Evidence map›Paper›PMID 25943181›Full record

ArticleLeukemia2015

Effectiveness of azacitidine in unselected high-risk myelodysplastic syndromes: results from the Spanish registry.

T Bernal, P Martínez-Camblor, J Sánchez-García, R de Paz, E Luño, B Nomdedeu, M T Ardanaz, C Pedro, M L Amigo, B Xicoy and 10 more

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Leukemia, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 1 pooled it
7.4field-weighted citation impact, top 2% 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

56 citing papers in PubMed, 1 synthesis or guideline pooled it, 104 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Article
  5. Article
  6. Therapy of high-risk myelodysplastic syndromes.Bone marrow transplantation · 2026
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Review
  16. Unveiling sex-based geographical disparities in myelodysplastic syndrome mortality trends in Spain (1999-2022).Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
    Article
  17. Article
  18. Clinical activity, pharmacokinetics, and pharmacodynamics of oral hypomethylating agents for myelodysplastic syndromes/neoplasms and acute myeloid leukemia: A multidisciplinary review.Journal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners · 2024
    Review
  19. Myelodysplastic syndromes mortality in Spain: a comprehensive age-period-cohort and joinpoint analysis.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
    Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 14 institutions in 2 countries.

T BernalServicio de Hematología, Hospital Universitario Central de Asturias, Departamento de Medicina, Universidad de Oviedo, Oviedo, Spain.
P Martínez-CamblorServicio de Hematología, Hospital Universitario Central de Asturias, Departamento de Medicina, Universidad de Oviedo, Oviedo, Spain.
J Sánchez-GarcíaIMIBIC, Hospital Universitario Reina Sofía, Universidad de Córdoba, Córdoba, Spain.
R de PazHospital Universitario La Paz, Madrid, Spain.
E LuñoServicio de Hematología, Hospital Universitario Central de Asturias, Departamento de Medicina, Universidad de Oviedo, Oviedo, Spain.
B NomdedeuHospital Clinic, Barcelona, Spain.
M T ArdanazHospital de Txagorritxu, Victoria-Gasteiz, Spain.
C PedroHospital del Mar, Barcelona, Spain.
M L AmigoHospital Universitario Morales Messeguer, Murcia, Spain.
B XicoyInstituto catalán de Oncología, Instituto de Investigación Josep Carreras, Instituto Catalán de Oncología, Hospital Germans Trias i Pujol, Badalona, Spain.
C del CañizoHospital Universitario de Salamanca, Salamanca, Spain.
M TormoHospital Clínico Universitario, Instituto de Investigación INCLIVA, Valencia, Spain.
J BargayHospital Son Llatzer, Palma de Mallorca, Spain.
D ValcárcelHospital Vall D'Hebrón, Barcelona, Spain.
S BrunetHospital Sant Pau, Universidad Autónoma de Barcelona, Barcelona, Spain.
L BenllochGrupo Español de Síndromes Mielodisplásicos, Valencia, Spain.
G SanzHospital Universitario y Politécnico La Fe, Valencia, Spain.
Spanish Group on Myelodysplastic Syndromes
PETHEMA Foundation
Spanish Society of Hematology
Universidad de Oviedo · ESComplejo Hospitalario de Salamanca · ESHospital Clínic de Barcelona · ESHospital Del Mar · ESHospital General Universitario Morales Meseguer · ESHospital Son Llatzer · ESHospital Txagorritxu · ESHospital Universitari i Politècnic La Fe · ESHospital Universitario La Paz · ESINCLIVA Health Research Institute · ESInstitut Català d'Oncologia · ESInstituto Maimónides de Investigación Biomédica de Córdoba · ESUniversitat Autònoma de Barcelona · ESVall d'Hebron Hospital Universitari · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The benefit of azacitidine treatment in survival of high-risk myelodysplastic syndromes (MDS) patients compared with conventional care treatment (CCT) has not been established outside clinical trials. To assess its effectiveness, we compared overall survival (OS) between azacitidine and conventional treatment (CCT) in high-risk MDS patients, excluding those undergoing stem cell transplantation, submitted to the Spanish MDS registry from 2000 to 2013. Several Cox regression and competing risk models, considering azacitidine as a time-dependent covariate, were used to assess survival and acute myeloblastic leukemia (AML) progression. Among 821 patients included, 251 received azacitidine. Median survival was 13.4 (11.8-16) months for azacitidine-treated patients and 12.2 (11-14.1) for patients under CCT (P=0.41). In a multivariate model, age, International prognostic scoring system and lactate dehydrogenase were predictors of OS whereas azacitidine was not (adjusted odds ratio 1.08, 95% confidence interval 0.86-1.35, P=0.49). However, in patients with chromosome 7 abnormalities, a trend toward a better survival was observed in azacitidine-treated patients (median survival 13.3 (11-18) months) compared with CCT (median survival 8.6 (5-10.4) months, P=0.08). In conclusion, our data show that, in spite of a widespread use of azacitidine, there is a lack of improvement in survival over the years. Identification of predicting factors of response and survival is mandatory.

Indexed as

AgedAged, 80 and overAntimetabolites, AntineoplasticAntineoplastic Combined Chemotherapy ProtocolsAzacitidineDisease ProgressionFemaleFollow-Up StudiesHumansIncidenceLeukemia, Myeloid, AcuteMaleMyelodysplastic SyndromesPrognosisRegistriesSpainAntimetabolites, AntineoplasticAzacitidine

Identifiers

PMID25943181
OpenAlexW1558398160

What OpenQuestion holds

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Registered trials

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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.