Evidence map›Paper›PMID 30286124›Full record

ArticlePloS one2018

The effect of naltrexone as a carboplatin chemotherapy-associated drug on the immune response, quality of life and survival of dogs with mammary carcinoma.

Marília Carneiro Machado, João Moreira da Costa-Neto, Ricardo Dias Portela, Mário Jorge Melhor Heine D'Assis, Olindo Assis Martins-Filho, Stella Maria Barrouin-Melo, Natalie Ferreira Borges, Fabiana Lessa Silva, Alessandra Estrela-Lima

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.7field-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

10 citing papers in PubMed, 32 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

9 authors at 4 institutions in 1 country.

Marília Carneiro MachadoDepartment of Anatomy, Pathology and Veterinary Clinics, Federal University of Bahia, Salvador, Bahia, Brazil.
João Moreira da Costa-NetoDepartment of Anatomy, Pathology and Veterinary Clinics, Federal University of Bahia, Salvador, Bahia, Brazil.
Ricardo Dias PortelaLaboratory of Immunology and Molecular Biology, Institute of Health Sciences, Federal University of Bahia, Salvador, Bahia, Brazil.
Mário Jorge Melhor Heine D'AssisDepartment of Anatomy, Pathology and Veterinary Clinics, Federal University of Bahia, Salvador, Bahia, Brazil.
Olindo Assis Martins-FilhoLaboratory of Diagnostic and Monitoring Biomarkers, Research Center René Rachou, Oswaldo Cruz Foundation, Belo Horizonte, Minas Gerais, Brazil.
Stella Maria Barrouin-MeloDepartment of Anatomy, Pathology and Veterinary Clinics, Federal University of Bahia, Salvador, Bahia, Brazil.
Natalie Ferreira BorgesCenter for Agrarian, Environmental and Biological Sciences, Federal University of Recôncavo da Bahia, Cruz das Almas, Bahia, Brazil.
Fabiana Lessa SilvaDepartment of Agrarian and Environmental Sciences, Estadual University of Santa Cruz, Ilhéus, Bahia, Brazil.
Alessandra Estrela-LimaDepartment of Anatomy, Pathology and Veterinary Clinics, Federal University of Bahia, Salvador, Bahia, Brazil.ORCID 0000-0002-9879-7999
Universidade Federal da Bahia · BRFundação Oswaldo Cruz · BRUniversidade Estadual de Santa Cruz · BRUniversidade Federal do Recôncavo da Bahia · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The objective of this study was to evaluate the effect of low-dose naltrexone (LDN) as a carboplatin chemotherapy-associated drug in female dogs with mammary carcinoma in benign mixed tumors (MC-BMT) after mastectomy and to assess its association with quality of life and survival rates. Sixty female dogs were included in this study, all of which had histopathological diagnosis of MC-BMT and were divided into three groups: G1 (control), consisting of animals submitted only to mastectomy with or without regional metastasis; G2, composed of treated animals that did not present with metastasis; and G3, treated dogs that presented with metastasis. G2 and G3 were also subdivided according to the treatment administered: chemotherapy alone (MC-BMT(-) C/MC-BMT(+) C) or LDN and chemotherapy (MC-BMT(-) C+LDN/MC-BMT(+) C+LDN). All animals were subjected to clinical evaluation, mastectomy, peripheral blood lymphocyte immunophenotyping, beta-endorphin and met-enkephalin quantification, and evaluation of survival rates and quality of life scores. The results showed higher serum concentrations of beta-endorphin and met-enkephalin, fewer chemotherapy-related side effects, and better quality of life and survival rates in the LDN-treated groups than in LDN-untreated groups (P < 0.05). Evaluation of clinical and pathological parameters indicated a significant association between the use of LDN and both prolonged survival and enhanced quality of life. These results indicate that LDN is a viable chemotherapy-associated treatment in female dogs with MC-BMT, maintaining their quality of life and prolonging survival rates.

Indexed as

Animalsbeta-EndorphinCarboplatinDogsDrug SynergismEnkephalin, MethionineFemaleImmunophenotypingLymphocytesMammary Neoplasms, AnimalMastectomyNaltrexoneNeoplasm MetastasisQuality of LifeSurvival AnalysisTreatment Outcomebeta-EndorphinCarboplatinEnkephalin, MethionineNaltrexone

Identifiers

PMID30286124
PMCPMC6171873
OpenAlexW2895145524

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LicenceCC BY
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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.