Evidence map›Paper›PMID 25954595›Full record

ArticleExperimental hematology & oncology2014

Effective long-term treatment with bevacizumab for relapsed glioblastoma: case report and review of the literature.

Katrin Schweneker, Christoph Clemm, Melanie Brügel, Michael Souvatzoglou, Mirjam Hermisson, Friederike Schmidt-Graf, Claus Zimmer, Christian Peschel, Philipp J Jost

Open access · goldAbstract readCase Reports
In one paragraph

Article in Experimental hematology & oncology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 44% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. 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

9 authors at 5 institutions in 1 country.

Katrin SchwenekerIII. Medizinische Klinik, München, Germany.
Christoph ClemmHämatologische Praxis, München, Germany.
Melanie BrügelInstitut für Diagnostische und Interventionelle Radiologie, München, Germany.
Michael SouvatzoglouNuklearmedizinische Klinik und Poliklinik, München, Germany.
Mirjam HermissonNeurologische Klinik und Poliklinik, München, Germany.
Friederike Schmidt-GrafNeurologische Klinik und Poliklinik, München, Germany.
Claus ZimmerAbteilung für Diagnostische und Interventionelle Neuroradiologie, Klinikum rechts der Isar, Technische Universität München, 81675 München, Germany.
Christian PeschelIII. Medizinische Klinik, München, Germany.
Philipp J JostIII. Medizinische Klinik, München, Germany.
München Klinik · DEKlinik und Poliklinik für Neurologie · DEKlinik und Poliklinik für Nuklearmedizin · DEPraxis für Hämatologie und Onkologie · DETechnical University of Munich · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma multiforme (GBM) is the most common malignant primary brain tumor in adults. Despite the use of optimized first-line therapy, GBM is still associated with a poor prognosis and an effective second-line therapy remains an important challenge in this patient population. In 2009, the US Food and Drug Administration (FDA) approved the monoclonal anti-VEGF-antibody bevacizumab for the treatment of relapsed GBM after two phase-II studies showed its efficacy and safety, alone or in combination with irinotecan, in relapsed GBM. In contrast, the European Medicines Agency (EMA) concluded from the same published data that a clear benefit in terms of overall survival was not shown and subsequently did not grant approval for bevacizumab in this setting. Here, we report on a 53-year old patient with relapsed GBM who was treated with bevacizumab as single agent. After three months, the tumor volume was reduced and the Karnofsky performance status was substantially improved compared to the baseline at the time of relapse. After continued long-term treatment for 26 months, the patient remains in an excellent general condition. Moreover, the measurement of the tumor volume using multiple imaging modalities shows a sustained treatment response. In conclusion, this case supports the notion that individual patients respond exceptionally well to treatment with anti-VEGF therapy and suggests that future trials are needed to better identify the patient population that responds to bevacizumab.

Indexed as

18 F-FET-PET/CT scanBevacizumabPseudoprogressionRelapsed glioblastoma

Identifiers

PMID25954595
PMCPMC4423626
OpenAlexW2156518873

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.