Evidence map›Paper›PMID 28824949›Full record

ArticleBladder cancer (Amsterdam, Netherlands)2017

Proceedings of the 3rd Annual Albert Institute for Bladder Cancer Research Symposium.

Thomas W Flaig, Ashish M Kamat, Donna Hansel, Molly A Ingersoll, H Barton Grossman, Cathy Mendelsohn, David DeGraff, Joseph C Liao, John A Taylor

Open access · bronzeAbstract read
In one paragraph

Article in Bladder cancer (Amsterdam, Netherlands), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
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 2 countries.

Thomas W FlaigDepartment of Medicine, University of Colorado, Aurora, CO, USA.
Ashish M KamatDepartment of Urology, MD Anderson Cancer Center, Houston, TX, USA.
Donna HanselDepartment of Pathology, University ofCalifornia San Diego, San Diego, CA, USA.
Molly A IngersollInstitut Pasteur, Dendritic Cell Immunology Unit, Paris, France.
H Barton GrossmanDepartment of Urology, MD Anderson Cancer Center, Houston, TX, USA.
Cathy MendelsohnDepartment of Pathology and Cell Biology, Columbia University, New York, NY, USA.
David DeGraffDepartment of Pathology, Penn State University, Hershey, PA, USA.
Joseph C LiaoDepartment of Urology, Stanford University, Stanford, CA, USA.
John A TaylorUniversity of Kansas, Department of Urology, Kansas City, KS, USA.
The University of Texas MD Anderson Cancer Center · USColumbia University · USInstitut Pasteur · FRPenn State Milton S. Hershey Medical Center · USStanford University · USUniversity of California San Diego · USUniversity of Colorado Anschutz Medical Campus · USUniversity of Kansas · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Third Annual Albert Institute Bladder Symposium was held on September 8-10th, 2016, in Denver Colorado. Participants discussed several critical topics in the field of bladder cancer: 1) Best practices for tissue analysis and use to optimize correlative studies, 2) Modeling bladder cancer to facilitate understanding and innovation, 3) Targeted therapies for bladder cancer, 4) Tumor phylogeny in bladder cancer, 5) New Innovations in bladder cancer diagnostics. Our understanding of and approach to treating urothelial carcinoma is undergoing rapid advancement. Preclinical models of bladder cancer have been leveraged to increase our basic and mechanistic understanding of the disease. With the approval of immune checkpoint inhibitors for the treatment of advanced urothelial carcinoma, the treatment approach for these patients has quickly changed. In this light, molecularly-defined subtypes of bladder cancer and appropriate pre-clinical models are now essential to the further advancement and appropriate application of these therapeutic improvements. The optimal collection and processing of clinical urothelial carcinoma tissues samples will also be critical in the development of predictive biomarkers for therapeutic selection. Technological advances in other areas including optimal imaging technologies and micro/nanotechnologies are being applied to bladder cancer, especially in the localized setting, and hold the potential for translational impact in the treatment of bladder cancer patients. Taken together, advances in several basic science and clinical areas are now converging in bladder cancer. These developments hold the promise of shaping and improving the clinical care of those with the disease.

Indexed as

animalmodelsMolecular Diagnostic TechniquesMolecular Targeted TherapyUrinary Bladder Neoplasms

Identifiers

PMID28824949
PMCPMC5545918
OpenAlexW2618418118

What OpenQuestion holds

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LicenceCC BY-NC
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.