New developments in brain metastases
- PMID: 30034538
- PMCID: PMC6048670
- DOI: 10.1177/1756286418785502
New developments in brain metastases
Abstract
Patients with brain metastases (BM) are a population of high clinical need for new therapeutic approaches due to, as yet, very impaired survival prognosis. However, only few clinical trials have specifically addressed this prognostically highly heterogeneous patient population. New developments in the treatment of BM patients aim to reduce the side effects of local therapies, for example, by redefining the indications for stereotactic radiosurgery and whole-brain radiotherapy (WBRT) or introducing new applications like hippocampal sparing WBRT. Furthermore, systemic therapies become a more important treatment approach in patients harboring targetable mutations, as recent BM-specific endpoints in several phase III trials have shown promising intracranial efficacy. In addition, immune-checkpoint inhibitors show promising intracranial efficacy, particularly in patients with melanoma and non-small lung cancer BM. Here, we provide a review on the recent new developments in the local and systemic therapy approaches in BM patients.
Keywords: ALK translocation; EGFR mutation; anti-HER2 therapy; brain metastases; immune-checkpoint inhibitors; targeted therapies.
Conflict of interest statement
Conflict of interest statement: Anna Berghoff: travel support from Roche and Bristol-Myers Squibb. Honoraria for lectures from Bristol-Myers Squibb. Matthias Preusser: research support from Boehringer-Ingelheim, GlaxoSmithKline, Merck Sharp & Dohme and Roche and honoraria for lectures, consultation or advisory board participation from Bristol-Myers Squibb, Novartis, Gerson Lehrman Group (GLG), CMC Contrast, GlaxoSmithKline, Mundipharma, Roche, AstraZeneca and AbbVie.
References
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- Preusser M, Winkler F, Collette L, et al. Trial design on prophylaxis and treatment of brain metastases: lessons learned from the EORTC brain metastases strategic meeting 2012. Eur J Cancer 2012; 48: 3439–3447. - PubMed
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