TY - JOUR A1 - Voß, Martin A1 - Wenger-Alakmeh, Katharina Johanna A1 - Fokas, Emmanouil A1 - Forster, Marie-Thérèse A1 - Steinbach, Joachim Peter A1 - Ronellenfitsch, Michael Wilfried T1 - Single-shot bevacizumab for cerebral radiation injury T2 - BMC neurology N2 - Background: Cerebral radiation injury, including subacute radiation reactions and later stage radiation necrosis, is a severe side effect of brain tumor radiotherapy. A protocol of four infusions of the monoclonal antibody bevacizumab has been shown to be a highly effective treatment. However, bevacizumab is costly and can cause severe complications including thrombosis, bleeding and gastrointestinal perforations. Methods: We performed a retrospective analysis of patients treated in our clinic for cerebral radiation injury who received only a singular treatment with bevacizumab. Single-shot was defined as a singular administration of bevacizumab without a second administration during an interval of at least 6 weeks. Results: We identified 11 patients who had received a singular administration of bevacizumab to treat cerebral radiation injury. Prior radiation had been administered to treat gliomas (ten patients) or breast cancer brain metastases (one patient). 9 of 10 patients with available MRIs showed a marked reduction of edema at first follow-up. Discontinuation of Dexamethasone was possible in 6 patients and a significant dose reduction could be achieved in all other patients. One patient developed pulmonary artery embolism 2 months after bevacizumab administration. The median time to treatment failure of any cause was 3 months. Conclusions: Single-shot bevacizumab therefore has meaningful activity in cerebral radiation injury, but durable control is rarely achieved. In patients where a complete protocol of four infusions with bevacizumab is not feasible due to medical contraindications or lack of reimbursement, single-shot bevacizumab treatment may be considered. KW - Radiation necrosis KW - Bevacizumab KW - Dexamethasone KW - Side effect KW - Edema Y1 - 2021 UR - http://publikationen.ub.uni-frankfurt.de/frontdoor/index/index/docId/63660 UR - https://nbn-resolving.org/urn:nbn:de:hebis:30:3-636604 SN - 1471-2377 N1 - The authors received no specific funding for this work. Open Access funding enabled and organized by Projekt DEAL. VL - 21.2021 IS - art. 77 SP - 1 EP - 7 PB - BioMed Central ; Berlin ; Heidelberg : Springer CY - London ER -