Evidence map›Paper›PMID 42859298›Full record

ArticleJournal of neuro-oncology2026

Comparative dosing of bevacizumab for radiation necrosis: impact of tumor type on edema response.

Sydney E Schultz, Milisia Labib, Jeff Breit, Jason N Barreto, Carolyn Mead-Harvey, Mohamad Behair, Aylin Nurioglu, Jessica White, Allison Valerius, Nishika Karbhari and 12 more

Abstract readMulticenter StudyComparative Study
PubMed Publisher
In one paragraph

Article in Journal of neuro-oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

22 authors.

Sydney E SchultzDepartment of Pharmacy, Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA. schultz.sydney@mayo.edu.ORCID https://orcid.org/0000-0001-9689-8123
Milisia LabibDepartment of Pharmacy, Cleveland Clinic, Cleveland, OH, USA.
Jeff BreitCADA Consulting, Portland OR, USA.
Jason N BarretoDepartment of Pharmacy, Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA.
Carolyn Mead-HarveyDepartment of Quantitative Health Sciences, Mayo Clinic, Scottsdale AZ, USA.
Mohamad BehairAlfaisal University, Riyadh, Saudi Arabia.
Aylin NuriogluAlfaisal University, Riyadh, Saudi Arabia.
Jessica WhiteDepartment of Neurology, Mayo Clinic, Rochester MN, USA.
Allison ValeriusDepartment of Neurology, Mayo Clinic, Rochester MN, USA.
Nishika KarbhariDepartment of Neurology, Mayo Clinic, Rochester MN, USA.
Jodi TarabaDepartment of Pharmacy, Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA.
Scott SoefjeDepartment of Pharmacy, Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA.
Gena HoefsDepartment of Pharmacy, Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA.
Samantha J CaronDepartment of Oncology, Mayo Clinic, Rochester MN, USA.
Michael W RuffDepartment of Neurology, Mayo Clinic, Rochester MN, USA.
Joon H UhmDepartment of Neurology, Mayo Clinic, Rochester MN, USA.
Daniel H LachanceDepartment of Neurology, Mayo Clinic, Rochester MN, USA.
Sani H KizilbashDepartment of Oncology, Mayo Clinic, Rochester MN, USA.
Jian L CampianDepartment of Oncology, Mayo Clinic, Rochester MN, USA.
Susan M GeyerDepartment of Quantitative Health Sciences, Rochester MN, USA.
Bryan J NethDepartment of Neurology, Mayo Clinic, Rochester MN, USA.
Ugur SenerDepartment of Neurology, Mayo Clinic, Rochester MN, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeBevacizumab is an effective treatment for radiation necrosis; however, dose -dependent radiographic and edema response data are lacking.

methodsMulticenter, retrospective cohort study of adult patients with primary central nervous system (CNS) tumors or brain metastases who received bevacizumab for radiation necrosis between June 2021 and July 2024. Patients were grouped by bevacizumab dose (7.5 mg/kg vs. 10 mg/kg administered every three weeks). Primary outcome was edema response, assessed by a blinded neuro-oncologist. Secondary outcomes included contrast enhancing disease response, clinical response, adverse events, treatment discontinuation, and re-dosing for recurrent radiation necrosis. Analyses were performed with and without adjustment for tumor type.

results104 patients were included (7.5 mg/kg, n = 53; 10 mg/kg, n = 51). Tumor type differed significantly between cohorts (p < 0.001), with more primary CNS tumors in the 10 mg/kg group. Edema response differed between dosing groups in unadjusted analyses (p = 0.032), favoring the 7.5 mg/kg cohort; however, this association was attenuated after adjustment for tumor type. Contrast enhancing disease response did not differ between groups in either unadjusted or adjusted analyses (p = 0.43). Clinical response was higher in the 7.5 mg/kg group (65.2% vs. 37.8%, p = 0.013). Rates of adverse events, treatment discontinuation, and re-dosing were similar.

conclusionsTaken together, both 7.5 mg/kg and 10 mg/kg dosing strategies achieved similar radiographic outcomes. Prospective, tumor-stratified studies incorporating edema-focused and patient-centered endpoints are needed to better define optimal dosing strategies in this heterogeneous population. These findings support an individualized approach to bevacizumab dosing in radiation necrosis and highlight the need for prospective, tumor-stratified studies.

Indexed as

Antineoplastic Agents, ImmunologicalBevacizumabBrain EdemaBrain NeoplasmsRadiation InjuriesAdultAgedDose-Response Relationship, DrugFemaleFollow-Up StudiesHumansMaleMiddle AgedNecrosisRetrospective StudiesAntineoplastic Agents, ImmunologicalBevacizumabBevacizumabCerebral edemaDosingRadiation necrosisVEGF

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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.