Evidence map›Paper›PMID 26872400›Full record

ReviewClinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association2016

Molecular Biomarkers in the Personalized Treatment of Colorectal Cancer.

Frank A Sinicrope, Koichi Okamoto, Pashtoon M Kasi, Hisato Kawakami

Open access · greenAbstract readReview
In one paragraph

Review in Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed, 1 pooled it
10.1field-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

63 citing papers in PubMed, 1 synthesis or guideline pooled it, 112 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Phenotype-Genotype Correlation in Colorectal Cancer: A Real-Life Study.GE Portuguese journal of gastroenterology · 2022
    Article
  18. Review
  19. Review
  20. Article

3 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

4 authors at 3 institutions in 1 country.

Frank A SinicropeDivision of Gastroenterology and Hepatology, Mayo Clinic and Mayo Cancer Center, Rochester, Minnesota; Division of Medical Oncology, Mayo Clinic and Mayo Cancer Center, Rochester, Minnesota. Electronic address: sinicrope.frank@mayo.edu.
Koichi OkamotoDivision of Gastroenterology and Hepatology, Mayo Clinic and Mayo Cancer Center, Rochester, Minnesota.
Pashtoon M KasiDivision of Medical Oncology, Mayo Clinic and Mayo Cancer Center, Rochester, Minnesota.
Hisato KawakamiDivision of Gastroenterology and Hepatology, Mayo Clinic and Mayo Cancer Center, Rochester, Minnesota.
Mayo Clinic in Arizona · USMayo Clinic · USWinnMed · US

Funding

Translational Research in Colon Cancer Prevention & TreatmentK05CA142885 · NCI · MAYO CLINIC ROCHESTER · PI SINICROPE, FRANK A. · 2009 to 2013
$808k
NCI NIH HHS K05 CA142885
6 · The paper itself

Abstract

Colorectal cancer (CRC) is a disease in which pathogenesis is influenced by genetic and epigenetic events that occur with tumor initiation and progression. Large variation exists in individual patient prognosis and response to chemotherapy, caused by molecular heterogeneity. Certain biomarkers have been identified that can predict clinical outcome beyond tumor staging, and inform treatment selection. Molecular testing is routinely performed in clinical practice for the selection of patients for targeted biological agents or immunotherapy, and is advocated for prognostic stratification. Estimating prognosis can avoid undertreatment or overtreatment and also guide the intensity of patient follow-up. Classifiers of CRC have been developed that integrate genetic and/or epigenetic features. The mutational status of KRAS and BRAF(V600E) oncogenes combined with analysis of the DNA mismatch repair system with/without the CpG island methylator phenotype (CIMP) has been shown to identify colon cancer subtypes with distinct clinical features and prognoses. Gene expression profiling has also been used to subtype CRCs and can overcome the limitations of single/limited gene testing. A recent effort identified 4 consensus molecular subtypes of biological relevance that were associated with different patient outcomes. Efforts to validate and refine these subtypes to include additional genomic features are ongoing. The focus of this article is to highlight molecular markers that can inform clinical decision-making in patients with CRC.

Indexed as

Genetic MarkersColorectal NeoplasmsDNA Repair EnzymesDrug TherapyGene Expression ProfilingHumansImmunotherapyPrecision MedicinePrognosisProto-Oncogene Proteins B-rafProto-Oncogene Proteins p21(ras)BRAF protein, humanDNA Repair EnzymesGenetic MarkersKRAS protein, humanProto-Oncogene Proteins B-rafProto-Oncogene Proteins p21(ras)Anti-EGFRAnti-VEGFBiologicsBRAFColorectal CancerDNA Mismatch RepairImmunotherapyMolecular SubtypesMSIPredictive MarkersPrognostic MarkersRASTargeted Therapy

Identifiers

PMID26872400
PMCPMC4836987
OpenAlexW2268912183

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.