Evidence map›Paper›PMID 25093488›Full record

ArticleBritish journal of cancer2014

Head and neck cancer relapse after chemoradiotherapy correlates with CD163+ macrophages in primary tumour and CD11b+ myeloid cells in recurrences.

P Balermpas, F Rödel, R Liberz, J Oppermann, J Wagenblast, S Ghanaati, P N Harter, M Mittelbronn, C Weiss, C Rödel and 1 more

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed, 1 pooled it
3.6field-weighted citation impact, top 6% 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

60 citing papers in PubMed, 1 synthesis or guideline pooled it, 100 citations in OpenAlex.

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  18. Radiotherapy resistance: identifying universal biomarkers for various human cancers.Journal of cancer research and clinical oncology · 2022
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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 at 1 institution in 1 country.

P BalermpasDepartment of Radiation Therapy and Oncology, Johann Wolfgang Goethe University, Frankfurt, Germany.
F RödelDepartment of Radiation Therapy and Oncology, Johann Wolfgang Goethe University, Frankfurt, Germany.
R LiberzSenckenberg Institute of Pathology, Goethe University, Frankfurt, Germany.
J OppermannDepartment of Radiation Therapy and Oncology, Johann Wolfgang Goethe University, Frankfurt, Germany.
J WagenblastDepartment of Head and Neck Surgery, Goethe University, Frankfurt, Germany.
S GhanaatiDepartment of Maxillofacial Surgery, Goethe University, Frankfurt, Germany.
P N HarterEdinger Institute, Institute of Neurology, Goethe University, Frankfurt, Germany.
M MittelbronnEdinger Institute, Institute of Neurology, Goethe University, Frankfurt, Germany.
C WeissDepartment of Radiation Therapy and Oncology, Johann Wolfgang Goethe University, Frankfurt, Germany.
C Rödel1] Department of Radiation Therapy and Oncology, Johann Wolfgang Goethe University, Frankfurt, Germany [2] German Cancer Consortium (DKTK), Partner Site Frankfurt and German Cancer Research Center (DKFZ), Heidelberg, Germany.
E FokasDepartment of Radiation Therapy and Oncology, Johann Wolfgang Goethe University, Frankfurt, Germany.
Goethe University Frankfurt · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWe investigated the prognostic role of tumour-associated macrophages (TAMs) in patients with head and neck squamous cell carcinoma (HNSCC) treated with definitive chemoradiotherapy (CRT).

methodsThe expression of CD68+, CD163+ and CD11b+ cells was assessed using immunohistochemistry in n=106 pre-treatment tumour biopsy samples and was correlated with clinicopathological characteristics, including T-stage, N-stage, grading, tumour localisation, age and sex as well as local failure-free survival (LFFS), distant metastases-free survival (DMFS), progression-free (PFS), and overall survival (OS). Finally, TAMs expression and vessel density (CD31) were examined in n=12 available early local recurrence samples and compared with their matched primary tumours . The diagnostic images and radiotherapy plans of these 12 patients were also analysed. All local recurrences occurred in the high radiation dose region (⩾70 Gy).

resultsWith a median follow-up of 40 months, OS at 2 years was 60.5%. High CD163 expression in primary tumours was associated with decreased OS (P=0.010), PFS (P=0.033), LFFS (P=0.036) and DMFS (P=0.038) in multivariate analysis. CD163 demonstrated a strong prognostic value only in human papillomavirus (p16(INK4))-negative patients. Early local recurrence specimens demonstrated a significantly increased infiltration of CD11b+ myeloid cells (P=0.0097) but decreased CD31-positive vessel density (P=0.0004) compared with their matched primary samples.

conclusionsAltogether, baseline CD163 expression predicts for an unfavourable clinical outcome in HNSCC after definitive CRT. Early local recurrences showed increased infiltration by CD11b+ cells. These data provide important insight on the role of TAMs in mediating response to CRT in patients with HNSCC.

Indexed as

RadiotherapyAntigens, CDAntigens, Differentiation, MyelomonocyticAntineoplastic AgentsBone Marrow CellsCD11b AntigenCD163 AntigenFemaleHead and Neck NeoplasmsHumansMacrophagesMaleMiddle AgedNeoplasm Recurrence, LocalReceptors, Cell SurfaceAntigens, CDAntigens, Differentiation, MyelomonocyticAntineoplastic AgentsCD11b AntigenCD163 AntigenITGAM protein, humanReceptors, Cell Surface

Identifiers

PMID25093488
PMCPMC4200089
OpenAlexW2074942026

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

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.