Untch 2008.
| Methods | randomized controlled trial, not placebo‐controlled | |
| Participants | n = 729, breast cancer (M0); concomitant treatment: chemotherapy | |
| Interventions | drug = Darbepoetin alpha dose = 4.5 µg/kg sc Q2W hb‐target = 13 g/dL planned ESA duration = during chemotherapy |
|
| Outcomes | Primary: relapse free survival time, overall survival; secondary: tumor control, safety and tolerability, transfusion, Hb level, QoL | |
| Notes | study number = 66960 | |
| Risk of bias | ||
| Bias | Authors' judgement | Support for judgement |
| Adequate sequence generation? | Unclear risk | no description |
| Allocation concealment? | Unclear risk | description is unclear |