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
Dickler M, Barry WT, Cirrincione C, Ellis MJ, Moynahan
ME, Innocenti F.
Phase III trial evaluating the additionof bevacizumab to letrozole as first-line endocrine therapyfor treatment of hormone-receptor positive advancedbreast cancer: CALGB 40503 (Alliance).
J Clin Oncol 2015;33 (suppl; abstr 501).
[PMID: ]
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[PMID: ]
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