Evidence map›Paper›PMID 20150372›Full record

Trial reportNeuro-oncology2010

A phase II trial of erlotinib in patients with recurrent malignant gliomas and nonprogressive glioblastoma multiforme postradiation therapy.

Jeffrey J Raizer, Lauren E Abrey, Andrew B Lassman, Susan M Chang, Kathleen R Lamborn, John G Kuhn, W K Alfred Yung, Mark R Gilbert, Kenneth A Aldape, Patrick Y Wen and 9 more

Open access · bronzeAbstract readClinical Trial, Phase II
In one paragraph

Trial report in Neuro-oncology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 149 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
149citing papers in PubMed, 4 pooled it
9.8field-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.

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

149 citing papers in PubMed, 4 syntheses or guidelines pooled it, 294 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Incorporation of biomarkers in phase II studies of recurrent glioblastoma.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2015
    Pooled it
  4. Guideline
  5. Trial
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  14. Review
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  16. Biodegradable nanofibrous scaffolds enhance standard of care for glioblastoma via localized targeted therapy.Journal of controlled release : official journal of the Controlled Release Society · 2025
    Article
  17. Review
  18. Review
  19. Review
  20. Review

89 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

19 authors at 10 institutions in 2 countries.

Jeffrey J RaizerDepartment of Neurology, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA. jraizer@nmff.org
Lauren E Abrey
Andrew B Lassman
Susan M Chang
Kathleen R Lamborn
John G Kuhn
W K Alfred Yung
Mark R Gilbert
Kenneth A Aldape
Patrick Y Wen
Howard A Fine
Minesh Mehta
Lisa M Deangelis
Frank Lieberman
Timothy F Cloughesy
H Ian Robins
Janet Dancey
Michael D Prados
North American Brain Tumor Consortium
University of California, San Francisco · USDana-Farber Brigham Cancer Center · USNational Institutes of Health · USNeurological Surgery · USNorthwestern University · USOntario Institute for Cancer Research · CAThe University of Texas MD Anderson Cancer Center · USMemorial Sloan Kettering Cancer Center · USNational Cancer Institute · USUW Health University Hospital · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
University of Pittsburgh Clinical and Translational Science InstituteUL1TR000005 · NCATS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI REIS, STEVEN E · 2012 to 2015
$50.8M
ZDV &3TC NEVIRAPINE COMBINATION THERAPY IN HIV 1 INFECTED INFANTS &M01RR000865 · NCRR · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI WASHINGTON, ARNOLD E. · 1985 to 2011
$43.4M
WITHIN SUBJ VARIABILITY IN MEASUREMENTS DRUG METABOL ENZYMES IN HLTY SUBJM01RR000056 · NCRR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LEVINE, ARTHUR S · 1985 to 2006
$29.2M
ZD1839 FOR MALIGNANT ASTROCYTOMA OR GLIOBLASTOMA AND MENINGIOMAM01RR000079 · NCRR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KESSLER, DAVID A · 1985 to 2006
$26.0M
ZOSUQUIDAR TRIHYDROCHLORIDE IN NEWLY DIAGNOSED AMLM01RR003186 · NCRR · UNIVERSITY OF WISCONSIN-MADISON · PI TRAYNOR, ANNE M · 1986 to 2007
$19.3M
Brain Tumor Clinical and Clinical Research ProgramZIDBC011098 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI GRESS, RONALD · 2009 to 2014
$19.3M
NABTC - Foreign AccrualU01CA062399 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI PRADOS, MICHAEL D · 1994 to 2008
$4.7M
Phase I/I I PK/PD Studies of Agents for CNS Malignancies (NABTC PK Center)U01CA062426 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI KUHN, JOHN G · 1994 to 2008
$1.4M
THERAPEUTIC STUDIES OF PRIMARY CNS MALIGNANCIESU01CA062422 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CHANG, SUSAN M · 1994 to 2008
$1.3M
THERAPIES OF PRIMARY CNS MALIGNANCIESU01CA062407 · NCI · DANA-FARBER CANCER INSTITUTE · PI WEN, PATRICK Y · 1994 to 2008
$1.2M
NABTC - M.D. Anderson Clinical CenterU01CA062412 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI GILBERT, MARK R. · 1994 to 2008
$1.1M
NCATS NIH HHS UL1 TR000005NCI NIH HHS 5-U01CA62399-09NCI NIH HHS CA16672NCI NIH HHS CA62399NCI NIH HHS CA62412NCI NIH HHS CA62422NCI NIH HHS CA62426NCI NIH HHS U01 CA62399NCI NIH HHS U01CA62405NCI NIH HHS U01CA62407-08NCI NIH HHS U01CA62421-08NCRR NIH HHS M01-RR00056NCRR NIH HHS M01-RR00079NCRR NIH HHS M01 RR003186NCRR NIH HHS M01-RR0865
6 · The paper itself

Abstract

Patients with (a) recurrent malignant glioma (MG): glioblastoma (GBM) or recurrent anaplastic glioma (AG), and (b) nonprogressive (NP) GBM following radiation therapy (RT) were eligible. Primary objective for recurrent MG was progression-free survival at 6 months (PFS-6) and overall survival at 12 months for NP GBM post-RT. Secondary objectives for recurrent MGs were response, survival, assessment of toxicity, and pharmacokinetics (PKs). Treatment with enzyme-inducing antiepileptic drugs was not allowed. Patients received 150 mg/day erlotinib. Patients requiring surgery were treated 7 days prior to tumor removal for PK analysis and effects of erlotinib on epidermal growth factor receptor (EGFR) and intracellular signaling pathways. Ninety-six patients were evaluable (53 recurrent MG and 43 NP GBM); 5 patients were not evaluable for response. PFS-6 in recurrent GBM was 3% with a median PFS of 2 months; PFS-6 in recurrent AG was 27% with a median PFS of 2 months. Twelve-month survival was 57% in NP GBMs post-RT. Primary toxicity was dermatologic. The tissue-to-plasma ratio normalized to nanograms per gram dry weight for erlotinib and OSI-420 ranged from 25% to 44% and 30% to 59%, respectively, for pretreated surgical patients. No effect on EGFR or intratumoral signaling was seen. Patients with NP GBM post-RT who developed rash in cycle 1 had improved survival (P < .001). Single-agent activity of erlotinib is minimal for recurrent MGs and marginally beneficial following RT for NP GBM patients. Development of rash in cycle 1 correlates with survival in patients with NP GBM after RT.

Indexed as

AdultAgedAntineoplastic AgentsBrain NeoplasmsDisease-Free SurvivalErlotinib HydrochlorideFemaleGlioblastomaGliomaHumansKaplan-Meier EstimateMaleMiddle AgedNeoplasm Recurrence, LocalQuinazolinesTissue DistributionAntineoplastic AgentsErlotinib HydrochlorideQuinazolines

Identifiers

PMID20150372
PMCPMC2940554
OpenAlexW2160137787

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.