Transfusion support and anaemia management
Red cell and platelet transfusions, iron and erythropoiesis-stimulating agents keep patients safe through chemotherapy and marrow failure; restrictive thresholds and ESA caution reflect trials showing more is not better.
Chemotherapy-induced anaemia affects most patients on myelosuppressive regimens; MDS and leukaemia patients are often transfusion-dependent. Evidence supports restrictive red cell thresholds (7-8 g/dL in stable patients; TRIST, Hb 7 vs 9 in haematologic malignancy) and prophylactic platelet transfusion at 10×10⁹/L (TOPPS showed prophylaxis still helps in most). ESAs (epoetin, darbepoetin) reduce transfusions but increased thromboembolism and mortality in several trials when Hb targets were high, so labels restrict them to palliative chemotherapy with Hb <10 g/dL (2007-08 FDA/EMA actions). IV iron improves ESA response and treats functional iron deficiency. Transfusional iron overload in MDS is treated with chelation (TELESTO). Newer agents: luspatercept and imetelstat (MDS), romiplostim/eltrombopag for chemotherapy-induced thrombocytopenia (off-label; avatrombopag trials), and thrombopoietin agonists after transplant. Blood supply and cost are limiting worldwide; pathogen-reduced platelets and cold-stored platelets are being adopted.
How it works
Replace or stimulate deficient blood components to prevent symptomatic anaemia, bleeding and infection while avoiding over-transfusion, alloimmunisation and ESA-related thrombosis.
- Life-saving in acute leukaemia and transplant
- Restrictive strategies proven safe and cheaper
- New MDS agents reduce transfusion burden
- Blood supply shortages, especially in LMICs
- ESA safety restricts use
- Iron overload and alloimmunisation with chronic transfusion
Imetelstat is the first telomerase-blocking drug approved for any cancer; it frees many lower-risk MDS patients from transfusions after growth factors have failed.
An injection that helps the marrow finish making red cells, reducing or removing the need for transfusions in lower-risk MDS and beta-thalassaemia.
Latest papers
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