Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2025 Jul;104(7):3855-3861.
doi: 10.1007/s00277-025-06462-3. Epub 2025 Jun 23.

Feasibility of allogeneic stem cell transplantation (HSCT) in patients with acute myeloid leukemia previously treated with CPX-351: report from a single center

Affiliations

Feasibility of allogeneic stem cell transplantation (HSCT) in patients with acute myeloid leukemia previously treated with CPX-351: report from a single center

Sabrina Giammarco et al. Ann Hematol. 2025 Jul.

Abstract

The increased use of CPX-351, a liposomal formulation of cytarabine and daunorubicin, in association with reduced intensity conditioning regimen and new strategies of GvHD prophylaxis such as PTCY, allows to proceed with HSCT in older patients or previously heavily treated, improving outcomes. Of 55 patients with s-AML treated with CPX-351 from February 2019 till December 2023, at our center, all 28 patients with an indication to proceed with HSCT, underwent to transplant to consolidate the obtained response. The median age was 62 yrs (range 43–69). They were all in complete remission except two. The median HCT-CI was 4 (range 0–7). The main conditioning regimen was the association of Thiotepa, Busulfan, and Fludarabine. A Prophylaxis Gvhd regimen was performed with cyclosporine and mycophenolic acid, and PTCY. Engraftment was reached in all patients treated with CPX-351, except one. Eight patients developed acute GVHD. 1 year’s OS was 66%. Comparing data with 59 patients, previously treated with 7 + 3 standard induction therapy, we found differences in terms of median age (p < 0.00001), HCT-CI (p = 0.01), and in terms of median CD34 + stem cells, which are significantly higher in the younger comparison population (p = 0.0002), with similar outcomes. The growing use of CPX-351 appears to be a safe and effective bridge therapy for HSCT in patients with a poorer prognosis, reproducing outcomes similar to younger populations.

Keywords: Allogeneic stem cell transplantation; CPX-351; Secondary acute myeloid leukemia.

PubMed Disclaimer

Conflict of interest statement

Declarations. Competing interests: The authors declare no competing interests.

Figures

Fig. 1
Fig. 1
a Overall survival according to induction therapy. b Disease free survival according to induction therapy. c Transplant related mortality according to induction therapy. d Cumulative Incidence of acute gvhd according to induction therapy

Similar articles

References

    1. Döhner H, Wei AH, Appelbaum FR, Craddock C, DiNardo CD, Dombret H et al (2022) Diagnosis and management of AML in adults: 2022 recommendations from an international expert panel on behalf of the ELN. Blood 140(12):1345–1377 - PubMed
    1. Shallis RM, Wang R, Davidoff A, Ma X, Zeidan AM (2019) Epidemiology of acute myeloid leukemia: recent progress and enduring challenges. Blood Rev 36:70–87 - PubMed
    1. Gupta V, Tallman MS, Weisdorf DJ (2011) Allogeneic hematopoietic cell transplantation for adults with acute myeloid leukemia: myths, controversies, and unknowns. Blood 117(8):2307–2318 - PubMed
    1. Ciurea SO, Zhang M-J, Bacigalupo AA, Bashey A, Appelbaum FR, Aljitawi OS et al (2015) Haploidentical transplant with posttransplant cyclophosphamide vs matched unrelated donor transplant for acute myeloid leukemia. Blood 126(8):1033–1040 - PMC - PubMed
    1. Lancet JE, Uy GL, Cortes JE, Newell LF, Lin TL, Ritchie EK et al (2018) CPX-351 (cytarabine and daunorubicin) liposome for injection versus conventional cytarabine plus Daunorubicin in older patients with newly diagnosed secondary acute myeloid leukemia. J Clin Oncol 36(26):2684–2692 - PMC - PubMed

LinkOut - more resources