Evidence map›Paper›PMID 26950372›Full record

Trial reportBone marrow transplantation2016

Toxicity and efficacy of busulfan and fludarabine myeloablative conditioning for HLA-identical sibling allogeneic hematopoietic cell transplantation in AML and MDS.

J De La Serna, J Sanz, A Bermúdez, M Cabrero, D Serrano, C Vallejo, V Gómez, J M Moraleda, S G Perez, M D Caballero and 3 more

Open access · bronzeAbstract readClinical TrialMulticenter Study
PubMed Publisher
In one paragraph

Trial report in Bone marrow transplantation, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-weighted citation impact, top 24% of its field
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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Stem cell therapies in the clinic.Bioengineering & translational medicine · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 9 institutions in 1 country.

J De La SernaHematology Department, Servicio de Hematología, Hospital Universitario 12 de Octubre, Madrid, Spain.
J SanzHematology Department, Hospital Universitario La Fe, Valencia, Spain.
A BermúdezHematology Department, Hospital Universitario Marques de Valdecilla, Santander, Spain.
M CabreroHematology Department, Hospital Universitario Clínico de Salamanca, Salamanca, Spain.
D SerranoHematology Department, Hospital Universitario Gregorio Marañón, Madrid, Spain.
C VallejoHematology Department, Hospital Universitario Central de Asturias, Oviedo, Spain.
V GómezHematology Department, Hospital Universitario de la Princesa, Madrid, Spain.
J M MoraledaHematology Department, Hospital Universitario Virgen de la Arrixaca, Murcia, Spain.
S G PerezHematology Department, Complejo Hospitalario Universitario de Santiago, Santiago de Compostela, Spain.
M D CaballeroHematology Department, Hospital Universitario Clínico de Salamanca, Salamanca, Spain.
E CondeHematology Department, Hospital Universitario Marques de Valdecilla, Santander, Spain.
J J LahuertaHematology Department, Servicio de Hematología, Hospital Universitario 12 de Octubre, Madrid, Spain.
G SanzHematology Department, Hospital Universitario La Fe, Valencia, Spain.
Complejo Hospitalario de Salamanca · ESHospital Universitari i Politècnic La Fe · ESHospital Universitario 12 De Octubre · ESMarqués de Valdecilla University Hospital · ESComplejo Hospitalario Universitario de Santiago · ESHospital General Universitario Gregorio Marañón · ESHospital Universitario Central de Asturias · ESHospital Universitario de La Princesa · ESHospital Universitario Virgen de la Arrixaca · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The safety and efficacy of a 4-day myeloablative conditioning (MAC) regimen consisting of Bu 3.2 mg/kg and fludarabine 40 mg/m(2)/day for HLA-identical sibling allogeneic hematopoietic cell transplantation (HCT) in myeloid malignancies was investigated in 133 patients (median age, 47 years; range 19-74 years) with de novo AML (60%), secondary AML (20%) or myelodysplastic syndrome (20%). All patients engrafted. Hepatic veno-occlusive disease occurred in five patients (4%), and severe toxicities, mostly mucositis, occurred in twenty-three (17%) patients. The non-relapse mortality (NRM) at 100 days was 1.5%. The incidences of acute GVHD grade 2-4 and grade 3-4 were 32 and 13%, respectively. At a median follow-up of 38 months, the cumulative incidence of chronic GVHD was 67%. The relapse incidence was 30% (27 and 31%, respectively, in patients with early- and late-stage disease), and the overall NRM was 15%. The actuarial 4-year disease-free survival (DFS) and overall survival (OS) were 54 and 62%, respectively. Patients aged <50 years had better outcomes compared with older patients (DFS 64 vs 42%, P=0.006; OS 73 vs 47%, P<0.001, respectively).

Indexed as

AdultAgedBusulfanGraft vs Host DiseaseHematopoietic Stem Cell TransplantationHepatic Veno-Occlusive DiseaseHistocompatibilityHumansLeukemia, Myeloid, AcuteMiddle AgedMucositisMyeloablative AgonistsMyelodysplastic SyndromesRecurrenceSurvival AnalysisTransplantation ConditioningBusulfanfludarabineMyeloablative AgonistsVidarabine

Identifiers

PMID26950372
OpenAlexW2295517063

What OpenQuestion holds

Textmetadata
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.