Evidence map›Paper›PMID 25263506›Full record

ArticleJournal of cutaneous pathology2014

Detection of mitotic figures and G2+ tumor nuclei with histone markers correlates with worse overall survival in patients with Merkel cell carcinoma.

Samuel A Henderson, Michael T Tetzlaff, Penvadee Pattanaprichakul, Patricia Fox, Carlos A Torres-Cabala, Roland L Bassett, Victor G Prieto, Hunter W Richards, Jonathan L Curry

Open access · greenAbstract read
In one paragraph

Article in Journal of cutaneous pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 22% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Merkel Cell Carcinoma, Version 1.2018, NCCN Clinical Practice Guidelines in Oncology.Journal of the National Comprehensive Cancer Network : JNCCN · 2018
    Guideline
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Update on Merkel Cell Carcinoma.Head and neck pathology · 2018
    Review
  9. Review
  10. Emerging clinical applications of selected biomarkers in melanoma.Clinical, cosmetic and investigational dermatology · 2015
    Review
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

9 authors at 4 institutions in 2 countries.

Samuel A HendersonThe University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Michael T Tetzlaff
Penvadee Pattanaprichakul
Patricia Fox
Carlos A Torres-Cabala
Roland L Bassett
Victor G Prieto
Hunter W Richards
Jonathan L Curry
The University of Texas MD Anderson Cancer Center · USIn-Q-Tel · USLawrence Berkeley National Laboratory · USMahidol University · TH

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

backgroundHigh mitotic figure count (MFC) correlates with low survival rate in Merkel cell carcinoma (MCC). However, the prognostic impact of histone biomarkers as surrogates of MFC in MCC is unknown. We evaluated the prognostic significance of the immunodetection of mitotic figures and of G2+ tumor nuclei with histone-associated mitotic markers H3K79me3T80ph (H3KT) and phosphohistone H3 (PHH3) in MCC.

methodsImmunohistochemical analyses of H3KT and PHH3 and proliferative marker Ki-67 were performed in a series of 21 cases of MCC. The significance of the pathologic data and immunoreactivity with these markers was evaluated with Pearson correlation and paired Student t-test. Univariate Cox proportional hazards regression models were performed to assess the relationships between these markers and survival.

resultsH3KT detected a higher number of mitotic figure (p<0.0001) and G2+ tumor nuclei (p<0.0052) than did PHH3. Furthermore, the MFC combined with G2+ tumor nuclei detected with H3KT compared to PHH3 and manual MFC was a significant predictor of impaired survival in patients with MCC (p=0.035; HR=1.0172), corresponding to a 1.72% increased risk of death for each unit increase in H3KT.

conclusionsBiomarker analysis of proliferative rates with histone markers may have relevance in stratifying risk in patients with MCC.

Indexed as

AgedAged, 80 and overBiomarkers, TumorCarcinoma, Merkel CellCell NucleusCell ProliferationFemaleHistonesHumansImmunohistochemistryMaleMiddle AgedMitosisPrognosisProportional Hazards ModelsSkin NeoplasmsBiomarkers, TumorHistonesbiomarkerH3K79me3T80phhistonesMerkel cell carcinomaPHH3

Identifiers

PMID25263506
PMCPMC4522694
OpenAlexW1899885034

What OpenQuestion holds

Textmetadata
LicenceTDM
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.