Evidence map›Paper›PMID 20154618›Full record

ReviewCurrent opinion in oncology2010

Recent updates in renal cell carcinoma.

W Kimryn Rathmell, Paul A Godley

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in oncology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.6field-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

15 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Tumor Associated Macrophages in Kidney Cancer.Analytical cellular pathology (Amsterdam) · 2016
    Review
  6. Article
  7. Review
  8. Review
  9. Eg5 inhibitor, a novel potent targeted therapy, induces cell apoptosis in renal cell carcinoma.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2014
    Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Solid renal masses in adults.The Indian journal of radiology & imaging
    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

2 authors at 2 institutions in 1 country.

W Kimryn RathmellDepartment of Medicine, Division of Hematology and Oncology, Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, North Carolina, USA. Rathmell@med.unc.edu
Paul A Godley
UNC Lineberger Comprehensive Cancer CenterUniversity of North Carolina at Chapel Hill · US

Funding

UNC-CH/SHAW: PARTNERSHIP FOR HEALTH DISPARITY RESEARCHP60MD000244 · NIMHD · UNIV OF NORTH CAROLINA CHAPEL HILL · PI GODLEY, PAUL A. · 2002 to 2011
$10.3M
Increasing Cancer Clinical Trial Enrollment in North Carolina CommunitiesU01CA114629 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI GODLEY, PAUL A. · 2005 to 2009
$4.2M
Genetic Events in the Development of Renal Cell CarcinomaR01CA121781 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI RATHMELL, WENDY KIMRYN · 2007 to 2011
$1.4M
NCI NIH HHS 1U01CA114629NCI NIH HHS R01 CA121781NCI NIH HHS U01 CA114629NIMHD NIH HHS 1P60MD00244NIMHD NIH HHS P60 MD000244
6 · The paper itself

Abstract

purpose of reviewThe review will examine the recent advances in our understanding of the genetic and molecular events that shape this cancer, and overview the emerging targeted therapies that have altered the landscape for renal cell carcinoma (RCC) patients. RECENT

findingsThe incidence of RCC continues to rise, making it the 7th and 8th most common cancer among men and women in the US, respectively. Von Hippel-Lindau (VHL) gene loss is an important factor in the development of clear cell RCC, however: loss of VHL can result in tumors which express both HIF1 and HIF2, or HIF2 alone, correlating with distinct pathway activities. Invasive tumors demonstrating loss of VHL consistently demonstrate additional genetic changes, which appear to be essential for tumor progression. Targeted therapies have demonstrated improvements in overall survival. New ways to radiographically measure the tumor response to these treatments may provide additional information about a drug's activity in an individual patient. Vascular endothelial growth factor receptor tyrosine kinase inhibitors are still being investigated in the adjuvant setting. SUMMARY: The field of RCC biology continues to rapidly change. As new targeted strategies to control this cancer evolve, so do both the clinical strategies, and the strategies to measure response and predict outcome.

Indexed as

Carcinoma, Renal CellChemotherapy, AdjuvantDrug Delivery SystemsHumansKidney NeoplasmsNeoadjuvant TherapyNephrectomy

Identifiers

PMID20154618
PMCPMC2906148
OpenAlexW1982329682

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.