Evidence map›Paper›PMID 28353668›Full record

ArticleInternational journal of molecular sciences2017

Bevacizumab for Patients with Recurrent Gliomas Presenting with a Gliomatosis Cerebri Growth Pattern.

Michael C Burger, Iris C Mildenberger, Marlies Wagner, Michel Mittelbronn, Joachim P Steinbach, Oliver Bähr

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 28% 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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Bevacizumab for Patients with Recurrent Multifocal Glioblastomas.International journal of molecular sciences · 2017
    Article
  4. 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

6 authors at 1 institution in 2 countries.

Michael C BurgerDr. Senckenberg Institute of Neurooncology, Goethe University, 60528 Frankfurt, Germany. michael.burger@kgu.de.
Iris C MildenbergerDr. Senckenberg Institute of Neurooncology, Goethe University, 60528 Frankfurt, Germany. iris.mildenberger@umm.de.
Marlies WagnerInstitute of Neuroradiology, Goethe University, 60528 Frankfurt, Germany. Marlies.Wagner@kgu.de.
Michel MittelbronnLuxembourg Centre of Neuropathology (LCNP), 3555 Dudelange, Luxembourg. michel.mittelbronn@lns.etat.lu.
Joachim P SteinbachDr. Senckenberg Institute of Neurooncology, Goethe University, 60528 Frankfurt, Germany. joachim.steinbach@med.uni-frankfurt.de.
Oliver BährDr. Senckenberg Institute of Neurooncology, Goethe University, 60528 Frankfurt, Germany. oliver.baehr@med.uni-frankfurt.de.
Goethe University Frankfurt · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bevacizumab has been shown to improve progression-free survival and neurologic function, but failed to improve overall survival in newly diagnosed glioblastoma and at first recurrence. Nonetheless, bevacizumab is widely used in patients with recurrent glioma. However, its use in patients with gliomas showing a gliomatosis cerebri growth pattern is contentious. Due to the marked diffuse and infiltrative growth with less angiogenic tumor growth, it may appear questionable whether bevacizumab can have a therapeutic effect in those patients. However, the development of nodular, necrotic, and/or contrast-enhancing lesions in patients with a gliomatosis cerebri growth pattern is not uncommon and may indicate focal neo-angiogenesis. Therefore, control of growth of these lesions as well as control of edema and reduction of steroid use may be regarded as rationales for the use of bevacizumab in these patients. In this retrospective patient series, we report on 17 patients with primary brain tumors displaying a gliomatosis cerebri growth pattern (including seven glioblastomas, two anaplastic astrocytomas, one anaplastic oligodendroglioma, and seven diffuse astrocytomas). Patients have been treated with bevacizumab alone or in combination with lomustine or irinotecan. Seventeen matched patients treated with bevacizumab for gliomas with a classical growth pattern served as a control cohort. Response rate, progression-free survival, and overall survival were similar in both groups. Based on these results, anti-angiogenic therapy with bevacizumab should also be considered in patients suffering from gliomas with a mainly infiltrative phenotype.

Indexed as

Angiogenesis InhibitorsBevacizumabBrain NeoplasmsCase-Control StudiesFemaleGliomaHumansMaleMiddle AgedNeoplasm Recurrence, LocalRetrospective StudiesSurvival AnalysisAngiogenesis InhibitorsBevacizumabanti-angiogenic therapybevacizumabglioblastomagliomagliomatosis cerebri growth patternprimary brain tumors

Identifiers

PMID28353668
PMCPMC5412312
OpenAlexW2602986461

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.