Evidence map›Paper›PMID 28684409›Full record

ArticleCancer discovery2017

Improving the Armamentarium of PI3K Inhibitors with Isoform-Selective Agents: A New Light in the Darkness.

Jordi Rodon, Josep Tabernero

Abstract readComment
PubMed Publisher
In one paragraph

Article in Cancer discovery, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

17 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Venous Malformations.Seminars in interventional radiology · 2022
    Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. PI3K Inhibitors in Breast Cancer Therapy.Current oncology reports · 2019
    Review
  10. Overview of the relevance of PI3K pathway in HR-positive breast cancer.Annals of oncology : official journal of the European Society for Medical Oncology · 2019
    Review
  11. Article
  12. Article
  13. PDK1 MediatesClinical cancer research : an official journal of the American Association for Cancer Research · 2019
    Article
  14. Review
  15. Review
  16. The Role of PI3K in Met Driven Cancer: A Recap.Frontiers in molecular biosciences · 2018
    Review
  17. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Jordi RodonInvestigational Cancer Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, Texas. JRodon@mdanderson.org.
Josep TaberneroMedical Oncology Department, Vall d'Hebron University Hospital and Vall d'Hebron Institute of Oncology (VHIO), Barcelona, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

<b/> Excitement and drug-development efforts aimed at targetable genetic aberrations in the PI3K/AKT/mTOR pathway have declined due to the limited clinical performance of these inhibitors as monotherapies. New, more isoform-selective treatments, such as taselisib, promise to both expand the therapeutic window and increase efficacy.

Indexed as

Molecular Targeted TherapyAntineoplastic AgentsHumansImidazolesNeoplasmsOxazepinesPhosphoinositide-3 Kinase InhibitorsProtein IsoformsProto-Oncogene Proteins c-aktSignal TransductionTOR Serine-Threonine Kinases2-(3-(2-(1-isopropyl-3-methyl-1H-1,2-4-triazol-5-yl)-5,6-dihydrobenzo(f)imidazo(1,2-d)(1,4)oxazepin-9-yl)-1H-pyrazol-1-yl)-2-methylpropanamideAntineoplastic AgentsImidazolesMTOR protein, humanOxazepinesPhosphoinositide-3 Kinase InhibitorsProtein IsoformsProto-Oncogene Proteins c-aktTOR Serine-Threonine Kinases

Identifiers

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.