Evidence map›Paper›PMID 16883305›Full record

ArticleNature reviews. Drug discovery2006

Current development of mTOR inhibitors as anticancer agents.

Sandrine Faivre, Guido Kroemer, Eric Raymond

2 registry-linked trialsAbstract read
PubMed Publisher
In one paragraph

Article in Nature reviews. Drug discovery, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 407 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
407citing papers in PubMed, 7 pooled it
26.3field-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.

NCT00770263 phase1completednot on this mapstarted 2009, after this paper: background citation

Phase I Study of Erlotinib and Temsirolimus in Resistant Solid Malignancies

TypeinterventionalSponsorWashington University School of MedicineRan2009 to 2014Enrolled46ConditionsSolid TumorsArmsErlotinib, Temsirolimus
NCT02008019 phase2suspendednot on this mapstarted 2014, after this paper: background citation

A Randomized Prospective, Multicentric, Open Label, Phase II Study Aiming to Evaluate the Efficacity and Safety of EVEROLIMUS as Neo-adjuvant Therapy in Patients With Primary or Relapsed Chondrosarcomas

TypeinterventionalSponsorCentre Leon BerardRan2014 to 2019Enrolled57ConditionsChondrosarcomaArmsEverolimus 2.5 mg/day, Everolimus 10 mg/day
3 · Its place in the literature

Who cites it

407 citing papers in PubMed, 7 syntheses or guidelines pooled it, 990 citations in OpenAlex.

  1. Rapamycin and rapalogs for tuberous sclerosis complex.The Cochrane database of systematic reviews · 2023
    Pooled it
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  4. Rapamycin and rapalogs for tuberous sclerosis complex.The Cochrane database of systematic reviews · 2016
    Pooled it
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  8. Trial
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  11. Article
  12. Review
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  14. Article
  15. Synthesis andACS omega · 2026
    Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. Article

347 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

3 authors at 2 institutions in 1 country.

Sandrine FaivreService Inter Hospitalier de Cancrologie, Beaujon University Hospital, 100 Boulevard du General Leclerc, 92118 Clichy Cedex, France.
Guido Kroemer
Eric Raymond
Hôpital Beaujon · FRInstitut Gustave Roussy · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mammalian target of rapamycin (mTOR) is a kinase that functions as a master switch between catabolic and anabolic metabolism and as such is a target for the design of anticancer agents. The most established mTOR inhibitors--rapamycin and its derivatives--showed long-lasting objective tumour responses in clinical trials, with CCI-779 being a first-in-class mTOR inhibitor that improved the survival of patients with advanced renal cell carcinoma. This heralded the beginning of extensive clinical programmes to further evaluate mTOR inhibitors in several tumour types. Here we review the clinical development of this drug class and look at future prospects for incorporating these agents into multitarget or multimodality strategies against cancer.

Indexed as

Protein KinasesAdaptor Proteins, Signal TransducingAnimalsAntineoplastic AgentsCell Cycle ProteinsDrug Resistance, NeoplasmEpigenesis, GeneticHumansNeoplasmsNeovascularization, PathologicPhosphatidylinositol 3-KinasesPhosphoproteinsProtein Kinase InhibitorsProto-Oncogene Proteins c-aktPTEN PhosphohydrolaseSignal TransductionAdaptor Proteins, Signal TransducingAntineoplastic AgentsCell Cycle ProteinsEIF4EBP1 protein, humanMTOR protein, humanPhosphatidylinositol 3-KinasesPhosphoproteinsProtein Kinase InhibitorsProtein KinasesProto-Oncogene Proteins c-aktPTEN PhosphohydrolaseTOR Serine-Threonine Kinases

Identifiers

PMID16883305
OpenAlexW1995197723

What OpenQuestion holds

Textmetadata
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.