Evidence map›Paper›PMID 25806222›Full record

ReviewTranslational lung cancer research2013

Activated RET and ROS: two new driver mutations in lung adenocarcinoma.

Marc Bos, Masyar Gardizi, Hans-Ulrich Schildhaus, Reinhard Buettner, Juergen Wolf

Abstract readReview
In one paragraph

Review in Translational lung cancer research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Comparison of the genomic background of MET-altered carcinomas of the lung: biological differences and analogies.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2019
    Article
  5. Article
  6. Article
  7. Antitumor Activity of RXDX-105 in Multiple Cancer Types withClinical cancer research : an official journal of the American Association for Cancer Research · 2017
    Article
  8. Review
  9. Article
  10. [Advances of driver gene and targeted therapy of non-small cell lung cancer].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2014
    Review
  11. 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 1 institution in 1 country.

Marc BosDepartment I of Internal Medicine, University Hospital Cologne, Cologne, Germany ; ; Center for Integrated Oncology Cologne/Bonn, Germany ;
Masyar GardiziCenter for Integrated Oncology Cologne/Bonn, Germany ; ; Institute of Pathology, University Hospital Cologne, Cologne, Germany.
Hans-Ulrich SchildhausCenter for Integrated Oncology Cologne/Bonn, Germany ; ; Institute of Pathology, University Hospital Cologne, Cologne, Germany.
Reinhard BuettnerCenter for Integrated Oncology Cologne/Bonn, Germany ; ; Institute of Pathology, University Hospital Cologne, Cologne, Germany.
Juergen WolfDepartment I of Internal Medicine, University Hospital Cologne, Cologne, Germany ; ; Center for Integrated Oncology Cologne/Bonn, Germany ;
University Hospital Cologne · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rearrangements of ROS1 and RET have been recently described as new driver mutations in lung adenocarcinoma with a frequency of about 1% each. RET and ROS1 rearrangements both represent unique molecular subsets of lung adenocarcinoma with virtually no overlap with other known driver mutations described so far in lung adenocarcinoma. Specific clinicopathologic characteristics have been described and several multitargeted receptor kinase inhibitors have shown in vitro activity against NSCLC cells harbouring these genetic alterations. In addition, the MET/ALK/ROS inhibitor crizotinib has already shown impressive clinical activity in patients with advanced ROS1-positive lung cancer. Currently, several early proof of concept clinical trials are testing various kinase inhibitors in both molecular subsets of lung adenocarcinoma patients. Most probably, personalized treatment of these genetically defined new subsets of lung adenocarcinoma will be implemented in routine clinical care of lung cancer patients in the near future.

Indexed as

adenocarcinomaLung cancerRETROS

Identifiers

PMID25806222
PMCPMC4369857
OpenAlexW2166589505

What OpenQuestion holds

Textmetadata
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.