Evidence map›Paper›PMID 26573425›Full record

ReviewVirchows Archiv : an international journal of pathology2016

RAS testing in metastatic colorectal cancer: advances in Europe.

J Han J M Van Krieken, Etienne Rouleau, Marjolijn J L Ligtenberg, Nicola Normanno, Scott D Patterson, Andreas Jung

Open access · hybridAbstract readReview
In one paragraph

Review in Virchows Archiv : an international journal of pathology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 14% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

  1. Pooled it
  2. Concordance of blood- and tumor-based detection of RAS mutations to guide anti-EGFR therapy in metastatic colorectal cancer.Annals of oncology : official journal of the European Society for Medical Oncology · 2017
    Trial
  3. Article
  4. International journal of molecular sciences · 2023
    Article
  5. Middle East and North Africa Registry to Characterize Rate of RAS Testing Status in Newly Diagnosed Patients with Metastatic Colorectal Cancer.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2023
    Observational
  6. Article
  7. Overcoming Resistance to Drugs TargetingInnovation (Cambridge (Mass.)) · 2020
    Article
  8. Article
  9. The predictive value of KRAS and NRAS mutations in metastatic colorectal cancer.Medical journal of the Islamic Republic of Iran · 2020
    Article
  10. High-resolution melting for detectingBiomedical reports · 2019
    Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Biomarker in Colorectal Cancer.Cancer journal (Sudbury, Mass.)
    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

6 authors at 6 institutions in 5 countries.

J Han J M Van KriekenDepartment of Pathology, Radboud University Medical Center, P.O. Box 9101, 6500 HB, Nijmegen, Netherlands. Han.vanKrieken@radboudumc.nl.
Etienne RouleauCurie Institute, Paris, France.
Marjolijn J L LigtenbergDepartment of Pathology, Radboud University Medical Center, P.O. Box 9101, 6500 HB, Nijmegen, Netherlands.
Nicola NormannoCell Biology and Biotherapy Unit, INT-Fondazione Pascale, Naples, Italy.
Scott D PattersonAmgen Inc., Thousand Oaks, CA, USA.
Andreas JungInstitute of Pathology, University of Munich, Munich, Germany.
Amgen (United States) · USInstitut Curie · FRIstituto Nazionale Tumori IRCCS "Fondazione G. Pascale" · ITLudwig-Maximilians-Universität München · DERadboud University Medical Center · NLRadboud University Nijmegen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Personalized medicine shows promise for maximizing efficacy and minimizing toxicity of anti-cancer treatment. KRAS exon 2 mutations are predictive of resistance to epidermal growth factor receptor-directed monoclonal antibodies in patients with metastatic colorectal cancer. Recent studies have shown that broader RAS testing (KRAS and NRAS) is needed to select patients for treatment. While Sanger sequencing is still used, approaches based on various methodologies are available. Few CE-approved kits, however, detect the full spectrum of RAS mutations. More recently, "next-generation" sequencing has been developed for research use, including parallel semiconductor sequencing and reversible termination. These techniques have high technical sensitivities for detecting mutations, although the ideal threshold is currently unknown. Finally, liquid biopsy has the potential to become an additional tool to assess tumor-derived DNA. For accurate and timely RAS testing, appropriate sampling and prompt delivery of material is critical. Processes to ensure efficient turnaround from sample request to RAS evaluation must be implemented so that patients receive the most appropriate treatment. Given the variety of methodologies, external quality assurance programs are important to ensure a high standard of RAS testing. Here, we review technical and practical aspects of RAS testing for pathologists working with metastatic colorectal cancer tumor samples. The extension of markers from KRAS to RAS testing is the new paradigm for biomarker testing in colorectal cancer.

Indexed as

Biomarkers, TumorColorectal NeoplasmsEuropeGene Expression ProfilingHumansPatient SelectionPrecision Medicineras ProteinsBiomarkers, Tumorras ProteinsBiomarkersColorectal cancerQuality assurance programsRASSequencing

Identifiers

PMID26573425
PMCPMC4830882
OpenAlexW2176041446

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.