Evidence map›Paper›PMID 27419179›Full record

ArticleOpen forum infectious diseases2016

Efficacy and Safety of a Preemptive Antiviral Therapy Strategy Based on Combined Virological and Immunological Monitoring for Active Cytomegalovirus Infection in Allogeneic Stem Cell Transplant Recipients.

David Navarro, Paula Amat, Rafael de la Cámara, Javier López, Lourdes Vázquez, David Serrano, José Nieto, Monserrat Rovira, José Luis Piñana, Estela Giménez and 1 more

Open access · goldAbstract read
In one paragraph

Article in Open forum infectious diseases, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
4.3field-weighted citation impact, top 6% 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

20 citing papers in PubMed, 43 citations in OpenAlex.

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  16. Observational
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  19. Immune Monitoring for CMV in Transplantation.Current infectious disease reports · 2018
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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

11 authors at 6 institutions in 2 countries.

David NavarroMicrobiology Service; Departments of Microbiology.
Paula AmatHematology and Medical Oncology Service, Hospital Clínico Universitario , Instituto de Investigación INCLIVA , Valencia.
Rafael de la CámaraHematology Service , Hospital de la Princesa , Madrid.
Javier LópezHematology Service , Hospital Ramón y Cajal , Madrid.
Lourdes VázquezHematoogy Service , Hospital General Universitario , Salamanca.
David SerranoHematology Unit , Hospital Morales Meseguer , Murcia.
José NietoHematology Unit , Hospital Morales Meseguer , Murcia.
Monserrat RoviraHematology Unit , Hospital Clinic , Barcelona , Spain.
José Luis PiñanaHematology and Medical Oncology Service, Hospital Clínico Universitario , Instituto de Investigación INCLIVA , Valencia.
Estela GiménezMicrobiology Service.
Carlos SolanoHematology and Medical Oncology Service, Hospital Clínico Universitario, Instituto de Investigación INCLIVA, Valencia; Medicine, School of Medicine, University of Valencia.
Hospital General Universitario Morales Meseguer · ESINCLIVA Health Research Institute · ESMicrobiology Society · GBHospital Clínic de Barcelona · ESHospital Universitario de La Princesa · ESUniversitat de València · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background.  Preemptive antiviral therapy for active cytomegalovirus (CMV) infection in allogeneic stem cell transplant recipients (Allo-SCT) results in overtreatment and a high rate of recurrences. Monitoring of CMV-specific T-cell immunity may help to individualize treatments and minimize these problems. Methods.  We conducted a prospective, multicenter, matched comparison-group study to evaluate the efficacy and safety of a novel strategy that consisted of interrupting anti-CMV therapy upon CMV DNAemia clearance and concurrent detection of phosphoprotein 65/immediate-early-1-specific interferon-γ-producing CD8(+) T cells at levels of >1 cell/µL (within 30 days after the initiation of therapy). Immunological monitoring was performed on days +7, +14, +21, and +28 after treatment initiation. The primary endpoint was the cumulative incidence of recurrent DNAemia within 2 months after treatment cessation. Secondary endpoints were the length of antiviral treatment courses and the incidence of hematological toxicity. Results.  Sixty-one patients were enrolled in the study group. Fifty-six patients were included in the matched-control group. Eleven patients (18%) fulfilled the criteria for antiviral treatment interruption. The cumulative incidence of recurrent CMV DNAemia was significantly lower (P = .02) in these patients than in patients in the comparative groups. Likewise, the length of antiviral treatment courses was significantly shorter in these patients than that in patients in the matched-control group (P = .003). No significant differences in the incidence of hematological toxicity was observed between the comparative groups. Conclusions.  Our data support the clinical utility of combining immunological and virological monitoring for the management of CMV infection in a subset of Allo-SCT recipients.

Indexed as

allogeneic stem cell transplantationcytomegalovirusIFN-γ CD8+ T cellsimmunological monitoringpreemptive antiviral therapy

Identifiers

PMID27419179
PMCPMC4943548
OpenAlexW2405311721

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.