Toxicity profile of bevacizumab in the UK Neurofibromatosis type 2 cohort

J Neurooncol. 2017 Jan;131(1):117-124. doi: 10.1007/s11060-016-2276-9. Epub 2016 Oct 28.

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.

Keywords: Bevacizumab; Cardiac failure; Hypertension; Neurofibromatosis type 2; Proteinuria; Toxicity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Antineoplastic Agents, Immunological / adverse effects*
  • Bevacizumab / adverse effects*
  • Child
  • Cohort Studies
  • Female
  • Heart Failure / chemically induced*
  • Humans
  • Hypertension / chemically induced*
  • Male
  • Middle Aged
  • Neurilemmoma / complications
  • Neurilemmoma / drug therapy*
  • Neurofibromatosis 2 / complications
  • Neurofibromatosis 2 / drug therapy*
  • Regression Analysis
  • United Kingdom
  • Young Adult

Substances

  • Antineoplastic Agents, Immunological
  • Bevacizumab