Evidence map›Paper›PMID 40549144›Full record

ArticleAnnals of hematology2025

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, Patrizia Chiusolo, Elisabetta Metafuni, Maria Assunta Limongiello, Federica Sorà, Filippo Frioni, Luca Di Marino, Livio Pagano, Simona Sica

Abstract read
In one paragraph

Article in Annals of hematology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Sabrina Giammarco *Dipartimento di Scienze di Laboratorio ed Ematologiche, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
Patrizia Chiusolo *Sezione di Ematologia, Università Cattolica del Sacro Cuore, Rome, Italy.
Elisabetta MetafuniDipartimento di Scienze di Laboratorio ed Ematologiche, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
Maria Assunta LimongielloDipartimento di Scienze di Laboratorio ed Ematologiche, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
Federica SoràSezione di Ematologia, Università Cattolica del Sacro Cuore, Rome, Italy.
Filippo FrioniSezione di Ematologia, Università Cattolica del Sacro Cuore, Rome, Italy.
Luca Di MarinoSezione di Ematologia, Università Cattolica del Sacro Cuore, Rome, Italy.
Livio PaganoSezione di Ematologia, Università Cattolica del Sacro Cuore, Rome, Italy.
Simona SicaSezione di Ematologia, Università Cattolica del Sacro Cuore, Rome, Italy. simona.sica@unicatt.it.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsDaunorubicinHematopoietic Stem Cell TransplantationLeukemia, Myeloid, AcuteTransplantation ConditioningAdultAgedBusulfanCyclosporineCytarabineFeasibility StudiesFemaleGraft vs Host DiseaseHumansMaleMiddle AgedBusulfanCPX-351CyclosporineCytarabineDaunorubicinfludarabineThiotepaVidarabineAllogeneic stem cell transplantationCPX-351Secondary acute myeloid leukemia

Identifiers

PMID40549144
PMCPMC12334473

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.