Evidence map›Paper›PMID 38824512›Full record

ArticleBMC cancer2024

The TEOGIC study project: a comprehensive characterization of early onset gastrointestinal cancer in the Northern area of Spain.

R Vera, N Castro, I Labiano, A Lecumberri, A E Huerta, H Arasanz, I Caseda, F Ruiz-Pace, C Viaplana, V Arrazubi and 15 more

Erratum issuedAbstract read
In one paragraph

Article in BMC cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

25 authors.

R VeraOncobiona Group, Navarrabiomed-Instituto de Investigación Sanitaria de Navarra (IdiSNA), Pamplona, Spain.
N CastroOncobiona Group, Navarrabiomed-Instituto de Investigación Sanitaria de Navarra (IdiSNA), Pamplona, Spain.
I LabianoOncobiona Group, Navarrabiomed-Instituto de Investigación Sanitaria de Navarra (IdiSNA), Pamplona, Spain.
A LecumberriOncobiona Group, Navarrabiomed-Instituto de Investigación Sanitaria de Navarra (IdiSNA), Pamplona, Spain.
A E HuertaOncobiona Group, Navarrabiomed-Instituto de Investigación Sanitaria de Navarra (IdiSNA), Pamplona, Spain.
H ArasanzOncobiona Group, Navarrabiomed-Instituto de Investigación Sanitaria de Navarra (IdiSNA), Pamplona, Spain.
I CasedaOncobiona Group, Navarrabiomed-Instituto de Investigación Sanitaria de Navarra (IdiSNA), Pamplona, Spain.
F Ruiz-PaceOncology Data Science Group, Vall d'Hebron Institute of Oncology (VHIO), Barcelona, Spain.
C ViaplanaOncology Data Science Group, Vall d'Hebron Institute of Oncology (VHIO), Barcelona, Spain.
V ArrazubiOncobiona Group, Navarrabiomed-Instituto de Investigación Sanitaria de Navarra (IdiSNA), Pamplona, Spain.
I Hernandez-GarciaOncobiona Group, Navarrabiomed-Instituto de Investigación Sanitaria de Navarra (IdiSNA), Pamplona, Spain.
E MataOncobiona Group, Navarrabiomed-Instituto de Investigación Sanitaria de Navarra (IdiSNA), Pamplona, Spain.
D GomezOncobiona Group, Navarrabiomed-Instituto de Investigación Sanitaria de Navarra (IdiSNA), Pamplona, Spain.
S LagunaDepartment of Medical Oncology, Hospital Universitario de Navarra (HUN), Pamplona, Spain.
J SuarezDepartment of Surgery, Hospital Universitario de Navarra (HUN), Pamplona, Spain.
I Fernandez-De-Los-ReyesDepartment of Pathology, Hospital Universitario de Navarra (HUN), Pamplona, Spain.
M RullanDepartment of Gastroenterology and Hepatology, Hospital Universitario de Navarra (HUN), Pamplona, Spain.
F EstremeraDepartment of Gastroenterology and Hepatology, Hospital Universitario de Navarra (HUN), Pamplona, Spain.
V AlonsoDepartment of Medical Oncology, Hospital Universitario Miguel Servet, IISA, Zaragoza, Spain.
R Pazo-CidDepartment of Medical Oncology, Hospital Universitario Miguel Servet, IISA, Zaragoza, Spain.
A Gil-NegreteDepartment of Medical Oncology, Hospital Universitario Donostia, San Sebastian, Spain.
A LafuenteDepartment of Medical Oncology, Hospital San Pedro, Logroño, Spain.
A Martin-CarniceroDepartment of Medical Oncology, Hospital San Pedro, Logroño, Spain.
R DienstmannOncology Data Science Group, Vall d'Hebron Institute of Oncology (VHIO), Barcelona, Spain.
M AlsinaOncobiona Group, Navarrabiomed-Instituto de Investigación Sanitaria de Navarra (IdiSNA), Pamplona, Spain. maria.alsina.maqueda@navarra.es.

Funding

Agencia Estatal de Investigación 8FJC2021-046521-IDepartamento de Salud, Gobierno de Navarra La Caixa ProgramFundación Científica Asociación Española Contra el Cáncer AECC SEED IDEAS 2023Fundación Científica Asociación Española Contra el Cáncer CLJUN19010ARASFundación Científica Asociación Española Contra el Cáncer CLJUN234885LECUMinisterio de Ciencia, Innovación y Universidades Knowledge Generation Proyects 2022
6 · The paper itself

Abstract

backgroundGastrointestinal cancers represent one of the most prevalent diseases worldwide. Strikingly, the incidence of Early Onset Gastrointestinal Cancer (EOGIC) has been rising during the last decades and changes in lifestyle and environmental exposure seem to play a role. EOGIC has been defined as a different entity compared to on-average gastrointestinal cancer, with distinct clinical and molecular characteristics. Inherent to the particularities of younger age, there is an unmet need for a tailored approach for the management of these patients. The TEOGIC proposes a comprehensive study to characterize EOGIC patients in the northern of Spain.

methodsPatients with histologically confirmed new diagnosis of colorectal, gastroesophageal and pancreatic adenocarcinoma will be considered for two cohorts: EOGIC (≤ 50 years old) and non-EOGIC (60-75 years old), with a ratio of 1:2. Two hundred and forty patients will be recruited in 4 Public Hospitals from northern Spain. After receiving unified informed consent, demographic and clinical data of the patients will be collected in a REDCap database. Lifestyle related data will be obtained in questionnaires assessing diet, physical activity and the general quality of life of the patients before diagnosis. Biological samples prior to any onco-specific treatment will be obtained for the analyses of circulating inflammatory proteins, gut microbiota, and the proteome of the tumor microenvironment. Histologic characteristics and routine biomarkers will be also collected. Thereafter, data will be integrated and analyzed to assess tumor specific, pan-tumor and sex-associated differential characteristics of EOGIC. DISCUSSION: The underlying risk factors and differential characteristics of EOGIC remain poorly studied, particularly in our geographical area. Although limited by the exploratory nature and the small sample size estimated to be recruited, TEOGIC represents the first attempt to comprehensively characterize these young patients, and thus attend to their special needs. Findings derived from this study could contribute to raise awareness and preventive behaviors in the population. In parallel, molecular studies could lead to the identification of potential novel non-invasive biomarkers and therapeutic targets that would help in the development of the tailored clinical management of these patients, focusing on screening programs for early diagnosis and precision medicine.

Indexed as

Gastrointestinal NeoplasmsAdenocarcinomaAdultAgedAge of OnsetBiomarkers, TumorEsophageal NeoplasmsFemaleHumansIncidenceLife StyleMaleMiddle AgedPancreatic NeoplasmsQuality of LifeSpainBiomarkers, TumorColorectal cancerEarly onset gastrointestinal cancerEnvironmental risk factorsGastroesophageal cancerGastrointestinal cancerMicrobiomePancreatic cancerPrecision medicineTumor microenvironment

Identifiers

PMID38824512
PMCPMC11143674

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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.