CPX-351 in Down syndrome–associated myeloid leukemia: results and prognostic factors from the phase 3 ML-DS 2018 trial
Myeloid leukemia of Down syndrome (ML-DS) is associated with an excellent prognosis but high treatment-related toxicity and mortality. The Phase 3 Clinical Trial for CPX-351 in ML-DS 2018 aimed to maintain the excellent event-free survival (EFS) achieved in the previous ML-DS 2006 trial while reducing the treatment intensity. Intensity-reduced induction and reinduction therapy with cytarabine and idarubicin with or without etoposide was replaced with CPX-351 (66 U/m2 on 3 days in course 1 and on 2 days in course 2). Risk stratification was based on flow cytometric measurable residual disease (MRD) after first induction. High-risk patients received high-dose cytarabine (3 g/m2 per 12 hour) in consolidation; standard-risk patients received cytarabine at a dose of 1 g/m2 per 12 hour. A total of 35 patients were enrolled until the trial was halted because of an unexpectedly high relapse rate. A per-protocol interim analysis revealed a significantly lower 24-month EFS when compared with the ML-DS 2006 trial (69% vs 90%; P< .001). In contrast with previous studies, most patients who relapsed responded to salvage therapy, leading to a comparable 24-month overall survival of 88% (vs 92%; P = .612). CPX-351 demonstrated a favorable toxicity profile with no treatment-related mortality. Positive MRD by error-corrected GATA1 next-generation sequencing, the presence of trisomy 8 or a complex karyotype were associated with an increased risk for relapse. In conclusion, replacing intensity-reduced induction therapy with CPX-351 in ML-DS led to a significantly lower EFS, highlighting the need for dose optimization to balance the efficacy and toxicity in this sensitive patient population. This trial was registered at https://www.clinicaltrialsregister.eu as EudraCT #2018-002988-25.
Authors
- Hermann Kreyenberg (ORCID: https://orcid.org/0000-0003-3575-9175)
- Melanie Bremm
- Heidrun Boztug
- Stephanie Laszig
- Bianca F. Goemans (ORCID: https://orcid.org/0000-0003-4030-3228)
- Jan‐Henning Klusmann (ORCID: https://orcid.org/0000-0002-1070-0727)
- Helena Kerp (ORCID: https://orcid.org/0000-0002-6036-0230)
- Katarzyna Pawińska-Wąsikowska (ORCID: https://orcid.org/0000-0002-1212-7629)
- K Schuschel (ORCID: https://orcid.org/0000-0002-5417-8950)
- Felicitas Thol (ORCID: https://orcid.org/0000-0001-5848-6152)
- Milica Miladinovic
- Eva Rettinger
- Hasan Issa (ORCID: https://orcid.org/0000-0002-9760-9618)
- Nastassja K. Scheidegger (ORCID: https://orcid.org/0000-0002-3091-2970)
- Barbara De Moerloose (ORCID: https://orcid.org/0000-0002-2449-539X)
- José Gonçalves-Dias (ORCID: https://orcid.org/0000-0001-9230-6004)
- Dirk Reinhardt (ORCID: https://orcid.org/0000-0002-7027-4483)
- Sabine Hünecke
- Emilia Salzmann‐Manrique
- Antonia Diederichs
- Katharina Waack-Buchholz
- Sibylle Wehner
Institutions
- Goethe University Frankfurt (DE)
- Jagiellonian University (PL)
- Ghent University Hospital (BE)
- Medizinische Hochschule Hannover (DE)
- Atrial Fibrillation NETwork (DE)
- Essen University Hospital (DE)
- Cancer Research Institute of the Slovak Academy of Sciences (SK)
- St Anna Children's Hospital (AT)
- Princess Máxima Center (NL)
- University Children's Hospital Zurich (CH)
Publication Details
- Journal
- Blood
- Published
- 2025-10-21
- DOI
- https://doi.org/10.1182/blood.2025030775
- Citations
- 2
- Primary Topic
- Acute Myeloid Leukemia Research
- Type
- article
- Field-Weighted Citation Impact
- 3.54
Funders
- Hilfe für krebskranke Kinder Frankfurt