Evidence map›Paper›PMID 28276433›Full record

ReviewNature reviews. Disease primers2017

Renal cell carcinoma.

James J Hsieh, Mark P Purdue, Sabina Signoretti, Charles Swanton, Laurence Albiges, Manuela Schmidinger, Daniel Y Heng, James Larkin, Vincenzo Ficarra

Abstract readReview
In one paragraph

Review in Nature reviews. Disease primers, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1,735 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1,735citing papers in PubMed, 3 pooled it
117.8field-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

1,735 citing papers in PubMed, 3 syntheses or guidelines pooled it, 2,697 citations in OpenAlex.

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1,675 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

9 authors at 8 institutions in 5 countries.

James J HsiehMolecular Oncology, Department of Medicine, Siteman Cancer Center, Washington University School of Medicine, 660 S. Euclid Avenue, Campus Box 8069, St. Louis, Missouri 63110, USA.
Mark P PurdueOccupational and Environmental Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland, USA.
Sabina SignorettiDepartment of Pathology, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Charles SwantonFrancis Crick Institute, UCL Cancer Institute, CRUK Lung Cancer Centre of Excellence, London, UK.
Laurence AlbigesDepartment of Cancer Medicine, Institut Gustave Roussy, Villejuif, France.
Manuela SchmidingerDepartment of Medicine I, Clinical Division of Oncology and Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
Daniel Y HengDepartment of Medical Oncology, Tom Baker Cancer Center, Calgary, Alberta, Canada.
James LarkinDepartment of Medical Oncology, Royal Marsden NHS Foundation Trust, London, UK.
Vincenzo FicarraDepartment of Experimental and Clinical Medical Sciences - Urologic Clinic, University of Udine, Udine, Italy.
Brigham and Women's Hospital · USCRUK Lung Cancer Centre of Excellence · GBInstitut Gustave Roussy · FRMedical University of Vienna · ATNational Cancer Institute · USRoyal Marsden NHS Foundation Trust · GBUniversity of Udine · ITWashington University in St. Louis · US

Funding

Integrated Analyses of Taspase 1 (MLL Cleaving Protease)R01CA119008 · NCI · WASHINGTON UNIVERSITY · PI HSIEH, JAMES J · 2006 to 2010
$1.3M
Molecular Mechanisms of Impaired DAN Damage Response in Leukemia PathogenesisR01CA138505 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI HSIEH, JAMES J · 2013 to 2015
$1.0M
NCI NIH HHS R01 CA119008NCI NIH HHS R01 CA138505
6 · The paper itself

Abstract

Renal cell carcinoma (RCC) denotes cancer originated from the renal epithelium and accounts for >90% of cancers in the kidney. The disease encompasses >10 histological and molecular subtypes, of which clear cell RCC (ccRCC) is most common and accounts for most cancer-related deaths. Although somatic VHL mutations have been described for some time, more-recent cancer genomic studies have identified mutations in epigenetic regulatory genes and demonstrated marked intra-tumour heterogeneity, which could have prognostic, predictive and therapeutic relevance. Localized RCC can be successfully managed with surgery, whereas metastatic RCC is refractory to conventional chemotherapy. However, over the past decade, marked advances in the treatment of metastatic RCC have been made, with targeted agents including sorafenib, sunitinib, bevacizumab, pazopanib and axitinib, which inhibit vascular endothelial growth factor (VEGF) and its receptor (VEGFR), and everolimus and temsirolimus, which inhibit mechanistic target of rapamycin complex 1 (mTORC1), being approved. Since 2015, agents with additional targets aside from VEGFR have been approved, such as cabozantinib and lenvatinib; immunotherapies, such as nivolumab, have also been added to the armamentarium for metastatic RCC. Here, we provide an overview of the biology of RCC, with a focus on ccRCC, as well as updates to complement the current clinical guidelines and an outline of potential future directions for RCC research and therapy.

Indexed as

AxitinibBevacizumabCarcinoma, Renal CellHumansImidazolesIndazolesIndolesKidneyKidney DiseasesNiacinamidePhenylurea CompoundsPyrimidinesPyrrolesQuality of LifeRisk FactorsSorafenibAxitinibBevacizumabImidazolesIndazolesIndolesNiacinamidepazopanibPhenylurea CompoundsPyrimidinesPyrrolesSorafenibSulfonamidesSunitinibVascular Endothelial Growth Factor AVEGFA protein, human

Identifiers

PMID28276433
PMCPMC5936048
OpenAlexW2726542547

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.