Evidence map›Paper›PMID 38662207›Full record

Observational studyAnnals of hematology2024

Systemic inflammatory autoimmune disease before allogeneic hematopoietic stem cell transplantation is a risk factor for death in patients with myelodysplastic syndrome or chronic myelomonocytic leukemia.

Kumiyo Tazoe, Naonori Harada, Yosuke Makuuchi, Masatomo Kuno, Teruhito Takakuwa, Hiroshi Okamura, Asao Hirose, Mika Nakamae, Mitsutaka Nishimoto, Yasuhiro Nakashima and 3 more

Abstract readObservational Study
PubMed Publisher
In one paragraph

Observational study in Annals of hematology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
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

13 authors at 3 institutions in 1 country.

Kumiyo TazoeDepartment of Hematology, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan.
Naonori HaradaDepartment of Hematology, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan. harada.naonori@omu.ac.jp.ORCID http://orcid.org/0000-0001-8585-1450
Yosuke MakuuchiDepartment of Hematology, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan.
Masatomo KunoDepartment of Hematology, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan.
Teruhito TakakuwaDepartment of Hematology, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan.
Hiroshi OkamuraDepartment of Hematology, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan.
Asao HiroseDepartment of Hematology, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan.
Mika NakamaeDepartment of Clinical Laboratory, Osaka Metropolitan University Hospital, Osaka, Japan.
Mitsutaka NishimotoDepartment of Hematology, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan.
Yasuhiro NakashimaDepartment of Hematology, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan.
Hideo KohDepartment of Preventive Medicine and Environmental Health, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan.
Masayuki HinoDepartment of Hematology, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan.
Hirohisa NakamaeDepartment of Hematology, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan.
Osaka Metropolitan University · JPFuchu Hospital · JPOsaka City University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myelodysplastic syndrome (MDS) is well known to be complicated by systemic inflammatory autoimmune disease (SIADs). However, it remains unclear how the prognosis after allogenic hematopoietic stem cell transplantation (allo-HSCT) in patients with MDS is impacted by SIADs that occur before allo-HSCT. Therefore, we hypothesized that SIADs before allo-HSCT may be a risk factor for negative outcomes after allo-HSCT in patients with MDS. We conducted a single-center, retrospective, observational study of sixty-nine patients with MDS or chronic myelomonocytic leukemia who underwent their first allo-HCT. Fourteen of the patients had SIADs before allo-HSCT. In multivariate analysis, the presence of SIADs before allo-HSCT was an independent risk factor for overall survival (HR, 3.36, 95% confidence interval: 1.34-8.42, p = 0.009). Endothelial dysfunction syndrome was identified in five of 14 patients with SIADs who required immunosuppressive therapy or intensive chemotherapy, and notably, all patients with uncontrollable SIADs at allo-HSCT developed serious endothelial dysfunction syndrome and died in the early phase after allo-HSCT. The development of SIADs in the context of MDS is thought to reflect the degree of dysfunction of hematopoietic cells in MDS and suggests a higher risk of disease progression. In addition, MDS patients with SIADs before allo-HSCT are considered to be at higher risk of endothelial dysfunction syndrome because of preexisting vascular endothelial dysfunction due to SIADs. In conclusion, SIADs before allo-HSCT constitute an independent risk factor for death in MDS patients undergoing allo-HSCT.

Indexed as

Hematopoietic Stem Cell TransplantationLeukemia, Myelomonocytic, ChronicMyelodysplastic SyndromesAdultAgedAllograftsAutoimmune DiseasesFemaleHumansMaleMiddle AgedRetrospective StudiesRisk FactorsSurvival RateTransplantation, HomologousAllogeneic hematopoietic stem cell transplantationInterleukin-6Myelodysplastic syndromeSystemic inflammatory autoimmune disease

Identifiers

PMID38662207
OpenAlexW4395463317

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.