Role of tipranavir in treatment of patients with multidrug-resistant HIV

Abstract

The worldwide emergence of multidrug-resistant human immunodeficiency virus (HIV)-1 strains has the driven the development of new antiretroviral (ARV) agents. Over the past 5 years, HIV-entry and integrase inhibitor ARVs, as well as improved non-nucleoside reverse transcriptase inhibitors (NRTIs) and protease inhibitors (PIs), have become available for treatment. It is important to assess how these new ARVs might be most judiciously used, paying close attention to viral susceptibility patterns, pharmacodynamic parameters, and the likelihood that patients will adhere to their therapy. Herein we review published material in Medline, EMBASE, and ISI for each antiretroviral agent/classes currently approved and summarize the available data on their efficacy, safety, and pharmacologic parameters. We focus on the role of tipranavir, a recently approved nonpeptidic PI, for treating HIV-infected children, adolescents, and adults with a history of multidrug-resistant HIV.

Introduction

One in 155 adults and adolescents are infected with human immunodeficiency virus (HIV) globally, with an astonishing rate of one in 21 in Sub-Saharan Africa.1 In the US alone, more than half a million people were living with HIV in 2007, and 44,000 new cases were reported in the same year.2 Although safe and effective antiretroviral (ARV) treatment is now available, the prevalence of genotypic resistance to protease inhibitors (PIs) and non-nucleoside reverse transcriptase inhibitors (NNRTIs) has steadily increased.3 In treatment-naïve adolescents, genotypic resistance has been reported to be as high as 15%.4 Given this scenario it is now more important than ever to understand how newer ARV agents may provide therapeutic alternatives for treatment-naïve and treatment-experienced HIV-infected patients.

The appearance of HIV-resistant strains for the most part is due to the development of point mutations in the HIV genome. Because HIV reverse transcriptase lacks the proofreading abilities of human DNA polymerase, 0.2 to 1 new point mutations may appear during each viral replication cycle.5 This translates into approximately 10,000 new mutations per day. Fortunately for the host, most of these mutations are lethal to the virus and thus do not result in added ARV resistance.5 Resistance only occurs when the mutation induces conformational changes which allow the virus to overcome the action of the inhibiting agent, while maintaining the activity of the enzyme. When HIV does develop a beneficial point mutation, the corresponding genetic sequence is amplified by selective pressures of ARV therapy. These genetic changes in the viral genome and their effects are also the basis for available resistance testing.

Resistance testing

Resistance testing helps to direct therapy by avoiding the use of ineffective or inappropriate ARV therapy. For this reason the current adult and adolescent HIV-1 guidelines recommend resistance testing for all new patients entering into care, HIV-positive women who are pregnant or planning to become pregnant, and when considering changes to a patient’s ARV regimen due to suboptimal viral load reduction or virologic failure.6 The pediatric HIV guidelines also recommend resistance testing prior to starting therapy in treatment-naïve children, for treatment failure, and when considering the start of a CCR5 antagonist.7

HIV-resistance patterns can be assessed by using either a genotypic assay or by determining its phenotypic susceptibility to ARVs. Genotypic assays screen viral genes for mutations which confer resistance to specific ARVs or entire classes of agents. This is done by either genomic mapping or the use of a DNA probe.6 The resulting list of mutations is interpreted using a regularly updated database containing mutations known to confer ARV resistance.8 Phenotypic testing involves the use of different concentrations of specific ARVs against the virus in vivo.6 Results of this test indicate the concentration at which 50% of the HIV viral replication is inhibited in culture (IC₅₀).6 A combination of phenotypic and genotypic tests, known as virtual phenotyping, has also been used.9 This method involves the use of a database, which matches a genotypic pattern to a known phenotypic profile.9

Rates of virologic success, defined as achieving a viral load of <200 copies/mL of blood, where compared between patients randomized to ARV therapy directed by genotyping, phenotyping, or standard of care (NARVAL trial).10,11 Patients allocated to therapy chosen by genotypic analysis (44/183) trended toward increased virologic success when compared with those whose therapy was chosen by phenotyping (36/183; P = 0.068) or standard of care (36/152; P = 0.052).10 Using multivariate analysis, patients in the genotypic regimen arm were found to have a higher likelihood of achieving virologic success than patients receiving standard of care (odds ratio [OR] 2.13 (95% confidence interval [CI] 1.20–3.79; P = 0.01)].11 In another study, ARV treatment was chosen according to virtual phenotype and then compared with treatment chosen based on genotype in 327 adult patients.12 At 48 weeks, no differences were found between patients achieving undetectable viral load in the virtual phenotype group and the genotype group (42% and 46%, respectively; P = 0.553).12 These discrepant results indicate that there are benefits and limitations to each type of resistance testing.13 Nevertheless, the adult and adolescent guidelines show preference for genotypic testing for treatment-naïve and pregnant patients.6

HIV life cycle and mechanism of drug action

In order to understand how ARVs function it is important to understand the HIV life cycle. The first step of viral entry is for HIV to locate a T lymphocyte via the CD4 receptor site.14 After the T lymphocyte is bound, the virus must also bind to either a CCR5 (site of action of maraviroc) or CXCR4 coreceptor. 15 The viral membrane then proceeds to fuse with the host cell membrane, via GP 41 (site of action of efuvirtide), enabling its RNA and proteins to enter the T lymphocyte. Inside the cell, viral reverse transcriptase produces HIV DNA using the viral RNA as a template (site of action of NRTIs and NNRTIs). Integrase enzyme then incorporates the HIV DNA into the human cell’s genome through several steps (site of action of integrase inhibitors). Viral DNA is then transcribed by human RNA polymerase, producing viral RNA. This RNA is translated into polyprotein precursors, which are then cleaved by protease into functional proteins (site of action of PIs).

Newer ARV treatment options for HIV-positive adults and children

There are several new ARV classes, as well as new agents from the older classes. In this study we performed an extensive literature search using Medline, EMBASE, and ISI, and collected data regarding efficacy, safety, and pharmacologic parameters of the relevant agents.

CCR5 antagonists

Maraviroc is the only currently approved CCR5 antagonist in clinical use. This agent acts through allosteric inhibition of the CCR5 receptor, preventing its interaction with gp120 and thus avoiding subsequent cellular entry by HIV. Data from two clinical trials, Maraviroc versus Optimized Therapy in Viremic Antiretroviral Treatment-Experienced Patients (MOTIVATE-1 [US and Canada; n = 585] and MOTIVATE-2 [US, Australia, and Europe; n = 464]), have been published.16 The study inclusion criteria were identical in both trials. Patients at least 16 years of age were enrolled into the studies if they were infected with a CCR5- tropic HIV strain and were receiving at least one NRTI, or one NNRTI, or a fusion inhibitor, two PIs, and had documented resistance to at least three of the aforementioned classes.16 When administered with an optimized background therapy (OBT), more patients in the combined once-daily or twice-daily maraviroc arms achieved an undetectable viral load (<50 copies/mL), than patients receiving placebo (43%, 46%, and 17%, respectively, P < 0.001).16

CCR5 antagonists only work against M-tropic strains of HIV, which are typically found in the early stages of infection. 17 This is due to their exclusive use of CCR5 coreceptors, rather than CXCR4, which is found in later stages of HIV.17 Therefore, maraviroc should only be used in patients with CCR5-tropic strains, and in not those which are CXCR4- tropic, dual-tropic, or mixed-tropic.

The most common adverse events reported for maraviroc were diarrhea, nausea, headache, fever, fatigue, and upper respiratory tract infection.16 Laboratory abnormalities were similar to those in the placebo arm.16 Maraviroc does carry a black box warning for hepatotoxicity preceded by an allergic reaction, as this had been reported in a healthy volunteer study.

Maraviroc has been approved by the US Food and Drug Administration (FDA) and European Medicines Agency (EMA) for use in patients with multidrug-resistant CCR5- tropic strains of HIV-1.18,19 A study evaluating safety, pharmacokinetics, and efficacy is currently enrolling children 2–18 years of age infected with CCR5-tropic HIV-1.20 Maraviroc-based regimens are not currently recommended for children younger than 16 years of age or for treatment-naïve patients.6 It is, however, recommended for use in treatment-experienced adults and adolescents infected with CCR5-tropic HIV-1 experiencing failure on their current regimen.6

Maraviroc is currently available as 150 mg and 300 mg tablets. A pediatric liquid formulation is currently under development.18–20 The monthly cost of maraviroc therapy is approximately $1000 USD. Because maraviroc is only efficacious in patients with CCR5-tropic HIV-1 strains, the adult and adolescent HIV-1 guidelines recommend a coreceptor tropism assay be performed prior to treatment initiation or upon failure while on maraviroc.6 The cost of the CCR5 tropism assay (about $1960) could limit the ability to screen patients for the use of maraviroc.21

Fusion inhibitors

One single fusion inhibitor, enfuvirtide, is approved for clinical use. Enfuvirtide acts by binding to a region of the HIV-1 gp41 envelope protein, resulting in its inhibition, and thereby inhibits the steps which lead to fusion of the viral envelope and the cell membrane.22 Due to its unique mechanism of activity, enfuvirtide maintains activity against isolates resistant to other ARV classes.

The efficacy of enfuvirtide was studied in two internationally conducted clinical trials of identical design, ie, the T-20 versus Optimized Regimen Only studies (TORO-1 [US, Canada, Mexico, and Brazil; n = 501] and TORO-2 [Australia and Europe; n = 512]).23,24 Patients 16 years of age and older who had previously documented ARV resistance, or who had received a minimum of 6 months of at least one NRTI and NNRTI, and at least two PIs, were eligible for participation. Patients were randomized to receive enfuvirtide plus an OBT or OBT alone. By 24 and 48 weeks, more patients in the enfuvirtide group achieved an undetectable viral load (< 50 copies/mL) than in the placebo group (15.9% versus 6.3% and 18.3% versus 7.8%, respectively).25

The most prevalent mutations associated with enfuvirtide resistance result from an alteration of the active site of gp41.26 Resistance against enfuvirtide is possible not only through mutations in gp41, but also in gp120.27 The most commonly reported adverse events experienced by the enfuvirtide group were injection site reaction, nausea, vomiting, fatigue, headache, insomnia, and peripheral neuropathy.28 Pneumonia and lymphadenopathy occurred at significantly higher rates in the enfuvirtide group. Hypersensitivity reactions can also occur.28

Enfuvirtide has been approved for use in treatment-experienced patients 6 years of age and older infected with HIV-1 in both Europe and in the US.18,19 Enfuvirtide is not recommended for use in treatment-naïve children, but should be considered as an additional ARV in patients who have failed NRTI, NNRTI, and PI regimens.7 Because enfuvirtide is a synthetic peptide, and therefore cannot be administered orally, it is currently available as a 90 mg/mL subcutaneous injection. The monthly cost of enfuvirtide is $2500 USD.

Nucleoside reverse transcriptase inhibitors

This class consists of DNA base analogs, which are reversible competitive inhibitors of reverse transcriptase, effectively preventing reverse transcription of viral RNA into DNA.29 There are currently 11 FDA-approved ARVs in this class.18 Dual NRTI therapy is recommended as part of therapy for treatment-naïve patients.6 The primary mechanism of resistance to NRTIs involves conformational changes at the active site.30 In a recent study from the US and Europe, 6.1% and 3.8%, respectively, had NRTI resistance mutations.31 The overall incidence of NRTI resistance has decreased now that patients use this class of ARV in combination with NNRTIs and/or PIs.

Non-nucleoside reverse transcriptase inhibitors

NNRTIs act noncompetitively to inhibit the formation of DNA from viral RNA.32 Resistance to NNRTIs occurs when mutations confer structural changes around the allosteric binding site of reverse transcriptase.33 In a study of 413 US and 500 Western European HIV-positive ARV-naïve patients, 7.3% and 3.2%, respectively, had NNRTI resistance mutations.31

There are currently four NNRTIs approved by the FDA, including delavirdine, efavirenz, nevirapine, and etravirine. As a class, NNRTIs have a lower genetic barrier to resistance than PIs, but are a line of therapy which can spare the use of PIs until later in life,6,7 and have much fewer drug interactions, as well as gastrointestinal and lipid-related adverse reactions.6 Of the available agents, efavirenz is recommended as first-line, with the exception of use in patients who are pregnant or likely to become pregnant, for whom nevirapine is preferred.6 For children under 3 years of age, nevirapine is preferred, because it is available in a liquid formulation.7 Efavirenz is the preferred NNRTI for use in HIV-infected children over the age of 3 years. Although not obtainable in a liquid formulation, it is available in capsules sized for pediatric dosing.7 As a class, the most common side effects of NNRTIs are rash, central nervous system effects, and lipoatrophy.6

Etravirine is the newest NNRTI. It is active against both wild-type and NNRTI-resistant HIV. Resistance is less likely to develop against etravirine because it is a flexible molecule and can bind reverse transcriptase in multiple conformations. 34 Decreased response to etravirine was associated with the presence of three or more NNRTI mutations (Val90Ile, Ala98Gly, Leu100Ile, Lys101Glu, Lys101Pro, Val106Ile, Val179Asp, Val179Phe, Tyr181Cys, Tyr181Ile, Tyr181Val, Gly190Ala, and Gly190Ser) concurrently.35

HIV-positive patients with documented resistance to NNRTIs, with three or more primary PI mutations and a history of having received 3 or more months of different NRTIs were enrolled into a Phase II etravirine clinical trial. The viral load had to be >1000 copies/mL. Patients were randomly assigned to receive either 400 mg or 800 mg of etravirine twice a day, or to serve as part of the control group. All patients on etravirine received a background regimen of at least two different ARVs (NRTI, lopinavir-ritonavir, or enfuvirtide). Patients in the control group received three or more similar ARVs. After 24 weeks, viral loads decreased by 1.04, 1.18, and 0.19 log₁₀ copies/mL in the 400 mg, 800 mg, and control groups, respectively. The decrease in viral load was greater in the patients receiving 800 mg of etravirine and those who were not using either enfuvirtide or lopinavir-ritonavir. The percentage of patients who had viral loads <400 copies/mL at 24 weeks was 30% in subjects receiving 400 mg of etravirine and 38% in those receiving 800 mg. By comparison, only 7.5% of subjects in the control group achieved a standard similar viral load.34

By 48 weeks, the viral load had decreased from baseline by 0.88, 1.01, and 0.14 log₁₀ copies/mL in the etravirine 400mg twice daily, etravirine 800 mg twice daily, and control groups, respectively. Approximately 20% of patients receiving either dose achieved viral loads <50 copies/mL whereas none of the patients in the control group had viral loads <50 copies/mL.36

The DUET-1 trial, a multicenter international trial, enrolled 612 patients on stable ARV therapy for at least 8 weeks prior to screening. To be included in the study, patients had to have a viral load >5000 copies/mL, three or more primary PI mutations, and at least one mutation associated with NNRTI resistance. Patients were randomized to receive etravirine 200 mg or placebo. All patients received a suitable NRTI, ritonavir-boosted darunavir, and also had the option of receiving enfuvirtide as part of their backbone therapy. Primarily as a result of virologic failure, 14% of patients in the etravirine group and 18% of patients in the placebo group discontinued participation in the study prior to 24 weeks. After 24 weeks, 56% of patients in the etravirine group and 39% in the placebo group had a viral load <50 copies/mL. Of note, 74% of subjects in the etravirine arm and 51% of patients in the placebo group achieved a viral load <400 copies/mL.35

The DUET-2 trial enrolled 591 patients in Australia, Belgium, Canada, France, Germany, Italy, Netherlands, Poland, Portugal, Spain, the UK, and the US. Patients were randomized to the same treatment or placebo arms as in the DUET-1 trial. Virologic failure led to early discontinuation in 17% of patients on etravirine and 25% of patients on placebo. After 24 weeks, 62% of patients on etravirine and 44% of those on placebo had achieved a viral load <50 copies/mL. Additionally, 75% of patients on etravirine achieved a viral load <400 copies/mL versus 54% of patients in the placebo group.37

Etravirine is currently approved for use in combination with other ARV agents for the treatment of adults who have tried other treatments and have evidence of HIV-1 strains resistant to NNRTIs and other ARV agents.18 The monthly cost of etravirine is $800 USD.

The most common adverse events were diarrhea (22.0%), injection site reaction (related to enfuvirtide, 20.1%), fever (20.1%), rash (20.1%), fatigue (15.7%), headache (15.7%), and nausea (15.1%). Rashes appeared early in therapy, usually during the first 2–4 weeks, and resolved in about 1–2 weeks with continued dosing. Rashes were mild to moderate in severity and were not dose-related.36 Psychiatric adverse events, including mood swings, nightmares, abnormal dreams, anxiety, and depression were reported in 10.7% versus 2.5% of patients on etravirine versus placebo, respectively. These did not lead to any patients discontinuing treatment. Headache and insomnia were the most common adverse events related to the nervous system.34

Integrase inhibitors

Currently, there is only one approved integrase inhibitor, raltegravir, which specifically inhibits strand transfer.38 This step is inhibited through allosteric modification of the integrase enzyme, preventing its binding to host DNA.39 Inhibition of the other steps of integration is currently in the preclinical research phase.

The efficacy of raltegravir was studied in two Merck Blocking Integrase in Treatment Experienced Patients with a Novel Compound against HIV, (BENCHMRK-1 [Europe, Asia, Australia, and Peru; n = 344] and BENCHMRK-2 [North and South America; n = 344]) trials, which both used the same study design.40 They enrolled patients at least 16 years old with HIV-1, a viral load >1000 copies/mL, and a documented resistance to at least one drug from each of the three major classes (NRTI, NNRTI, and PI). Each patient was randomized to an optimized background regimen or optimized background regimen plus raltegravir. After 16 weeks of therapy, significantly more patients receiving the raltegravir-containing regimen achieved an undetectable viral load (less than 50 copies/mL) than in the placebo group in the BENCHMRK-1 trial (61.8% versus 34.7%, respectively, P < 0.001).40 Similar results were seen in the BENCHMRK-2 trial.40 At 48 weeks, a combined analysis showed a significantly higher number of patients with undetectable viral load (<50 copies/mL) in the raltegravir group than in the placebo group (62.1% versus 32.9%, respectively).40

Although the mechanism of resistance is not well understood, it is known that there is no cross-resistance with other ARV classes. Within the class, cross-resistance with as yet unavailable integrase inhibitors appears to be substantial. Additionally, as supported by a Phase III trial, clinical failures were generally seen in patients who had developed a point mutation at one of three amino acid residues.41 Specifically, in one trial that enrolled patients older than 16 years showed that 64% of the 462 raltegravir group versus 34% of the 228 treatment-experienced patients were counted as treatment failures.40

Raltegravir was generally well tolerated in the BENCHMRK trials, with diarrhea, nausea, headache, and fatigue being the most common adverse events.40 Elevated total cholesterol and triglyceride levels were the most common laboratory abnormalities reported. It is important to note that elevated creatine kinase levels were observed in the clinical trials, and that cases of myopathy and rhabdomyolysis have been reported since that time.40

Raltegravir has FDA and EMA approval for use in HIV-infected adult patients.18,19 Raltegravir has also been recently recommended as a preferred regimen for treatment-naïve patients in the current adult and adolescent guidelines, and is considered a fully active ARV agent in patients naïve to integrase inhibitors. 6 Currently, a Phase I/II trial assessing the efficacy, safety, and pharmacokinetics of raltegravir is enrolling HIV-infected children 4 weeks to 18 years of age.42 Raltegravir is presently available in 400 mg tablets, with a pediatric formulation under investigation.18,42 The monthly cost of raltegravir is $972.00.

Protease inhibitors

There are currently 10 approved PIs, which are based on an analog of a peptide bond which the protease normally cleaves.43 This, in turn, prevents gag and gag-pol polyproteins from being synthesized into structural proteins and viral enzymes. PI-based regimens are known to confer an additional benefit in decreasing the development of genotypic mutations.44–46 By decreasing mutation rates, the likelihood of developing new resistance is also decreased.

Resistance to PIs generally involves a mutation affecting the structure of the active site of protease.47 In a recent study in ARV-naïve HIV-infected patients from the US and Western Europe, 3.6% and 0.8% of screened subjects, respectively, had PI resistance mutations.31

Ten PIs have been approved by the FDA, including saquinavir, indinavir, ritonavir, nelfinavir, amprenavir, lopinavir, fosamprenavir, atazanavir, darunavir, and tipranavir.6 Of these, ritonavir-boosted atazanvir, darunavir, fosamprenavir, and lopinavir regimens are preferred, with alternative regimens of ritonavir-boosted saquinavir or unboosted fosamprenavir or atazanavir.6 Only ritonavir-boosted lopinavir is recommended as a preferred PI for children.7 Alternatively, ritonavir-boosted atazanavir or fosamprenavir, as well as unboosted nelfinavir, are recommended.7 Of these agents, lopinavir coformulated with ritonavir is available as a pediatric oral solution and as tablets, and is approved for children 2 weeks of age and older.7 Fosamprenavir and nelfinavir are also available as pediatric suspensions, and are approved for use in children 2 years of age and older.7 Atazanavir is available in a pediatric capsule formulation, and is approved for use in children 6 years of age and older.7

The PIs are generally known to produce adverse effects related to gastrointestinal intolerance, dyslipidemia, and drug metabolism.6 Of the PIs, atazanavir is known to have the fewest effects on lipids.6

Darunavir

Of the PIs, both darunavir and tipranavir are able to maintain antiviral activity against many PI-resistant HIV-1 strains. Resistance to darunavir has been associated with 11 mutations (V11I, V32I, L33F, I47V, I50V, I54L, I54M, G73S, L76V, I84V, and L89V).48 One study demonstrated that over 20% of treatment failures were associated with the V32I and I54L mutations.49 Darunavir exhibits high-affinity binding properties, in addition to strong chain interactions and potential hydrogen bonding with both the HIV-1 protease, as well as mutant proteases.50,51 This allows for greater activity against resistant strains as compared with other PIs. Furthermore, darunavir-resistant strains need to undergo multiple simultaneous mutations to overcome darunavir binding affinity.50

A darunavir-ritonavir combination is FDA-approved for the treatment of HIV infection in children 6 years and older weighing at least 20 kg.52 In adult and adolescent patients, darunavir–ritonavir is recommended as a preferred PI therapy to start in ARV-naïve patients.6 In pediatric patients, darunavir is recommended as a second-line treatment option after failure of initial therapy due to the high pill burden required in children weighing less than 40 kg.7 However, it is also suggested that darunavir may be an option for ARV-experienced pediatric patients.7 Currently, darunavir is available as 75 mg, 150 mg, 300 mg, 400 mg, and 600 mg.52 The monthly cost of darunavir for a patient receiving 600 mg twice daily is $990.

The most commonly reported adverse events with darunavir include diar rhea (32%), nausea (18%), nasopharyngitis (12%), headache (11%), and upper respiratory tract infection (10%).53

Tipranavir

Like darunavir, tipranavir is a nonpeptidic PI, with an increased flexibility at the binding portion of the molecule.54 This increased flexibility results in a greater ability to overcome conformational changes in the protease enzyme due to mutations. Nonpeptidic PIs also act to prevent dimerization of the protease, preventing its activity through multiple pathways.55 These advantages have been demonstrated in its maintenance of a relatively low IC₉₀ when tested against HIV-1 strains which had been made highly resistant to ritonavir.56 Interestingly, tipranavir, like other PIs, has been shown to modulate Pneumocystis carinii growth.57

Several predictors of response have been evaluated for tipranavir. One of the earliest predictors studied was the number of baseline PI mutations. There are seven mutations which are major determinants of tipranavir resistance, ie, L33F, I47V, Q58E, T74P, V82L, V82T, and I84V.8 There are also 14 mutations which play a minor role in conferring tipranavir resistance, ie, L10V, I13V, K20M, K20R, E35G, M36I, K43T, M46L, I54A, I54M, I54V, H69K, N83D, and L90M.8 It has been found that patients with viruses with two or fewer universal PI-associated mutations are significantly more likely to achieve virologic response.58,59 A derivation of counting mutations is the tipranavir mutation score, whereby a genotyping is performed, and the mutations conferring reduced in vitro or in vivo tipranavir susceptibility or response are counted.60 This measure was found to be highly variable, and had poor correlation with virologic response.60 Patients achieving a trough concentration of at least 15 μM achieved a −1.1 log₁₀ viral load reduction.61 In a small retrospective analysis of 29 adult patients, tipranavir trough levels were found to be significantly higher in patients achieving a virologic response (P = 0.03).62 This, however, was not significantly associated with virologic response when analyzed using logistic regression (P = 0.17).63 The unbound tipranavir IC₉₀ and IC₅₀ are 0.1 μM and 0.03–0.07 μM, respectively.54,64

Less traditional predictors of response have also been assessed. The genotypic sensitivity score, sometimes referred to as an optimized background score considers the number of drugs in the optimized background regimen which have been shown to be active through genotypic testing.65–67 For adult patients with a genotypic sensitivity score of ≥2, 64.2% achieved a virologic response, compared with a 20% virologic response rate for those with a score <2.66 This trend was not observed in pediatric patients, possibly due to the small number of patients enrolled, and very few having a genotypic sensitivity score of ≥2.67 An inhibitory quotient is calculated by dividing the tipranavir trough by the tipranavir IC₅₀.68–70 A general breakpoint might be thought of as >50–60, because two analyses found that most patients (81%) above this level achieved at least a −1 log₁₀ viral load reduction.68,69 Another analysis found that an inhibitory quotient of ≥76 had a response rate of 64%, whereas an inhibitory quotient <76 had a response rate of 29%.70

The genotypic inhibitory quotient (gIQ) is calculated by dividing the tipranavir serum trough concentration by the number of tipranavir resistance conferring mutations genotyped from the patient’s HIV strain.62,63,66,67,70 The measure of gIQ had the highest correlation with virologic success in both children and adults. When correlating gIQ, tipranavir trough, tipranavir mutation score, use of enfuvirtide, and genotypic sensitivity score with virologic response in adult patients using logistic regression, gIQ was found to be the most significant predictor of virologic response (P = 0.03).63 At 48 weeks, a significantly greater reduction in viral load was observed in adult patients who had a gIQ > 14,500 ng/mL/mutation (83.3% versus 38.4%).66 At 48 weeks, pediatric patients with a gIQ above the first quartile (0.56–7.19) were more likely to achieve a viral load of <400 copies/mL (8% versus 52–68%).67 A more recent assessment of gIQ found that patients with more than eight tipranavir resistance mutations were unlikely to achieve a virologic response, regardless of the tipranavir trough level.62

The pharmacokinetics of a tipranavir–ritonavir combination have been studied in both adult and pediatric patients. Like many other PIs, tipranavir is metabolized via the cytochrome (CYP) p450 3A4 isozyme.71 Tipranavir should always be coadministered with ritonavir because of its known inhibition of CYP 3A4 metabolism, resulting in a boosting effect. This is important because tipranavir alone strongly induces its own metabolism, producing trough concentrations less than 5% of those produced by the combination.72 The understanding of the overall effects of the tipranavir–ritonavir combination on CYP p450 has been recently expanded to include an initial and steady-state phase.73 Upon initiating tipranavir–ritonavir, the ritonavir component results in strong inhibition of hepatic and, possibly, intestinal CYP 3A4 and 5, along with p-glycoprotein.73 This eventually balances with the inductive effects of tipranavir to a moderate inhibition of hepatic and strong inhibition of intestinal CYP 3A4 and 5, with little effect on p-glycoprotein.73

Tipranavir is highly protein-bound, with >99.9% of the drug bound to albumin or α-1-acid glycoproteins.56 In order to assure adequate absorption, the capsule formulation of tipranavir should be administered with a high-fat meal.74 The oral solution has been found to be unaffected by this dietary consideration.75

The primary adult efficacy data comes from two Randomized Evaluation of Strategic Intervention in multiresistant patients with Tipranavir (RESIST-1 [US and Australia; n = 620] and RESIST-2 [Europe and Latin America; n = 539]) trials, both of which had the same study design.76,77 Patients included were HIV-1 infected adults with a baseline viral load of at least 1000 copies/mL, at least one primary PI mutation corresponding to baseline PI therapy, with no more than two resistance-associated PI mutations. All patients were assessed by clinicians prior to randomization using genotypic testing to determine an appropriate PI, NRTI, and NNRTI regimen. They were then randomized to receive an unblinded regimen of either tipranavir boosted with ritonavir or their previously selected comparator PI. The primary efficacy endpoint measured was the proportion of patients achieving at least a −1 log₁₀ viral load decrease. A higher proportion of patients receiving tipranavir achieved the primary endpoint in both the RESIST-1 (41.5% versus 22.3%; P < 0.0001) and RESIST-2 trials (41% versus 14.9%; P < 0.0001) at 24 weeks.

The efficacy of tipranavir has been studied in pediatric patients from the US, Europe, and Latin America.78 This trial enrolled children 2–18 years of age who had a baseline viral load of more than 1500 copies/mL. Unlike the adult trial, treatment-naïve patients were also included and no resistance profile requirements were placed as criteria for enrollment. Children in this study were stratified by age into three categories, ie, 2–5, 6–11, and 12–18 years of age. The primary outcome for this study was safety and therefore it was not designed with sufficient power to measure efficacy outcomes. Nonetheless, viral loads as well as CD4 cell counts, were performed as secondary endpoints. As in the adult trial, patients were assigned an optimized background regimen prior to randomization. Patients in this noncomparator study received an unblinded regimen consisting of an optimized background regimen, including at least two other non-PIs as well as either low- (290/115 mg/m²) or high-dose (375/150 mg/m²) tipranavir–ritonavir, with an upper dosing limit equal to the adult dose of 500/200 mg.

At 48 weeks, 42.6% of all patients achieved a viral load of <400 copies/mL. In the high-dose group, 45.6% achieved viral loads <400 copies/mL compared with only 39.7% in the low-dose group. A mean viral load decrease of 1.24 log₁₀ copies/mL and 0.8 log₁₀ copies/mL was seen in the high- and low-dose groups, respectively. A trend toward better efficacy was seen in the high-dose group with respect to viral load reduction, although it was not statistically significant. As for immunologic response to therapy, a median increase in CD4⁺ T cell percentages was seen in both the high- (5% increase) and low-dose group (3% increase), although these values were not statistically different (P = 0.11). The immunologic response to therapy was greatest in the 2–5 year age group (10% and 6% for the low- and high-dose groups, respectively), likely due to the less resistant HIV strains of the younger children. Over the 48-week period, four patients developed AIDS-defining illnesses; all four had been receiving the low-dose regimen. The investigators concluded that there was a potential benefit of the high-dose regimen over the low-dose regimen.

A total of 78 study patients were continued on or switched to the high-dose regimen after 48 weeks. An abstract has been published to summarize the long-term safety and efficacy data gained from these patients over 100 weeks of high-dose therapy.79 Overall, 38% of patients maintained a viral load of <400 copies/mL and 34% maintained an undetectable viral load of <50 copies/mL. The 2–5-year-old age group experienced the greatest virologic response, with 56% achieving a viral load of <400 copies/mL and 48% achieving an undetectable viral load of <50 copies/mL.

Tipranavir carries a black box warning for both fatal and nonfatal intracranial hemorrhage, because these have been seen in the adult population,18 although these have not been observed in the pediatric or adolescent populations.78 Black box warnings also indicate a risk for clinical hepatitis and hepatic decompensation in patients with chronic hepatitis B or C coinfection.18 This subset of patients has been excluded from pediatric and adolescent tipranavir studies, and should apply to these populations as well. Recently, a study analyzing electrocardiograms demonstrated only clinically insignificant changes in corrected QT interval, with a maximum observation of 8.3 milliseconds for healthy patients receiving a supratherapeutic dose of tipranavir 750 mg.18

For the pediatric and adolescent populations, safety endpoints have been reported based on the Division of AIDS standardized toxicity grading table.80 The 48-week safety outcomes were not out of the ordinary, with 53.9% of patients experiencing a drug-related adverse event, 25.2% of patients experiencing a serious adverse event, and 8.7% patients discontinuing use of the study drug due to an adverse event.78 The most commonly reported adverse events were nausea, vomiting, diarrhea, and headache. An increased risk of bleeding was also described in the pediatric and adolescent study.78 When considering laboratory abnormalities, elevations in gamma-glutamyl transpeptidase and alanine transaminase led to discontinuation of tipranavir in four patients.78

A subanalysis from the RESIST trials assessed health-related quality of life in patients receiving tipranavircontaining regimens versus those receiving a comparator protease.81 It was found that changes in health-related quality of life from baseline were similar between groups.

Currently, tipranavir in combination with ritonavir is FDA-approved for use in patients 2 years of age and older, who are treatment-experienced and infected with an HIV-1 strain clinically resistant to more than one PI.18 The European Medicines Agency has given a positive opinion for tipranavir use in highly pretreated adolescents (>12 years old) with evidence of resistance to multiple PIs, and also in highly pretreated children aged 2–12 years. The tipranavir–ritonavir combination is not currently recommended as initial therapy according to the adult and adolescent guidelines.6

Conclusions

The tipranavir–ritonavir combination provides another promising line of therapy for patients infected with viruses exhibiting PI resistance. Tipranavir has been proven to be relatively safe in both the adult and pediatric populations, giving a valuable alternative for these patients. The PI class effect in decreasing the formation of new mutations makes tipranavir agent more desirable for HIV strains already highly resistant to other ARV therapies.