Visceral Leishmaniasis patients and the monitoring of their response to treatment. PLoS One 2017; 12 (9): e0185606. pmid:28957391
- 12. Hossain MS, Kumar A, Hossain AFMA, Mahshin M, Sharma A, Hossain MA et al. Using focused pharmacovigilance for ensuring patient safety against antileishmanial drugs in Bangladesh’s National Kala-azar Elimination Programme. Infect Dis Poverty 2018; 7 (1): 80. pmid:30099967
- 13. Uranw S, Ostyn B, Rijal A, Devkota S, Khanal B, Menten J et al. Post-kala-azar dermal leishmaniasis in Nepal: a retrospective cohort study (2000–2010). PLoS Negl Trop Dis 2011; 5 (12): e1433. pmid:22206030
- 14. Das S, Mandal R, Rabidas VN, Verma N, Pandey K, Ghosh AK et al. Chronic arsenic exposure and risk of post kala-azar dermal leishmaniasis development in India: a retrospective cohort study. PLoS Negl Trop Dis 2016; 10 (10): e0005060. pmid:27776123
- 15. Farouk S, Salih MA, Musa AM, Blackwell JM, Miller EN, Khalil EA et al. Interleukin 10 gene polymorphisms and development of post kala-azar dermal leishmaniasis in a selected Sudanese population. Public Health Genomics 2010; 13 (6): 362–7. pmid:20051670
- 16. Croft SL. PKDL—a drug related phenomenon? Indian J Med Res 2008; 128 (1): 10–1. pmid:18820352
- 17. Koley S, Mandal RK, Choudhary S, Bandyopadhyay A. Post-kala-azar dermal leishmaniasis developing in miltefosine-treated visceral leishmaniasis. Indian J Dermatol 2013; 58 (3): 241.
- 18. Pandey K, Das VN, Singh D, Das S, Lal CS, Verma N et al. Post-kala-azar dermal leishmaniasis in a patient treated with injectable paromomycin for visceral leishmaniasis in India. J Clin Microbiol 2012; 50 (4): 1478–9. pmid:22278840
- 19. Das VN, Pandey K, Singh D, Forwood C, Lal CS, Das P. Development of post-kala-azar dermal leishmaniasis in AmBisome treated visceral leishmaniasis: a possible challenge to elimination program in India. J Postgrad Med 2013; 59 (3): 226–8. pmid:24029204
- 20. Mondal D, Alvar J, Hasnain MG, Hossain MS, Ghosh D, Huda MM et al. Efficacy and safety of single-dose liposomal amphotericin B for visceral leishmaniasis in a rural public hospital in Bangladesh: a feasibility study. Lancet Glob Health. 2014; 2 (1): e51–7. pmid:25104636
- 21. Sundar S, Chakravarty J, Agarwal D, Rai M, Murray HW. Single-dose liposomal amphotericin B for visceral leishmaniasis in India. N Engl J Med 2010; 362: 504–12. pmid:20147716
- 22. Rahman R, Goyal V, Haque R, Jamil K, Faiz A, Samad R et al. Safety and efficacy of short course combination regimens with AmBisome, miltefosine and paromomycin for the treatment of visceral leishmaniasis (VL) in Bangladesh. PLoS Negl Trop Dis 2017; 11 (5): e0005635. pmid:28558062
- 23. Jamil KM, Haque R, Rahman R, Faiz MA, Bhuiyan AT, Kumar A et al. Effectiveness study of Paromomycin IM Injection (PMIM) for the treatment of visceral leishmaniasis (VL) in Bangladesh. PLoS Negl Trop Dis 2015; 9 (10): e0004118. pmid:26496648
- 24.
Ahmed B-N, chief ed. National guideline for kala-azar case management May, 2013. Dhaka: Kala-azar Elimination Program, Directorate General of Health Services, Ministry of Health and Family Welfare, Government of the Peoples Republic of Bangladesh; 2013. pp. 5–12. http://kalacorebd.com/wp-content/uploads/2016/04/KA-Managment-Guideline-18-05-2013_v10-1.pdf (accessed March, 24, 2019).
- 25.
Control of the leishmaniases: report of a meeting of the WHO Expert Committee on the Control of Leishmaniases, Geneva, 22–26 March 2010. Geneva: World Health Organization; 2010. WHO Technical Report Series 949. https://apps.who.int/iris/bitstream/handle/10665/44412/WHO_TRS_949_eng.pdf;jsessionid=1D498E949591171BAD06D9B0F0149DC8?sequence=1 (accessed month, date, year).
- 26. Rahman M, Ahmed BN, Faiz MA, Chowdhury MZ, Islam QT, Sayeedur R et al. Phase IV trial of miltefosine in adults and children for treatment of visceral leishmaniasis (kala-azar) in Bangladesh. Am J Trop Med Hyg 2011; 85 (1): 66–9. pmid:21734127
- 27. Bhattacharya SK, Sinha PK, Sundar S, Thakur CP, Jha TK, Pandey K et al. Phase 4 trial of miltefosine for the treatment of Indian visceral leishmaniasis. J Infect Dis 2007; 196 (4): 591–8. pmid:17624846
- 28. Mondal D, Singh SP, Kumar Narendra, Joshi A, Sundar S, Das P et al. Visceral leishmaniasis elimination programme in India, Bangladesh, and Nepal: Reshaping the case finding/case management strategy. PLoS Negl Trop Dis 3(1): e355. (accessed August, 06, 2019) pmid:19159009
- 29. Wijnant GJ, Van Bocxlaer K, Yardley V, Harris A, Murdan S, Croft SL. Relation between skin pharmacokinetics and efficacy in AmBisome treatment of murine cutaneous leishmaniasis. Antimicrobial Agents and Chemotherapy 2018; 62: 1–9.
- 30. Burza S, Sinha PK, Mahajan R, Sanz MG, Lima MA, Mitra G et al. Post Kala-Azar dermal leishmaniasis following treatment with 20 mg/kg liposomal amphotericin B (Ambisome) for primary visceral leishmaniasis in Bihar, India. PLoS Negl Trop Dis 2014; 8 (1): e2611. pmid:24392171