Evidence map›Paper›PMID 25101620›Full record

ArticlePloS one2014

Expression and immune responses to MAGE antigens predict survival in epithelial ovarian cancer.

Sayeema Daudi, Kevin H Eng, Paulette Mhawech-Fauceglia, Carl Morrison, Anthony Miliotto, Amy Beck, Junko Matsuzaki, Takemasa Tsuji, Adrienne Groman, Sacha Gnjatic and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

54 citing papers in PubMed, 78 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Nucleic acid vaccination strategies for ovarian cancer.Frontiers in bioengineering and biotechnology · 2022
    Review
  20. Article
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

13 authors at 4 institutions in 2 countries.

Sayeema DaudiDepartment of Gynecologic Oncology, Roswell Park Cancer Institute, Buffalo, New York, United States of America.
Kevin H EngDepartment of Biostatisticsm, Roswell Park Cancer Institute, Buffalo, New York, United States of America.
Paulette Mhawech-FaucegliaDepartment of Pathology, University Southern California, Los Angeles, California, United States of America.
Carl MorrisonDepartment of Pathology, Roswell Park Cancer Institute, Buffalo, New York, United States of America.
Anthony MiliottoDepartment of Gynecologic Oncology, Roswell Park Cancer Institute, Buffalo, New York, United States of America; Center for Immunotherapy, Roswell Park Cancer Institute, Buffalo, New York, United States of America.
Amy BeckCenter for Immunotherapy, Roswell Park Cancer Institute, Buffalo, New York, United States of America.
Junko MatsuzakiCenter for Immunotherapy, Roswell Park Cancer Institute, Buffalo, New York, United States of America; Department of Immunology, Roswell Park Cancer Institute, Buffalo, New York, United States of America.
Takemasa TsujiCenter for Immunotherapy, Roswell Park Cancer Institute, Buffalo, New York, United States of America; Department of Immunology, Roswell Park Cancer Institute, Buffalo, New York, United States of America.
Adrienne GromanDepartment of Biostatisticsm, Roswell Park Cancer Institute, Buffalo, New York, United States of America.
Sacha GnjaticDepartment of Medicine, Mount Sinai Hospital, New York, New York, United States of America.
Guillo SpagnoliDepartment of Biomedicine, University Hospital Basel, Basel, Switzerland.
Shashikant LeleDepartment of Gynecologic Oncology, Roswell Park Cancer Institute, Buffalo, New York, United States of America.
Kunle OdunsiDepartment of Gynecologic Oncology, Roswell Park Cancer Institute, Buffalo, New York, United States of America; Center for Immunotherapy, Roswell Park Cancer Institute, Buffalo, New York, United States of America; Department of Immunology, Roswell Park Cancer Institute, Buffalo, New York, United States of America.
Roswell Park Comprehensive Cancer Center · USMount Sinai Hospital · USUniversity Hospital of Basel · CHUniversity of Southern California · US

Funding

Two-Spirit Films in Indigenous Cancer HealthP30CA016056 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI MARK G FRATTINI · 1985 to 2026
$116.6M
RPCI-UPCI Ovarian Cancer SPOREP50CA159981 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI MOYSICH, KIRSTEN B. · 2013 to 2025
$19.6M
Postdoctoral Research Training in Surgical OncologyT32CA108456 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI YENDAMURI, SAIKRISHNA · 2006 to 2020
$2.8M
mTOR inhibition for generating memory T cells to enhance ovarian tumor immunityR01CA158318 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI ODUNSI, KUNLE, SHRIKANT, PROTUL · 2011 to 2015
$1.7M
NCI NIH HHS 5T32 CA 108456NCI NIH HHS P30 CA016056NCI NIH HHS P50 CA159981NCI NIH HHS P50CA159981-01A1NCI NIH HHS R01 CA158318NCI NIH HHS R01CA158318-01A1NCI NIH HHS T32 CA108456
6 · The paper itself

Abstract

The MAGE cancer-testis antigens (CTA) are attractive candidates for immunotherapy. The aim of this study was to determine the frequency of expression, humoral immunity and prognostic significance of MAGE CTA in human epithelial ovarian cancer (EOC). mRNA or protein expression frequencies were determined for MAGE-A1, -A3, -A4, -A10 and -C1 (CT7) in tissue samples obtained from 400 patients with EOC. The presence of autologous antibodies against the MAGE antigens was determined from 285 serum samples. The relationships between MAGE expression, humoral immunity to MAGE antigens, and clinico-pathologic characteristics were studied. The individual frequencies of expression were as follows: A1: 15% (42/281), A3: 36% (131/390), A4: 47% (186/399), A10: 52% (204/395), C1: 16% (42/267). Strong concordant expression was noted with MAGE-A1:-A4, MAGE-A1:-C1 and MAGE-A4:-A10 (p<0.0005). Expression of MAGE-A1 or -A10 antigens resulted in poor progression free survival (PFS) (OR 1.44, CI 1.01-2.04, p = 0.044 and OR 1.3, CI 1.03-1.64, p = 0.03, respectively); whereas, MAGE-C1 expression was associated with improved PFS (OR 0.62, CI 0.42-0.92, p = 0.016). The improved PFS observed for MAGE-C1 expression, was diminished by co-expression of MAGE-A1 or -A10. Spontaneous humoral immunity to the MAGE antigens was present in 9% (27/285) of patients, and this predicted poor overall survival (log-rank test p = 0.0137). These findings indicate that MAGE-A1, MAGE-A4, MAGE-A3, and MAGE-A10 are priority attractive targets for polyvalent immunotherapy in ovarian cancer patients.

Indexed as

AdultAgedAged, 80 and overAntigens, NeoplasmDisease ProgressionEnzyme-Linked Immunosorbent AssayFemaleHumansImmunity, HumoralImmunohistochemistryImmunotherapyKaplan-Meier EstimateMiddle AgedNeoplasm ProteinsOvarian NeoplasmsReverse Transcriptase Polymerase Chain ReactionAntigens, NeoplasmNeoplasm Proteins

Identifiers

PMID25101620
PMCPMC4125181
OpenAlexW1998426661

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.