Evidence map›Paper›PMID 25949868›Full record

ArticleOncoimmunology2015

Immune signature of tumor infiltrating immune cells in renal cancer.

Katharina Geissler, Paolo Fornara, Christine Lautenschläger, Hans-Jürgen Holzhausen, Barbara Seliger, Dagmar Riemann

2 registry-linked trialsOpen access · goldAbstract read
In one paragraph

Article in Oncoimmunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 114 papers.

0numbers the graph read from it
0cells of the map it votes in
114citing papers in PubMed
4.3field-weighted citation impact, top 4% 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.

NCT03354884 phase2completednot on this mapstarted 2018, after this paper: background citation

caBozantinib in cOllectiNg ductS Renal Cell cArcInoma (BONSAI)

TypeinterventionalSponsorFondazione IRCCS Istituto Nazionale dei Tumori, MilanoRan2018 to 2020Enrolled23ConditionsCollecting Duct Carcinoma (Kidney)Armscabozantinib
NCT04891055 unknown statusnot on this mapstarted 2018, after this paper: background citation

Prospective Translational Study Investigating Predictors of Outcome in Metastatic Renal Cell Carcinoma Patients Treated With Nivolumab (I-Rene Trial)

TypeobservationalSponsorFondazione IRCCS Istituto Nazionale dei Tumori, MilanoRan2018 to 2021Enrolled90ConditionsMetastatic Renal Cell Carcinoma
3 · Its place in the literature

Who cites it

114 citing papers in PubMed, 181 citations in OpenAlex.

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  20. Integrative bioinformatics andOncology research · 2024
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54 more citing papers are in PubMed but not listed here.

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

6 authors at 3 institutions in 4 countries.

Katharina GeisslerInstitute of Medical Immunology; Martin Luther-University Halle-Wittenberg ; Halle, Germany.
Paolo FornaraClinic of Urology; Martin Luther-University Halle-Wittenberg ; Halle, Germany.
Christine LautenschlägerInstitute of Med. Epidemiology and Biometry and Medical Informatics; Martin Luther-University Halle-Wittenberg ; Halle, Germany.
Hans-Jürgen HolzhausenInstitute of Pathology; Martin Luther-University Halle-Wittenberg ; Halle, Germany.
Barbara SeligerInstitute of Medical Immunology; Martin Luther-University Halle-Wittenberg ; Halle, Germany.
Dagmar RiemannInstitute of Medical Immunology; Martin Luther-University Halle-Wittenberg ; Halle, Germany.
Institute of Immunology · HRLuther University · KRMartin Luther University Halle-Wittenberg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor-associated immune cells have been discussed as an essential factor for the prediction of the outcome of tumor patients. Lymphocyte-specific genes are associated with a favorable prognosis in colorectal cancer but with poor survival in renal cell carcinoma (RCC). Flow cytometric analyses combined with immunohistochemistry were performed to study the phenotypic profiles of tumor infiltrating lymphocytes (TIL) and the frequency of T cells and macrophages in RCC lesions. Data were correlated with clinicopathological parameters and survival of patients. Comparing oncocytoma and clear cell (cc)RCC, T cell numbers as well as activation-associated T cell markers were higher in ccRCC, whereas the frequency of NK cells was higher in oncocytoma. An intratumoral increase of T cell numbers was found with higher tumor grades (G1:G2:G3/4 = 1:3:4). Tumor-associated macrophages slightly increased with dedifferentiation, although the macrophage-to-T cell ratio was highest in G1 tumor lesions. A high expression of CD57 was found in T cells of early tumor grades, whereas T cells in dedifferentiated RCC lesions expressed higher levels of CD69 and CTLA4. TIL composition did not differ between older (>70 y) and younger (<58 y) patients. Enhanced patients' survival was associated with a higher percentage of tumor infiltrating NK cells and Th1 markers, e.g. HLA-DR+ and CXCR3+ T cells, whereas a high number of T cells, especially with high CD69 expression correlated with a worse prognosis of patients. Our results suggest that immunomonitoring of RCC patients might represent a useful tool for the prediction of the outcome of RCC patients.

Indexed as

CD13CD57CD69flow cytometryimmunohistochemistryimmunophenotypemAb, monoclonal antibodyMDSC, myeloid-derived suppressor cellsMFI, mean fluorescence intensityNK, natural killer cellsoncocytomaPE, phycoerythrineRCC, renal cell carcinomarenal cell carcinomasurvivalTIL, tumor-infiltrating lymphocytestumor-associated macrophages (TAM)tumor infiltrating lymphocytes (TIL)

Identifiers

PMID25949868
PMCPMC4368143
OpenAlexW1986935067

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.