Evidence map›Paper›PMID 29490977›Full record

Observational studyBlood advances2018

CDA as a predictive marker for life-threatening toxicities in patients with AML treated with cytarabine.

Raphaelle Fanciullino, Laure Farnault, Mélanie Donnette, Diane-Charlotte Imbs, Catherine Roche, Geoffroy Venton, Yael Berda-Haddad, Vadim Ivanov, Joseph Ciccolini, L'Houcine Ouafik and 2 more

Erratum issuedOpen access · goldAbstract readObservational Study
In one paragraph

Observational study in Blood advances, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
4.1field-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

18 citing papers in PubMed, 42 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 5 institutions in 1 country.

Raphaelle FanciullinoSMARTc Unit, Pharmacokinetics Laboratory, Unité Mixte de Recherche (UMR) INSERM U1068 Centre de Recherche en Cancerologie de Marseille, Aix Marseille University, Marseille, France.
Laure FarnaultHematology and Cellular Therapy Department, La Conception University Hospital of Marseille, Marseille, France.
Mélanie DonnetteSMARTc Unit, Pharmacokinetics Laboratory, Unité Mixte de Recherche (UMR) INSERM U1068 Centre de Recherche en Cancerologie de Marseille, Aix Marseille University, Marseille, France.
Diane-Charlotte ImbsSMARTc Unit, Pharmacokinetics Laboratory, Unité Mixte de Recherche (UMR) INSERM U1068 Centre de Recherche en Cancerologie de Marseille, Aix Marseille University, Marseille, France.
Catherine RocheLaboratoire de Biologie Médicale, Assistance Publique-Hôpitaux de Marseille, Marseille, France; and.
Geoffroy VentonHematology and Cellular Therapy Department, La Conception University Hospital of Marseille, Marseille, France.
Yael Berda-HaddadLaboratoire de Biologie Médicale, Assistance Publique-Hôpitaux de Marseille, Marseille, France; and.
Vadim IvanovHematology and Cellular Therapy Department, La Conception University Hospital of Marseille, Marseille, France.
Joseph CiccoliniSMARTc Unit, Pharmacokinetics Laboratory, Unité Mixte de Recherche (UMR) INSERM U1068 Centre de Recherche en Cancerologie de Marseille, Aix Marseille University, Marseille, France.
L'Houcine OuafikLaboratoire de Biologie Médicale, Assistance Publique-Hôpitaux de Marseille, Marseille, France; and.
Bruno LacarelleSMARTc Unit, Pharmacokinetics Laboratory, Unité Mixte de Recherche (UMR) INSERM U1068 Centre de Recherche en Cancerologie de Marseille, Aix Marseille University, Marseille, France.
Regis CostelloHematology and Cellular Therapy Department, La Conception University Hospital of Marseille, Marseille, France.
Hôpital de la Conception · FRAix-Marseille Université · FRAssistance Publique Hôpitaux de Marseille · FRCentre de Recherche en Cancérologie de Marseille · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cytarabine (Ara-C) is the backbone of acute myeloid leukemia (AML) chemotherapy. Little is known about possible risk factors predictive for the frequent (ie, up to 16%) life-threatening or lethal toxicities caused by Ara-C. Ara-C is detoxified in the liver by a single enzyme, cytidine deaminase (CDA), coded by a gene known to be highly polymorphic. In this proof-of-concept study, we particularly investigated the role of the CDA poor metabolizer (PM) phenotype in Ara-C toxicities. CDA phenotyping (measurement of CDA residual activity in serum) and genotyping (search for the

Indexed as

AdultAgedAged, 80 and overAntimetabolites, AntineoplasticBiomarkersCytarabineCytidine DeaminaseDown-RegulationFemaleHumansLeukemia, Myeloid, AcuteMaleMiddle AgedPredictive Value of TestsYoung AdultAntimetabolites, AntineoplasticBiomarkersCytarabineCytidine Deaminase

Identifiers

PMID29490977
PMCPMC5851420
OpenAlexW2789635619

What OpenQuestion holds

Textmetadata
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.