Vansteenkiste 2002.
Methods | randomized controlled trial, placebo‐controlled | |
Participants | n = 320, small cell lung cancer (limited and extensive), and non‐small lung cancer (stage I‐IV); concomitant treatment: chemotherapy | |
Interventions | drug = Darbepoetin alpha dose = 2.25 mg/kg sc weekly hb‐target = 13‐14 g/dL (women), 13‐15 g/dL (men) planned ESA duration = 12 weeks |
|
Outcomes | Primary: transfusion; secondary: Hb response, Hb, transfusion timing and quantity, QoL | |
Notes | study number = 49684 | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Adequate sequence generation? | Unclear risk | based on a schedule specified by Amgen before the start of the study |
Allocation concealment? | Low risk | central randomization |