Evidence map›Paper›PMID 28520590›Full record

ReviewCurrent opinion in endocrinology, diabetes, and obesity2017

Role of tyrosine kinase inhibitors in the treatment of pituitary tumours: from bench to bedside.

Anat Ben-Shlomo, Odelia Cooper

Abstract readReview
In one paragraph

Review in Current opinion in endocrinology, diabetes, and obesity, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing 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

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

  1. Pooled it
  2. EGFR/ErbB2-Targeting Lapatinib Therapy for Aggressive Prolactinomas.The Journal of clinical endocrinology and metabolism · 2021
    Trial
  3. Article
  4. Review
  5. Article
  6. Review
  7. New Trends in Treating Cushing's Disease.TouchREVIEWS in endocrinology · 2024
    Article
  8. Review
  9. Review
  10. Pituitary Tumorigenesis-Implications for Management.Medicina (Kaunas, Lithuania) · 2023
    Review
  11. Review
  12. Review
  13. [Targeted Drug Therapy for Intracranial Tumors].Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2022
    Review
  14. Article
  15. Review
  16. Molecular targets in acromegaly.Frontiers in endocrinology · 2022
    Review
  17. Aggressive pituitary tumours and pituitary carcinomas.Nature reviews. Endocrinology · 2021
    Review
  18. Article
  19. Review
  20. 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

2 authors.

Anat Ben-ShlomoPituitary Center, Cedars-Sinai Medical Center, Los Angeles, California, USA.
Odelia Cooper

Funding

ErbB receptor tyrosine kinase inhibitor therapy for aggressive prolactinomasR21DK105405 · NIDDK · CEDARS-SINAI MEDICAL CENTER · PI COOPER, ODELIA · 2015 to 2016
$429k
NIDDK NIH HHS R21 DK105405
6 · The paper itself

Abstract

purpose of reviewTreatment of aggressive pituitary tumours often yields suboptimal control of the tumour and confers significant morbidity. Lactotroph and corticotroph-derived tumours express ErbB receptors and ligands, and mutations in ubiquitin-specific protease 8 (USP8), which alters epidermal growth factor receptor (EGFR) degradation, have been implicated in Cushing disease pathogenesis. EGFR tyrosine kinase inhibitor (TKI) therapy has emerged as a potential new therapeutic approach for patients with aggressive prolactinomas and Cushing disease. RECENT

findingsUsing EGFR or human epidermal growth factor receptor 2-driven prolactin (PRL) promoters, transgenic mice develop large tumours that respond to TKI inhibition. In human corticotroph primary cultures, treatment with the pan-ErbB TKI canertinib as well as the EGFR TKI gefitinib suppresses proopiomelanocortin mRNA. USP8 mutations, detected in up to two-thirds of Cushing disease, may underlie the increase in EGFR signalling in these tumours. Human prolactinomas have differential ErbB receptor expression associated with aggressive behaviour and data from an ongoing clinical trial suggest that resistant prolactinomas may respond to the EGFR TKI lapatinib. SUMMARY: Preclinical and clinical models substantiate the role of the EGFR pathway in corticotroph and lactotroph adenomas. Although further study is needed, results to date suggest that targeting the ErbB pathway may be an effective therapeutic approach for patients with aggressive pituitary tumours.

Indexed as

Translational Research, BiomedicalAnimalsCell Line, TumorErbB ReceptorsGefitinibHumansLapatinibMiceMice, TransgenicPituitary NeoplasmsProlactinomaProtein Kinase InhibitorsQuinazolinesEGFR protein, humanErbB ReceptorsGefitinibLapatinibProtein Kinase InhibitorsQuinazolines

Identifiers

PMID28520590
PMCPMC5815830

What OpenQuestion holds

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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.