Evidence map›Paper›PMID 42008176›Full record

ArticleAnnals of hematology2026

HLA-matched versus haploidentical donor transplantation with post-transplant cyclophosphamide: a study on behalf of the donor/source working group of the Japanese society for transplantation and cellular therapy.

Yosuke Nakaya, Hirohisa Nakamae, Junichi Sugita, Junya Kanda, Yuta Hasegawa, Tetsuya Eto, Takahiro Fukuda, Naoki Kurita, Nobuhiro Hiramoto, Koji Nagafuji and 10 more

Abstract readComparative Study
In one paragraph

Article in Annals of hematology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

20 authors.

Yosuke NakayaDepartment of Hematology, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan.ORCID http://orcid.org/0000-0003-3337-1599
Hirohisa NakamaeDepartment of Hematology, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan. hirohisa@omu.ac.jp.ORCID http://orcid.org/0000-0003-4203-990X
Junichi SugitaDepartment of Hematology, Sapporo Hokuyu Hospital, Sapporo, Japan.ORCID http://orcid.org/0000-0003-3852-5075
Junya KandaDepartment of Hematology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.ORCID http://orcid.org/0000-0002-6704-3633
Yuta HasegawaDepartment of Hematology, Hokkaido University Hospital, Sapporo, Japan.ORCID http://orcid.org/0000-0002-9925-2093
Tetsuya EtoDepartment of Hematology, Hamanomachi Hospital, Fukuoka, Japan.ORCID http://orcid.org/0000-0002-2630-493X
Takahiro FukudaDepartment of Hematopoietic Stem Cell Transplantation, National Cancer Center Hospital, Tokyo, Japan.
Naoki KuritaDepartment of Hematology, University of Tsukuba Hospital, Tsukuba, Japan.ORCID http://orcid.org/0000-0002-1283-4307
Nobuhiro HiramotoDepartment of Hematology, Kobe City Medical Center General Hospital, Kobe, Japan.ORCID http://orcid.org/0000-0002-0472-6680
Koji NagafujiDivision of Hematology and Oncology, Department of Medicine, Kurume University Hospital, Kurume, Japan.ORCID http://orcid.org/0000-0003-4795-121X
Shuichi OtaDepartment of Hematology, Sapporo Hokuyu Hospital, Sapporo, Japan.ORCID http://orcid.org/0000-0002-3631-244X
Noboru AsadaDepartment of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.ORCID http://orcid.org/0000-0002-0148-644X
Toshihiko AndoDivision of Hematology, Respiratory Medicine and Oncology, Department of Internal Medicine, Faculty of Medicine, Saga University, Saga, Japan.
Toshiro KawakitaDepartment of Hematology, NHO Kumamoto Medical Center, Kumamoto, Japan.
Takashi AkasakaDepartment of Hematology, Tenri Hospital, Tenri, Japan.ORCID http://orcid.org/0000-0002-0131-2570
Yasuo Mori14. Hematology, Oncology & Cardiovascular medicine, Kyushu University Hospital, Fukuoka, Japan.ORCID http://orcid.org/0000-0001-6425-1720
Tomohiko KamimuraDepartment of Hematology, Harasanshin Hospital, Fukuoka, Japan.
Makoto OnizukaDepartment of Hematology/Oncology, Tokai University School of Medicine, Isehara, Japan.ORCID http://orcid.org/0000-0003-3864-0823
Yoshiko AtsutaJapanese Data Center for Hematopoietic Cell Transplantation, Nagoya, Japan.ORCID http://orcid.org/0000-0003-4404-2870
Hideki NakasoneDivision of Hematology, Jichi Medical University Saitama Medical Center, Saitama, Japan.ORCID http://orcid.org/0000-0001-5812-9315

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Post-transplant cyclophosphamide (PTCy) is now being increasingly applied to HLA-matched donor (MD) transplantation. Prior studies in Western countries have demonstrated that allogeneic hematopoietic cell transplantation (allo-HCT) employing PTCy yields better outcomes with HLA-matched donors (MDs) than with haploidentical donors (HIDs). However, the effect of HLA mismatch may differ among racial groups. We retrospectively analyzed adult patients with hematological malignancies who underwent their first allo-HCT with PTCy from MDs or HIDs registered to the Japanese registry database between 2013 and 2021. Among 63 (related, n = 33; unrelated, n = 30) and 1261 patients who received MD and HID allo-HCT with PTCy, 50 (related, n = 30; unrelated, n = 20) and 100 patients were assigned to MD and HID groups by 1:2 propensity score matching (PSM). The results showed that MD recipients had better neutrophil recovery (hazard ratio [HR], 1.48; 95% confidence interval [CI], 1.04–2.10; P = 0.031) and lower risk of non-relapse mortality (NRM) (HR, 0.19; 95% CI, 0.05–0.81; P = 0.024) than HID recipients. Multivariable analyses in the entire cohort before PSM confirmed these findings. Fatal infection was the primary cause of NRM in the HID group. This study is the first to demonstrate that, within a homogeneous Asian cohort, MD may have an advantage over HID in PTCy-based allo-HCT in facilitating neutrophil engraftment and reducing the risk of NRM.

Indexed as

CyclophosphamideHematologic NeoplasmsHematopoietic Stem Cell TransplantationHLA AntigensTransplantation, HaploidenticalAdultAgedEast Asian PeopleFemaleHistocompatibility TestingHumansImmunosuppressive AgentsJapanMaleMiddle AgedRegistriesCyclophosphamideHLA AntigensImmunosuppressive AgentsGraft-versus-host diseaseHaploidentical donorHematological malignancies.Matched donorPost-transplant cyclophosphamide

Identifiers

PMID42008176
PMCPMC13095949

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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.