Evidence map›Paper›PMID 26893618›Full record

ArticleExperimental and therapeutic medicine2016

Efficacy and safety of bevacizumab for the treatment of glioblastoma.

Zhiyun Yu, Gang Zhao, Zhonghua Zhang, Yunqian Li, Yong Chen, Nan Wang, Zhongying Zhao, Guifang Xie

Open access · diamondAbstract read
In one paragraph

Article in Experimental and therapeutic medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

10 citing papers in PubMed, 19 citations in OpenAlex.

  1. Bevacizumab: The future of chronic subdural hematoma.Interventional neuroradiology : journal of peritherapeutic neuroradiology, surgical procedures and related neurosciences · 2026
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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

8 authors at 2 institutions in 1 country.

Zhiyun YuDepartment of Neurosurgery, First Hospital of Jilin University, Changchun, Jilin 130021, P.R. China.
Gang ZhaoDepartment of Neurosurgery, First Hospital of Jilin University, Changchun, Jilin 130021, P.R. China.
Zhonghua ZhangDepartment of Neurosurgery, First Hospital of Jilin University, Changchun, Jilin 130021, P.R. China.
Yunqian LiDepartment of Neurosurgery, First Hospital of Jilin University, Changchun, Jilin 130021, P.R. China.
Yong ChenDepartment of Neurosurgery, First Hospital of Jilin University, Changchun, Jilin 130021, P.R. China.
Nan WangDepartment of Neurosurgery, First Hospital of Jilin University, Changchun, Jilin 130021, P.R. China.
Zhongying ZhaoDepartment of Neurosurgery, Siping Central People's Hospital, Siping, Jilin 136000, P.R. China.
Guifang XieDepartment of Obstetrics and Gynecology, First Hospital of Jilin University, Changchun, Jilin 130021, P.R. China.
Jilin University · CNFirst Hospital of Jilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma (GBM) is the most common and devastating primary malignant intracranial tumor in adults. The current first-line treatment for patients with newly diagnosed GBM is surgical resection followed by radiotherapy plus concomitant and adjuvant temozolomide. This treatment protocol may prolong the survival period of the patient, however it is not curative and more effective therapeutic strategies are required. GBM is a type of highly vascularized tumor with increased expression levels of vascular endothelial growth factor (VEGF), which is a significant mediator of angiogenesis. Since angiogenesis is essential for tumor growth, anti-angiogenic therapies hold potential for the treatment of GBM, and targeting VEGF has demonstrated promising results in previous studies. Bevacizumab (BEV) is a recombinant humanized monoclonal antibody that inhibits VEGF and is approved by the US Food and Drug Administration as a monotherapy treatment for patients with recurrent GBM and is associated with manageable toxicity. Previous studies have demonstrated that BEV may be an effective treatment for recurrent GBM, with prolonged progression-free survival and overall survival, and maintained patient quality of life and functional status. The present review article briefly outlines the mechanism of action of BEV and summarizes the current literature and clinical trial research on the role of BEV for the treatment of patients with recurrent and newly diagnosed GBM.

Indexed as

anti-angiogenicbevacizumabglioblastomavascular endothelial growth factor

Identifiers

PMID26893618
PMCPMC4733960
OpenAlexW2204053148

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.