Anticancer Drugs in the Adjuvant Setting Have Considerable Costs Per Event Averted, Raising Questions of Sustainability
Adjuvant therapies are often approved based on composite, surrogate endpoints with high costs per event averted
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Adjuvant therapies are often approved based on composite, surrogate endpoints with high costs per event averted
Data from a median of 6 years follow-up from the ECHELON-1 study
Clinical study publications frequently frame unimproved quality of life outcomes in a positive way
New indication concerns its use in combination with venetoclax for the treatment of adult patients with previously untreated chronic lymphocytic leukaemia
Practice changing results of the DESTINY-Breast04 study
Findings from the GAIN/iCat2 Study in patients with extracranial solid tumours
Evidence for efficacy is based on the results from the TRANSFORM and PILOT studies
Findings from a large-scale computational analysis
It is a new therapeutic option for adults with Philadelphia chromosome‑positive chronic myeloid leukaemia in chronic phase, previously treated with two or more tyrosine kinase inhibitors
Findings from the Dutch Pharmacology Oncology Group - Therapeutic Drug Monitoring study show that pharmacokinetically guided dose-adjustments of oral targeted therapies are feasible in clinical practice
Findings from the PRO-TECT (Alliance AFT-39) cluster randomised study should be interpreted provisionally pending results of the primary outcome of overall survival
Vegzelma is highly similar to the reference product Avastin, which was authorised in the EU in January 2005
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