Evidence map›Paper›PMID 26488159›Full record

Observational studyPloS one2015

Potential for Drug-Drug Interactions between Antiretrovirals and HCV Direct Acting Antivirals in a Large Cohort of HIV/HCV Coinfected Patients.

Isabelle Poizot-Martin, Alissa Naqvi, Véronique Obry-Roguet, Marc-Antoine Valantin, Lise Cuzin, Eric Billaud, Antoine Cheret, David Rey, Christine Jacomet, Claudine Duvivier and 4 more

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.7field-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

19 citing papers in PubMed, 35 citations in OpenAlex.

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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

14 authors at 12 institutions in 2 countries.

Isabelle Poizot-MartinAix-Marseille University, APHM Hôpital Sainte-Marguerite, Immuno-Hematology Clinic, Marseille, France; Inserm U912 (SESSTIM), Marseille, France.
Alissa NaqviCHU de Nice, Hôpital Archet 1, Service de Maladies Infectieuses, Unité de Virologie Clinique, Nice, France.
Véronique Obry-RoguetAix-Marseille University, APHM Hôpital Sainte-Marguerite, Immuno-Hematology Clinic, Marseille, France.
Marc-Antoine ValantinSorbonne Universités, UPMC Université Paris 06, UMR_S 1136, Institut Pierre Louis d'Epidémiologie et de Santé Publique, F-75013, Paris, France; APHP, Groupe hospitalier Pitié-Salpêtrière-Université Pierre et Marie Curie, Service de Maladies Infectieuses et Tropicales, Paris, France.
Lise CuzinINSERM, UMR 1027, Toulouse, F-31000, France; Université de Toulouse III, Toulouse, F-31000, France; CHU Toulouse, COREVIH Toulouse, F-31000, France.
Eric BillaudService des maladies infectieuses, CHU, Hôtel-Dieu, Nantes, France.
Antoine CheretCentre Hospitalier de Tourcoing, Service Universitaire de Maladies Infectieuses, Tourcoing, France; CHU Bicêtre, Service de Médecine Interne, Le Kremlin-Bicêtre, France; Laboratoire de Virologie, Hôpital Necker EA 7327 Université Paris Descartes, Paris, France.
David ReyHôpitaux Universitaires de Strasbourg, Center for HIV care, Strasbourg, France.
Christine JacometCHU Clermont-Ferrand, Service des Maladies Infectieuses et tropicales, Clermont-Ferrand, France.
Claudine DuvivierLaboratoire de Virologie, Hôpital Necker EA 7327 Université Paris Descartes, Paris, France; APHP-Hopital Necker, Service de Maladies Infectieuses et Tropicales, Centre d'Infectiologie Necker-Pasteur IHU Imagine, Paris, France; Institut Pasteur, Centre Médical-Centre d'Infectiologie Necker-Pasteur, Paris, France.
Pascal PuglieseCHU de Nice, Hôpital Archet 1, Service de Maladies Infectieuses, Unité de Virologie Clinique, Nice, France.
Pierre PradatHospices civils de Lyon, Hôpital de la Croix Rousse, Service d'Hépatologie, Centre de recherche clinique, Lyon, France; Inserm U1052, Lyon, France.
Laurent CotteInserm U1052, Lyon, France; Hospices civils de Lyon, Hôpital de la Croix Rousse, Service des maladies infectieuses, Lyon, France.
Hepadat'AIDS Study Group
Centre Hospitalier Universitaire de Nice · FRCentre de Recherche en Cancérologie de Lyon · FRCentre d'Investigation Clinique de Nantes · FRCentre Hospitalier de Tourcoing · FRCentre Hospitalier Universitaire de Clermont-Ferrand · FRCNR de la Résistance aux Antibiotiques · FREconomic & Social Sciences, Health Systems & Medical Informatics · FRHôpital Sainte-Marguerite · FRHôpitaux Universitaires de Strasbourg · FRHospices Civils de Lyon · FRInserm · FRSorbonne Université · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesDevelopment of direct acting antivirals (DAA) offers new benefits for patients with chronic hepatitis C. The combination of these drugs with antiretroviral treatment (cART) is a real challenge in HIV/HCV coinfected patients. The aim of this study was to describe potential drug-drug interactions between DAAs and antiretroviral drugs in a cohort of HIV/HCV coinfected patients.

methodsCross-sectional study of all HIV/HCV coinfected patients attending at least one visit in 2012 in the multicenter French Dat'AIDS cohort. A simulation of drug-drug interactions between antiretroviral treatment and DAAs available in 2015 was performed.

resultsOf 16,634 HIV-infected patients, 2,511 had detectable anti-HCV antibodies, of whom 1,196 had a detectable HCV-RNA and were not receiving HCV treatment at the time of analysis. 97.1% of these patients were receiving cART and 81.2% had a plasma HIV RNA <50 copies/mL. cART included combinations of nucleoside reverse transcriptase inhibitors with a boosted protease inhibitor in 43.6%, a non-nucleoside reverse transcriptase inhibitor in 17.3%, an integrase inhibitor in 15.4% and various combinations or antiretroviral drugs in 23.7% of patients. A previous treatment against HCV had been administered in 64.4% of patients. Contraindicated associations/potential interactions were expected between cART and respectively sofosbuvir (0.2%/0%), sofosbuvir/ledipasvir (0.2%/67.6%), daclatasvir (0%/49.4%), ombitasvir/boosted paritaprevir (with or without dasabuvir) (34.4%/52.2%) and simeprevir (78.8%/0%).

conclusionsSignificant potential drug-drug interactions are expected between cART and the currently available DAAs in the majority of HIV/HCV coinfected patients. Sofosbuvir/ledipasvir and sofosbuvir/daclatasvir with or without ribavirin appeared the most suitable combinations in our population. A close collaboration between hepatologists and HIV/AIDS specialists appears necessary for the management of HCV treatment concomitantly to cART.

Indexed as

Anti-HIV AgentsCoinfectionCross-Sectional StudiesDrug InteractionsDrug Therapy, CombinationFemaleHepacivirusHepatitis C AntibodiesHepatitis C, ChronicHIV InfectionsHumansMaleMiddle AgedProtease InhibitorsAnti-HIV AgentsHepatitis C AntibodiesProtease Inhibitors

Identifiers

PMID26488159
PMCPMC4619009
OpenAlexW2156716616

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.