Evidence map›Paper›PMID 26802023›Full record

ReviewOncotarget2016

ALK and ROS1 as targeted therapy paradigms and clinical implications to overcome crizotinib resistance.

Mingxiang Ye, Xinxin Zhang, Nan Li, Yong Zhang, Pengyu Jing, Ning Chang, Jianxiong Wu, Xinling Ren, Jian Zhang

Open access · diamondAbstract readReview
In one paragraph

Review in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
5.4field-weighted citation impact, top 4% 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

13 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Cancers · 2020
    Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Treating patients with ALK-rearranged non-small-cell lung cancer: mechanisms of resistance and strategies to overcome it.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2017
    Review
  12. Review
  13. 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

9 authors at 2 institutions in 1 country.

Mingxiang YeDepartment of Pulmonary Medicine, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Xinxin ZhangDepartment of Pulmonary Medicine, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Nan LiDepartment of Pulmonary Medicine, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Yong ZhangDepartment of Pulmonary Medicine, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Pengyu JingDepartment of Thoracic Surgery, Tangdu Hospital, Fourth Military Medical University, Xi'an, China.
Ning ChangDepartment of Pulmonary Medicine, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Jianxiong WuDepartment of Pulmonary Medicine, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Xinling RenDepartment of Pulmonary Medicine, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Jian ZhangDepartment of Pulmonary Medicine, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Xijing Hospital · CNAir Force Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During the past decade, more than 10 targetable oncogenic driver genes have been validated in non-small cell lung cancer (NSCLC). Anaplastic lymphoma kinase (ALK) and ROS1 kinase are two new driver genes implicated in ALK- and ROS1-rearranged NSCLC. Inhibition of ALK and ROS1 by crizotinib has been reported to be highly effective and well tolerated in these patients. However, resistance to crizotinib emerges years after treatment, and increasing efforts have been made to overcome this issue. Here, we review the biology of ALK and ROS1 and their roles in cancer progression. We also summarize the ongoing and completed clinical trials validating ALK and ROS1 as targets for cancer treatment. In the last section of the review, we will discuss the molecular mechanisms of crizotinib resistance and focus approaches to overcome it. This review describes an exciting new area of research and may provide new insights for targeted cancer therapies.

Indexed as

Anaplastic Lymphoma KinaseAnimalsCarcinoma, Non-Small-Cell LungCrizotinibDrug Resistance, NeoplasmHumansLung NeoplasmsMolecular Targeted TherapyProtein Kinase InhibitorsProtein-Tyrosine KinasesProto-Oncogene ProteinsPyrazolesPyridinesReceptor Protein-Tyrosine KinasesALK protein, humanAnaplastic Lymphoma KinaseCrizotinibProtein Kinase InhibitorsProtein-Tyrosine KinasesProto-Oncogene ProteinsPyrazolesPyridinesReceptor Protein-Tyrosine KinasesROS1 protein, humananaplastic lymphoma kinasecrizotinibdrug resistancenon-small cell lung cancerROS1 kinase

Identifiers

PMID26802023
PMCPMC4914285
OpenAlexW2289922904

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.