Evidence map›Paper›PMID 29455666›Full record

ReviewMolecular cancer2018

KRAS oncogene in non-small cell lung cancer: clinical perspectives on the treatment of an old target.

Marta Román, Iosune Baraibar, Inés López, Ernest Nadal, Christian Rolfo, Silvestre Vicent, Ignacio Gil-Bazo

Open access · goldAbstract readReview
In one paragraph

Review in Molecular cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 167 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
167citing papers in PubMed, 1 pooled it
33.0field-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

167 citing papers in PubMed, 1 synthesis or guideline pooled it, 300 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. A KRASMolecular therapy. Oncology · 2025
    Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. Emerging Targets in Non-Small Cell Lung Cancer.Lung Cancer (Auckland, N.Z.) · 2025
    Review
  17. Article
  18. Article
  19. Article
  20. Review

107 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

7 authors at 5 institutions in 2 countries.

Marta RománDepartment of Oncology, Clínica Universidad de Navarra, 31008, Pamplona, Spain.
Iosune BaraibarDepartment of Oncology, Clínica Universidad de Navarra, 31008, Pamplona, Spain.
Inés LópezProgram of Solid Tumors and Biomarkers, Center for Applied Medical Research, Pamplona, Spain.
Ernest NadalThoracic Oncology Unit, Department of Medical Oncology, Catalan Institute of Oncology (ICO), L'Hospitalet del Llobregat, Barcelona, Spain.
Christian RolfoPhase I-Early Clinical Phase I-Early Clinical Trials Unit, Oncology Department, Antwerp University Hospital, Edegem, Belgium.
Silvestre VicentProgram of Solid Tumors and Biomarkers, Center for Applied Medical Research, Pamplona, Spain.
Ignacio Gil-BazoDepartment of Oncology, Clínica Universidad de Navarra, 31008, Pamplona, Spain. igbazo@unav.es.
Clinica Universidad de Navarra · ESUniversidad de Navarra · ESAntwerp University Hospital · BECentro de Investigación Biomédica en Red de Cáncer · ESInstitut Català d'Oncologia · ES

Funding

FP7 People: Marie-Curie Actions 618312 KRASmiR FP7-PEOPLE-2013-CIGInstituto de Salud Carlos III PI11/00976Instituto de Salud Carlos III PI15/02223Instituto de Salud Carlos III SAF2013-46423-RMinisterio de Educación, Gobierno de España FPU15/00173RTICC RD12/0036/0040Worldwide Cancer Research 16-0224
6 · The paper itself

Abstract

Lung neoplasms are the leading cause of death by cancer worldwide. Non-small cell lung cancer (NSCLC) constitutes more than 80% of all lung malignancies and the majority of patients present advanced disease at onset. However, in the last decade, multiple oncogenic driver alterations have been discovered and each of them represents a potential therapeutic target. Although KRAS mutations are the most frequently oncogene aberrations in lung adenocarcinoma patients, effective therapies targeting KRAS have yet to be developed. Moreover, the role of KRAS oncogene in NSCLC remains unclear and its predictive and prognostic impact remains controversial. The study of the underlying biology of KRAS in NSCLC patients could help to determine potential candidates to evaluate novel targeted agents and combinations that may allow a tailored treatment for these patients. The aim of this review is to update the current knowledge about KRAS-mutated lung adenocarcinoma, including a historical overview, the biology of the molecular pathways involved, the clinical relevance of KRAS mutations as a prognostic and predictive marker and the potential therapeutic approaches for a personalized treatment of KRAS-mutated NSCLC patients.

Indexed as

AnimalsAntineoplastic AgentsCarcinoma, Non-Small-Cell LungGenes, rasHumansLung NeoplasmsMutationAntineoplastic Agents

Identifiers

PMID29455666
PMCPMC5817724
OpenAlexW2795913084

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.