Evidence map›Paper›PMID 34216177›Full record

Trial reportThe oncologist2021

A Pragmatic Study Evaluating NEPA Versus Aprepitant for Prevention of Chemotherapy-Induced Nausea and Vomiting in Patients Receiving Moderately Emetogenic Chemotherapy.

Laurent Zelek, Philippe Debourdeau, Hugues Bourgeois, Jean Philippe Wagner, Fabien Brocard, Claudia Lefeuvre-Plesse, Bruno Chauffert, Marianne Leheurteur, Jean-Baptiste Bachet, Hélène Simon and 2 more

Open access · bronzeAbstract readMulticenter StudyRandomized Controlled TrialPragmatic Clinical Trial
In one paragraph

Trial report in The oncologist, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 4 pooled it
2.9field-weighted citation impact, top 9% 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

17 citing papers in PubMed, 4 syntheses or guidelines pooled it, 23 citations in OpenAlex.

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  4. Prevalence and predictors of long-delayed (> 120 h) chemotherapy-induced nausea and vomiting (CINV)-a systematic review and individual patient data meta-analysis.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2023
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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

12 authors at 10 institutions in 1 country.

Laurent ZelekHôpital Avicenne, Bobigny, France.ORCID 0000-0001-7455-2009
Philippe DebourdeauInstitut Sainte-Catherine, Avignon, France.
Hugues BourgeoisClinique Victor Hugo, Le Mans, France.
Jean Philippe WagnerInstitut Andrée Dutreix and Clinique de Flandre, Dunkerque, France.
Fabien BrocardPolyclinique De Gentilly, Nancy, France.
Claudia Lefeuvre-PlesseCentre Eugène Marquis, Rennes Cedex, France.
Bruno ChauffertCentre Hospitalier Universitaire Amiens, Amiens, France.
Marianne LeheurteurCentre Henri Becquerel, Rouen, France.
Jean-Baptiste BachetHôpital La Pitié Salpêtrière, Paris, France.
Hélène SimonCentre Hospitalier Universitaire Morvan, Brest, France.
Didier MayeurCentre George Francois Leclerc, Dijon, France.
Florian ScottéInterdisciplinary Cancer Course Department, Gustave Roussy Cancer Center, Villejuif, France.
Centre Eugène Marquis · FRCentre Georges François Leclerc · FRCentre Henri BecquerelCentre Hospitalier Régional Universitaire de Brest · FRCentre Hospitalier Universitaire Amiens-Picardie · FRClinique Victor Hugo · FRHôpital Avicenne · FRInstitut Gustave Roussy · FRInstitut Sainte Catherine · FRSorbonne Université · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNeurokinin (NK) 1 receptor antagonists (RAs), administered in combination with a 5-hydroxytryptamine-3 (5-HT MATERIALS AND

methodsThis was a pragmatic, multicenter, randomized, single-cycle, open-label, prospective study designed to demonstrate noninferiority of single-dose NEPA to a 3-day aprepitant regimen in preventing CINV in chemotherapy-naive patients receiving AC/non-AC MEC in a real-life setting. The primary efficacy endpoint was complete response (no emesis/no rescue) during the overall (0-120 hour) phase. Noninferiority was achieved if the lower limit of the 95% confidence interval (CI) of the difference between NEPA and the aprepitant group was greater than the noninferiority margin set at -10%.

resultsNoninferiority of NEPA versus aprepitant was demonstrated (risk difference 9.2%; 95% CI, -2.3% to 20.7%); the overall complete response rate was numerically higher for NEPA (64.9%) than aprepitant (54.1%). Secondary endpoints also revealed numerically higher rates for NEPA than aprepitant.

conclusionThis pragmatic study in patients with cancer receiving AC and non-AC MEC revealed that a single dose of oral NEPA plus DEX was at least as effective as a 3-day aprepitant regimen, with indication of a potential efficacy benefit for NEPA. IMPLICATIONS FOR PRACTICE: In the absence of comparative neurokinin 1 (NK

Indexed as

AntiemeticsAntineoplastic AgentsAntibiotics, AntineoplasticAprepitantDouble-Blind MethodHumansIsoquinolinesNauseaPalonosetronProspective StudiesQuinuclidinesVomitingAntibiotics, AntineoplasticAntiemeticsAntineoplastic AgentsAprepitantIsoquinolinesPalonosetronQuinuclidinesChemotherapy-induced nausea and vomiting • Netupitant • Palonosetron • Aprepitant • NEPA

Identifiers

PMID34216177
PMCPMC8488783
OpenAlexW3176272029

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.