Evidence map›Paper›PMID 20959478›Full record

ArticleCancer research2010

Antibodies to merkel cell polyomavirus T antigen oncoproteins reflect tumor burden in merkel cell carcinoma patients.

Kelly G Paulson, Joseph J Carter, Lisa G Johnson, Kevin W Cahill, Jayasri G Iyer, David Schrama, Juergen C Becker, Margaret M Madeleine, Paul Nghiem, Denise A Galloway

Open access · hybridAbstract readComparative Study
In one paragraph

Article in Cancer research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 106 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
106citing papers in PubMed, 2 pooled it
9.7field-weighted citation impact, top 1% 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

106 citing papers in PubMed, 2 syntheses or guidelines pooled it, 234 citations in OpenAlex.

  1. Guideline
  2. Merkel Cell Carcinoma, Version 1.2018, NCCN Clinical Practice Guidelines in Oncology.Journal of the National Comprehensive Cancer Network : JNCCN · 2018
    Guideline
  3. Trial
  4. Trial
  5. Trial
  6. Neoadjuvant Nivolumab for Patients With Resectable Merkel Cell Carcinoma in the CheckMate 358 Trial.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2020
    Trial
  7. Durable Tumor Regression and Overall Survival in Patients With Advanced Merkel Cell Carcinoma Receiving Pembrolizumab as First-Line Therapy.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2019
    Trial
  8. Intratumoral G100, a TLR4 Agonist, Induces Antitumor Immune Responses and Tumor Regression in Patients with Merkel Cell Carcinoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2019
    Trial
  9. Trial
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. Merkel Cell Carcinoma.Hematology/oncology clinics of North America · 2024
    Review
  18. Article
  19. Article
  20. Observational

46 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

10 authors at 4 institutions in 3 countries.

Kelly G PaulsonDivision of Human Biology, Fred Hutchinson Cancer Research Center, University of Washington, Seattle, Washington 98109, USA.
Joseph J Carter
Lisa G Johnson
Kevin W Cahill
Jayasri G Iyer
David Schrama
Juergen C Becker
Margaret M Madeleine
Paul Nghiem
Denise A Galloway
University of Graz · ATFred Hutch Cancer Center · USUniversity of Washington · USUniversitätsklinikum Würzburg · DE

Funding

VIROLOGIC/GENETIC FACTORS OF HPV NEOPLASMSP01CA042792 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI GALLOWAY, DENISE A. · 1987 to 2011
$21.0M
Interdisciplinary Tranining in Cancer ResearchT32CA080416 · NCI · UNIVERSITY OF WASHINGTON · PI STODDARD, BARRY L. · 1998 to 2023
$9.7M
HPV CAPSID ANTIBODIESR01AI038382 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI GALLOWAY, DENISE A. · 1995 to 2020
$4.4M
Pathogenetic and prognostic studies for improved therapy of Merkel cell carcinomaK24CA139052 · NCI · UNIVERSITY OF WASHINGTON · PI NGHIEM, PAUL · 2009 to 2018
$1.8M
Targeting MCPyV to Overcome Immune Evasion in Merkel Cell CarcinomaRC2CA147820 · NCI · UNIVERSITY OF WASHINGTON · PI NGHIEM, PAUL · 2009 to 2010
$1.0M
The replication checkpoint and genomic fidelity in skinK02AR050993 · NIAMS · UNIVERSITY OF WASHINGTON · PI NGHIEM, PAUL · 2004 to 2008
$509k
Pathogenetics of Merkel cell cancer: a disease linked to UV damage & a new virusF30ES017385 · NIEHS · UNIVERSITY OF WASHINGTON · PI PAULSON, KELLY GARNESKI · 2009 to 2010
$65k
NCI NIH HHS 2P01CA042792NCI NIH HHS K24 CA139052NCI NIH HHS K24-CA139052-1NCI NIH HHS P01 CA042792NCI NIH HHS RC2 CA147820NCI NIH HHS RC2CA147820NCI NIH HHS T32 CA080416NCI NIH HHS T32-CA80416-10NIAID NIH HHS R01 AI038382NIAID NIH HHS R01AI38382NIAMS NIH HHS K02 AR050993NIEHS NIH HHS F30 ES017385NIEHS NIH HHS F30ES017385
6 · The paper itself

Abstract

Merkel cell polyomavirus (MCPyV) is a common infectious agent that is likely involved in the etiology of most Merkel cell carcinomas (MCC). Serum antibodies recognizing the MCPyV capsid protein VP1 are detectable at high titer in nearly all MCC patients and remain stable over time. Although antibodies to the viral capsid indicate prior MCPyV infection, they provide limited clinical insight into MCC because they are also detected in more than half of the general population. We investigated whether antibodies recognizing MCPyV large and small tumor-associated antigens (T-Ag) would be more specifically associated with MCC. Among 530 population control subjects, these antibodies were present in only 0.9% and were of low titer. In contrast, among 205 MCC cases, 40.5% had serum IgG antibodies that recognize a portion of T-Ag shared between small and large T-Ags. Among cases, titers of T-Ag antibodies fell rapidly (∼8-fold per year) in patients whose cancer did not recur, whereas they rose rapidly in those with progressive disease. Importantly, in several patients who developed metastases, the rise in T-Ag titer preceded clinical detection of disease spread. These results suggest that antibodies recognizing T-Ag are relatively specifically associated with MCC, do not effectively protect against disease progression, and may serve as a clinically useful indicator of disease status.

Indexed as

AdultAgedAged, 80 and overAntibodiesAntigens, Polyomavirus TransformingCarcinoma, Merkel CellCase-Control StudiesDNA, ViralFemaleHumansImmunoenzyme TechniquesMaleMerkel CellsMiddle AgedMutagenesis, Site-DirectedPlasmidsAntibodiesAntigens, Polyomavirus TransformingDNA, Viral

Identifiers

PMID20959478
PMCPMC2970647
OpenAlexW2110947977

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.