Evidence map›Paper›PMID 29488330›Full record

ReviewThoracic cancer2018

ALK-rearrangement in non-small-cell lung cancer (NSCLC).

Xue Du, Yun Shao, Hai-Feng Qin, Yan-Hong Tai, Hong-Jun Gao

Registry-linked trialOpen access · goldAbstract readReview
In one paragraph

Review in Thoracic cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04137718 (Multicenter Observational Study for Clinicopathological Characteristics and Clinical Efficacy of Chinese Non-Small Cell Lung Cancer), which is not on this map. Cited by 160 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
160citing papers in PubMed, 1 pooled it
17.8field-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.

NCT04137718 unknown statusnot on this mapstarted 2019, after this paper: background citation

Multicenter Observational Study for Clinicopathological Characteristics and Clinical Efficacy of Chinese Non-Small Cell Lung Cancer (NSCLC) Patients With Rare Driver Gene Mutation

TypeobservationalSponsorShanghai Pulmonary Hospital, Shanghai, ChinaRan2019 to 2024Enrolled50,000ConditionsChinese, Non-Small Cell Lung CancerArmsnonIntervention
3 · Its place in the literature

Who cites it

160 citing papers in PubMed, 1 synthesis or guideline pooled it, 265 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. Review

100 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

5 authors at 1 institution in 1 country.

Xue DuDepartment of Pathology, Cancer Center of People's Liberation Army of China, Affiliated Hospital of Academy of Military Medical Sciences, Beijing, China.ORCID 0000-0001-9424-0520
Yun ShaoDepartment of Pathology, Cancer Center of People's Liberation Army of China, Affiliated Hospital of Academy of Military Medical Sciences, Beijing, China.
Hai-Feng QinDepartment of Lung Cancer, Cancer Center of People's Liberation Army of China, Affiliated Hospital of Academy of Military Medical Sciences, Beijing, China.
Yan-Hong TaiDepartment of Pathology, Cancer Center of People's Liberation Army of China, Affiliated Hospital of Academy of Military Medical Sciences, Beijing, China.
Hong-Jun GaoDepartment of Lung Cancer, Cancer Center of People's Liberation Army of China, Affiliated Hospital of Academy of Military Medical Sciences, Beijing, China.
Academy of Military Medical Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ALK gene encodes a transmembrane tyrosine kinase receptor. ALK is physiologically expressed in the nervous system during embryogenesis, but its expression decreases postnatally. ALK first emerged in the field of oncology in 1994 when it was identified to fuse to NPM1 in anaplastic large-cell lymphoma. Since then, ALK has been associated with other types of cancers, including non-small-cell lung cancer (NSCLC). More than 19 different ALK fusion partners have been discovered in NSCLC, including EML4, KIF5B, KLC1, and TPR. Most of these ALK fusions in NSCLC patients respond well to the ALK inhibitor, crizotinib. In this paper, we reviewed fusion partner genes with ALK, detection methods for ALK-rearrangement (ALK-R), and the ALK-tyrosine kinase inhibitor, crizotinib, used in NSCLC patients.

Indexed as

Anaplastic Lymphoma KinaseCarcinoma, Non-Small-Cell LungCell Cycle ProteinsCrizotinibDrug Resistance, NeoplasmHumansKinesinsMicrotubule-Associated ProteinsNuclear Pore Complex ProteinsNucleophosminOncogene Proteins, FusionProtein Kinase InhibitorsProto-Oncogene ProteinsSerine EndopeptidasesALK protein, humanAnaplastic Lymphoma KinaseCell Cycle ProteinsCrizotinibEML4 protein, humanKIF5B protein, humanKinesinsKLC1 protein, humanMicrotubule-Associated ProteinsNPM1 protein, humanNuclear Pore Complex ProteinsNucleophosminOncogene Proteins, FusionProtein Kinase InhibitorsProto-Oncogene ProteinsSerine EndopeptidasesTPR protein, humanALK-rearrangement (ALK-R)ALK-tyrosine kinase inhibitor (TKI)anaplastic lymphoma kinase (ALK)detection platformsnon-small-cell lung cancer (NSCLC)

Identifiers

PMID29488330
PMCPMC5879058
OpenAlexW2791498761

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

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.