Evidence map›Paper›PMID 39487701›Full record

ArticleCancer medicine2024

xCT as a Predictor for Survival in a Population-Based Cohort of Head and Neck Squamous Cell Carcinoma.

Linda Nissi, Sanni Tuominen, Johannes Routila, Teemu Huusko, Petra Ketonen, Maria Sundvall, Ilmo Leivo, Heikki Irjala, Heikki Minn, Tove J Grönroos and 1 more

Abstract read
In one paragraph

Article in Cancer medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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

1 citing paper in PubMed.

  1. 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

11 authors.

Linda NissiDepartment of Oncology, and FICAN West Cancer Centre, Turku University Hospital and University of Turku, Turku, Finland.ORCID https://orcid.org/0000-0001-6971-2274
Sanni TuominenPreclinical Imaging Turku PET Centre, University of Turku, Turku, Finland.
Johannes RoutilaDepartment of Otorhinolaryngology-Head and Neck Surgery, Turku University Hospital and University of Turku, Turku, Finland.
Teemu HuuskoDepartment of Otorhinolaryngology-Head and Neck Surgery, Turku University Hospital and University of Turku, Turku, Finland.
Petra KetonenPreclinical Imaging Turku PET Centre, University of Turku, Turku, Finland.
Maria SundvallDepartment of Oncology, and FICAN West Cancer Centre, Turku University Hospital and University of Turku, Turku, Finland.ORCID https://orcid.org/0000-0002-0494-2965
Ilmo LeivoDepartment of Pathology, Turku University Hospital and University of Turku, Turku, Finland.
Heikki IrjalaDepartment of Otorhinolaryngology-Head and Neck Surgery, Turku University Hospital and University of Turku, Turku, Finland.
Heikki MinnDepartment of Oncology, and FICAN West Cancer Centre, Turku University Hospital and University of Turku, Turku, Finland.ORCID https://orcid.org/0000-0002-5878-4333
Tove J GrönroosDepartment of Oncology, and FICAN West Cancer Centre, Turku University Hospital and University of Turku, Turku, Finland.
Sami VenteläDepartment of Otorhinolaryngology-Head and Neck Surgery, Turku University Hospital and University of Turku, Turku, Finland.

Funding

Cancer Foundation FinlandGovernmental Research Funding for Turku University HospitalJane ja Aatos Erkon SäätiöMoikoisten SyöväntutkimussäätiöResearch Council of FinlandSuomen KulttuurirahastoSuomen Lääketieteen SäätiöSwedish Cultural Foundation in FinlandTurku Doctoral Programme of Molecular Medicine of University of Turku
6 · The paper itself

Abstract

backgroundxCT, also known as SLC7A11 (solute carrier Family 7 Member 11), is a cystine/glutamate antiporter protein that mediates regulated cell death and antioxidant defense. The aim of this study was to investigate the effect of xCT on the outcome of patients diagnosed with new head and neck squamous cell carcinoma (HNSCC).

methodsThis retrospective cohort study utilized a population-based dataset, comprising all patients (n = 1033) diagnosed with new HNSCC during 2005-2015 in a population of 697,000 people. All patients (n = 585) with a tumor tissue sample available for immunohistochemical (IHC) staining were included. The follow-up rates were 97% and 81% at 3 and 5 years, respectively. Also, the specificity of the anti-xCT antibody was validated.

resultsThe expression level and prognostic significance of xCT were strongly dependent on tumor location. In oropharyngeal squamous cell carcinoma (OPSCC) patients, xCT expression was a significant prognostic factor for 5-year overall survival (OAS) (HR: 2.71; 95% CI 1.67-4.39; p < 0.001), disease-specific survival (DSS) (HR: 2.58; 95% CI 1.47-4.54; p = 0.001), and disease-free survival (DFS) (HR: 2.69; 95% CI 1.55-4.64; p < 0.001). Five-year survival rates for OPSCC patients with high and low levels of xCT were OAS 34% versus 62%; DSS 51% versus 73%; DFS 43% versus 73%, respectively. According to a multivariate model adjusted for age, T-class, nodal positivity, and tobacco consumption, xCT was an independent prognostic factor for 3-year survival, in which it outperformed p16 IHC. Similar associations were not observed in squamous cell carcinomas of oral cavity or larynx. Regarding treatment modalities, xCT was most predictive in HNSCC patients who received radiotherapy.

conclusionsHigh xCT expression was associated with poor prognosis in OPSCC. Our findings suggest that joint analysis of xCT and p16 may add significant value in OPSCC treatment stratification.

Indexed as

Amino Acid Transport System y+Biomarkers, TumorHead and Neck NeoplasmsSquamous Cell Carcinoma of Head and NeckAdultAgedAged, 80 and overFemaleHumansImmunohistochemistryMaleMiddle AgedPrognosisRetrospective StudiesAmino Acid Transport System y+Biomarkers, TumorSLC7A11 protein, human

Identifiers

PMID39487701
PMCPMC11530867

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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.