Evidence map›Paper›PMID 30376108›Full record

Trial reportThe Journal of antimicrobial chemotherapy2019

Effect of valaciclovir on CD4 count decline in untreated HIV: an international randomized controlled trial.

Darrell H S Tan, Janet M Raboud, Leah Szadkowski, Beatriz Grinsztejn, José Valdez Madruga, Maria Ines Figueroa, Pedro Cahn, Simon E Barton, Amanda Clarke, Julie Fox and 3 more

Open access · hybridAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in The Journal of antimicrobial chemotherapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.1field-weighted citation impact, top 55% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 9 institutions in 4 countries.

Darrell H S TanDivision of Infectious Diseases, St. Michael's Hospital, Toronto, Canada.
Janet M RaboudDalla Lana School of Public Health, University of Toronto, Toronto, Canada.
Leah SzadkowskiBiostatistics Research Unit, University Health Network, Toronto, Canada.
Beatriz GrinsztejnInstituto de Pesquisa Clínica Evandro Chagas (IPEC), Fundaçao Oswaldo Cruz, Rio de Janeiro, Brazil.
José Valdez MadrugaCentro de Referência e Treinamento em DST/AIDS-SP, São Paulo, Brazil.
Maria Ines FigueroaFundación Huesped, Buenos Aires, Argentina.
Pedro CahnFundación Huesped, Buenos Aires, Argentina.
Simon E BartonChelsea and Westminster Hospital, London, UK.
Amanda ClarkeBrighton & Sussex University Hospital NHS Trust, Brighton, UK.
Julie FoxGuy's & St. Thomas' NHS Foundation Trust, London, UK.
Wendy ZubykCIHR Canadian HIV Trials Network, Vancouver, Canada.
Sharon L WalmsleyDepartment of Medicine, University of Toronto, Toronto, Canada.
VALIDATE Study Group
Fundación Huésped · ARUniversity Health Network · CAChelsea and Westminster Hospital · GBFundação Oswaldo Cruz · BRGuy's and St Thomas' NHS Foundation Trust · GBHIV Legal Network · CASt. Michael's Hospital · CAUniversity Hospitals Sussex NHS Foundation Trust · GBUniversity of Toronto · CA

Funding

CIHR MCT 94245CIHR NEB 136629
6 · The paper itself

Abstract

Objectives: To determine the impact of valaciclovir on HIV disease progression in treatment-naive HIV-positive adults. Methods: In this fully blind, multicentre, 1:1 randomized placebo-controlled trial, treatment-naive HIV-1-positive adults with CD4 counts 400-900 cells/mm3 and not meeting contemporaneous recommendations for combination ART (cART) were randomized to valaciclovir 500 mg or placebo twice daily, and followed quarterly until having two consecutive CD4 counts ≤350 cells/mm3 or initiating cART for any reason. The primary analysis compared the rate of CD4 count decline by study arm after adjusting for baseline CD4 count and viral load (VL). Secondary analyses compared the rate of CD4 percentage decline, HIV VL, herpes simplex virus (HSV) recurrences and drug-related adverse events. The trial closed after release of the START trial results in August 2015. Results: We enrolled 198 participants in Canada, Brazil, Argentina and the UK. Median (IQR) age was 35 (30-43) years. Baseline CD4 count was 592 (491-694) cells/mm3 and VL was 4.04 (3.5-4.5) log10 copies/mL. Over 276 person-years of follow-up, CD4 counts declined by 49 cells/mm3/year in the valaciclovir arm versus 58 cells/mm3/year in the placebo arm (P = 0.65). No differences were seen in the rate of change in CD4 percentage (-1.2%/year versus -1.7%/year, P = 0.34). VL was 0.27 log10 copies/mL lower in valaciclovir participants overall (P<0.001). Placebo participants had more HSV recurrences (62 versus 21/100 person-years, P < 0.0001) but similar rates of grade ≥2 drug-related adverse events. Conclusions: Unlike prior trials using aciclovir, we found that valaciclovir did not slow CD4 count decline in cART-untreated adults, although power was limited due to premature study discontinuation. Valaciclovir modestly lowered HIV VL.

Indexed as

CD4 Lymphocyte CountAdultAnti-HIV AgentsArgentinaBrazilCanadaDisease ProgressionFemaleHIV InfectionsHIV SeropositivityHumansInternationalityMaleMiddle AgedTreatment OutcomeUnited KingdomAnti-HIV AgentsValacyclovir

Identifiers

PMID30376108
PMCPMC6337901
OpenAlexW2898697105

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.