Evidence map›Paper›PMID 41034408›Full record

ArticleBone marrow transplantation2025

Sequential versus standard conditioning in untreated MDS patients with blasts undergoing allogeneic HSCT.

Radwan Massoud, Evgeny Klyuchnikov, Normann Steiner, Maroly Bohorquez Manjarres, Gaby Zeck, Rolf Krause, Silke Heidenreich, Claudia Langebrake, Adrin Dadkhah, Ina Rudolph and 15 more

Abstract read
In one paragraph

Article in Bone marrow transplantation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

25 authors.

Radwan MassoudDepartment of Stem cell transplantation, University Medical Center Hamburg Eppendorf, Hamburg, Germany.ORCID 0000-0001-9275-3840
Evgeny KlyuchnikovDepartment of Stem cell transplantation, University Medical Center Hamburg Eppendorf, Hamburg, Germany.
Normann SteinerDepartment of Stem cell transplantation, University Medical Center Hamburg Eppendorf, Hamburg, Germany.ORCID 0000-0001-9829-1309
Maroly Bohorquez ManjarresDepartment of Stem cell transplantation, University Medical Center Hamburg Eppendorf, Hamburg, Germany.
Gaby ZeckDepartment of Stem cell transplantation, University Medical Center Hamburg Eppendorf, Hamburg, Germany.
Rolf KrauseDepartment of Stem cell transplantation, University Medical Center Hamburg Eppendorf, Hamburg, Germany.
Silke HeidenreichDepartment of Stem cell transplantation, University Medical Center Hamburg Eppendorf, Hamburg, Germany.
Claudia LangebrakeDepartment of Stem cell transplantation, University Medical Center Hamburg Eppendorf, Hamburg, Germany.
Adrin DadkhahDepartment of Stem cell transplantation, University Medical Center Hamburg Eppendorf, Hamburg, Germany.ORCID 0000-0002-3301-0059
Ina RudolphDepartment of Stem cell transplantation, University Medical Center Hamburg Eppendorf, Hamburg, Germany.
Rusudan SabauriDepartment of Stem cell transplantation, University Medical Center Hamburg Eppendorf, Hamburg, Germany.
Christian NiederwieserDepartment of Stem cell transplantation, University Medical Center Hamburg Eppendorf, Hamburg, Germany.ORCID 0000-0002-0114-1011
Tetiana PerekhrestenkoDepartment of Stem cell transplantation, University Medical Center Hamburg Eppendorf, Hamburg, Germany.
Mirjam ReichardDepartment of Stem cell transplantation, University Medical Center Hamburg Eppendorf, Hamburg, Germany.
Mathias SchäfersküpperDepartment of Stem cell transplantation, University Medical Center Hamburg Eppendorf, Hamburg, Germany.
Franziska E MarquardDepartment of Stem cell transplantation, University Medical Center Hamburg Eppendorf, Hamburg, Germany.
Sofia OechslerDepartment of Stem cell transplantation, University Medical Center Hamburg Eppendorf, Hamburg, Germany.
Gunnar WeiseDepartment of Stem cell transplantation, University Medical Center Hamburg Eppendorf, Hamburg, Germany.
Kristin RathjeDepartment of Stem cell transplantation, University Medical Center Hamburg Eppendorf, Hamburg, Germany.
Maraike HarfmannDepartment of Stem cell transplantation, University Medical Center Hamburg Eppendorf, Hamburg, Germany.
Nico GagelmannDepartment of Stem cell transplantation, University Medical Center Hamburg Eppendorf, Hamburg, Germany.
Catherina LückDepartment of Stem cell transplantation, University Medical Center Hamburg Eppendorf, Hamburg, Germany.
Christine WolschkeDepartment of Stem cell transplantation, University Medical Center Hamburg Eppendorf, Hamburg, Germany.
Francis AyukDepartment of Stem cell transplantation, University Medical Center Hamburg Eppendorf, Hamburg, Germany.ORCID 0000-0001-6297-1847
Nicolaus KrögerDepartment of Stem cell transplantation, University Medical Center Hamburg Eppendorf, Hamburg, Germany. nmkroeger@outlook.de.ORCID 0000-0001-5103-9966

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myelodysplastic syndromes (MDS) can progress to AML and often require allogeneic hematopoietic stem cell transplantation (allo-SCT). The sequential FLAMSA-FB regimen, featuring a cytoreductive FLAMSA phase followed by fludarabine-busulfan (FB) conditioning, may enhance disease control. We retrospectively analyzed 106 untreated MDS patients with blasts 5-19% at the University Medical Center Hamburg who received either FLAMSA-FB (n = 45) or standard conditioning (n = 61: Thiotepa-Busulfan (n = 30), Fludarabine-Busulfan (n = 16), Treosulfan-Fludarabine (n = 15)). Median follow-up was 24 months. The FLAMSA group was younger (median age 56 vs. 62, p = 0.02), but baseline IPSS risk scores (p = 0.16) and donor types (p = 0.43) were comparable. Engraftment rates were similar. At two years, overall survival (OS) was 62% with FLAMSA and 68% with standard conditioning (p = 0.92), while progression-free survival (PFS) was 56% vs. 59% (p = 0.92). Non-relapse mortality (22% vs. 25%, p = 0.78) and cumulative incidence of relapse (22% vs. 13%, p = 0.12) did not differ significantly, nor did grade II-IV acute graft-versus-host disease (GVHD). Propensity score matching in 18 pairs confirmed no significant differences in OS, PFS, NRM, or CIR. However, moderate-to-severe chronic GVHD was higher with FLAMSA-FB (50% vs. 17%, p = 0.04). Thus, FLAMSA-FB did not improve transplant outcomes over standard conditioning but was linked to an increased risk of chronic GVHD.

Indexed as

Hematopoietic Stem Cell TransplantationMyelodysplastic SyndromesTransplantation ConditioningAdultAgedBusulfanFemaleGraft vs Host DiseaseHumansMaleMiddle AgedRetrospective StudiesTransplantation, HomologousVidarabineBusulfanfludarabineVidarabine

Identifiers

PMID41034408
PMCPMC12672364

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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.