FormalPara Key Summary Points
Drug-drug interactions between antiretrovirals and immunosuppressors in HIV-infected patients undergoing solid organ transplantation are extremely complex
Data are lacking on the clinical and pharmacological management of HIV-infected transplant recipients receiving cobicistat-containing ART regimens and tacrolimus or mTOR inhibitors
Favourable outcomes are possible in these patients if tacrolimus doses are significantly reduced and daily therapeutic-drug monitoring performed
Despite careful therapeutic drug monitoring some level of tacrolimus toxicity, e.g., chronic renal failure, may be difficult to avoid

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Introduction

Managing HIV-infected patients undergoing solid-organ transplantation (SOT) represents a major challenge due to the potential drug-drug interactions (DDI) between antiretroviral (ART) drugs and immunosuppressive agents, some of which have a narrow therapeutic index [1]. Data about interactions and dose adjustment are still limited. Where possible, ART drugs with lower potential for DDIs are used, such as regimens based on non-boosted integrase-strand-transfer inhibitors (InSTI), but when ART resistance is known or suspected, other families of ART are required.

With the improvements in hepatitis C virus (HCV) therapy in the past few years, the proportion of patients with HIV/HCV co-infection who will need a liver transplantation may decrease [2,3,4]. On the other hand, HIV-infected patients now have a near-normal life span, and comorbidities such as end-stage kidney disease, non-alcoholic-steatohepatitis or cardiovascular disease are on the rise [5]. Thus, the numbers of experienced ART patients requiring SOT may increase in the coming years.

Cobicistat is a potent and selective inhibitor of cytochrome P450 3A (CYP3A), used as pharmacokinetic booster for first-generation integrase inhibitors (e.g., elvitegravir) and protease inhibitors (PIs) (e.g., darunavir or DRV) in the management of HIV infections [6]. Calcineurin inhibitors, such as cyclosporine and tacrolimus, which are frequently used in SOT recipients, and mTOR inhibitors, such as sirolimus and everolimus, are both CYP3A substrates [7]. Thus, careful therapeutic drug monitoring (TDM) is recommended when these drugs are used together. Although there is some experience with ritonavir, another PI booster, clinical experience with cobicistat and immunosuppressants is extremely scarce, since it has only recently been developed. It offers, however, the benefit of a more selective cytochrome inhibition and co-formulation [6, 8].

We report three cases of cobicistat-tacrolimus co-administration, including one also with sirolimus and one with everolimus co-administration, in HIV-positive patients who underwent SOT and review previously reported cases. The Institutional Ethics Committee approved the Liver Transplant and Kidney Transplant in HIV Infection Cohorts in Hospital Clinic-IDIBAPS of Barcelona as medical records were used to identify cases. Patients provided their informed consent for the publication of their data.

Clinical cases and review of previously reported cases

Case 1

A 40-year-old man with end-stage renal disease on peritoneal dialysis was referred to our centre for evaluation for kidney transplantation. He had a history of HIV infection, diagnosed in 2006, due to HIV-associated nephropathy. There was no history of opportunistic infections, nor was HCV co-infection reported. Hepatitis B core antibody (Anti-HBc), CMV and toxoplasmosis IgG were positive. He had had received several ART regimens since 2006 with poor compliance, although HIV resistance was not documented. Previous ART included atazanavir/ritonavir (ATV/r)-lamivudine (3TC)–zidovudine (AZT), DRV/ritonavir (DRV/r)–3TC-AZT, DRV/r–3TC-abacavir (ABC) and DRV/r–raltegravir (RAL), ongoing at the time of referral. Persistently detectable HIV viral load (VL), around 200–300 copies/ml, was documented while receiving DRV/r-RAL over several months and 595 CD4 T cells/µl, during pre- transplant evaluation. HBV VL was undetectable.

A genotypic resistance performed on plasma samples test did not amplify the virus. A pro-viral resistance test was then performed. Protease and reverse transcriptase (RT) genes were amplified, with no detectable mutations; integrase gene was not amplified. Given the low genetic barrier to resistance of raltegravir and the inability to exclude resistance to InSTIs, the decision taken was to modify ART to DRV/r 600/100 mg BID + dolutegravir (DTG) 50 mg BID. Kidney transplantation was deferred until undetectable VL and proper adherence to ARTs were achieved. The patient became rapidly undetectable (< 50 copies/ml). Later, the regimen was simplified to darunavir/cobicistat (DRV/c) 800/150 mg QD + DTG 50 mg BID to reduce the pill burden. He maintained good adherence and VL remained undetectable at subsequent checkups. The patient received a living-donor kidney transplantation in June 2017.

Immunosuppression consisted of induction with basiliximab, mycophenolate mofetil (MMF) and tacrolimus. Initially, 1.5 mg of tacrolimus was given with TDM performed 48 and 72 h post-dose. Trough concentrations increased up to 34.8 ng/ml. Thus, doses were adapted and the patient was finally discharged on tacrolimus 1.5 mg/48 h. Creatinine serum levels were between 2.0 and 2.4 mg/dl. Later, tacrolimus was modified to 0.5 mg/72 h maintaining whole blood concentrations between 7 and 14 ng/ml (Fig. 1a). Post-transplantation course was uncomplicated without rejection episodes.

Fig. 1
figure 1

a Case 1. Tacrolimus and sirolimus whole blood concentrations and dosing interval after kidney transplantation. b Case 2. Tacrolimus and everolimus whole blood concentrations and dosing interval after kidney transplantation. c Case 3. Tacrolimus whole blood concentrations and dosing interval after liver transplantation

Fourteen months after kidney transplantation, not having changed the ART regimen, the patient developed cutaneous Kaposi sarcoma (KS). He received local treatment and, as there is evidence that sirolimus can delay progression of cutaneous KS, MMF was switched to sirolimus [9, 10]. The initial dose was 1 mg/48 h, then 0.5 mg/4 days. Levels ranged between 3.2 and 6 ng/ml, while tacrolimus doses were continued 0.5 mg/72 h (Fig. 1a).

Three years later, the patient is well, with no evidence of KS progression, stable renal function (serum creatinine around 1.8 mg/dl), undetectable plasma HIV VL and CD4 T cells > 1000/µl.

Case 2

A 59-year-old man had been HIV infected since 1994 with end-stage renal disease due to focal segmental glomerulosclerosis. He had a history of pulmonary tuberculosis in 1994 and cutaneous KS in 2012. He had a 23-year history of ART. Initially receiving zidovudine monotherapy and then other sub-optimal ART regimens based on a combination of thymidine analogues (nucleoside RT inhibitors) and the first protease inhibitors, which led to virological failures and ART-related complications, e.g., lipodystrophy, dyslipidaemia and gynecomastia. A genotypic resistance test in 2009 revealed the presence of mutations in the reverse transcriptase region and in the protease region that limited the available treatment options.

At the time of kidney-transplant evaluation, he was receiving DRV/c 800/150 mg QD and DTG 50 mg QD with stable virological suppression (HIV VL < 50 copies/ml) and CD4 T cells of 247/µl. Thus, in November 2019 he underwent kidney transplantation from an HLA-identical living donor.

Immunosuppression consisted of basiliximab, prednisone, tacrolimus and everolimus. The last two immunosuppressants were initiated 1 week before kidney transplantation, 1 mg/week and 0.5 mg/48 h, respectively, with careful TDM. After transplantation, tacrolimus was modified to 1.5 mg/week. The patient experienced delayed graft function and proteinuria (protein/creatinine ratio > 2000 mg/g). Therefore, a biopsy was performed 2 weeks after transplantation. It revealed acute tubular necrosis. Graft rejection and segmental hyalinosis lesions were ruled out. Then, due to the possible association of acute tubular necrosis with everolimus [11], the latter was substituted with mycophenolate mofetil.

During the following months, additional tacrolimus dose adjustments were necessary. Stable whole blood concentrations between 3.8 and 7.2 ng/ml were achieved with 0.5 mg/week (Fig. 1b). Eleven months after kidney transplantation the patient is still on the same ART regimen, serum creatinine is stable between 1.9 and 2.2 mg/dl, HIV VL remains undetectable and the last CD4 T cell count was 477/µl. A new KS was diagnosed, and then it was decided to discontinue tacrolimus.

Case 3

A 57-year-old man had been HIV/HCV co-infected for 30 years due to intravenous drug abuse. He had a history of chronic renal failure (creatinine serum level 1.7 mg/dl, GFR 42 ml/min), cirrhosis due to HCV, treated with direct-acting antivirals (DAAs) and ribavirin for 6 months with sustained virological response (SVR). He had presented opportunistic infections, including Pneumocystis jirovecii pneumonia and genitourinary tuberculosis several years ago, both of which were adequately treated. There was no history of HBV co-infection or vaccination. During the months leading up to the referral to our centre, he had several hepatic encephalopathy episodes and refractory ascites. Therefore, liver transplant evaluation was performed.

He received multiple ART regimens. At the time of referral, he was receiving DRV/c 800/150 mg QD and RAL 400 mg BID. HIV VL was < 50 copies/ml and CD4 T cells 124/µl. Resistance to other families of ART was suspected although not detected in previous genotypic tests. To reduce the pill burden and increase the genetic barrier of the ART regimen, RAL was switched to DTG 50 mg QD while DRV/c was continued. CD4 T cells increased up to 213/µl (30%), and 3 months later, in June 2019, the patient underwent liver transplantation.

Immunosuppression consisted of MMF, basiliximab, prednisone and tacrolimus. Initially, 1 mg of tacrolimus was given with daily TDM. He continued with 2 mg/day until target concentrations were reached and was discharged on 1.5 mg/day. Subsequently, doses were adjusted and stable whole blood levels between 6.7 and 10.4 ng/ml were maintained with 1 mg/48 h. Post-transplantation, he presented partial portal vein thrombosis, treated with acenocoumarol. Transient transaminase elevations suggestive of graft rejection occurred, decreasing with tacrolimus dose adjustment and leading to tacrolimus nephrotoxicity (creatinine levels rose to 2.3 mg/dl). HBV vaccination was completed post-transplantation.

Fourteen months later, the patient remains on the same ART regimen; HIV VL is undetectable. Tacrolimus was reduced to 0.5 mg/72 h (Fig. 1c). Liver function is normal. Creatinine serum levels were around 2.1 mg/dl. There were no signs of graft rejection or pharmacologic toxicity.

Previously Reported Cases

Three additional cases of tacrolimus and cobicistat co-administration (all kidney recipients) were previously published. The main characteristics of these cases and those reported here are summarized in Table 1.

Table 1 Main characteristics, clinical course and outcome of HIV-positive solid organ-transplant recipients receiving cobicistat-based regimens

Discussion

Although there is some experience with tacrolimus and mTOR inhibitors co-administered with ritonavir boosted PIs, most data on how to manage DDIs with cobicistat are theoretical. Cobicistat has been developed more recently, and thus, there are fewer cases using this booster, since other more convenient ARV drugs, e.g., non-boosted InSTIs, have become available in recent years. However, when PIs are required, cobicistat offers several advantages, such as co-formulation and a more favourable DDI profile. In contrast to ritonavir, cobicistat is a more specific CYP3A inhibitor and its affinity to other cytochrome P450 isoenzymes is different. It is a weak inhibitor of CYP2D6 and does not inhibit or induce other CYP enzymes [6, 12, 13].

However, the absence of clinical studies providing information about dose adjustment represents a major challenge in terms of pharmacological management.

Not only were significant tacrolimus (and mTOR inhibitors in cases 1 and 2) dose reductions necessary in the three cases presented here, but also prolongation of the dosing interval with careful TDM to maintain the target concentration and avoid toxicity. It is worth noting that tacrolimus doses were slightly higher than those used when ritonavir is given [14,15,16,17,18,19].

Finding appropriate tacrolimus doses to avoid graft rejection without harming kidney function, especially in patients with a history of chronic renal disease as in case 3, is another important issue in these complex scenarios. Although the three patients had successful outcomes, it was difficult to stabilize creatinine serum levels and a slight deterioration of renal function in the three cases due to tacrolimus nephrotoxicity could not be excluded.

To our knowledge, only three additional cases of tacrolimus and cobicistat co-administration have been published previously (cases 1–3 in Table 1) and all of them reported serious tacrolimus toxicity. Han et al. and Patel et al. reported significant increases in tacrolimus serum levels when Stribild (tenofovir–emtricitabine–elvitegravir–cobicistat) was initiated in two HIV infected kidney transplant recipients, which led to tacrolimus discontinuation and ART substitution with a non-boosted integrase-based regimen in both cases (2 mg BID and 3 mg BID of tacrolimus were administered, respectively) [20, 21]. Likewise, Bartiromo et al. published a case of a kidney transplant recipient, receiving tacrolimus 5 mg BID, who developed COVID-19 pneumonia at the beginning of the SARS-CoV-2 pandemic and was medicated with DRV/c as an antiviral for SARS-CoV-2 (and 1 day of lopinavir/ritonavir before DRV/c, with the same indication), with tacrolimus dose reduction to 3 mg BID. The whole blood concentration of tacrolimus reached 90.5 ng/ml causing serious drug toxicity. Thus, both medications were suspended [22]. It is worth mentioning that recent evidence shows no activity of darunavir-cobicistat against SARS-CoV-2 but it was under consideration at the time of this reported case [23].

These situations with extremely complex DDIs are becoming more frequent since transplantation has become the standard of care for patients with HIV and end-stage kidney or liver disease. In fact, kidney and liver transplants are the most common transplant procedures performed in patients with HIV [24]. Current criteria for SOT in people living with HIV (PLWH) state that patients must be on stable ART therapy with proper compliance, HIV plasmatic VL must be undetectable, there should be an absence of active opportunistic infections and the CD4 T cell count should ideally be > 200 cells/µl when there is a history of opportunistic infection [24]. As previously explained, given the near-normal life expectancy of HIV-infected individuals, end-stage organ dysfunction due to causes other than HCV may increase.

Outcomes of liver and kidney transplant in PLWH have been consistent with those in HIV-uninfected people, especially in the absence of HCV co-infection [24]. Although higher rates of acute graft rejection in PLWH undergoing SOT are still a matter of concern (in part consequent to difficulties in adapting immunosuppressors concomitantly with certain ARTs), several studies have reported patient and graft survival rates in long-term follow-up of HIV-positive kidney-transplant recipients similar to those who were HIV negative [25,26,27]. Regarding liver transplantation in HIV/HCV co-infected patients, since DAAs became available, SVRs prior to and post liver transplantation are comparable to those of HCV-mono-infected patients [28, 29]. Thereby, graft and patient survival has shown improvement over time and outcomes of co-infected liver recipients are expected to match those of HCV-mono-infected patients.

Nevertheless, the inadequate management of DDIs can impact in HIV control and graft survival, including increased HIV viremia or graft rejection due to sub-therapeutic ART or immunosuppressant levels as well as the emergence of opportunistic infections or toxicity due to over-immunosuppression [30]. To the best of our knowledge, this is the first report of a successful outcome in patients receiving tacrolimus and cobicistat. A multidisciplinary approach and frequent communication between health care providers are mandatory to avoid dosage errors and prescription issues and to ensure successful management.

Given our own experience with these three cases and those reported, we suggest that, in patients already taking cobicistat, tacrolimus (and other calcineurin and mTOR inhibitors) should be started as a single low dose (e.g., 1 mg) and daily TDM performed, only repeating doses when levels reach the lowest desired target levels. Then, a single dose should be repeated and TDM performed daily again until establishing an initial appropriate dose interval. If the situation is the opposite (a patient already taking tacrolimus initiates a cobicistat-based regimen), tacrolimus should be stopped and only resumed when levels decrease to the minimum therapeutic level, following the same principle described above. Since cobicistat lengthens the half-life of immunosuppressants, it will take longer to reach steady-state pharmacokinetics. Early dosage changes before it has been achieved may contribute to greater difficulty in dose adjustment.

In conclusion, for HIV-infected transplant recipients on tacrolimus where it is impossible to avoid ART regimens containing cobicistat, a significant dose reduction made on a case-by-case basis with close TDM remains essential, as the final doses of tacrolimus are difficult to predict. Despite the difficulties in establishing the final doses of immunosuppressants, the outcome seems favourable, although some level of chronic renal toxicity may be present as a consequence of dose adjustments.