Evidence map›Paper›PMID 32062493›Full record

ReviewCancer treatment reviews2020

KRAS as a druggable target in NSCLC: Rising like a phoenix after decades of development failures.

Alex Friedlaender, Alexander Drilon, Glen J Weiss, Giuseppe L Banna, Alfredo Addeo

Abstract readReview
In one paragraph

Review in Cancer treatment reviews, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
7.2field-weighted citation impact, top 2% 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

59 citing papers in PubMed, 115 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Observational
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Targeting KRASDrugs · 2024
    Review
  12. Review
  13. Review
  14. Article
  15. Review
  16. Review
  17. Prognostic Implication ofJTO clinical and research reports · 2023
    Article
  18. Review
  19. Article
  20. Article
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 3 institutions in 3 countries.

Alex FriedlaenderOncology Department, University Hospital of Geneva, Switzerland.
Alexander DrilonMemorial Sloan Kettering Cancer Center and Weill Cornell Medical College, NY, USA.
Glen J WeissMiRanostics Consulting, Oro Valley, AZ, United States.
Giuseppe L BannaUnited Lincolnshire NHS Hospital Trust, United Kingdom.
Alfredo AddeoOncology Department, University Hospital of Geneva, Switzerland. Electronic address: Alfredo.addeo@hcuge.ch.
University Hospital of Geneva · CHMemorial Sloan Kettering Cancer Center · USUnited Lincolnshire Hospitals NHS Trust · GB

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Cancers of nearly all lineages harbor alterations that deregulate mitogen-activated protein kinase signaling, a crucial signaling pathway for tumor formation and maintenance. Of these, KRAS mutations are the most frequent gain-of-function alterations found in patients with cancer. In particular they represents the most common molecular alteration detected in non-small cell lung cancer (NSCLC) accounting for up to 25% of all oncogenic mutations. They were identified decades ago and prior efforts to target these proteins have been unsuccessful. KRAS mutation profiles (i.e. frequency of specific codon substitutions) in smokers and never-smokers are distinct and not all KRAS alterations are driver mutations. KRAS has evolved from a mutation with possible predictive value to a therapeutic target with great promise. Here, we will discuss the biology of KRAS in lung cancer and its clinical implications in oncology today and in the foreseeable future.

Indexed as

Molecular Targeted TherapyAntineoplastic AgentsCarcinoma, Non-Small-Cell LungFemaleForecastingGene Expression Regulation, NeoplasticHumansImmunotherapyLung NeoplasmsMaleMutationProto-Oncogene Proteins p21(ras)Survival AnalysisTreatment OutcomeAntineoplastic AgentsKRAS protein, humanProto-Oncogene Proteins p21(ras)Checkpoint inhibitorsKRASNSCLC

Identifiers

PMID32062493
PMCPMC7448574
OpenAlexW3004931546

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.