Evidence map›Paper›PMID 34224367›Full record

ArticleMolecular cancer therapeutics2021

Phase 0 Clinical Trial of Everolimus in Patients with Vestibular Schwannoma or Meningioma.

Matthias A Karajannis, Audrey Mauguen, Ekrem Maloku, Qingwen Xu, Erin M Dunbar, Scott R Plotkin, Anna Yaffee, Shiyang Wang, J Thomas Roland, Chandranath Sen and 12 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.7field-weighted citation impact, top 13% 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

16 citing papers in PubMed, 19 citations in OpenAlex.

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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

22 authors at 6 institutions in 1 country.

Matthias A KarajannisPediatric Neuro-Oncology Service, Department of Pediatrics, Memorial Sloan Kettering Cancer Center, New York, New York. karajanm@mskcc.org.ORCID 0000-0002-7151-6528
Audrey MauguenDepartment of Epidemiology & Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0003-3236-6093
Ekrem MalokuDivision of Neuropathology, Department of Pathology, NYU Langone Health, New York, New York.
Qingwen XuDepartment of Cancer Biology, MD Anderson Cancer Center, Houston, Texas.
Erin M DunbarNeuro-Oncology, Piedmont Brain Tumor Center, Atlanta, Georgia.
Scott R PlotkinDepartment of Neurology, Massachusetts General Hospital, Boston, Massachusetts.ORCID 0000-0002-6109-6419
Anna YaffeeDepartment of Pediatrics, NYU Langone Health, New York, New York.
Shiyang WangDepartment of Pediatrics, NYU Langone Health, New York, New York.
J Thomas RolandDepartment of Otolaryngology, NYU Langone Health, New York, New York.
Chandranath SenDepartment of Neurosurgery, NYU Langone Health, New York, New York.
Dimitris G PlacantonakisDepartment of Neurosurgery, NYU Langone Health, New York, New York.ORCID 0000-0003-1950-2978
John G GolfinosDepartment of Neurosurgery, NYU Langone Health, New York, New York.ORCID 0000-0003-4221-0180
Jeffrey C AllenDepartment of Pediatrics, NYU Langone Health, New York, New York.
Nicholas A VitanzaDepartment of Pediatrics, NYU Langone Health, New York, New York.ORCID 0000-0002-3966-4985
Luis A ChiribogaDepartment of Pathology, NYU Langone Health, New York, New York.ORCID 0000-0002-2028-6873
Robert J SchneiderDepartment of Microbiology, NYU Langone Health, New York, New York.ORCID 0000-0001-5807-5564
Jingjing DengDepartment of Cell Biology and Skirball Institute, NYU Langone Health, New York, New York.
Thomas A NeubertDepartment of Cell Biology and Skirball Institute, NYU Langone Health, New York, New York.ORCID 0000-0001-7049-2088
Judith D GoldbergDepartment of Population Health, NYU Langone Health, New York, New York.ORCID 0000-0001-8351-6376
David ZagzagDivision of Neuropathology, Department of Pathology, NYU Langone Health, New York, New York.
Filippo G GiancottiDepartment of Cancer Biology, MD Anderson Cancer Center, Houston, Texas.
Jaishri O BlakeleyDepartment of Neurology, Johns Hopkins Hospital, Baltimore, Maryland.ORCID 0000-0002-1049-0993
NYU Langone Health · USMemorial Sloan Kettering Cancer Center · USThe University of Texas MD Anderson Cancer Center · USJohns Hopkins Hospital · USMassachusetts General Hospital · USPiedmont Cancer Institute · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ANIRBAN MAITRA · 1985 to 2026
$83.1M
Therapeutic efficacy of the CRL inhibitor MLN4924 in NF2 mutant mesotheliomaR01CA191222 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI GIANCOTTI, FILIPPO G, ZAUDERER, MARJORIE G. · 2016 to 2020
$2.5M
Exploration of Activity of RAD001 in vivo in Vestibular Schwannomas and MeningiomR01CA164295 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI KARAJANNIS, MATTHIAS ANGELOS, ZAGZAG, DAVID · 2012 to 2017
$1.5M
Mass Spectrometer For Small Molecule AnalysisS10OD023659 · OD · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI NEUBERT, THOMAS A · 2017 to 2017
$596k
Ventana Medical Systems Discovery XTS10OD010584 · OD · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI CHIRIBOGA, LUIS A · 2013 to 2013
$127k
Sandy Recovery Ventana Medical Systems Discovery XTS10OD018338 · OD · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI CHIRIBOGA, LUIS A · 2014 to 2014
$123k
NCI NIH HHS P30 CA008748NCI NIH HHS P30 CA016087NCI NIH HHS R01 CA164295NCI NIH HHS R01 CA191222NIH HHS S10 OD010584NIH HHS S10 OD018338NIH HHS S10 OD023659
6 · The paper itself

Abstract

Inhibition of mTORC1 signaling has been shown to diminish growth of meningiomas and schwannomas in preclinical studies, and clinical data suggest that everolimus, an orally administered mTORC1 inhibitor, may slow tumor progression in a subset of patients with neurofibromatosis type 2 (NF2) with vestibular schwannoma. To assess the pharmacokinetics, pharmacodynamics, and potential mechanisms of treatment resistance, we performed a presurgical (phase 0) clinical trial of everolimus in patients undergoing elective surgery for vestibular schwannoma or meningiomas. Eligible patients with meningioma or vestibular schwannoma requiring tumor resection enrolled on study received everolimus 10 mg daily for 10 days immediately prior to surgery. Everolimus blood levels were determined immediately before and after surgery. Tumor samples were collected intraoperatively. Ten patients completed protocol therapy. Median pre- and postoperative blood levels of everolimus were found to be in a high therapeutic range (17.4 ng/mL and 9.4 ng/mL, respectively). Median tumor tissue drug concentration determined by mass spectrometry was 24.3 pg/mg (range, 9.2-169.2). We observed only partial inhibition of phospho-S6 in the treated tumors, indicating incomplete target inhibition compared with control tissues from untreated patients (

Indexed as

AdultAgedAntineoplastic AgentsClinical Trials as TopicEverolimusFemaleFollow-Up StudiesHumansMaleMeningeal NeoplasmsMeningiomaMiddle AgedNeuroma, AcousticPrognosisProspective StudiesAntineoplastic AgentsEverolimus

Identifiers

PMID34224367
PMCPMC8419097
OpenAlexW3173610131

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.