Quirt 1996.
Methods | randomized controlled trial, placebo‐controlled | |
Participants | n = 56, lung, gynecological, hematological malignancies, other cancer; concomitant treatment: chemotherapy | |
Interventions | drug = Epoetin alpha dose = 150 IU/kg sc TIW hb‐target = 12.5‐14 g/dL planned ESA duration = 16 weeks |
|
Outcomes | Primary: transfusion; secondary: QoL, costs from societal perspective, tumor response | |
Notes | study number = 80214 | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Adequate sequence generation? | Unclear risk | no description |
Allocation concealment? | Unclear risk | no description |