Evidence map›Paper›PMID 27796735›Full record

ArticleJournal of neuro-oncology2017

Toxicity profile of bevacizumab in the UK Neurofibromatosis type 2 cohort.

Katrina A Morris, John F Golding, Claire Blesing, D Gareth Evans, Rosalie E Ferner, Karen Foweraker, Dorothy Halliday, Raj Jena, Catherine McBain, Martin G McCabe and 6 more

Abstract read
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In one paragraph

Article in Journal of neuro-oncology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 2 pooled it
–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

24 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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  2. Pooled it
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  4. Efficacy and safety of bevacizumab for vestibular schwannomas in neurofibromatosis type-2: a systematic review and meta-analysis.European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery · 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

16 authors.

Katrina A MorrisNuffield Department of Neurosciences and NF2 Unit, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.ORCID 0000-0003-1075-8424
John F GoldingUniversity of Westminster, London, UK.
Claire BlesingJohn Radcliffe Hospital, Oxford Cancer Centre, The Churchill Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
D Gareth EvansGenomic Medicine, Institute of Human Development, MAHSC, University of Manchester, St Mary's Hospital, Manchester, UK.
Rosalie E FernerDepartment of Neurology, Neurofibromatosis Service, Guy's & St Thomas' Hospital, Great Maze Pond, London, SE1 9RT, UK.
Karen FowerakerNottingham University Hospitals NHS Trust, Nottingham, UK.
Dorothy HallidayDepartment of Genetics and NF2 Unit, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
Raj JenaDepartment of Oncology, University of Cambridge, Addenbrooke's Hospital, Cambridge, UK.
Catherine McBainThe Christie NHS Foundation Trust, Manchester, UK.
Martin G McCabeCentre for Paediatric, Teenage and Young Adult Cancer, Institute of Cancer Sciences, University of Manchester, Manchester, UK.
Angela SwampillaiDepartment of Neurology, Neurofibromatosis Service, Guy's & St Thomas' Hospital, Great Maze Pond, London, SE1 9RT, UK.
Nicola WarnerJohn Radcliffe Hospital, Oxford Cancer Centre, The Churchill Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
Shaun WilsonDepartment of Paediatric Oncology, The West Wing, John Radcliffe Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
Allyson ParryNuffield Department of Neurosciences and NF2 Unit, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
Shazia K AfridiDepartment of Neurology, Neurofibromatosis Service, Guy's & St Thomas' Hospital, Great Maze Pond, London, SE1 9RT, UK. Shazia.Afridi@gstt.nhs.uk.
UK NF2 research group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bevacizumab is considered an established part of the treatment strategies available for schwannomas in patients with Neurofibromatosis type 2 (NF2). In the UK, it is available through NHS National Specialized Commissioning to NF2 patients with a rapidly growing target schwannoma. Regrowth of the tumour on suspension of treatment is often observed resulting in prolonged periods of exposure to bevacizumab to control the disease. Hypertension and proteinuria are common events with bevacizumab use and there are concerns with regards to the long-term risks of prolonged treatment. Dosing, demographic and adverse event (CTCAE 4.03) data from the UK NF2 bevacizumab cohort are reviewed with particular consideration of renal and cardiovascular complications. Eighty patients (48 male:32 female), median age 24.5 years (range 11-66 years), were followed for a median of 32.7 months (range 12.0-60.2 months). The most common adverse events were fatigue, hypertension and infection. A total of 19/80 patients (24 %) had either a grade 2 or grade 3 hypertension event and 14/80 patients (17.5 %) had proteinuria. Of 36 patients followed for 36 months, 78 % were free from hypertension and 86 % were free of proteinuria. Logistic regression modeling identified age and induction dosing regime to be independent predictors of development of hypertension with dose of 7.5 mg/kg 3 weekly and age >30years having higher rates of hypertension. Proteinuria persisted in one of three patients after cessation of bevacizumab. One patient developed congestive heart failure and the details of this case are described. Further work is needed to determine optimal dosing regimes to limit toxicity without impacting on efficacy.

Indexed as

AdolescentAdultAgedAntineoplastic Agents, ImmunologicalBevacizumabChildCohort StudiesFemaleHeart FailureHumansHypertensionMaleMiddle AgedNeurilemmomaNeurofibromatosis 2Regression AnalysisAntineoplastic Agents, ImmunologicalBevacizumabBevacizumabCardiac failureHypertensionNeurofibromatosis type 2ProteinuriaToxicity

Identifiers

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.