Evidence map›Paper›PMID 31657156›Full record

ArticleCancer medicine2019

Effects of different doses of erythropoietin in patients with myelodysplastic syndromes: A propensity score-matched analysis.

Enrico Balleari, Rosa Angela Filiberti, Chiara Salvetti, Bernardino Allione, Emanuele Angelucci, Marco Bruzzone, Tullio Calzamiglia, Marina Cavaliere, Maurizio Cavalleri, Daniela Cilloni and 20 more

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.5field-weighted citation impact, top 31% 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

8 citing papers in PubMed, 9 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. 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

30 authors at 8 institutions in 2 countries.

Enrico BalleariFondazione Italiana Sindromi Mielodisplastiche (FISM), Bologna, Italy.ORCID 0000-0003-2186-8012
Rosa Angela FilibertiUO Clinical Epidemiology, Ospedale Policlinico San Martino-IRCCS, Genova, Italy.
Chiara SalvettiFondazione Italiana Sindromi Mielodisplastiche (FISM), Bologna, Italy.
Bernardino AllioneFondazione Italiana Sindromi Mielodisplastiche (FISM), Bologna, Italy.
Emanuele AngelucciFondazione Italiana Sindromi Mielodisplastiche (FISM), Bologna, Italy.
Marco BruzzoneUO Clinical Epidemiology, Ospedale Policlinico San Martino-IRCCS, Genova, Italy.
Tullio CalzamigliaFondazione Italiana Sindromi Mielodisplastiche (FISM), Bologna, Italy.
Marina CavaliereFondazione Italiana Sindromi Mielodisplastiche (FISM), Bologna, Italy.
Maurizio CavalleriFondazione Italiana Sindromi Mielodisplastiche (FISM), Bologna, Italy.
Daniela CilloniFondazione Italiana Sindromi Mielodisplastiche (FISM), Bologna, Italy.
Marino ClavioFondazione Italiana Sindromi Mielodisplastiche (FISM), Bologna, Italy.
Elena CrisàFondazione Italiana Sindromi Mielodisplastiche (FISM), Bologna, Italy.
Anna Da ColFondazione Italiana Sindromi Mielodisplastiche (FISM), Bologna, Italy.
Paolo DaniseFondazione Italiana Sindromi Mielodisplastiche (FISM), Bologna, Italy.
Federica PiloFondazione Italiana Sindromi Mielodisplastiche (FISM), Bologna, Italy.
Dario FerreroFondazione Italiana Sindromi Mielodisplastiche (FISM), Bologna, Italy.
Carlo FinelliFondazione Italiana Sindromi Mielodisplastiche (FISM), Bologna, Italy.
Daniela GioiaFondazione Italiana Sindromi Mielodisplastiche (FISM), Bologna, Italy.
Roberto Massimo LemoliFondazione Italiana Sindromi Mielodisplastiche (FISM), Bologna, Italy.
Elisa MasieraFondazione Italiana Sindromi Mielodisplastiche (FISM), Bologna, Italy.
Emanuela MessaFondazione Italiana Sindromi Mielodisplastiche (FISM), Bologna, Italy.
Maurizio MiglinoFondazione Italiana Sindromi Mielodisplastiche (FISM), Bologna, Italy.
Pellegrino MustoFondazione Italiana Sindromi Mielodisplastiche (FISM), Bologna, Italy.
Esther Natalie OlivaFondazione Italiana Sindromi Mielodisplastiche (FISM), Bologna, Italy.
Antonella PoloniFondazione Italiana Sindromi Mielodisplastiche (FISM), Bologna, Italy.
Flavia SalviFondazione Italiana Sindromi Mielodisplastiche (FISM), Bologna, Italy.
Alessandro SannaFondazione Italiana Sindromi Mielodisplastiche (FISM), Bologna, Italy.
Marco ScudelettiFondazione Italiana Sindromi Mielodisplastiche (FISM), Bologna, Italy.
Rodolfo TassaraFondazione Italiana Sindromi Mielodisplastiche (FISM), Bologna, Italy.
Valeria SantiniFondazione Italiana Sindromi Mielodisplastiche (FISM), Bologna, Italy.
Italian Foundation of Myelodysplastic Syndromes · ITOspedale Policlinico San Martino · ITCentro di Riferimento Oncologico della Basilicata · ITFondazione Ricerca Molinette · ITIRCCS Azienda Ospedliero-Universitaria di Bologna Policlinico di Sant'Orsola · ITMarche Polytechnic University · ITOspedale di Sanremo · ITTracer Technologies (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundErythropoiesis-stimulating agents effectively improve the hemoglobin levels in a fraction of anemic patients with myelodysplastic syndromes (MDS). Higher doses (HD) of recombinant human erythropoietin (rhEPO) have been proposed to overcome suboptimal response rates observed in MDS patients treated with lower "standard doses" (SD) of rhEPO. However, a direct comparison between the different doses of rhEPO is lacking.

methodsA cohort of 104 MDS patients treated with HD was retrospectively compared to 208 patients treated with SD in a propensity score-matched analysis to evaluate hematological improvement-erythroid (HI-E) rate induced by the different doses of rhEPO. The impact of rhEPO doses on survival and progression to leukemia was also investigated.

resultsOverall HI-E rate was 52.6%. No difference was observed between different rhEPO doses (P = .28) in matched cohorts; in a subgroup analysis, transfusion-dependent patients and patients with higher IPSS-R score obtained a higher HI-E rate with HD, although without significant impact on overall survival (OS). Achievement of HI-E resulted in superior OS. At univariate analysis, a higher HI-E rate was observed in transfusion-independent patients (P < .001), with a lower IPSS-R score (P < .001) and lower serum EPO levels (P = .027). Multivariate analysis confirmed that rhEPO doses were not significantly related to HI-E (P = .26). There was no significant difference in OS or progression to leukemia in patients treated with HD vs SD.

conclusionSD are substantially equally effective to HD to improve anemia and influencing survival in MDS patients stratified according to similar propensity to be exposed to rhEPO treatment.

Indexed as

AgedAged, 80 and overAnemiaDisease ProgressionErythrocyte IndicesErythropoietinFemaleHumansMaleMiddle AgedMyelodysplastic SyndromesPropensity ScoreProportional Hazards ModelsRecombinant ProteinsRetrospective StudiesTreatment OutcomeErythropoietinRecombinant Proteinsanemiaerythropoietinmyelodysplastic syndromes

Identifiers

PMID31657156
PMCPMC6912022
OpenAlexW2981631177

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.