Ruel, Theodore D. MD*; Kakuru, Abel MD†; Ikilezi, Gloria MD†; Mwangwa, Florence MD†; Dorsey, Grant MD, PhD‡; Rosenthal, Philip J. MD‡; Charlebois, Edwin MPH, PhD‡; Havlir, Diane MD‡; Kamya, Moses MMed, PhD§; Achan, Jane MPeds, PhD‖
*Department of Pediatrics, University of California, San Francisco, CA;
†Infectious Diseases Research Collaboration, Kampala, Uganda;
‡Department of Medicine, University of California, San Francisco, San Francisco, CA; and
Departments of §Medicine;
‖Pediatrics and Child Health, Makerere University College of Health Sciences, Kampala, Uganda.
Correspondence to: Theodore D. Ruel, MD, Division of Infectious Disease, Department of Pediatrics, UCSF-Benioff Children's Hospital, University of California, San Francisco, 500 Parnassus Avenue, San Francisco, CA 94143-0136, (e-mail: firstname.lastname@example.org).
Supported by the Eunice Kennedy Shriver National Institute of Child Health and Human Development (P01HD059454 and T.D.R.: K23HD60459) at the National Institutes of Health. Lopinavir/ritonavir was donated by AbbVie.
Presented in part at the 18th (March 2, 2011, Boston, MA) and 20th (March 5, 2013, Atlanta, GA) Conferences on Retrovirus and Opportunistic Infections.
T.D.R. and J.A. contributed significantly to the design of the study, acquisition and interpretation of data, and drafted/edited the article. A.K., G.I., and F.M. contributed significantly to the acquisition of data and edited the article. G.D., P.J.R., D.H., and M.K. contributed significantly to the design of the study, acquisition and interpretation of data, and edited the article. All authors approved the final version.
The authors have no conflicts of interest to disclose.
Clinical Trial Registration: Prevention of Malaria and HIV disease in Tororo (PROMOTE) pediatrics trial registration: NCT00978068.
Supplemental digital content is available for this article. Direct URL citations appear in the printed text and are provided in the HTML and PDF versions of this article on the journal's Web site (www.jaids.com).
Received July 25, 2013
Accepted November 10, 2013
In the Prevention of Malaria and HIV disease in Tororo (PROMOTE) pediatrics trial, HIV-infected Ugandan children randomized to receive lopinavir/ritonavir (LPV/r)-based antiretroviral therapy (ART) experienced a lower incidence of malaria compared with children receiving nonnucleoside reverse transcriptase inhibitor (NNRTI)-based ART.1 Although LPV/r has direct antiplasmodial activity in vitro,2 the decreased malaria incidence in the LPV/r arm of PROMOTE was driven primarily by a reduction in the recurrence of malaria after treatment with artemether–lumefantrine, stemming from a beneficial pharmacologic interaction that prolonged the half-life of lumefantrine.1 Children receiving LPV/r also had a lower prevalence of gametocytemia, suggesting that wider use could lead to decreased malaria transmission.3
The results of PROMOTE-pediatrics suggest that expanded use of LPV/r for the treatment of HIV-infected children living in areas of high malaria endemicity settings could be a rational policy. However, the HIV-related outcomes of LPV/r- compared with NNRTI-based ART must also be considered. In 1 randomized trial of infants aged less than 36 months, LPV/r-based ART led to superior virologic outcomes compared with NNRTI-based ART, but results from trials in older children were equivocal, and some data have suggested that LPV/r may be associated with impaired CD4 recovery.4,5
In this study, we report results of the protocol-specified noninferiority comparison of the proportion of children with HIV RNA levels <400 copies per milliliter after 48 weeks of ART. To assess the durability of virologic efficacy, we compared time to confirmed virologic failure over 96 weeks. We additionally compared changes in CD4+ T-cell measures and adverse event incidence during the follow-up period.
Details about the PROMOTE-pediatrics trial, including eligibility criteria and the study protocol have been published (Clinical Trial Registration: NCT00978068).1 In brief, this was an open-label randomized clinical trial designed to determine if the use of LPV/r-based ART would reduce malaria incidence compared with the use of NNRTI-based ART. Subjects were HIV-infected children aged at least 2 months but less than 6 years living in Tororo, Uganda, who were either ART-naive and ART-eligible per Ugandan guidelines or ART-experienced, receiving NNRTI-based first line ART with an HIV RNA level <400 copies per milliliter in the preceding 6 months. Children aged less than 2 years who had been exposed to maternal nevirapine (NVP) and/or received NVP as perinatal transmission prophylaxis were excluded because use of an NNRTI as treatment would be clinically contraindicated.
At enrollment, children were randomized 1:1 to receive LPV/r plus 2 nucleoside reverse transcriptase inhibitors (NRTIs) or an NNRTI plus 2 NRTIs. In the NNRTI arm, NVP was used for all children aged <3 years and efavirenz (EFV) for most children aged >3 years. NRTIs were zidovudine or abacavir plus lamivudine (3TC); stavudine was also used initially, but then replaced by AZT or abacavir after 2009, in accordance with changes in Ugandan and WHO guidelines.6 NVP was dosed at 160-200 mg/m2 (maximum 200 mg) once daily for the first 14 days and then twice daily.7,8 EFV was dosed as 15 mg/kg (maximum 600 mg) once daily.8 LPV/r was dosed by weight bands per 2008 United States Department of Health and Human Services guidelines.7
Children were followed at the study clinic with monthly routine visits and for all acute illnesses at the study clinic. CD4 counts and percentages (FACS Calibur; BD Biosciences, San Jose, CA) and HIV RNA levels (COBAS Amplicor HIV-1 Monitor Test v1.5 and Ampliprep Taqman Assay; Roche Molecular Diagnostics, Pleasanton, CA, and Abbott m2000 RealTime PCR; Abbott Molecular Diagnostics, Wiesbaden, Germany) were determined every 12 weeks for the first year and every 24 weeks thereafter. Adherence was assessed using 3-day recall at each routine visit and calculated as the percentage of prescribed doses reportedly taken. Children who had persistent HIV RNA levels of >400 copies per milliliter had in-depth adherence assessments, with changes to second-line ART made on a case-by-case basis, per Ugandan guidelines.
The primary outcome for this analysis, the proportion of children with virologic suppression (HIV RNA level <400 copies/mL) after 48 weeks was compared by test of proportions. Because the primary aim of the PROMOTE-pediatrics trial was to compare efficacy in malaria prevention, the study sample size was based on estimates of malaria incidence. To compare virologic efficacy between arms, we chose to use a noninferiority analysis and prespecified a noninferiority margin of −11% in the difference between arms in the proportion with HIV RNA level <400 copies per milliliter with a 95% confidence interval (CI). Analyses were per-protocol to minimize the risk of falsely concluding no difference between arms (type II error). However, we also analyzed the primary outcome using modified intention-to-treat techniques, in which children were categorized according to originally assigned study arm, and those who died, were lost to follow-up, or had missing data at 48 weeks were considered to have not suppressed. The proportions with virologic suppression were also compared at 96 weeks per-protocol. To assess the durability of virologic efficacy up to 96 weeks, we generated a Kaplan–Meir survival model of time to virologic failure, stratified by ART status at enrollment, with virologic failure defined at the time of the first of 2 successive HIV RNA >400 copies per milliliter (after a minimum of 24 weeks of treatment for ART-naive children), and compared risk of failure by arm using a log-rank test. Means of CD4 measures and adherence were compared using Student t test with 2-tailed P values. The incidence of Division of AIDS (National Institute of Allergy and Infectious Diseases)9 grade III or IV adverse events was compared using negative binomial regression using all available follow-up time and per-protocol approaches. Children were enrolled from September 2009 through October 2011; data accumulated up to October 1, 2012 were included in these analyses. Stata Version 11 was used for all analyses (StataCorp, College Station, TX).
PROMOTE-pediatrics was approved by the Makerere University School of Medicine Research and Ethics Committee, the Uganda National Council for Science and Technology, and the University of California, San Francisco, Committee for Human Research.
After screening 421 children, 185 children were enrolled (Fig. 1) with 91 initiating LPV/r-based ART and 92 initiating or continuing NNRTI-based ART (33 EFV, 59 NVP). At enrollment, the median age of the cohort was 3.1 years (range, 0.4–5.9) and 131 (71%) were ART-naive. Baseline characteristics of the children who initiated therapy were similar between arms (Table 1). The mean (range) of total follow-up time per subject was 109 (0–156) weeks. At monthly routine assessments, mean reported adherence was 99.5% in both arms (P = 0.99).
A total of 91 (99%) of children in the LPV/r arm and 85 (89%) of children in the NNRTI arm remained in follow-up at 48 weeks, the time point of the primary analysis. One child discontinued study medication due to an adverse reaction (Stevens–Johnson Syndrome after 3 weeks of therapy with NVP). Eight children withdrew from the NNRTI arm and 1 from the LPV/r arm (Fig. 1), all due to inability to comply with study procedures, and none related to medication tolerance. HIV RNA levels at 48 weeks were missing from 13 children (7 LPV/r and 6 NNRTI) due to missed study visits or laboratory problems.
The proportion of children with virologic suppression at 48 weeks was 80% (67/84) in the LPV/r arm compared with 76% (59/78) in the NNRTI arm, corresponding to a difference of 4.1% with a 95% CI of –8.7% to 17%, thereby excluding the prespecified noninferiority margin of −11%. In modified intention-to-treat analysis, the proportion of children with virologic suppression was 74% (67/91) in the LPV/r arm compared with 65% (60/92) in the NNRTI arm (difference of 8.4%; 95% CI: −4.9% to +22%).
The proportion of children with virologic suppression at 96 weeks was 89% (46/52) in the LPV/r arm vs. 84% (41/49) in the NNRTI arm (difference: 4.8%, 95% CI: −9% to 18%) in per-protocol analysis. Of the 124 children enrolled with at least 96 weeks of follow-up (Fig. 1), 6 had changed from NNRTI to LPV/r and 18 children were missing HIV RNA levels due to laboratory error or missed visits (LPV/r: 10, NNRTI: 8).
A total of 37 children developed confirmed virologic failure by 96 weeks (Fig. 2; see Figure S1, Supplemental Digital Content, http://links.lww.com/QAI/A491). Among the ART-naive, the 96-week virologic failure rate was 26% (95% CI: 17% to 39%) in the LPV/r arm and 28% (18% to 41%) in the NNRTI arm (Log-rank test P = 0.8) in survival modeling. Among the ART-experienced, the 96-week virologic failure rate was 8% (95% CI: 2% to 27%) in the LPV/r arm and 12% (4% to 32%) in the NNRTI arm (Log-rank test P = 0.6).
Compared with the NNRTI arm, a greater portion of the children who developed virologic failure in the LPV/r arm subsequently achieved virologic suppression after adherence counseling. Of the 18 children with virologic failure in the LPV/r arm, 14 (78%) subsequently achieved virologic suppression after adherence counseling. In contrast, of the 19 with virologic failure in the NNRTI arm, only 4 (21%) subsequently achieved virologic suppression (P = 0.0006). A total of 6 children switched to second-line ART (all from NNRTI to LPV/r); 5 achieved virologic suppression and 1 did not yet have follow-up viral load testing.
ART-naive children experienced comparable increases in CD4 counts, with mean change from baseline to 48 weeks of 405 cells per microliter (SD, 324) for the LPV/r arm and 426 cells per microliter (498) for the NNRTI arm (P = 0.7); similar recovery in CD4 percentage was also seen, with mean (SD) change of 11.8 (7.4) in the LPV/r arm and 13.3 (7.1) in the NNRTI arm (P = 0.27). Among the ART-experienced, there were mean (SD) losses in CD4 count at 48 weeks for both the LPV/r [−296 (610)] and NNRTI arms [−5.8 (733)] (P = 0.13), but CD4 percentages showed mean improvements: LPV/r [0.5 (8.8)], NNRTI [3.5 (9.5)] (P = 0.23). There were no significant differences in mean CD4 number or percentage between arms at any time point (all P values >0.05) (Figs. 3A, B; see Figure S2a and 2b, Supplemental Digital Content, http://links.lww.com/QAI/A491). There was a trend toward lower mean CD4 counts among ART-experienced children randomized to LPV/r vs. NNRTI at 48–96 weeks, but CD4 percentages remained comparable at all time points.
Division of AIDS grade 3 or 4 adverse events were rare, and there were no significant differences in their incidence between the 2 ART arms (see Table S1, Supplemental Digital Content, http://links.lww.com/QAI/A491). Neutropenia (<750 cells/μL) and thrombocytopenia (<50,000/μL) were the most commonly reported adverse events. There were 47 neutropenia events (24.0 per 100 person-years) in the LPV/r arm and 51 (28.3 per 100 person-years) in the NNRTI arm. The rate of grade 3 or 4 elevated alanine aminotransferase was slightly higher in children in the NNRTI arm compared with the LPV/r arm (3.32 vs. 1.53 events per person-year, respectively, P = 0.26). There was 1 permanent ART change in a patient who developed Stevens–Johnson Syndrome while receiving NVP. One patient changed from NVP to EFV due to hepatitis. Two children (1 from each arm) temporarily changed to EFV to avoid interactions with therapy for tuberculosis. There were 4 deaths, none attributed to study medications. Two children with severe malnutrition (1 each randomized to NVP and LPV/r) died within 6 weeks of enrollment of unclear causes; they had been admitted to the hospital and provided with nutritional supplementation. One child died of measles complicated by pneumonia (NVP) despite measles vaccination. One child experienced a sudden death of unclear etiology (EFV).
Our finding of comparable virologic outcomes in children receiving LPV/r and NNRTI-based ART supports to the idea that LPV/r-based ART could be used to treat HIV-infected African children while also preventing malaria. We previously showed that children in the LPV/r arm of this study experienced a lower incidence of malaria,1 primarily due to a reduction in the incidence of recurrent malaria after treatment with artemether–lumefantrine. It is thus important to note that the benefits of LPV/r in malaria prevention would only apply to areas where artemether–lumefantrine is in use. But, artemether–lumefantrine is recommended by the WHO as first line treatment for malaria and is in use throughout much of Africa.10 With the results present here, we show that the antimalarial benefits of LPV/r for HIV-infected children in this setting did not come at a cost of virologic or CD4+ T-cell recovery.
Comparable virologic outcomes for protease inhibitor (PI) vs. NNRTI-based ART have been reported from larger randomized trials in adults and children. In the optimal combination therapy after NVP exposure (A5208) trial, NVP and LPV/r-based ART lead to the same rate of virologic failure or death (14% vs. 14%, hazard ratio, 0.97; 95% CI: 0.6 to 1.6) among 500 ART-naive HIV-infected African women without previous exposure to single-dose NVP.11 In the PENPACT 1 trial, 263 HIV-infected children randomized to either NNRTI- or PI-based ART had similar proportions with HIV RNA <400 copies per milliliter throughout follow-up.12 However, in the IMPAACT p1060 trial, the HIV-infected infants (without perinatal exposure to NVP) randomized to receive NVP had an elevated risk of virologic failure (confirmed HIV RNA >400 copies/mL) or death by 24 weeks (hazard ratio, 2.51; 95% CI: 1.41 to 4.47) and a trend toward lower rates of suppression (HIV RNA <400 copies/mL) at 48 weeks (75% vs. 85%, respectively, P = 0.06) compared with infants receiving LPV/r.5 Our study did not confirm the superiority of LPV/r reported in the p1060 trial, but we did note trends in favor of the LPV/r. Differences between our results and those of p1060 are likely explained, at least in part, by the age differences between our and their cohorts (median 3.1 vs. 1.8 years, respectively). If we restrict our analyses to include only children aged <3 years (n = 75), the rates of virologic suppression are more in favor of LPV/r as reported in p1060 (data not shown). Also of note, the older children in the NNRTI arm of our study received EFV, which has been associated with superior outcomes compared with NVP in African children.13
The good outcomes of children switching from NNRTI to LPV/r-based ART in our study add to limited data on the safety of switching ART in children with virologic control.14–18 HIV-infected children occasionally need to change ART due to adverse events, anticipated drug interactions, or formulation availability. Previous studies have demonstrated safety in changing from PI to EFV15 or NVP4,18-based ART, but to the best of our knowledge, no randomized trials have previously reported on the safety of switching from NNRTI- to PI-based ART among children with virologic suppression.
We observed a notable difference between treatment arms in the outcomes of children recognized to have virologic failure. Most children in the LPV/r arm ultimately achieved suppression with adherence counseling and without a change in ART, but most children in the NNRTI arm continued to fail despite counseling. This could be the result of the lower barrier to resistance seen with NNRTI's compared with PIs such as LPV/r19 or reflect ongoing issues of poorer tolerance and adherence to NNRTI's. This finding highlights the importance of early recognition of adherence problems and the role that frequent HIV RNA level testing could play in identifying those at risk for resistance.
Virologic failure rates by 96 weeks were >25% in both treatment arms. The reasons for such high failure rates are uncertain, but adherence issues were identified in the majority of cases. Caregivers received adherence counseling before treatment initiation and at every monthly visit. Adherence was reported at 99.5% over all clinic visits, but we believe that caregiver reports were inflated. When a case of virologic failure was identified, additional counseling was performed and in difficult cases, counselors visited the homes of families to help them problem solve. In some cases, adherence was improved with simple changes in practice such as substituting tablets for liquids. But, in other cases, socioeconomic factors presented greater challenge and no clear solution, such as the case of the single mothers who assigned responsibility for medication administration to young siblings. Our experience suggests that treatment programs in similar settings should devote as much effort as resources allow to adherence support to optimize ART outcomes.
Consideration of the optimal first line ART for HIV-infected African children must take into account not only the response to initial therapy but also the consequences of failure on resistance mutation accumulation and the response to second-line therapy. Our ability to assess the long-term implications of study regimens would have been improved with information about the accumulation of resistance mutations and additional data about the outcomes of children on the second-line therapy. Some studies have shown good responses to PI-based therapy after NNRTI-based ART in Africa, but data are limited in children.20–22 One small retrospective study showed poorer virologic responses when NNRTIs were used as second-line following PIs, compared with when PIs followed NNRTIs.23 However, in PENPACT 1, which took place in Europe and North and South America, children who received PIs (vs. NNRTI) as first line had fewer NRTI mutations at the time of virologic failure and good suppression rates in response to NNRTI-based second-line treatment.4
We also compared changes in CD4 measures by treatment arm. In HIV-infected adults, several studies have suggested that PIs,24–26 and LPV/r in particular,27 may be associated with improved CD4 count recovery. Conversely, some data suggest impaired CD4 responses in children receiving LPV/r compared with NNRTI-based ART. Among the NVP-exposed infants in the p1060 trial, the LPV/r arm demonstrated a trend toward lower CD4 percentages recovery at 48 weeks28 compared with the NNRTI arm. In the NEVEREST trial, ART-experienced infants receiving LPV/r were randomized to either continue LPV/r or switch to NVP; a greater portion of those who stayed on LPV/r experienced a 10% decline in CD4 percentage at 52 weeks (15% vs. 3%).4 The marginal differences in CD4 measures that have been reported are of unclear clinical significance, but suggest the possibility of an interaction of LPV/r with lymphocyte recovery. In this trial, we did not find significant differences in CD4 count or percentage between the arms of our study. ART-experienced LPV/r-treated children had lower median CD4 counts, with a net decline from baseline to 48 weeks but CD4 percentages remained notably stable.
Both NNRTIs and LPV/r were well tolerated in our study, with only 1 grade III/IV adverse event leading to permanent discontinuation. As in other trials of NNRTIs and PIs in children, the most common adverse event was neutropenia, but the clinical consequences of these events seem to have been minor.5,28 All cases resolved without complications in our study. Indeed, high rates of reported neutropenia may also reflect genetic and/or geographic differences that lead to relatively low neutrophil levels in Ugandan, compared with North American children.29 There is some concern that LPV/r may impair growth; greater change in weight-for-age Z score was seen in children receiving NNRTIs compared with those receiving PIs in the p1060 trial. In our trial, severe malnutrition was noted in only 1 patient, who died before initiating medications, but detailed analyses of impacts of study drugs on growth are ongoing.
Considering our results, what is the role for LPV/r in the treatment of HIV-infected African children? The cost of LPV/r has declined dramatically over the past decade, and there is wider access to pediatric formulations.30 Clinical trials have yielded varying results about whether LPV/r is superior to NNRTIs. At the moment, it may be that LPV/r use should be targeted to the populations of children in which it has shown particular benefit. The World Health Organization now recommends LPV/r over NNRTIs as the first-line therapy for all HIV-infected children aged younger than 3 years.31 The results of PROMOTE-pediatrics suggest that the use of LPV/r- over NNRTI-based ART could lower the incidence of malaria for HIV-infected children aged up to 6 years living in malaria-endemic regions where artemether–lumefantrine is the malaria treatment of choice.1 And for a malaria-endemic country, the relatively higher cost of LPV/r compared with NNRTs may be offset by the avoidance of malaria-associated medications, hospitalizations, and mortality. As the use of LPV/r expands in Africa, it will be important that data about clinical outcomes and the declining cost of LPV/r continue to be evaluated in the development of treatment guidelines.
The authors would like to acknowledge the children and families and study team of PROMOTE-pediatrics for the time and effort that made the trial possible. The authors thank Albert Plenty for his assistance with statistical analysis.
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