Evidence map›Paper›PMID 40540702›Full record

ArticleJCO precision oncology2025

Molecular Correlates of Long-Term Response to Bevacizumab in Glioblastoma.

John L Villano, Catherine R Garcia, Rachael M Morgan, Shulin Zhang, Jill Kolesar, Farhan A Mirza, Timothy Samec, Joanne Xiu, Stephanie Rock, Santosh Kesari and 4 more

Abstract read
In one paragraph

Article in JCO precision oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

14 authors.

John L VillanoDepartment of Medicine, University of Kentucky, Lexington, KY.ORCID 0000-0001-5583-0093
Catherine R GarciaDepartment of Neuro-Oncology, University of Texas, MD Anderson Cancer Center, Houston, TX.ORCID 0000-0002-6361-0127
Rachael M MorganDepartment of Pharmacy, University of Kentucky, Lexington, KY.
Shulin ZhangDepartment of Pathology and Laboratory Medicine, University of Kentucky, Lexington, KY.ORCID 0000-0003-2118-2475
Jill KolesarCollege of Pharmacy, University of Iowa, Iowa City, IA.ORCID 0000-0001-8575-4546
Farhan A MirzaDepartment of Neurosurgery, University of Kentucky, Lexington, KY.ORCID 0000-0001-8203-8608
Timothy SamecCaris Life Sciences, Phoenix, AZ.ORCID 0000-0003-3468-7165
Joanne XiuCaris Life Sciences, Phoenix, AZ.
Stephanie RockCaris Life Sciences, Phoenix, AZ.ORCID 0000-0001-5700-6954
Santosh KesariPacific Neuroscience Institute and Saint John's Cancer Institute at Providence Saint John's Health Center, Santa Monica, CA.ORCID 0000-0003-3772-6000
Emil LouUniversity of Minnesota, Masonic Cancer Center, Minneapolis, MN.ORCID 0000-0002-1607-1386
Sonikpreet AulakhDepartment of Medical Oncology, West Virginia University, Morgantown, WV.ORCID 0000-0001-7150-5805
Michael J GlantzDepartment of Medicine, Neurology, and Neurosurgery Penn State Milton S. Hershey Medical Center, Hershey, PA.ORCID 0000-0003-4877-5094
Eric T WongDepartment of Neurology, Medicine, Neurosurgery & Radiation Oncology, Rhode Island Hospital, Providence, RI.ORCID 0000-0001-7112-6207

Funding

University of Kentucky Markey Cancer Center Support Grant ECIA SupplementP30CA177558 · NCI · UNIVERSITY OF KENTUCKY · PI Bernard Mark Evers · 2013 to 2026
$38.3M
NCI NIH HHS P30 CA177558
6 · The paper itself

Abstract

purposeThe use of bevacizumab in glioblastoma has been associated with increased progression-free survival and improvement in symptoms and quality of life. There are no clinical indicators on how to choose patients who would benefit the most from this agent. We aim to describe molecular markers in patients with glioblastoma who may benefit from treatment.

methodsWe analyzed glioblastoma tumor samples that underwent comprehensive molecular profiling analysis at Caris Life Sciences.

resultsThe data set consisted of 3,106 glioblastoma tumor samples, of which 571 were from patients treated with bevacizumab. The majority were males (65%) and older than 60 years. Median survival was 17.5 months in patients receiving bevacizumab. In patients who were treated with bevacizumab for ≥1 year, median survival was 33.8 months, compared with 15 months in those treated for ≤6 months. Patients who received bevacizumab for ≥1 year had higher prevalence of

conclusion

Indexed as

Antineoplastic Agents, ImmunologicalBevacizumabBrain NeoplasmsGlioblastomaAdultAgedBiomarkers, TumorFemaleHumansMaleMiddle AgedAntineoplastic Agents, ImmunologicalBevacizumabBiomarkers, Tumor

Identifiers

PMID40540702
PMCPMC12539333

What OpenQuestion holds

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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.