Evidence map›Paper›PMID 31255173›Full record

ArticleBMC cancer2019

Impact of genetic mutations and nutritional status on the survival of patients with colorectal cancer.

Mariana Abe Vicente Cavagnari, Tiago Donizetti Silva, Marco Antonio Haddad Pereira, Luísa Jacques Sauer, David Shigueoka, Sarhan Sydney Saad, Katia Barão, Carla Caroline Dias Ribeiro, Nora Manoukian Forones

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 2 pooled it
2.5field-weighted citation impact, top 10% 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, 2 syntheses or guidelines pooled it, 38 citations in OpenAlex.

  1. Pooled it
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    Review
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  17. Germline MICA Polymorphism Is Associated with the Long-Term Outcomes in Patients Undergoing Hepatectomy for Colorectal Liver Metastases.Journal of gastrointestinal surgery : official journal of the Society for Surgery of the Alimentary Tract · 2020
    Article
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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 2 institutions in 1 country.

Mariana Abe Vicente CavagnariDepartment of Medicine. Gastroenterology Division. Oncology Group, Universidade Federal de São Paulo - SP. Brazil, R Botucatu 740, 2° andar CEP 04023900, Vila Clementino, São Paulo, Brazil. marianaav@hotmail.com.ORCID http://orcid.org/0000-0003-4352-4659
Tiago Donizetti SilvaDepartment of Medicine. Gastroenterology Division. Oncology Group, Universidade Federal de São Paulo - SP. Brazil, R Botucatu 740, 2° andar CEP 04023900, Vila Clementino, São Paulo, Brazil.
Marco Antonio Haddad PereiraDepartment of Radiology, Universidade Federal de São Paulo, São Paulo, Brazil.
Luísa Jacques SauerDepartment of Radiology, Universidade Federal de São Paulo, São Paulo, Brazil.
David ShigueokaDepartment of Radiology, Universidade Federal de São Paulo, São Paulo, Brazil.
Sarhan Sydney SaadDepartment of Surgery, Universidade Federal de São Paulo, São Paulo, Brazil.
Katia BarãoDepartment of Medicine. Gastroenterology Division. Oncology Group, Universidade Federal de São Paulo - SP. Brazil, R Botucatu 740, 2° andar CEP 04023900, Vila Clementino, São Paulo, Brazil.
Carla Caroline Dias RibeiroDepartment of Medicine. Gastroenterology Division. Oncology Group, Universidade Federal de São Paulo - SP. Brazil, R Botucatu 740, 2° andar CEP 04023900, Vila Clementino, São Paulo, Brazil.
Nora Manoukian ForonesDepartment of Medicine. Gastroenterology Division. Oncology Group, Universidade Federal de São Paulo - SP. Brazil, R Botucatu 740, 2° andar CEP 04023900, Vila Clementino, São Paulo, Brazil.
Universidade Federal de São Paulo · BRUniversidade Federal de Santa Maria · BR

Funding

Fundação de Amparo à Pesquisa do Estado de São Paulo (BR) 2013/19268-3
6 · The paper itself

Abstract

backgroundThe prognosis of colorectal cancer (CRC) patients can be influenced by genetic mutations and nutritional status. The relationship between these variables is unclear. The objective of the study was to verify the variables involved in the nutritional status and genetic mutations, which correlate with survival of CRC patients.

methodsPatients with surgical intervention for tumor resection were evaluated using body mass index, nutritional screening, patient self-produced global subjective assessment, phase angle, and computed tomography to calculate the areas of visceral adipose tissue (VAT) and subcutaneous adipose tissue, and muscle mass for the determination of sarcopenia. Ten gene mutations involved in CRC carcinogenesis were studied (PIK3CA, KRAS, BRAF, EGFR, NRAS, TP53, APC, PTEN, SMAD4, and FBXW7). DNA was extracted from fresh tumor or paraffin tissues.

resultsOf the 46 patients, 29 (64.4%) were at nutritional risk and 21 (45.7%) were moderately malnourished. However, there was a high percentage of VAT in 24 (61.5%) and sarcopenia in 19 (48.7%) patients. These variables were associated with a higher risk of mortality. Nutritional risk, moderate or severe malnutrition, phase angle < 5°, VAT < 163.8 cm

conclusionsPatients with positive indicators for malnutrition or risk of malnutrition had an increased risk of death. No relationship was identified between the presence of mutations and survival.

Indexed as

Nutritional StatusAgedBody CompositionColorectal NeoplasmsFemaleHumansIntra-Abdominal FatMaleMiddle AgedMutationNeoplasm ProteinsPrognosisSarcopeniaSurvival AnalysisNeoplasm ProteinsBody compositionOncogenePhase angleSarcopeniaTumor supressor geneVisceral adipose tissue

Identifiers

PMID31255173
PMCPMC6599287
OpenAlexW2954759366

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.