Milroy 2003.
Methods | randomized controlled trial, not placebo‐controlled | |
Participants | n = 424, non‐small cell lung cancer (stage IIIb or IV, advanced); concomitant treatment: chemotherapy | |
Interventions | drug = Epoetin alpha dose = if body weight > 45 kg 10000 IU sc TIW, if body weight < 45 kg 5000 IU sc TIW hb‐target = 12.5‐14 g/dL (women), 13.5‐15 g/dL (men) planned ESA duration = during chemotherapy |
|
Outcomes | Primary: QoL; secondary: Hb, tumor response, survival, transfusion | |
Notes | study number = 67954 | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Adequate sequence generation? | Unclear risk | no description |
Allocation concealment? | Low risk | central randomization |