Studied treatment 
                                    
                                     
                                 
                                
                                    Control treatment 
                                    
                                     
                                 
                            
                            
                         
                        
                            
                            
                            
                                
                                    Patients 
                                    
                                     
                                 
                                
                                    Group sizes -9 / -9 
                                 
                            
                            
                         
                        
                            
                            
                            
                                
                                    Blindness 
                                      
                                    Inclusion period 
                                      
                                 
                                
                                    Follow-up duration 
                                      
                                    Centers 
                                      
                                 
                                
                                    Lost to FU 
                                      
                                    geographical localisation 
                                      
                                 
                                
                                    Primary endpoint 
                                      
                                    Design 
                                      
                                 
                            
                            
                         
                        
                            
                            
                             Endpoint X1 N1 X0 N0 TE 95% CI objective response   -   -9   -   -9  no data  progression-free survival (PFS)   -   -9   -   -9  no data overall survival (OS)   -   -9   -   -9  no data  wound-healing complications (grade 3)   -   -9   -   -9  no data treatment-related deaths   -   -9   -   -9  no data  hypertension (grade 3)   -   -9   -   -9  no data arterial thromboembolic event   -   -9   -   -9  no data  gastrointestinal perforation (grade 3)   -   -9   -   -9  no data left ventricular systolic dysfunction (grade 2 or 3)   -   -9   -   -9  no data  high-grade congestive heart failure   -   -9   -   -9  no data serious adverse events   -   -9   -   -9  no data  arterial/venous thromboembolism (grade 3)   -   -9   -   -9  no data pulmonary embolism (grade 3)   -   -9   -   -9  no data  bleeding (grade 3)   -   -9   -   -9  no data cardiomyopathy (grade 3)   -   -9   -   -9  no data  permanent discontinuation   -   -9   -   -9  no data adverse events grade 3   -   -9   -   -9  no data  venous thromboembolic event (grade 3)   -   -9   -   -9  no data proteinuria (grade 3)   -   -9   -   -9  no data 0,2 2,0 1,0 
                         
                        
                            
                                De Jong RS, Sonke GS, Maass N et al.
                                Fulvestrant (FUL)plus enzastaurin (ENZA) vs FUL plus placebo (PBO) inaromatase inhibitor (AI)-resistant metastatic breast cancer(MBC): a randomized, double-blind, phase 2 trial.
                                AnnOncol2012; 23: ix124.	
                           
                        [PMID: ]
                         
                                 
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