Evidence map›Paper›PMID 24309981›Full record

Trial reportThe oncologist2014

Low incidence of pseudoprogression by imaging in newly diagnosed glioblastoma patients treated with cediranib in combination with chemoradiation.

Marco C Pinho, Pavlina Polaskova, Jayashree Kalpathy-Cramer, Dominique Jennings, Kyrre E Emblem, Rakesh K Jain, Bruce R Rosen, Patrick Y Wen, A Gregory Sorensen, Tracy T Batchelor and 1 more

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

Trial report in The oncologist, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

11 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Pseudoprogression of brain tumors.Journal of magnetic resonance imaging : JMRI · 2018
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
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

11 authors at 4 institutions in 2 countries.

Marco C PinhoDepartments of Radiology, Neurology, and Radiation Oncology, Massachusetts General Hospital, Boston, Massachusetts, USA; Athinoula A. Martinos Center for Biomedical Imaging, Charlestown, Massachusetts, USA; The Intervention Centre, Oslo University Hospital, Oslo, Norway; Center for Neuro-Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts, USA.
Pavlina Polaskova
Jayashree Kalpathy-Cramer
Dominique Jennings
Kyrre E Emblem
Rakesh K Jain
Bruce R Rosen
Patrick Y Wen
A Gregory Sorensen
Tracy T Batchelor
Elizabeth R Gerstner
Athinoula A. Martinos Center for Biomedical Imaging · USMassachusetts General Hospital · USCenter for Neuro-Oncology · USOslo University Hospital · NO

Funding

Vascular Normalization: Rolse of Perivascular CellsP01CA080124 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI JAIN, RAKESH K. · 2000 to 2016
$35.0M
Targeting the Vasular SystemP50CA165962 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI Benjamin Harris Kann · 2013 to 2026
$33.5M
Harvard Clinical and Translational Science Center (UL1)UL1TR000170 · NCATS · HARVARD MEDICAL SCHOOL · PI NADLER, LEE MARSHALL · 2012 to 2013
$31.4M
Oregon Clinical and Translational Research InstituteUL1TR000128 · NCATS · OREGON HEALTH & SCIENCE UNIVERSITY · PI ELLISON, DAVID H · 2012 to 2015
$28.7M
Training Program in Nervous System TumorsK12CA090354 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI PLOTKIN, SCOTT R · 2001 to 2025
$16.3M
AZD2171 and chemoradiation for newly diagnosed glioblastomaR01CA129371 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI BATCHELOR, TRACY T · 2007 to 2017
$6.2M
Quantitative MRI of Glioblastoma ResponseU01CA154601 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI KALPATHY-CRAMER, JAYASHREE · 2011 to 2016
$3.4M
Clinical and Molecular Studies of Novel Therapeutics in Malignant Brain TumorsK24CA125440 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI BATCHELOR, TRACY T · 2007 to 2016
$1.9M
Toward Multi-Center MR Brain PerfusionR01NS060918 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI SCHMAINDA, KATHLEEN MARIE, STUFFLEBEAM, STEVEN · 2010 to 2014
$1.8M
Clinical Image Retrieval: User needs assessment toolbox development & evaluationR00LM009889 · NLM · MASSACHUSETTS GENERAL HOSPITAL · PI KALPATHY-CRAMER, JAYASHREE · 2011 to 2013
$690k
NCATS NIH HHS 8UL1TR000170-05NCATS NIH HHS UL1 TR000128NCATS NIH HHS UL1 TR000170NCI NIH HHS 1U01CA154601NCI NIH HHS K12 CA090354NCI NIH HHS K24 CA125440NCI NIH HHS K24CA125440ANCI NIH HHS N01CM-2008-00060CNCI NIH HHS P01-CA080124NCI NIH HHS P50 CA165962NCI NIH HHS R01 CA129371NCI NIH HHS R01CA129371NCI NIH HHS U01 CA154601NINDS NIH HHS 5R01NS060918NLM NIH HHS R00 LM009889
6 · The paper itself

Abstract

backgroundChemoradiation (CRT) can significantly modify the radiographic appearance of malignant gliomas, especially within the immediate post-CRT period. Pseudoprogression (PsP) is an increasingly recognized phenomenon in this setting, and is thought to be secondary to increased permeability as a byproduct of the complex process of radiation-induced tissue injury, possibly enhanced by temozolomide. We sought to determine whether the addition of a vascular endothelial growth factor (VEGF) signaling inhibitor (cediranib) to conventional CRT had an impact on the frequency of PsP, by comparing two groups of patients with newly diagnosed glioblastoma before, during, and after CRT.

methodsAll patients underwent serial magnetic resonance imaging as part of institutional review board-approved clinical studies. Eleven patients in the control group received only chemoradiation, whereas 29 patients in the study group received chemoradiation and cediranib until disease progression or toxicity. Response assessment was defined according to Response Assessment in Neuro-Oncology criteria, and patients with enlarging lesions were classified into true tumor progressions (TTP) or PsP, based on serial radiographic follow-up.

resultsTwo patients in the study group (7%) showed signs of apparent early tumor progression, and both were subsequently classified as TTP. Six patients in the control group (54%) showed signs of apparent early tumor progression, and three were subsequently classified as TTP and three as PsP. The frequency of PsP was significantly higher in the control group.

conclusionAdministration of a VEGF inhibitor during and after CRT modifies the expression of PsP by imaging.

Indexed as

AdultAgedAntineoplastic Combined Chemotherapy ProtocolsBrain NeoplasmsChemoradiotherapyDacarbazineDisease ProgressionFemaleGlioblastomaHumansIncidenceIndolesMagnetic Resonance ImagingMaleMiddle AgedQuinazolinescediranibDacarbazineIndolesQuinazolinesTemozolomideCediranibGlioblastomaPseudoprogressionVascular endothelial growth factor

Identifiers

PMID24309981
PMCPMC3903059
OpenAlexW2109604886

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.