Current experience with treatment of prognostically unfavourable acute myeloid leukaemias with CPX-351 at the Institute of Haematology and Blood Transfusion
Authors:
J. Valka
Authors‘ workplace:
Ústav hematologie a krevní transfuze, Praha
Published in:
Transfuze Hematol. dnes,30, 2024, No. 4, p. 253-259.
Category:
Original Papers
doi:
https://doi.org/10.48095/cctahd2024prolekare.cz20
Overview
The therapeutic agent CPX-351, Vyxeos liposomal, is a newly approved drug intended for therapy of high-risk subtypes of acute myeloid leukaemia (AML) such as AML arising from antecedent myelodysplastic syndrome or associated with previous anticancer therapy. In the Czech Republic, CPX-351 is reimbursed for patients aged 60 and over with the above-mentioned AML subtypes. The following paper describes the indication and dosage schedule of CPX-351, its mechanism of action and also briefly mentions the therapeutic results and safety profile of CPX-351 according to the product registration study. The article then focuses on current clinical experience with CPX-351 since 2022 at the UHKT Prague and analyses in detail the case reports of two patients treated at the UHKT in the last months. CPX-351 therapy represents, according to our experience so far, a relatively effective option for treating high-risk AML in which treatment with standard chemotherapy often fails.
Keywords:
acute myeloid leukaemia – myelodysplastic syndrome – CPX-351 – therapy-related AML
Sources
Labels
Haematology Internal medicine Clinical oncologyArticle was published in
Transfusion and Haematology Today
2024 Issue 4
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