Evidence map›Paper›PMID 32203259›Full record

Observational studyBone marrow transplantation2020

Prospective evaluation of alternative donor from unrelated donor and cord blood in adult acute leukemia and myelodysplastic syndrome.

Seitaro Terakura, Tetsuya Nishida, Masashi Sawa, Tomonori Kato, Kotaro Miyao, Yukiyasu Ozawa, Tatsunori Goto, Akio Kohno, Kazutaka Ozeki, Yasushi Onishi and 22 more

Abstract readObservational Study
PubMed Publisher
In one paragraph

Observational study in Bone marrow transplantation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

4 citing papers in PubMed, 11 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. 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

32 authors at 17 institutions in 1 country.

Seitaro TerakuraDepartment of Hematology and Oncology, Nagoya University Graduate School of Medicine, Nagoya, Japan. tseit@med.nagoya-u.ac.jp.ORCID http://orcid.org/0000-0002-1194-8046
Tetsuya NishidaDepartment of Hematology and Oncology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Masashi SawaDepartment of Hematology and Oncology, Anjo Kosei Hospital, Anjo, Japan.
Tomonori KatoDepartment of Hematology and Oncology, Anjo Kosei Hospital, Anjo, Japan.
Kotaro MiyaoDepartment of Hematology and Oncology, Anjo Kosei Hospital, Anjo, Japan.
Yukiyasu OzawaDepartment of Hematology, Japanese Red Cross Nagoya First Hospital, Nagoya, Japan.
Tatsunori GotoDepartment of Hematology, Japanese Red Cross Nagoya First Hospital, Nagoya, Japan.
Akio KohnoDepartment of Hematology and Oncology, JA Aichi Konan Kosei Hospital, Konan, Japan.
Kazutaka OzekiDepartment of Hematology and Oncology, JA Aichi Konan Kosei Hospital, Konan, Japan.
Yasushi OnishiDepartment of Hematology and Rheumatology, Tohoku University Hospital, Sendai, Japan.
Noriko FukuharaDepartment of Hematology and Rheumatology, Tohoku University Hospital, Sendai, Japan.
Nobuharu FujiiDepartment of Hematology and Oncology, Okayama University Graduate School of Medicine, Okayama, Japan.
Hisayuki YokoyamaDepartment of Hematology, National Hospital Organization Sendai Medical Center, Sendai, Japan.
Masanobu KasaiDepartment of Hematology and Oncology, Japanese Red Cross Nagoya Daini Hospital, Nagoya, Japan.
Hiroatsu IidaDepartment of Hematology, Meitetsu Hospital, Nagoya, Japan.
Nobuhiro KanemuraDepartment of Hematology, Gifu University Graduate School of Medicine, Gifu, Japan.
Tomoyuki EndoDepartment of Hematology, Hokkaido University Hospital, Sapporo, Japan.
Hiroatsu AgoDepartment of Hematology and Oncology, Shimane Prefectural Central Hospital, Izumo, Japan.
Makoto OnizukaDepartment of Hematology and Oncology, Tokai University Hospital, Isehara, Japan.
Satoshi IyamaDepartment of Hematology, Sapporo Medical University Hospital, Sapporo, Japan.
Yuichiro NawaDepartment of Hematology, Ehime Prefectural Central Hospital, Matsuyama, Japan.
Mika NakamaeDepartment of Hematology, Osaka City University Graduate School of Medicine, Osaka, Japan.
Yasuyuki NagataDepartment of Hematology, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Shingo KurahashiDivision of Hematology and Oncology, Toyohashi Municipal Hospital, Toyohashi, Japan.
Yasuo TomiyaDepartment of Hematology, Miyagi Cancer Center, Natori, Japan.
Atsumi YanagisawaJapanese Data Center for Hematopoietic Cell Transplantation, Nagoya, Japan.
Ritsuro SuzukiDepartment of Oncology and Hematology, Shimane University Hospital, Izumo, Japan.
Yachiyo KuwatsukaJapanese Data Center for Hematopoietic Cell Transplantation, Nagoya, Japan.
Yoshiko AtsutaJapanese Data Center for Hematopoietic Cell Transplantation, Nagoya, Japan.
Koichi MiyamuraDepartment of Hematology, Japanese Red Cross Nagoya First Hospital, Nagoya, Japan.
Makoto MurataDepartment of Hematology and Oncology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Nagoya Blood and Marrow Transplantation Group
Anjo Kosei Hospital · JPKonan Kosei Hospital · JPNagoya University · JPHamamatsu University School of Medicine · JPMeitetsu Hospital · JPMiyagi Prefectural Hospital Organization · JPNagoya University Hospital · JPOkayama University · JPShimane University Hospital · JPTokai University Hospital · JPHokkaido University Hospital · JPOsaka City University · JPSapporo Medical University Hospital · JPSendai Medical Center · JPShimane Prefectural Central Hospital · JPThe Japanese Data Center for Hematopoietic Cell Transplantation · JPTohoku University Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A prospectively registered observational study was conducted to assess the significance of allogeneic hematopoietic stem cell transplantation from highly HLA-matched unrelated donors (UD) and cord blood (CB) on outcomes in adult acute leukemia (AL) and myelodysplastic syndrome (MDS). Between 2007 and 2015, 231 transplant-eligible patients were registered for a phase 2 study of alternative donor transplantation. After registration, a sufficient time period was given to find appropriate UD. Patients received CB transplantation (CBT) if an appropriate UD was unavailable. In total, 119 patients received CBT (106 AL and 13 MDS) and 91 patients received UD transplantation (UDT) (86 AL and 5 MDS). The median age was 39 years in both groups. The primary objective was overall survival (OS); secondary objectives included cumulative incidences of non-relapse mortality (NRM) and relapse, and disease-free survival. Diagnosis, disease status at transplantation, refined disease risk index, and hematopoietic cell transplant-specific comorbidity index did not differ between UDT and CBT. In multivariate analyses, graft source was not a significant risk factor for all objectives. In adjusted analyses, UDT and CBT showed similar OS, NRM, and relapse in this prospective study. CB can be a comparable alternative stem cell source to UD by achieving a timely transplant.

Indexed as

Graft vs Host DiseaseHematopoietic Stem Cell TransplantationLeukemia, Myeloid, AcuteMyelodysplastic SyndromesAdultFetal BloodHumansProspective StudiesRetrospective StudiesUnrelated Donors

Identifiers

PMID32203259
OpenAlexW3010731801

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.