Evidence map›Paper›PMID 28050146›Full record

ArticleCurrent oncology (Toronto, Ont.)2016

Personalized oncogenomics in the management of gastrointestinal carcinomas-early experiences from a pilot study.

B S Sheffield, B Tessier-Cloutier, H Li-Chang, Y Shen, E Pleasance, K Kasaian, Y Li, S J M Jones, H J Lim, D J Renouf and 5 more

Open access · goldAbstract read
In one paragraph

Article in Current oncology (Toronto, Ont.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

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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

15 authors at 4 institutions in 1 country.

B S SheffieldDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC.
B Tessier-CloutierDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC.
H Li-ChangRoyal Victoria Regional Health Centre, Department of Pathology and Laboratory Medicine, Barrie, ON.
Y ShenCanada's Michael Smith Genome Sciences Centre, BC Cancer Agency, Vancouver, BC.
E PleasanceCanada's Michael Smith Genome Sciences Centre, BC Cancer Agency, Vancouver, BC.
K KasaianCanada's Michael Smith Genome Sciences Centre, BC Cancer Agency, Vancouver, BC.
Y LiCanada's Michael Smith Genome Sciences Centre, BC Cancer Agency, Vancouver, BC.
S J M JonesCanada's Michael Smith Genome Sciences Centre, BC Cancer Agency, Vancouver, BC.
H J LimDivision of Medical Oncology, BC Cancer Agency, Vancouver, BC.
D J RenoufDivision of Medical Oncology, BC Cancer Agency, Vancouver, BC.
D G HuntsmanDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC.
S YipDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC.
J LaskinDivision of Medical Oncology, BC Cancer Agency, Vancouver, BC.
M MarraCanada's Michael Smith Genome Sciences Centre, BC Cancer Agency, Vancouver, BC.; Department of Medical Genetics, University of British Columbia, Vancouver, BC.
D F SchaefferDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC.
BC Cancer Agency · CAUniversity of British Columbia · CACanada's Michael Smith Genome Sciences Centre · CARoyal Victoria Regional Health Centre · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGastrointestinal carcinomas are genomically complex cancers that are lethal in the metastatic setting. Whole-genome and transcriptome sequencing allow for the simultaneous characterization of multiple oncogenic pathways.

methodsWe report 3 cases of metastatic gastrointestinal carcinoma in patients enrolled in the Personalized Onco-Genomics program at the BC Cancer Agency. Real-time genomic profiling was combined with clinical expertise to diagnose a carcinoma of unknown primary, to explore treatment response to bevacizumab in a colorectal cancer, and to characterize an appendiceal adenocarcinoma.

resultsIn the first case, genomic profiling revealed an SUMMARY: We show that whole-genome and transcriptome sequencing can be achieved within clinically effective timelines, yielding clinically useful and actionable information.

Indexed as

appendiceal adenocarcinomabevacizumabcholangiocarcinomacolonic adenocarcinomagenomicsOncogenomicspersonalized medicinetargeted therapy

Identifiers

PMID28050146
PMCPMC5176383
OpenAlexW2566181313

What OpenQuestion holds

Textmetadata
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.