Evidence map›Paper›PMID 26076664›Full record

ArticleCancer immunology, immunotherapy : CII2015

Immune biomarkers are more accurate in prediction of survival in ulcerated than in non-ulcerated primary melanomas.

Ellen H de Moll, Yichun Fu, Yingzhi Qian, Sara H Perkins, Shira Wieder, Sacha Gnjatic, Romain Remark, Sebastian G Bernardo, Marina Moskalenko, Jonathan Yao and 7 more

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Systematic Multiomic Analysis ofInternational journal of molecular sciences · 2023
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. 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

17 authors at 3 institutions in 1 country.

Ellen H de MollDepartment of Dermatology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Yichun Fu
Yingzhi Qian
Sara H Perkins
Shira Wieder
Sacha Gnjatic
Romain Remark
Sebastian G Bernardo
Marina Moskalenko
Jonathan Yao
Tammie Ferringer
Rui Chang
Jerry Chipuk
Basil A Horst
Miriam B Birge
Robert G Phelps
Yvonne M Saenger
Icahn School of Medicine at Mount Sinai · USColumbia University · USGeisinger Medical Center · US

Funding

Function and regulation of the BCL-2 familyR01CA157740 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CHIPUK, JERRY EDWARD · 2011 to 2015
$1.7M
NCI NIH HHS R01 CA157740
6 · The paper itself

Abstract

introductionUlcerated melanomas may have a unique biology and microenvironment. We test whether markers of immune infiltration correlate with clinical outcome in ulcerated compared to non-ulcerated primary melanoma tumors.

methodsSixty-two stage II-III cutaneous melanomas, 32 ulcerated and 30 non-ulcerated, were analyzed for tumor-infiltrating lymphocytes (TILs). Immunohistochemistry (IHC) was performed for CD2, a marker previously shown to correlate with overall survival (OS) and recurrence-free survival (RFS) in this patient population. IHC using antibody, VE1, to BRAF V600E was also performed on a subset of 41 tumors to assess the relationship of BRAF mutation to immune markers.

resultsWe found, using Cox regression models, that the presence of TILs was associated with improved OS (p = 0.034) and RFS (p = 0.002) in ulcerated melanoma tumors, but not in non-ulcerated melanoma (p = 0.632, 0.416). CD2 expression also was correlated with improved OS (p = 0.021) and RFS (p = 0.001) in ulcerated melanoma, but no relationship was seen in non-ulcerated melanoma (p = 0.427, 0.682). In this small population, BRAF status did not correlate with TILs or CD2+ count.

conclusionOur data show that immune markers including TILs and CD2 count correlate more closely with survival in ulcerated melanomas than that in non-ulcerated melanomas. We propose that immune biomarkers may be particularly relevant to ulcerated, as compared to non-ulcerated, melanomas and that this merits study in larger populations.

Indexed as

AdultAgedAged, 80 and overBiomarkers, TumorCutaneous Malignant MelanomaHumansImmunohistochemistryLymphocytes, Tumor-InfiltratingMelanomaMiddle AgedRetrospective StudiesSkin NeoplasmsSurvival AnalysisBiomarkers, Tumor

Identifiers

PMID26076664
PMCPMC4581435
OpenAlexW615967542

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.