Advertisement

TheBodyPRO.com Covers IAS 2015

News

Tenofovir Alafenamide (TAF) in People With Kidney Dysfunction

October/November 2015

 1  |  2  |  Next > 

As mentioned previously in this issue of TreatmentUpdate, clinical trials assessing the new formulation of tenofovir (tenofovir alafenamide, or TAF) and sometimes comparing it to the original formulation (tenofovir disoproxil fumarate, or TDF) are ongoing. Studies have found that TAF is as effective as TDF and is very likely safer, particularly for the kidneys and bones. Participants enrolled in these studies had relatively good kidney health.

But will TAF be safe in people with pre-existing kidney dysfunction? To try to answer this question, researchers conducted study 292-0112. In this study, researchers sought participants who had mild-to-moderate kidney dysfunction graded with the use of eGFR (estimated glomerular filtration rate). After screening, researchers recruited 242 HIV-positive participants who had an eGFR between 30 and 69 mL/minute, who were on stable combination anti-HIV therapy (commonly called ART) and who had a viral load less than 50 copies/ml. All participants were switched to a TAF-containing regimen and monitored for 48 weeks. In general, TAF was safe and when this formulation of tenofovir was substituted for TDF, improvements in bone density and kidney health were seen. However, not every participant who switched from TDF to TAF had improvement in kidney injury, particularly in cases of severe injury to these organs.


Study Details

All 242 participants were switched from their current regimen to the following regimen:

  • TAF + FTC + elvitegravir + cobicistat (this fixed-dose combination pill is called Genvoya)
Advertisement

The average profile of participants when they entered the study was as follows:

  • age -- 58 years (note that 28% of participants were at least 65 years old)
  • 79% men, 21% women
  • CD4+ count -- 632 cells/mm3
  • HIV viral load -- less than 50 copies/ml
  • 40% had hypertension
  • 14% had type 2 diabetes
  • eGFR -- 56 mL/minute (note that 34% of participants had an eGFR of at least 60 mL/min)
  • 33% had mild-to-moderate levels of protein in their urine, suggestive of kidney injury

Overall, 158 participants were taking TDF as part of their regimen and 84 participants were taking other nukes.


Results

In the everyday world outside a clinical trial, when assessing kidney health, doctors usually request lab analyses of blood, and in particular the amount of the waste product creatinine. They can then put the amount of creatinine detected into a formula and get an estimate of the functioning of the kidneys. This is called the estimated glomerular filtration rate (eGFR). Doctors routinely use eGFR because assessing the actual GFR (written as aGFR) would be cumbersome for patients. Note that the eGFR is an estimate and it is useful for routine laboratory analyses requested by doctors.

However, in the present research setting, it was important to find out about the aGFR because eGFR is a calculated value (not a measured one). In the present study, researchers were able to assess the actual GFR. They found that there were no significant changes in the aGFR and only minor ones with eGFR after participants switched to a TAF-based regimen. Overall, this suggests that TAF does not have a major impact on the kidneys' ability to filter blood.

The researchers also had laboratories analyse participants' urine and they assessed certain proteins in the urine, as follows:

  • protein to creatinine ratio
  • albumin to creatinine ratio
  • retinol-binding protein to creatinine ratio
  • beta2-microglobulin to creatinine ratio

They found significant reductions in these proteins among TAF users but not TDF users. Overall, this suggests that TAF helped to reduce kidney injury compared to TDF.


A Moderate-to-Severe Degree of Kidney Injury

Researchers focused on people with high levels of total protein in their urine samples (more than 200 mg/gram,) as this sub-group would likely have a higher level of kidney injury than other participants.


Switching From TDF to TAF

In conducting their analyses, researchers found that among participants who had been on a TDF-containing regimen at the start of the study, 47% had high levels of protein in their urine, suggestive of kidney injury. After switching from TDF to TAF, 48 weeks later the proportion with a high level of protein in their urine was 13%. This difference was statistically significant. It shows that switching from TDF to TAF is associated with significant improvements in kidney health. However, note that this switch does not help everyone who used TDF. Perhaps not everyone's kidneys recovered after the switch because of the severity of kidney injury, or there may have been other factors that could have affected kidney health that were unrelated to TAF, such as the presence of higher-than-normal blood pressure, type 2 diabetes and so on.

 1  |  2  |  Next > 


Related Stories

Genvoya, New Single-Tablet HIV Regimen Containing Tenofovir Alafenamide, Approved By FDA
Tenofovir Alafenamide (TAF) Still Noninferior to Current Tenofovir -- With Better Bone/Kidney Signals



This article was provided by Canadian AIDS Treatment Information Exchange. It is a part of the publication TreatmentUpdate. Visit CATIE's Web site to find out more about their activities, publications and services.
 


No comments have been made.
 

Add Your Comment:
(Please note: Your name and comment will be public, and may even show up in
Internet search results. Be careful when providing personal information! Before
adding your comment, please read TheBody.com's Comment Policy.)

Your Name:


Your Location:

(ex: San Francisco, CA)

Your Comment:

Characters remaining:


Please note: Knowledge about HIV changes rapidly. Note the date of this summary's publication, and before treating patients or employing any therapies described in these materials, verify all information independently. If you are a patient, please consult a doctor or other medical professional before acting on any of the information presented in this summary. For a complete listing of our most recent conference coverage, click here.

Advertisement

The content on this page is free of advertiser influence and was produced by our editorial team. See our content and advertising policies.