Evidence map›Paper›PMID 28485375›Full record

Observational studyThe pharmacogenomics journal2018

Impact of NADPH oxidase functional polymorphisms in acute myeloid leukemia induction chemotherapy.

J E Megías-Vericat, P Montesinos, M J Herrero, F Moscardó, V Bosó, L Rojas, D Martínez-Cuadrón, R Rodríguez-Veiga, L Sendra, J Cervera and 3 more

Abstract readObservational Study
PubMed Publisher
In one paragraph

Observational study in The pharmacogenomics journal, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.6field-weighted citation impact, top 16% 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, 23 citations in OpenAlex.

  1. Review
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  8. Autophagy and Metabolism in Normal and Malignant Hematopoiesis.International journal of molecular sciences · 2021
    Review
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  11. Review
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  13. Adult patients withHaematologica · 2019
    Article
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  16. Article
  17. Reactive oxygen species in haematopoiesis: leukaemic cells take a walk on the wild side.Journal of experimental & clinical cancer research : CR · 2018
    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 2 institutions in 1 country.

J E Megías-VericatUnidad de Farmacogenética, Instituto Investigación Sanitaria La Fe and Área del Medicamento, Hospital Universitario y Politécnico La Fe, Valencia, Spain.
P MontesinosServicio de Hematología y Hemoterapia, Hospital Universitario y Politécnico La Fe, Valencia, Spain.
M J HerreroUnidad de Farmacogenética, Instituto Investigación Sanitaria La Fe and Área del Medicamento, Hospital Universitario y Politécnico La Fe, Valencia, Spain.
F MoscardóServicio de Hematología y Hemoterapia, Hospital Universitario y Politécnico La Fe, Valencia, Spain.
V BosóUnidad de Farmacogenética, Instituto Investigación Sanitaria La Fe and Área del Medicamento, Hospital Universitario y Politécnico La Fe, Valencia, Spain.
L RojasUnidad de Farmacogenética, Instituto Investigación Sanitaria La Fe and Área del Medicamento, Hospital Universitario y Politécnico La Fe, Valencia, Spain.
D Martínez-CuadrónServicio de Hematología y Hemoterapia, Hospital Universitario y Politécnico La Fe, Valencia, Spain.
R Rodríguez-VeigaServicio de Hematología y Hemoterapia, Hospital Universitario y Politécnico La Fe, Valencia, Spain.
L SendraUnidad de Farmacogenética, Instituto Investigación Sanitaria La Fe and Área del Medicamento, Hospital Universitario y Politécnico La Fe, Valencia, Spain.
J CerveraServicio de Hematología y Hemoterapia, Hospital Universitario y Politécnico La Fe, Valencia, Spain.
J L PovedaServicio de Farmacia, Área del Medicamento, Hospital Universitario y Politécnico La Fe, Valencia, Spain.
M Á SanzServicio de Hematología y Hemoterapia, Hospital Universitario y Politécnico La Fe, Valencia, Spain.
S F AliñoUnidad de Farmacogenética, Instituto Investigación Sanitaria La Fe and Área del Medicamento, Hospital Universitario y Politécnico La Fe, Valencia, Spain.
Hospital Universitari i Politècnic La Fe · ESInstituto de Investigación Sanitaria La Fe · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Efficacy and toxicity of anthracycline treatment in acute myeloid leukemia (AML) is mediated by reactive oxygen species (ROS). NADPH oxidase is the major endogenous source of ROS and a key mediator of oxidative cardiac damage. The impact of NADPH oxidase polymorphisms (CYBA:rs4673, NCF4:rs1883112, RAC2:rs13058338) was evaluated in 225 adult de novo AML patients. Variant alleles of NCF4 and RAC2 were related to higher complete remission (P=0.035, P=0.016), and CYBA homozygous variant showed lower overall survival with recessive model (P=0.045). Anthracycline-induced cardiotoxicity was associated to NCF4 homozygous variant (P=0.012) and CYBA heterozygous genotype (P=0.027). Novel associations were found between variant allele of CYBA and lower lung and gastrointestinal toxicities, and a protective effect in nephrotoxicity and RAC2 homozygous variant. Moreover, RAC2 homozygous variant was related to delayed thrombocytopenia recovery. This study supports the interest of NADPH oxidase polymorphisms regarding efficacy and toxicity of AML induction therapy, in a coherent integrated manner.

Indexed as

AgedAntineoplastic Combined Chemotherapy ProtocolsFemaleHumansInduction ChemotherapyLeukemia, Myeloid, AcuteMaleMiddle AgedNADPH OxidasesPolymorphism, Single NucleotideRAC2 GTP-Binding Proteinrac GTP-Binding ProteinsReactive Oxygen SpeciesRemission InductionRetrospective StudiesNADPH OxidasesRAC2 GTP-Binding Proteinrac GTP-Binding ProteinsReactive Oxygen Species

Identifiers

PMID28485375
OpenAlexW2613014145

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.