Evidence map›Paper›PMID 22149431›Full record

ReviewExpert review of anticancer therapy2012

Development of targeted therapy in uterine serous carcinoma, a biologically aggressive variant of endometrial cancer.

Karim S El-Sahwi, Peter E Schwartz, Alessandro D Santin

Open access · greenAbstract readReview
In one paragraph

Review in Expert review of anticancer therapy, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

18 citing papers in PubMed, 42 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Uterine serous carcinoma.Gynecologic oncology · 2021
    Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Mutational landscape of uterine and ovarian carcinosarcomas implicates histone genes in epithelial-mesenchymal transition.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  12. Improved i.p. drug delivery with bioadhesive nanoparticles.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  13. Article
  14. Dual HER2 targeting impedes growth of HER2 gene-amplified uterine serous carcinoma xenografts.Clinical cancer research : an official journal of the American Association for Cancer Research · 2014
    Article
  15. Review
  16. Landscape of somatic single-nucleotide and copy-number mutations in uterine serous carcinoma.Proceedings of the National Academy of Sciences of the United States of America · 2013
    Article
  17. Article
  18. 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

3 authors at 2 institutions in 2 countries.

Karim S El-SahwiDepartment of Obstetrics, Gynecology and Reproductive Sciences, Yale University School of Medicine, CT, USA.
Peter E Schwartz
Alessandro D Santin
Yale University · USSanten (Japan) · JP

Funding

CPE Peptide-Based Nanoparticles for the Diagnosis and Therapy of Chemotherapy ResR01CA154460 · NCI · YALE UNIVERSITY · PI SANTIN, ALESSANDRO D · 2011 to 2015
$1.7M
Treatment of Chemotherapy-Resistant Human Ovarian Cancer by Administration of CPER01CA122728 · NCI · YALE UNIVERSITY · PI SANTIN, ALESSANDRO D · 2008 to 2011
$1.4M
NCI NIH HHS 1R01CA122728-01A4NCI NIH HHS CA154460-01A1NCI NIH HHS R01 CA122728NCI NIH HHS R01 CA154460
6 · The paper itself

Abstract

Endometrial cancer (EC) is the most common female genital malignancy in the USA. Most carcinomas arising from the uterus are estrogen dependent and are associated with obesity and hypertension. They are designated type I ECs and typically, due to their early diagnosis secondary to postmenopausal bleeding, have a good prognosis. By contrast, type II ECs develop in older patients, are not hormone dependent and are responsible for most recurrences and deaths from EC. Uterine serous cancer constitutes up to 10% of all endometrial tumors, and represents the most biologically aggressive variant of type II EC. This article will describe the most salient molecular markers that have been identified in uterine serous cancer, thus far with emphasis on the use of erbB2 (HER2/neu) as the first of a series of therapeutic markers for the treatment of this highly-aggressive subset of ECs.

Indexed as

Antineoplastic AgentsClinical Trials, Phase II as TopicCystadenocarcinoma, SerousEndometrial NeoplasmsFemaleHumansMolecular Targeted TherapyNeoplasm Recurrence, LocalRandomized Controlled Trials as TopicUterine NeoplasmsAntineoplastic Agents

Identifiers

PMID22149431
PMCPMC3287395
OpenAlexW2133797921

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.