Evidence map›Paper›PMID 28787661›Full record

ReviewEuropean journal of cancer (Oxford, England : 1990)2017

Understanding the role of primary tumour localisation in colorectal cancer treatment and outcomes.

Sebastian Stintzing, Sabine Tejpar, Peter Gibbs, Lars Thiebach, Heinz-Josef Lenz

Open access · bronzeAbstract readReview
In one paragraph

Review in European journal of cancer (Oxford, England : 1990), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 162 papers, 10 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
162citing papers in PubMed, 10 pooled it
12.4field-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

162 citing papers in PubMed, 10 syntheses or guidelines pooled it, 289 citations in OpenAlex.

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  8. Diagnostic Value and Clinical Significance of Methylated SEPT9 for Colorectal Cancer: A Meta-Analysis.Medical science monitor : international medical journal of experimental and clinical research · 2019
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  14. Impact of Consensus Molecular Subtype on Survival in Patients With Metastatic Colorectal Cancer: Results From CALGB/SWOG 80405 (Alliance).Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2019
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102 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

5 authors at 5 institutions in 5 countries.

Sebastian StintzingDepartment of Medicine III, University Hospital, LMU Munich, Germany. Electronic address: sebastian.stintzing@med.uni-muenchen.de.
Sabine TejparMolecular Digestive Oncology Unit, University Hospital Gasthuisberg, Leuven, Belgium. Electronic address: sabine.tejpar@uzleuven.be.
Peter GibbsSystems Biology and Personalised Medicine, The Walter and Eliza Hall Institute of Medical Research, Melbourne, Australia. Electronic address: gibbs.p@wehi.EDU.AU.
Lars ThiebachRoche Pharma AG, Grenzach-Wyhlen, Germany. Electronic address: lars.thiebach@roche.com.
Heinz-Josef LenzUSC Norris Comprehensive Cancer Center, University of Southern California, Los Angeles, CA, USA. Electronic address: LENZ@med.usc.edu.
KU Leuven · BELMU Klinikum · DERoche (Switzerland) · CHUniversity of Southern California · USWalter and Eliza Hall Institute of Medical Research · AU

Funding

USC/NORRIS COMPREHENSIVE CANCER CENTER (CORE) SUPPORTP30CA014089 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI MYLES G COCKBURN · 1985 to 2026
$181.4M
NCI NIH HHS P30 CA014089
6 · The paper itself

Abstract

Metastatic colorectal carcinoma (mCRC) is a heterogeneous disease with differing outcomes and clinical responses and poor prognosis. CRCs can be characterised by their primary tumour location within the colon. The left-sided colon, derived from the hindgut, includes the distal third of the transverse colon, splenic flexure, descending colon, sigmoid colon and rectum. The right-sided colon, derived from the midgut, includes the proximal two-thirds of the transverse colon, ascending colon and caecum. Sometimes, the rectum is described separately, despite originating from the hindgut, and in many clinical series, the left-sided colon includes only tumours within and distal to the splenic flexure. Differences in the microbiome, clinical characteristics and chromosomal and molecular characteristics have been reported between the right and left side of the colon, regardless of how this is defined. There is now strong evidence from clinical studies in patients with mCRC for the prognostic effect of primary tumour location. The impact of primary colonic tumour location on response to treatment is now under investigation in a large number of clinical studies in patients with mCRC. In this review, we summarise the microbiome, clinical, chromosomal and molecular differences associated with the primary location of CRC. We present an overview of the proven prognostic impact of primary tumour location for patients with mCRC and discuss emerging data for the predictive impact of primary tumour location on clinical outcome.

Indexed as

Antineoplastic AgentsBiomarkers, TumorColonic NeoplasmsColorectal NeoplasmsErbB ReceptorsGastrointestinal MicrobiomeHumansMolecular Diagnostic TechniquesMutationNeoplasm MetastasisPrecision MedicinePredictive Value of TestsProtein Kinase InhibitorsRectal NeoplasmsTreatment OutcomeAntineoplastic AgentsBiomarkers, TumorEGFR protein, humanErbB ReceptorsProtein Kinase InhibitorsColonColorectal carcinomaHindgutMetastaticMidgutPredictivePrognostic

Identifiers

PMID28787661
PMCPMC7505124
OpenAlexW2744203203

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.