Evidence map›Paper›PMID 32761342›Full record

ArticleInternational urology and nephrology2020

Prognostic value of immunological profile based on CD8+ and FoxP3+ T lymphocytes in the peritumoral and intratumoral subsites for renal cell carcinoma.

Kerem Teke, Busra Yaprak Bayrak, Mustafa Yuksekkaya, Ali Kemal Uslubas, Mehmet Esat Kosem, Hasan Yilmaz, Onder Kara, Ozdal Dillioglugil

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In one paragraph

Article in International urology and nephrology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
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  3. Redistribution of CD8+ T cell subsets in metastatic renal cell carcinoma patients treated with anti-PD-1 therapy.Cytometry. Part A : the journal of the International Society for Analytical Cytology · 2022
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Kerem TekeDepartment of Urology, Kocaeli University School of Medicine, Umuttepe Campus, 41380, Kocaeli, Turkey. drtekekerem@gmail.com.ORCID http://orcid.org/0000-0001-9030-4662
Busra Yaprak BayrakDepartment of Pathology, Kocaeli University School of Medicine, Kocaeli, Turkey.
Mustafa YuksekkayaDepartment of Urology, Kocaeli University School of Medicine, Umuttepe Campus, 41380, Kocaeli, Turkey.
Ali Kemal UslubasDepartment of Urology, Kocaeli University School of Medicine, Umuttepe Campus, 41380, Kocaeli, Turkey.
Mehmet Esat KosemDepartment of Urology, Kocaeli University School of Medicine, Umuttepe Campus, 41380, Kocaeli, Turkey.
Hasan YilmazDepartment of Urology, Kocaeli University School of Medicine, Umuttepe Campus, 41380, Kocaeli, Turkey.
Onder KaraDepartment of Urology, Kocaeli University School of Medicine, Umuttepe Campus, 41380, Kocaeli, Turkey.
Ozdal DillioglugilDepartment of Urology, Kocaeli University School of Medicine, Umuttepe Campus, 41380, Kocaeli, Turkey.
Kocaeli Üniversitesi · TR

Funding

Kocaeli Üniversitesi Grant number 2018/138
6 · The paper itself

Abstract

purposeWe aimed to assess an "Immunological Profile (IP)" including CD8+ and FoxP3+ T lymphocytes for renal cell carcinoma (RCC) to evaluate its effects on tumor pathological characteristics, disease progression, and survival.

methodsAdjacent normal and intratumoral specimens from 42 patients who had undergone radical nephrectomy for RCC were analyzed for counts of CD8+ and FoxP3+ T lymphocytes by immunohistochemistry. Tissue from both sites were evaluated and scored separately according to low (0) or high (1) expression of CD8 and FoxP3. A total score (min: 0, max: 4) was assigned to each patient. Thereafter, patients were divided into two groups for clinicopathologic and survival stratification based on score (IP

resultsThe mean follow-up was 54.73 ± 21.34 months. Poor RCC characteristics including pT3-T4, tumor necrosis, lymphovascular invasion, lymph node involvement, and larger tumor size were significantly more common in the IP

conclusionAssessment of IP including CD8+ and FoxP3+ T lymphocytes in adjacent normal and intratumoral sites in RCC may serve as a good predictive marker for PFS.

Indexed as

CD8-Positive T-LymphocytesAdultAgedCarcinoma, Renal CellCohort StudiesDisease ProgressionFemaleForkhead Transcription FactorsHumansKidney NeoplasmsMaleMiddle AgedPrognosisSurvival RateT-LymphocytesForkhead Transcription FactorsFOXP3 protein, humanCD8FoxP3Immune scoringImmunologic profileRCCRenal cell carcinoma

Identifiers

PMID32761342
OpenAlexW3047172440

What OpenQuestion holds

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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.