Evidence map›Paper›PMID 41368188›Full record

ArticleBlood cell therapy2025

Successful Neutrophil Engraftment with Continued Ruxolitinib in Cord Blood Transplantation.

Tomohiro Nagano, Takumi Kondo, Ryuichiro Hiyama, Daisuke Ikeda, Kenta Hayashino, Yusuke Inoue, Masaya Ueno, Yayoi Ueda, Saya Kubota, Hiroki Kobayashi and 8 more

Abstract readCase Reports
In one paragraph

Article in Blood cell therapy, 2025. 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

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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

18 authors.

Tomohiro NaganoDepartment of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.
Takumi KondoDepartment of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.
Ryuichiro HiyamaDepartment of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.
Daisuke IkedaDepartment of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.
Kenta HayashinoDepartment of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.
Yusuke InoueDepartment of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.
Masaya UenoDepartment of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.
Yayoi UedaDepartment of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.
Saya KubotaDepartment of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.
Hiroki KobayashiDepartment of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.
Keisuke SeikeDepartment of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.
Hideaki FujiwaraDepartment of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.
Noboru AsadaDepartment of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.
Daisuke EnnishiDepartment of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.
Keiko FujiiDepartment of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.
Nobuharu FujiiDepartment of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.
Ken-Ichi MatsuokaDepartment of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.
Yoshinobu MaedaDepartment of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Janus kinase (JAK)-signal transducer and activator of transcription (STAT) pathway is crucial for immune function and hematopoiesis, which partly explains why cytopenia is a major adverse effect of ruxolitinib, a selective JAK1/2 inhibitor. Hematologic toxicity restricts the use of ruxolitinib during the pre-engraftment phase of allogeneic hematopoietic stem cell transplantation for myelofibrosis and graft-versus-host disease (GVHD) prophylaxis. While some reports have described its use in peripheral blood and bone marrow transplantation, its application in cord blood transplantation (CBT) remains unknown. Herein, we report two cases of CBT in which ruxolitinib was administered to treat GVHD after prior allogeneic transplantation. In Case 1, a patient underwent a third transplant for acute myeloid leukemia, and in Case 2, a patient received CBT for post-transplant lymphoproliferative disorder following transplantation for classic Hodgkin lymphoma. Neutrophil engraftment was achieved in both cases, and Case 2 developed a pre-engraftment immune reaction. Platelet and red blood cell engraftment did not occur in either case, likely due to underlying comorbidities or limited survival, rather than the effects of ruxolitinib. This is the first report documenting successful neutrophil engraftment in CBT with concurrent ruxolitinib administration, suggesting its potential feasibility during the pre-engraftment phase. Further studies are warranted to evaluate its effects on multilineage hematopoietic recovery, infections, GVHD, and relapse risk.

Indexed as

case reportcord blood transplantationgraft-versus-host diseaseneutrophil engraftmentruxolitinib

Identifiers

PMID41368188
PMCPMC12682611

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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.