Single-Tablet Regimens in HIV Therapy

Abstract

Combined antiretroviral therapy (cART) has evolved considerably over the past decades leading to a better control of human immunodeficiency virus replication. Recently, regimens have evolved so as to simplify dosing frequency and reduce pill burden to improve adherence. Several national and international guidelines suggest antiretroviral (ARV) regimen simplification as a method of improving adherence. Decreased cART adherence has been associated with both patient-related factors and regimen-related factors. Adherence rates are statistically higher when simpler, once-daily (OD) regimens are combined with smaller daily regimen pill burdens. The avoidance of selective non-adherence, where a patient takes part of a regimen but not the full regimen, is a further potential benefit offered by single-tablet regimens (STRs). Simplification of cART has been associated with a better quality of life (QoL). Although tempered by other factors, better adherence, higher QoL and patients’ preferences are all key points which might combine to assure long-lasting efficacy and durability of cART. All studies underlined the favorable tolerability profile of newer STRs. Three STRs are currently available. Tenofovir (TDF) plus emtricitabine (FTC)/efavirenz (EFV) was the first OD complete ARV regimen available as a STR. TDF plus FTC/rilpivirine is a second-generation STR. The most recently approved STR, TDF plus FTC/cobicistat/elvitegravir, is the first non-nucleoside reverse transcriptase inhibitor-based STR. All of them have shown excellent efficacy; safety and tolerability have been improved by more recent formulations. Several other STRs are anticipated both combining completely different drugs, abacavir (ABC) plus lamivudine (3TC)/dolutegravir, utilizing innovative formulations of older drugs, tenofovir alafenamide fumarate, or taking advance of bioequivalent drugs, lamivudine (3TC) plus ABC/EFV. The future challenge would be to develop completely alternative STRs (including for example protease inhibitors or new molecules) to extend the advantages of simplicity to heavily pre-treated individuals.

Electronic supplementary material

The online version of this article (doi:10.1007/s40121-014-0024-z) contains supplementary material, which is available to authorized users.

Introduction

Combination antiretroviral therapy (cART) has evolved considerably over the past two decades leading to better control of human immunodeficiency virus (HIV), preservation of the immune system and decreased incidence of opportunistic infections, malignancies and deaths. However, successful implementation of cART has been hampered by complicated regimens, high pill burden, drug–drug interactions and frequent short- and long-term adverse effects, leading to decreased adherence to prescribed regimens. Over time, the development of better-tolerated drugs with low or no dietary restrictions and fewer drug interactions has favored the success of cART and to further improve adherence, regimens have evolved so as to simplify dosing frequency and reduce pill burden. Early cART regimens were based on the administration of more than 25 pills, 3 times per day. Combination products consisted initially of partial regimens mostly combining two nucleoside reversed transcriptase inhibitors (NRTIs) such as zidovudine/lamivudine (3TC), abacavir (ABC)/3TC or tenofovir (TDF)/emtricitabine (FTC) or a boosted protease inhibitor (PI) lopinavir/ritonavir (RTV), but, in 2006, the first single-tablet regimen (STR), a combination of TDF/FTC/efavirenz (EFV) became available [1] and, since then, STRs have been regarded as relevant tools to manage chronic HIV infection. The most advanced regimens used nowadays involve a single pill administered daily. The US guidelines now recommend that providers, when choosing between regimens of similar efficacy and tolerability, use once-daily (OD) regimens for treatment-naïve patients beginning cART, switch treatment-experienced patients receiving complex or poorly tolerated regimens to OD regimens, and use fixed-dose combinations (FDCs) and STRs to decrease pill burden [2].

The analysis in this article is based on previously conducted studies, and does not involve any new studies of human or animal subjects performed by any of the authors.

STR and Adherence

Several national and international guidelines underscore the importance of simplifying antiretroviral (ARV) regimens. The Spanish guidelines suggest that switching to a STR in stable patients currently receiving 2 NRTIs and a PI and RTV offers added advantages in terms of treatment adherence and that the use of STRs is the most efficient strategy to prevent selective treatment non-adherence [3], that is the possibility for a patient to consume less pills than those effectively prescribed. The Italian guidelines recommend the use of STRs and FDCs to improve durability of virologic suppression and to reduce the risk of developing resistance [4]. The European AIDS Clinical Society (EACS) guidelines recommend switching virologically suppressed patients for toxicity, to prevent long-term toxicity, and for simplification of a regimen.

Therapeutic switches must always be performed within a context of known viral resistance and it must always be kept in mind that any drug combination has its toxicological profile and that by switching it, it is possible to replace one set of toxicities with another. Nevertheless, it has been shown that the performance of patients who switched to an STR compared to patients remaining on a more complex regimen is superior, both in terms of virological response and persistence [5, 6].

Patient adherence is a problem in any chronic illness. A review of 76 studies across a wide range of therapeutic areas that measured adherence using electronic monitoring has revealed that compliance rates in clinical trials are lower than previously assumed and that the number of prescribed doses per day is inversely related to compliance. According to electronic monitoring methods, the overall adherence rate was 71 ± 17%. Adherence to OD regimens was significantly higher than with 3-times-daily and 4-times-daily regimens, which reinforces the principle of simplicity [7].

Decreased cART adherence is associated either with patient-related factors such as substance abuse, stress and depression, and with regimen-related factors. Regimen complexity includes the number of pills (pill burden), pill size, frequency and timing of doses, dietary and/or water requirements or restrictions, adverse events (AEs), medication storage requirements, number of prescriptions, number of copayments, refills, and medication bottles as well as the influence of these or other factors on the patient’s lifestyle. Pill count, dosing frequency, and AEs have the greatest impact on patients’ perceived ability to adhere to ARV medication regimens [8]. The exact rate of adherence necessary for cART treatment success is uncertain. Some studies indicate a minimum effective adherence rate of 80%, although a higher level (at least 95%) is considered ideal [9, 10]. More recent experience has shown that the relationship between treatment adherence and viral load suppression as well as resistance development can vary among drug classes [11–13].

Several studies have shown that patients prefer OD regimens and simpler schedules [14–18]. A meta-analysis of 11 randomized, controlled trials on a total of 3029 subjects revealed that the adherence rate to cART was better with OD regimens, although the difference in adherence between OD and twice-daily (BID) regimens was modest (2.9%) [19].

Nevertheless, adherence rates are statistically higher when simpler (OD) regimens are combined with smaller daily regimen pill burdens [20]. This statement is well elucidated by results of the ADONE (ADherence ONE pill; NCT #00990600) study which just simplified treatment in HIV-controlled patients by reducing the number of pills without changing the pharmacological content. One month after the simplification from TDF + 3TC/FTC + EFV to TDF/FTC/EFV STR, the adherence rate increased significantly to 96.1% from a baseline value of 93.8% (p < 0.01); the increment was steadily maintained throughout the study (96.2% at 6 months) [21].

It has been shown that patients on a fixed-dose regimen of EFV/FTC/TDF were 2.1 times more likely to have complete adherence than patients on other regimens [22], that patients on a OD STR consistently achieve higher adherence levels than patients on ≥2 pills per day regimens [23] and that STR was significantly better at achieving ≥90% adherence rates when compared with other multi-pill regimens (MPRs) (p < 0.05 all comparisons), despite an OD schedule or the use of FDCs [24].

With the methodological limits of a cohort study, in a commercially insured population of patients with HIV starting first-line cART, those beginning treatment with TDF/FTC/EFV had significantly better adherence and were more likely to be persistent with therapy than those beginning treatment with an EFV-based regimen other than TDF/FTC/EFV or a nevirapine (NVP)-based regimen [25]. Even among homeless or marginally housed patients, those receiving a single pill per day (TDF/FTC/EFV) had better virologic outcomes and a 26% increase in adherence, compared with those on MPRs [12].

The avoidance of selective non-adherence (taking some, but not all components in a given regimen) should be regarded as a further potential benefit of STRs. Selective non-adherence has been related to several clinical and economic drawbacks [14, 26, 27]. The COMPACT study [27] has shown that, independently from the type of cART, patients reported a complete non-adherence rate of about 20%; however, patients on multi-drug regimens added an adjunctive 3–13% (according to the regimen) selective non-adherence. That made the difference statistically significant in favor of STRs. More relevant, patients receiving a STR had a more effective control of HIV replication (96% of subjects below the limit of detection) and a better immune status (61% above 500 cells/mcl). Comparing partial (or selective) adherence of MPRs to STRs it has been demonstrated that complete non-adherence is relatively similar across regimens, while partial adherence is present with any MPR and doubles the risk of incomplete daily dosing [23].

Although the reduction of pill burden and dosing frequency has been associated to higher adherence rates, this may be only partially effective as drugs’ tolerability and the occurrence of drug-related AEs may strongly undermine adherence. [16, 28–33].

Interestingly, a study in the Balearic Islands, showed a higher risk of AEs, some more severe in intensity as a consequence of the decision to administer ARV FDCs as separate components to reduce costs. Many of these AEs were neuropsychiatric disorders possibly related to EFV in stable patients who previously tolerated this drug. As a result, unlike the desired objective of cost saving, the disruption of ARV FDCs led to an increase of health care expenditure [34].

Adherence is also a cornerstone of persistence. Persistence is the length of time patients remain on a specific ARV regimen and is a key tenet to achieve long-term treatment success. NNRTI-based regimens exhibited greater persistence than PI-based ones. Among the specific regimens, TDF/FTC/EFV provided the longest persistence [35]. As successive ARV regimens have exhibited progressively shorter durability, optimizing the duration of the first regimen in treatment-naïve patients is of utmost importance. OD regimens had greater longevity than those taken BID or more frequently and the shift to newer, more convenient and better-tolerated therapeutic options has induced, over the last few years, a remarkable increase in the durability of first regimens [36].

STR and Quality of Life (QoL)

As cART options have increased and HIV-infected patients are living longer, the improvement or maintenance of health-related QoL has become an increasingly important goal of the management of chronic HIV infection. The maintenance of QoL passes through HIV medications use [37]. Simplification of cART has been shown to maintain or increase the QoL. Switching virologically suppressed subjects from their existing PI-based or NNRTI-based regimen to TDF/FTC/EFV STR was associated with maintained QoL and better treatment adherence. Patients referred an improved ease of use and an increment of treatment satisfaction after the switch to STR that was associated to a sustained improvement of several commonly encountered HIV-related symptoms [5].

One of the secondary objectives of the ADONE study was to verify the effect of the simplification strategy on QoL. The results confirmed an improvement of QoL over time from 68.8% to 72.7% (p = 0.042) and this change was significantly associated with the perception of health status and presence, number and intensity of reported AEs (p < 0.0001). Also, QoL significantly influenced adherence (p < 0.0001) [21].

The switching boosted PI to rilpivirine (RPV) in combination with truvada as a STR (SPIRIT) study evaluated the switch from a PI-based cART to a STR (TDF/FTC/RPV) in chronically suppressed HIV patients. The study explored several patient-reported outcomes mostly dealing with symptoms often related to chronic therapies. After switching to STR, a general significant improvement of these symptoms was observed [6].

Better adherence, higher QoL and patients’ preferences are all key points which may combine to assure long-lasting efficacy of cART.

STR and Cost-Effectiveness

Adherence is strictly correlated to hospitalization, as demonstrated in different studies. Completely adherent patients are less likely to be hospitalized or to require emergency room care than non-adherent patients [22].

Patients who achieve a 95% adherence threshold have a significantly lower rate of hospitalization compared with patients who are non-adherent to therapy, regardless of their pill burden. Furthermore, patients who received a single pill per day were shown to be significantly less likely to be hospitalized than patients who received three or more pills per day [38].

In the COMPACT study [27], the type of therapy also influenced the total cost of illness. Patients treated with a STR showed association with the lowest cost. A selective non-adherence in a MPR of 3.5% increased the risk of hospitalization by 39% thus further increasing management costs.

Patients on a STR have been associated with significantly lower monthly health care cost (US $605 per patient per month) (p < 0.001) compared to patients on MPR. Differences were even greater (US $922 per patient) (p < 0.001) when only treatment-naïve patients were examined. The use of OD STRs was associated with a 17% reduction in total health care costs, partly due to the significant reduction of hospitalization costs [23]. As already pointed out, cohort analyses have a few limitations and these results must be evaluated with caution as selection biases could play a role in the final outcome. As an example, patients with a lower CD4 nadir could have preferentially received a MPR and as the CD4 nadir is related to the risk of AEs and development of opportunistic pathologies their health care costs would naturally be higher. However, these concerns are somehow tempered by the consistency of results among different cohorts [23, 27].

The economic value of the switch from a two-pills-a-day TDF/FTC + EFV therapy to a STR (TDF/FTC/EFV) was evaluated by means of incremental cost-effectiveness ratio (ICER). The STR was the most cost-effective treatment strategy, with an ICER of €22,017 vs. €26,558 for the two-pills-a-day regimen [19]. Besides improving adherence and QoL as perceived by the patients, STRs allowed a 17% reduction of costs, corresponding to a € 4,541 lower cost-effectiveness ratio per quality-adjusted life-years (QALY) [39].

Similarly, the SPIRIT study showed that the use of the STR TDF/FTC/RPV was associated with an overall 16% cost reduction per subject through 24 weeks [6].

Current STRs

Three STRs are currently available. TDF/FTC/EFV is a STR containing 300 mg of TDF, 200 mg of FTC and 600 mg of EFV. It was the first OD complete ARV regimen available as a STR and is approved for use in all HIV patients, treatment naïve or experienced (alone as a complete regimen or in combination with other ARV agents for the treatment of HIV-1 infection in adults and pediatric patients 12 years of age and older) in the US, while only use in patients virologically suppressed more than 3 months is approved by the European Medicines Agency (EMA). TDF/FTC/RPV is a second-generation STR containing 300 mg of TDF, 200 mg of FTC and 25 mg of RPV. It is licensed both in the US and in Europe for the use in HIV-infected subjects naïve or experienced (with a limitation referring to a viral load <100,000 copies/ml). More recently, TDF/FTC/COBI (cobicistat)/EVG (elvitegravir) has been approved. It is the first non-NNRTI-based STR containing 300 mg of TDF, 200 mg of FTC, 150 mg of EVG and 150 mg of COBI. EVG is an integrase inhibitor that selectively inhibits the strand-transfer step of integration process of viral DNA into the nucleic acid of the host [40, 41]. COBI is a pharmacokinetic enhancer that does not exert any ARV activity [42].

TDF/FTC/EFV is currently one of the first choices for the treatment of HIV infection both in the US [43] and in the main European Guidelines [3, 44, 45]. It is the STR most widely used in clinical practice and the experience gained over years on the single components is much more extensive if compared to newer STR formulations. The US Guidelines have recently added TDF/FTC/COBI/EVG as a preferred regimen and the European Guidelines have added TDF/FTC/RPV as a recommended regimen as well. Different studies have demonstrated that virologically suppressed patients receiving a wide array of NRTI backbones given with NNRTI- or PI-based therapies can be safely switched to the TDF/FTC/EFV STR [16, 20, 21, 46].

Longer term data up to week 144 support the high durability of the use of TDF/FTC/EFV STR and a continued immunological recovery [41, 47].

TDF/FTC/EFV STR has been considered as the comparator arm in the trials leading to registration of new STRs. It showed high efficacy in naïve subjects coupled with a favorable toxicological profile (Tables 1, 2; [48–59]).

Table 1.

Tolerability profile of single-tablet regimens (STRs)

Reason for drug discontinuation	TDF/FTC/EFV STaR (%) (n = 392)	TDF/FTC/EFV 102 (%) (n = 352)	TDF/FTC/RPV STaR (%) (n = 394)	TDF/FTC/COBI/EVG 102 (%) (n = 348)	TDF/FTC/COBI/EVG 103 (%) (n = 353)
Renal events	0	0	0	2.0	0.8
Rash and skin reactions	0.5	1.4	0	0	0
Diarrhea	0.5	0	0	0	0.6
Nausea	0	0	0	0	0.3
Vomiting	0	0	0	0	0.3
Fatigue	0.5	0.6	0	0.3	0
Pyrexia	0.5	0	0	0	0.6
Hepatitis C	0	0	0	0	0.3
Dizziness	1.5	0	0	0	0
Abnormal dreams	1.8	0.6	0	0	0
Insomnia	1.0	0.6	0.3	0	0
Depression	2.0	1.1	0	0.3	0
Suicidal ideation	0.8	0	0	0	0

Reasons for drug discontinuation due to intolerance (%) as reported by the studies STaR, 102 and 103. 96 week results

COBI cobicistat, EFV efavirenz, EVG elvitegravir, FTC emtricitabine, RPV rilpivirine, STaR single-tablet RPV, TDF tenofovir

Table 2.

Efficacy profile of different single-tablet regimens (STRs) or regimens potentially leading to a STR in naïve patients

Reference	STR regimen	Success rate (%)	Control arm	Success rate (%)	Follow-up (weeks)
Cohen et al. (ECHO, THRIVE) [48]	2 NRTIs + RPV	84	2NRTIs + EFV	82	48
Cohen et al. (STaR) [49]	TDF/FTC/RPV	86	TDF/FTC/EFV	82	48
Cohen et al. [50]	TDF/FTC/RPV	78	TDF/FTC/EFV	78	96
Cohen et al. [41]	TDF/FTC/COBI/EVG	90	TDF/FTC/EFV	83	48
Sax et al. [51]	TDF/FTC/COBI/EVG	88	TDF/FTC/EFV	84	48
Zolopa et al. [52]	TDF/FTC/COBI/EVG	84	TDF/FTC/EFV	82	96
Wohl et al. [53]	TDF/FTC/COBI/EVG	80	TDF/FTC/EFV	75	144
De Jesus et al. [54]	TDF/FTC/COBI/EVG	90	TDF + FTC + ATV/rtv	87	48
Rockstroh et al. [55]	TDF/FTC/COBI/EVG	83	TDF + FTC + ATV/rtv	82	96
Clumeck et al. [56]	TDF/FTC/COBI/EVG	78	TDF + FTC + ATV/rtv	75	144
Raffi et al. (SPRING 2) [57]	2NRTIs + DTG	81	2 NRTIs + RAL	76	48
Feinberg et al. (FLAMINGO) [58]	2NRTIs + DTG	90	2 NRTIs + DRV/rtv	83	48
Walmsley et al. (SINGLE) [59]	3TC/ABC + DTG	88	TDF/FTC/TDF	81	48

Success rate is virologic success evaluated according to the US Food and Drug Administration snapshot analysis definition

ABC abacavir, ATV atazanavir, COBI cobicistat, DRV darunavir, DTG dolutegravir, EFV efavirenz, EVG elvitegravir, FTC emtricitabine, NRTI nucleoside reversed transcriptase inhibitors, RAL raltegravir, RPV rilpivirine, rtv ritonavir, STR single-tablet regimens, TDF tenofovir, 3TC lamivudine

All components of the STRs were developed to be administered OD and possess long plasma and intracellular half-lives that are congruent one to the other which may provide an additional pharmacologic advantage in the case of occasionally missed doses as the unintentional functional monotherapy is prevented and the regimen genetic barrier is enhanced.

Two cohort studies [60, 61] have considered this aspect drawing similar conclusion. They studied the change in the prevalence of mutations for any component of the TDF/FTC/EFV STR after the introduction in the market of the STR itself compared to the prevalence of the same viral mutations in the period these drugs were used as single components. Although both studies may suffer methodological drawbacks and selection bias impossible to rule out, they both concluded that there was a temporal association between the incremental use of the STR and the decreased prevalence of signature mutations. The French study conducted between 2005 and 2010 showed that the overall prevalence of resistance associated mutations to TDF, 3TC/FTC and EFV decreased over time, in the same period the use of TDF almost doubled without any increment of the K65R mutation; the use of 3TC was more than halved while the use of FTC increased from 8% to 53% with a decrease in M184 V/I prevalence; the introduction and the expansion of the use of EFV as a STR was associated with a decrease of the prevalence of the K103N [60]. These decreases may show the importance of utilizing FTC instead of 3TC in combination with TDF, as well as to the importance of the STR combination.

The virological efficacy of RPV has been demonstrated in naïve patients in different studies [48, 49] (Table 2). The pooled data of the early capture HIV cohort study (ECHO) and [treatment of HIV RPV vs. EFV trials (THRIVE)] indicated RPV as non-inferior to EFV both at 48 and 96 weeks. A slightly higher incidence of virologic failures was observed with RPV (14%) vs. EFV (8%), this difference mostly accumulated in the first 48 weeks of therapy, while failures were comparable afterwards, and occurred primarily in those with VL >100,000 c/mL. The virologic failure difference reduced in the open-label single-tablet RPV (STaR) study that used the STR formulation, suggesting the relevance of the STR on adherence [49]. In the registrative studies, the subgroups of patients with baseline HIV-RNA >100,000 copies/mL showed higher rates of virological failures and more frequent emergence of NNRTI and NRTI resistance including the E138K resistance mutation that causes cross-resistance with etravirine (ETR) [50]. These studies have justified the approved indication limiting the use of TDF/FTC/RPV STR to patients with lower baseline viremia. In the open-label STaR study, the TDF/FTC/RPV STR favorably compared with the TDF/FTC/EFV STR. Considering the totality of patients the second-generation STR was non-inferior to the control arm and a post hoc analysis stratified according to the baseline viral load, revealed that TDF/FTC/RPV was superior to TDF/FTC/EFV in patients with viral load <100,000 copies/mL [49].

All studies underlined the favorable tolerability profile of TDF/FTC/RPV (see Table 1) [48, 49]. RPV was well tolerated, demonstrating fewer drug discontinuations, and reduction in central nervous system (CNS) and rash AEs, when compared to EFV.

These characteristics were further explored in a few small switch studies. In a cohort of patients chronically and successfully treated with TDF/FTC/EFV STR, the switch to TDF/FTC/RPV STR obtained a significant and steady reduction of CNS-related symptoms such as dizziness (p = 0.008), depression (p = 0.029), insomnia (p = 0.001), anxiety (p = 0.021), confusion (p = 0.005), impaired concentration (p = 0.008), somnolence (p = 0.003), aggressive mood (p = 0.034) and abnormal dreams (p < 0.001) that turned out in a significant improvement in the quality of sleep (p < 0.001) [62]. A similar experience conducted in the US concluded that switching from TDF/FTC/EFV to TDF/FTC/RPV appears to be a safe and efficacious option in virologically suppressed HIV-1-infected subjects who experience EFV intolerance and wish to remain on a STR [63].

In a larger controlled study in experienced patients, switching to TDF/FTC/RPV was non-inferior to remaining on a PI/RTV + 2NRTIs regimen with a lower rate of virological failure in the TDF/FTC/RPV arm. Mutations developed in <1% of subjects switched to TDF/FTC/RPV and after the switch an improvement in fasting lipids, including total cholesterol, low-density lipoproteins (LDL) cholesterol, triglycerides and total cholesterol/high-density lipoproteins (HDL) ratio was observed at week 24 and week 48 [6].

TDF/FTC/COBI/EVG is the most recent available STR, recommended as preferred in the Department of Health and Human services (DHHS) Guidelines for naïve HIV-infected patients with creatinine clearance (CrCl) >70 mL/min [43, 45, 64].

The integrase inhibitor EVG can be administered OD. The speed of viral suppression observed with TDF/FTC/COBI/EVG is consistent with the potency of HIV integrase inhibitors and robust COBI-boosted EVG exposures [41, 65]. TDF/FTC/COBI/EVG has shown to be non-inferior for safety and efficacy to TDF/FTC/EFV at 48 [51], 96 [52] and 144 weeks [53] in a controlled, randomized trial enrolling 700 HIV-positive cART-naïve subjects (Table 2). At week 48, 87.6% of the patients receiving TDF/FTC/COBI/EVG had HIV-RNA concentrations <50 copies/mL vs. 84.1% of those receiving TDF/FTC/EFV [57]. HIV-RNA concentrations <50 copies/mL were maintained at week 144 in 80% of the TDF/FTC/COBI/EVG arm vs. 75% in the TDF/FTC/EFV arm, testifying for durability [53]. Very few patients in the TDF/FTC/COBI/EVG arm discontinued because of AEs, 4% at week 48 [51] and 5% at week 96 and 6% at week 144 [52, 53]. The most common AEs observed in the TDF/FTC/COBI/EVG arm were nausea and an increase of serum creatinine concentration with a decrease in estimated glomerular filtration rate (eGFR). COBI is associated with reduced active secretion of creatinine in the renal tubules leading to initial rises in creatinine levels in the first 2–4 weeks [52]. Because of this, only patients with a CrCl >70 mL/min were included in the registrative studies and consequently the use of COBI is currently allowed only in patients with CrCl >70 mL/min. Large pharmacovigilance programs on this enhancer should be considered to look at its long-term impact on renal function, not limiting data to just eGFR changes.

A second, large (715 enrolled patients), non-inferiority double-blind trial compared TDF/FTC/COBI/EVG to atazanavir (ATV)/RTV + FTC/TDF. The primary endpoint was the proportion of patients suppressed at week 48 [54], but secondary endpoint week 96 [55] and 144 [62] data are available. At week 48, 89.5% of the patients receiving TDF/FTC/COBI/EVG had HIV-RNA concentrations <50 copies/mL vs. 86.8% of those receiving ATV/RTV + FTC/TDF [60]. At week 144, the figures were 78% and 75% [56]. As for the previous study, the rate of discontinuation in the TDF/FTC/COBI/EVG arm due to AEs was very low (3.7% at week 48) [54] (Table 1). Furthermore, the TDF/FTC/COBI/EVG-treated patients had statistically lower increases in fasting triglycerides, and a lower percentage of subjects experienced alanine aminotransferase (ALT), aspartate aminotransferase (AST) or bilirubin elevations when compared with ATV/RTV + TDF/FTC-treated patients.

As for resistances, in the 102 study [51], 2% of patients in the TDF/FTC/COBI/EVG arm failed with resistance inducing mutations, usually to both NRTIs and EVG. The result was comparable to that observed in the TDF/FTC/EFV arm. The integrase gene resistance mutations observed were E92Q, Q148R and N155H, which confer decreased susceptibility both to EVG and raltegravir and a potential low-level resistance to dolutegravir, and T66I, which preserves both raltegravir and dolutegravir (DTG).

Future Perspectives

An interesting STR that is anticipated is the combination ABC/3TC/DTG.

Dolutegravir is an unboosted integrase inhibitor that has been effectively and safely used for the treatment of HIV-infected naïve (with 2 NRTIs) and experienced patients (with optimized background regimen) [57–59, 66, 67], (Table 2). DTG has shown to be effective with ABC/3TC or TDF/FTC regardless of blood level HIV-1 RNA [66], although the number of patients on ABC/3TC with high viral load is limited. The efficacy of DTG has been compared to raltegravir in the SPRING-2 (NCT#01227824) study; both associated with 2 NRTIs in cART-naïve patients: DTG 50 mg OD was as effective as raltegravir 400 mg BID at 96 weeks (81% vs. 76%). In the NRTI backbone comparison at 96 weeks those on DTG with ABC/3TC had efficacy rates of 74% compared to those on TDF/FTC of 86%. [57]. DTG has also been compared to a boosted-PI, both associated with 2 NRTIs (TDF/FTC or ABC/3TC). The open-label FLAMINGO (NCT#01449929) study has shown the superiority in efficacy of DTG compared to darunavir (DRV)/RTV at week 48, driven by higher discontinuations in the DRV arm. Virologic failure was observed in 2 patients (1%) on each arm without treatment-emergent resistance in either arm. The most common AEs were diarrhea with DRV/RTV and headache with DTG, while treatment-related study discontinuations were low (1% on DTG arm, 4% on DRV/RTV arm) [58].

In the SINGLE (NCT#01263015) study, enrolling naïve patients, DTG 50 mg + ABC/3TC had a better safety profile and was more effective through 48 weeks than TDF/FTC/EFV. The time to reach HIV-RNA <50 copies/mL was 28 days with DTG vs. 84 days with EFV (p < 0.0001) and the increase in CD4 cells count was 267 with DTG vs. 208 with EFV (p < 0.001). The main AEs observed in the DTG arm were insomnia and a mild, non-progressive increase in the serum creatinine without any effect on the actual glomerular filtration rate. Discontinuation due to AEs was observed in 10% of the patients in the EFV arm vs. 2% in the DTG arm and the higher discontinuation rate in the EFV arm drove the overall greater efficacy. Moreover, in patients failing cART in the DTG arm, resistance to any of the regimen components did not develop [59]. The SINGLE study supported the idea of co-formulating ABC/3TC/DTG as a new promising STR whose limits might be related to the backbone: restricted use to patients HLAB*5701 negative.

Dolutegravir is, since August 2013, approved in the US for the treatment of HIV-1 infection in combination with other ARV drugs, but studies exploring the potential of the ABC/3TC/DTG STR are ongoing, such as the ARV treatment in ART-naïve women (ARIA Study, NCT#01910402) [68].

Tenofovir alafenamide (TAF) is an investigational pro-drug of TDF with lower plasma concentrations and increased delivery to hepatocytes and lymphoid cells. The potential advantages of TAF vs. TDF are the reduction in AEs as TAF induces smaller changes in body mineral density (BMD) and median serum creatinine, further, higher concentration in the peripheral blood mononuclear cells (PBMCs) may overcome resistance (e.g., K65R) [69].

A 25 mg dose of TAF has shown greater ARV activity than a standard 300 mg dose of TDF [70]. Clinically, in Phase 2 studies in cART-naïve patients, TAF resulted in non-inferior efficacy to TDF both co-formulated with FTC/EVG/COBI.

The possibility to use small doses of TAF instead of TDF could further widen the STR options as bulky molecules such as PIs could be successfully co-formulated (e.g., FTC/TAF/COBI/DRV and other third agents). Studies on STR including TAF such as FTC/TAF/COBI/EVG or FTC/TAF/COBI/DRV are already ongoing.

In the next few months, the patents of several relevant ARV drugs will expire and the possibility to combine bioequivalent drugs will become a reality, it has been hypothesized the possibility to obtain a fully bioequivalent STR combining ABC/3TC/EFV.

Limits of STRs in Clinical Practice

STRs, through regimen simplification, offer major advantages in the management of HIV-positive individual, but cannot be the answer to all problems. Intrinsic to the concept of STR are some potential limitations to their use.

STRs are based on FDCs not allowing, therefore, for dose adjustment of single components unless breaking the regimen to more pills. This may be the case in patients with impaired renal function in which the need to adjust specific drug dosages exist (e.g., 3TC; FTC; TDF) [44]. The same may be true to limit the occurrence of adverse effects in populations with genetic backgrounds that reduce the metabolic pathways of specific drugs (e.g., EFV) [71].

A second limit may be the occurrence of intolerance as well as genetic predisposition to intolerance (e.g., HLAB*5701) to one of the components of the STR.

A third variable could be co-infections such as Hepatitis B that force clinicians to prefer, as far as possible, drugs able to control both HIV and hepatitis B virus (HBV) replication (FTC/TDF and not 3TC/ABC) thus limiting the therapeutic options.

In deciding on the use of an STR, the clinician should pay attention to the resistance profile of any component of the STR itself remembering that transmitted resistance occurs mainly among NRTIs and NNRTIs [72, 73], shows a steady prevalence trend (of about 10–12%) [73, 74] and is less frequent for newly developed compounds even if tested with high sensitivity methods [75].

A further variable to consider are drug–drug kinetic interactions that may expose the risk of a functional dual therapy if blood concentrations of one of the STR components are reduced, this might be the case of RPV and proton pump inhibitors co-administration [76] or dolutegravir and antacids co-administration [77]. Polypharmacy is a growing problem in the aging HIV population and besides exposing to the risk of drug–drug interactions, polypharmacy may exert a non-specific negative effect by reducing adherence [78] and therefore, partially vanishing the advantages of STRs.

Finally, the cost of the newest compound, often higher than older ones, may constitute a drawback to the use of STRs, forcing national regulatory agencies to put limitations on their prescriptions [79] or ceilings to their use.

Conclusion

One of the challenges of HIV infection management remains to encourage and enable patients to take ARV drugs correctly for a lifetime. Selection of a regimen should be individualized on the basis of virologic efficacy, toxicity, pill burden, dosing frequency, drug–drug interaction potential, resistance testing results, and comorbid conditions [43].

Simplicity of treatment is a key point and the combination of several active ARV agents in a single pill is a way to comply with the above considerations and offers potential advantages. These advantages, besides the improved all-around adherence, include a reduced risk of selective non-compliance, a reduced risk of prescription error, a reduced risk to expose the patient to general stigma by allowing an improved privacy and an increased acceptability, all of which might decrease the likelihood of treatment failure and subsequent selection of drug resistance.

Results of surveys show that patients prefer to take fewer daily pills, and look for compact easy-to-use regimens; observational and controlled studies indicate that virological and clinical outcomes are improved in individuals treated with single vs. MPRs, even among difficult-to-treat populations. In many cases, STRs also show economic benefit compared to other available regimens.

The choice of the initial ARV regimen is a cornerstone of the correct management of HIV infection as it may influence all the subsequent choices and residual options. Individualization of therapy is of utmost importance. It may be counterintuitive to claim the possibility to individualize treatment through the use of fixed-dose combinations, however, excluding infrequent cases (e.g., severe renal impairment or specific drug interactions); individualization is not based on the reduction/increment of doses, but rather on the choice of pharmacological components of the regimen. Therefore, the available STRs, based on the combination of different drug classes, allow prescribers to individualize treatment in naïve patients. As an example: TDF/FTC/COBI/EVG could be used in a wide variety of naïve subjects without limitations based on their pre-treatment viral load or their immunological status. In the event of a reduced eGFR (<70 ml/min), TDF/FTC/RPV [71] appears a good alternative choice for the treatment of naïve patients, provided their baseline viral load is ≤100,000 copies/mL, in the latter case TDF/FTC/EFV could result in being the preferred STR.

A further advantage is that a switch from a given STR to another is possible, in the case of individual intolerance to a specific component or to further tailor cART to the individual preferences and lifestyles.

A possible limit of the STRs currently available is that they share a common backbone, thus limiting the possibility of drug sequencing in the case of selection of a viral clone resistant to one of the NRTI components. Patients forced to abandon their STR because of emergence of resistance to the backbone are generally obliged to switch to MPRs, often requiring more frequent dosing. STR combinations currently in development may change this situation but the future challenge would be to develop completely alternative STRs so as to extend the advantages of simplicity to heavily pre-treated individuals.

Electronic supplementary material

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