Evidence map›Paper›PMID 34036223›Full record

ArticleJCO precision oncology2021

Impact of ALK Inhibitors in Patients With

Yuki Takeyasu, Hitomi S Okuma, Yuki Kojima, Tadaaki Nishikawa, Maki Tanioka, Kazuki Sudo, Tatsunori Shimoi, Emi Noguchi, Ayumu Arakawa, Taisuke Mori and 6 more

Open access · hybridAbstract read
In one paragraph

Article in JCO precision oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

26 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
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  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Update of Diagnosis and Targeted Therapy for ALKCurrent treatment options in oncology · 2023
    Review
  16. Article
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  18. Article
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  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 2 institutions in 1 country.

Yuki TakeyasuDepartment of Breast and Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.
Hitomi S OkumaDepartment of Breast and Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.
Yuki KojimaDepartment of Breast and Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.
Tadaaki NishikawaDepartment of Breast and Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.
Maki TaniokaDepartment of Breast and Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.
Kazuki SudoDepartment of Breast and Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.
Tatsunori ShimoiDepartment of Breast and Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.
Emi NoguchiDepartment of Breast and Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.
Ayumu ArakawaDepartment of Pediatric Oncology, National Cancer Center Hospital, Tokyo, Japan.
Taisuke MoriDepartment of Diagnostic Pathology, National Cancer Center Hospital, Tokyo, Japan.
Kuniko SunamiDepartment of Laboratory Medicine, National Cancer Center Hospital, Tokyo, Japan.
Takashi KuboDivision of Translational Genomics, Exploratory Oncology Research and Clinical Trial Center, National Cancer Center, Tokyo, Japan.
Takashi KohnoDivision of Translational Genomics, Exploratory Oncology Research and Clinical Trial Center, National Cancer Center, Tokyo, Japan.
Yoshida AkihikoDepartment of Pediatric Oncology, National Cancer Center Hospital, Tokyo, Japan.
Noboru YamamotoDepartment of Experimental Therapeutics, National Cancer Center Hospital, Tokyo, Japan.
Kan YonemoriDepartment of Breast and Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.
Tokyo National Hospital · JPJuntendo University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeAnaplastic lymphoma kinase ( PATIENTS AND

methodsBetween April 2012 and April 2019, clinical outcomes and characteristics of patients with

resultsWe identified seven patients (inflammatory myofibroblastic tumors, n = 3; ALK-positive histiocytosis, n = 1; histiocytic sarcoma, n = 1; osteosarcoma, n = 1; and parotid adenocarcinoma, n = 1), with a median age of 17 years. Two rare

conclusionThis study highlights the potential benefit of ALK-TKIs, especially alectinib, in patients with

Indexed as

Gene RearrangementAdolescentAdultAnaplastic Lymphoma KinaseAntineoplastic AgentsCarbazolesCrizotinibFemaleHumansMaleMiddle AgedNeoplasmsPiperidinesRetrospective StudiesTreatment OutcomeYoung AdultalectinibALK protein, humanAnaplastic Lymphoma KinaseAntineoplastic AgentsCarbazolesCrizotinibPiperidines

Identifiers

PMID34036223
PMCPMC8140781
OpenAlexW3159313740

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.