Just a moment, the page is loading...
Browse ALL STUDIES
Keyword Search
View All Selected
Clear All
Login / Create Account
Login
Create Account
Home
About Us
Privacy Policy
Minimum System Requirements
How To Join
Mission
Data Sponsors
Researchers
How It Works
How to Request Data
Review of Requests
Data Sharing Agreement
Access to Data
Independent Review Panel
Metrics
FAQs
News
Help/Contact Us
Comparative effect of dolutegravir and raltegravir on CD4+/CD8+ ratio, CD4%, and multiple T-cell marker recovery. SPRING-2 study.
Proposal
1633
Title of Proposed Research
Comparative effect of dolutegravir and raltegravir on CD4+/CD8+ ratio, CD4%, and multiple T-cell marker recovery. SPRING-2 study.
Lead Researcher
Jose Ramon Blanco
Affiliation
Hospital San Pedro - Center for Biomedical Research of La Rioja (CIBIR), SPAIN
Funding Source
Potential Conflicts of Interest
R Blanco has carried out consulting work for Abbvie, Bristol-Myers Squibb, Gilead Sciences, Janssen, Merck, and ViiV Healthcare; has received compensation for lectures from Abbvie, Bristol-Myers Squibb, Gilead Sciences, Janssen, Merck, and ViiV Healthcare, as well as grants and payments for the development of educational presentations for Gilead Sciences and Bristol-Myers Squibb, and ViiV Healthcare.S Moreno has carried out consulting work for Abbvie, Boehringer Ingelheim, Bristol-Myers Squibb, Gilead Sciences, Janssen, Merck, Roche and ViiV Healthcare; has received clinical grants and compensation for lectures from Abbvie, Boehringer Ingelheim, Bristol-Myers Squibb, Gilead Sciences, Janssen, Merck, Roche and ViiV Healthcare.
Data Sharing Agreement Date
26 July 2017
Lay Summary
The immune system is composed of a variety of different cell types and proteins. One
of these types of cells are lymphocytes (included among the white blood cell). There
are two main types of T-lymphocytes (CD4 and CD8). Because the CD4 count is so
variable, some researchers look at the CD4/CD8 ratio and the CD4%. Healthy persons
generally have a CD4/CD8 ratio >1 and a CD4% >29%.
HIV-1 infection has a negative impact in the immunological status. Since CD4 cells are
the main targets of HIV, the CD4 count falls after the infection while the CD8 count
increases causing a decrease in the CD4/CD8 ratio. There is a direct correlation
between the CD4 count and the risk of morbidity and mortality.
The goal of antiretroviral therapy (ART) is to inhibit viral replication so that the patient
can improve its immune response trying to revert it to 'normal'. However, achieving an
apparent normal or even high CD4 count may not translate into a fully restored health.
To realize its importance, HIV-infected patients on stable antiretroviral therapy with
durable viral control that had a high CD4 count but a low CD4/CD8 ratio or a low
CD4% have a higher morbi-mortality risk. Meanwhile, those patients with a high CD4
count and a higher CD4/CD8 ratio and a higher CD4% have a lower morbi-mortality
risk, similar to the healthy people.
At present, not all the antiretroviral treatments have the same immunological recovery
efficacy. Even, the normalization of CD4/CD8 ratio and CD4% is uncommon following
ART. Indeed, immunological recovery could be dependent on the drug class used.
INSTIs are an effective and well-tolerated class of antiretroviral drugs that currently are
included in all the HIV treatment guidelines. Recently it has been showed that
raltegravir (RAL), the first available INSTIs, showed a faster CD4/CD8 ratio
normalization than efavirenz [1], a finding with potential clinical implications. Whether
other INSTIs have a similar impact for this outcome remains to be explored. So, in the
SPRING-2 study, patients who initiated their first treatment with the INSTIs-containing
regimen dolutegrair (DTG) or RAL showed a similar CD4+ recovery after 48 [2] and 96
[3] weeks of treatment.
Undoubtedly, if DTG were able to achieve a higher immunological recovery (CD4/CD8
ratio, CD4 percentage,…) it could strengthen the role of DTG in the quality of immune
recovery.
Study Data Provided
[{ "PostingID": 1387, "Title": "VIIV-ING113086", "Description": "A randomized, double blind study of the safety and efficacy of GSK1349572 50mg once daily to raltegravir 400mg twice daily both administered with fixed-dose dual nucleoside reverse transcriptase inhibitor therapy over 96 weeks in HIV-1 infected antiretroviral therapy naive adult subjects" }]
Statistical Analysis Plan
This exploratory post hoc analysis will be performed in the intention-to-treat population that included all participants who underwent randomization and received at least one dose of study drug. The primary approach to handle missing data will be observed-cases approach that included only cases with available data at a particular timepoint; an observed-cases approach allows the evaluation of immunological normalization without confounding by discontinuations or lack of observation. A sensitivity analysis of the primary endpoints will be performed restricting the analysis to subjects who had achieved an HIV-1 RNA level <50 copies/mL at a particular timepoint. Treatment group balance in the main baseline covariates will be assessed using independent samples t-test and chi-squared correspondingly. Percentage difference (“RAL” - “DTG”) and corresponding precision based on 95% confidence intervals (CI) and p-values will be calculated for i) CD4+/CD8+ ratio normalization at cut-offs (0.5 and 1) at 48 weeks and 96 weeks, ii) the achievement of CD4 percentage normalization at cut-off 29% at 48 weeks and 96 weeks, and iii) the achievement of complete normalization, comprising a CD4 =500, a CD4+/CD8+ ratio =1 and %CD4 =29%. To assess possible differences across subgroups or baseline covariates we will perform a multivariable (adjusted) analyses. To evaluate the impact of the cut-offs selection in our findings, we will also calculate the mean changes and 95% CI [ANCOVA] in CD4+/CD8 ratio and CD4+% from cART initiation by treatment arm and the estimated mean differences [95% CI] in mean changes. A sensitivity analysis of the missing data approach will include the endpoint time to CD4+/CD8+ and CD4+% normalization.
Publication Citation
Blanco JR, Alejos B, Moreno S. Immune recovery markers in a double blind clinical trial comparing dolutegravir and raltegravir based regimens as initial therapy (SPRING-2). PLoS One. 2020 Jan 16;15(1):e0226724.
https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0226724
© 2024 ideaPoint. All Rights Reserved.
Powered by ideaPoint.
Help
Privacy Policy
Cookie Policy
Help and Resources