Evidence map›Paper›PMID 39190255›Full record

ArticleInternational journal of hematology2024

Clinical impact of airflow obstruction after allogeneic hematopoietic stem cell transplantation.

Sanshiro Nakao, Shokichi Tsukamoto, Yusuke Takeda, Chikako Ohwada, Chihiro Ri, Shintaro Izumi, Yuri Kamata, Shinichiro Matsui, Asuka Shibamiya, Arata Ishii and 9 more

Abstract read
In one paragraph

Article in International journal of hematology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

19 authors.

Sanshiro NakaoDepartment of Hematology, Chiba University Hospital, 1-8-1 Inohana, Chuo-Ku, Chiba, 260-8677, Japan.
Shokichi TsukamotoDepartment of Hematology, Chiba University Hospital, 1-8-1 Inohana, Chuo-Ku, Chiba, 260-8677, Japan.
Yusuke TakedaDepartment of Hematology, Chiba University Hospital, 1-8-1 Inohana, Chuo-Ku, Chiba, 260-8677, Japan.
Chikako OhwadaDepartment of Hematology, Chiba University Hospital, 1-8-1 Inohana, Chuo-Ku, Chiba, 260-8677, Japan.
Chihiro RiDepartment of Hematology, Chiba University Hospital, 1-8-1 Inohana, Chuo-Ku, Chiba, 260-8677, Japan.
Shintaro IzumiDepartment of Hematology, Chiba University Hospital, 1-8-1 Inohana, Chuo-Ku, Chiba, 260-8677, Japan.
Yuri KamataDepartment of Hematology, Chiba University Hospital, 1-8-1 Inohana, Chuo-Ku, Chiba, 260-8677, Japan.
Shinichiro MatsuiDepartment of Hematology, Chiba University Hospital, 1-8-1 Inohana, Chuo-Ku, Chiba, 260-8677, Japan.
Asuka ShibamiyaDepartment of Hematology, Chiba University Hospital, 1-8-1 Inohana, Chuo-Ku, Chiba, 260-8677, Japan.
Arata IshiiDepartment of Hematology, Chiba University Hospital, 1-8-1 Inohana, Chuo-Ku, Chiba, 260-8677, Japan.
Koji TakaishiDepartment of Hematology, Chiba University Hospital, 1-8-1 Inohana, Chuo-Ku, Chiba, 260-8677, Japan.
Kohei TakahashiBiostatistics Section, Clinical Research Centre, Chiba University Hospital, Chiba, Japan.
Yuki ShikoBiostatistics Section, Clinical Research Centre, Chiba University Hospital, Chiba, Japan.
Nagisa Oshima-HasegawaDepartment of Hematology, Chiba University Hospital, 1-8-1 Inohana, Chuo-Ku, Chiba, 260-8677, Japan.
Tomoya MutoDepartment of Hematology, Chiba University Hospital, 1-8-1 Inohana, Chuo-Ku, Chiba, 260-8677, Japan.
Naoya MimuraDepartment of Hematology, Chiba University Hospital, 1-8-1 Inohana, Chuo-Ku, Chiba, 260-8677, Japan.
Koutaro YokoteDepartment of Endocrinology, Hematology and Gerontology, Chiba University Graduate School of Medicine, Chiba, Japan.
Chiaki NakasekoDepartment of Hematology, International University of Health and Welfare, Narita, Japan.
Emiko SakaidaDepartment of Hematology, Chiba University Hospital, 1-8-1 Inohana, Chuo-Ku, Chiba, 260-8677, Japan. esakaida@faculty.chiba-u.jp.ORCID http://orcid.org/0000-0002-7254-1928

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Criteria for airflow obstruction (AFO) at one year after allogeneic hematopoietic stem cell transplantation (allo-HSCT) in pulmonary function tests (PFTs) are more stringent than the bronchiolitis obliterans syndrome (BOS) criteria of the National Institutes of Health. This single-center, retrospective cohort study evaluated the clinical impact of the AFO criteria at any time after transplantation. In 132 patients who underwent allo-HSCT from 2006 to 2016, the 2-year cumulative incidence of AFO was 35.0%, and the median time to diagnosis of AFO was 101 days after transplantation (range 35-716 days). Overall chronic graft-versus-host disease (cGVHD) incidence was significantly higher in patients with AFO than in those without AFO (80.4% vs. 47.7%, P < 0.01); notably, 37.0% of patients with AFO developed cGVHD after AFO diagnosis. AFO patients developed BOS with a 5-year cumulative incidence of 49.1% after AFO onset. The 5-year cumulative incidence of non-relapse mortality in the AFO group was higher than that in the non-AFO group (24.7% vs. 7.1%, P < 0.01). These results suggest that closely monitoring PFTs within two years after allo-HSCT, regardless of cGVHD status, is important for early detection of AFO and prevention of progression to BOS. (192words).

Indexed as

Bronchiolitis ObliteransGraft vs Host DiseaseHematopoietic Stem Cell TransplantationTransplantation, HomologousAdolescentAdultAgedFemaleHumansIncidenceMaleMiddle AgedRespiratory Function TestsRetrospective StudiesYoung AdultAirflow obstruction (AFO)Allogeneic hematopoietic stem cell transplantationBronchiolitis obliterans syndromeChronic graft-versus-host disease

Identifiers

PMID39190255
PMCPMC11415471

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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.