Evidence map›Paper›PMID 28597239›Full record

ArticleLa Radiologia medica2017

Relationship between reticuloendothelial systems' FDG uptake level and clinicopathological features in patient with invasive ductal breast cancer.

Ertan Şahin, Umut Elboğa

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Article in La Radiologia medica, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

9 citing papers in PubMed.

  1. Trial
  2. Organ Crosstalk: The Role of Spleen.Phenomics (Cham, Switzerland) · 2025
    Review
  3. BaselineLa Radiologia medica · 2025
    Article
  4. Advances in PET/CT Imaging for Breast Cancer.Journal of clinical medicine · 2023
    Review
  5. Article
  6. Article
  7. Spleen glucose metabolism on [European journal of nuclear medicine and molecular imaging · 2021
    Article
  8. [EJNMMI research · 2020
    Article
  9. Article
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

2 authors.

Ertan ŞahinDepartment of Nuclear Medicine, Namık Kemal University Hospital, Tekirdağ, Turkey. er_ahin@yahoo.com.
Umut ElboğaDepartment of Nuclear Medicine, Gaziantep University Hospital, Gaziantep, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe reticuloendothelial system (RES) is a part of the immune system and plays a major role in the protection of against diseases. We thought that FDG-PET/CT may show the degree of systemic immune response induced with malignancy in the organs with the high RES activity. Our objective is to investigate FDG uptake levels of high RES activity organs (liver, spleen, bone marrow) in invasive ductal breast cancer and to evaluate the association with the clinicopathological features.

methodsIn the present study, 193 patients with invasive ductal breast cancer who performed FDG-PET/CT were categorized according to the clinicopathological features including age, tumor size, axillary nodal status, histological grade, the presence of lymphavascular invasion, receptor status, Ki-67 proliferation index and biological subgroup. Also, a control group of 100 subjects were identified for comparison with breast cancer patients. We analyzed the relation of FDG uptake levels in high RES activity organs and clinicopathological features in patients.

resultsThere was a statistically significant difference of SUVmax of the liver, spleen, and bone marrow between cancer and control groups (P < 0.0001). We found that high SUVmax in liver, spleen and bone marrow were significantly correlated with worse prognostic clinicopathological features in patient with invasive ductal breast cancer.

conclusionsFDG uptake level in high RES activity organs is associated with the presence of tumor, and also directly relating clinicopathological features for patients with invasive ductal breast cancer.

Indexed as

Positron Emission Tomography Computed TomographyAdultAgedBreast NeoplasmsCarcinoma, Ductal, BreastCross-Sectional StudiesFemaleFluorodeoxyglucose F18HumansMiddle AgedMononuclear Phagocyte SystemNeoplasm InvasivenessRadiopharmaceuticalsFluorodeoxyglucose F18RadiopharmaceuticalsBreast cancerClinicopathological featuresFDGReticuloendothelial system

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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.