Evidence map›Paper›PMID 38486829›Full record

ArticleBlood cell therapy2024

Efficacy of off-the-shelf bone marrow mesenchymal stem cells for pediatric steroid-refractory acute graft-versus-host disease.

Hirohito Kubota, Yuki Arakawa, Yoshitaka Mizushima, Tomoya Irikura, Mai Watakabe, Takahiro Ishikawa, Ryota Kaneko, Mamoru Honda, Yuichi Mitani, Kohei Fukuoka and 3 more

Abstract read
In one paragraph

Article in Blood cell therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Observational
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.

Hirohito KubotaDepartment of Hematology/Oncology, Saitama Children's Medical Center, Saitama, Japan.
Yuki ArakawaDepartment of Hematology/Oncology, Saitama Children's Medical Center, Saitama, Japan.
Yoshitaka MizushimaDepartment of Hematology/Oncology, Saitama Children's Medical Center, Saitama, Japan.
Tomoya IrikuraDepartment of Hematology/Oncology, Saitama Children's Medical Center, Saitama, Japan.
Mai WatakabeDepartment of Hematology/Oncology, Saitama Children's Medical Center, Saitama, Japan.
Takahiro IshikawaDepartment of Hematology/Oncology, Saitama Children's Medical Center, Saitama, Japan.
Ryota KanekoDepartment of Hematology/Oncology, Saitama Children's Medical Center, Saitama, Japan.
Mamoru HondaDepartment of Hematology/Oncology, Saitama Children's Medical Center, Saitama, Japan.
Yuichi MitaniDepartment of Hematology/Oncology, Saitama Children's Medical Center, Saitama, Japan.
Kohei FukuokaDepartment of Hematology/Oncology, Saitama Children's Medical Center, Saitama, Japan.
Makiko MoriDepartment of Hematology/Oncology, Saitama Children's Medical Center, Saitama, Japan.
Koichi OshimaDepartment of Hematology/Oncology, Saitama Children's Medical Center, Saitama, Japan.
Katsuyoshi KohDepartment of Hematology/Oncology, Saitama Children's Medical Center, Saitama, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Temcell is a mesenchymal stem cell (MSC) product approved for steroid-refractory acute graft-versus-host disease (SR-aGVHD) in Japan. However, reports regarding Temcell's efficacy in pediatric patients have been scarce, and the appropriate use of MSC therapy against pediatric SR-aGVHD also remains to be determined. Patients and Methods: We retrospectively assessed a cohort of pediatric patients treated with Temcell for SR-aGVHD following allogeneic hematopoietic transplantation. MSCs were infused intravenously at a dose of 2 × 10 Results: Twelve patients received eighteen cycles of MSC therapy (median age, 10.3 [1.7-17.8] years), with four receiving additional cycles (one cycle: n = 3, three cycles: n = 1). The severity of aGVHD before MSC therapy was grade I-II in three patients and grade III-IV in nine patients (gut stage 3-4, n= 7; liver stage 3-4; n =2). The median number of immunosuppressive therapy regimens received prior to MSC administration was two (range: 1-5). The first MSC cycle displayed the best overall response rate of 83%, including six patients with a complete response (CR) and with a 49% reduction in the mean daily dose of prednisone after eight weeks. The median time to first response was 3.5 days (range: 2-15 days). Two of the four patients who were re-administered MSCs for recurrent or persistent GVHD achieved a CR. The three-year overall survival rate was 69.4%, while the three-year failure free survival (FFS) rate was 22.2%, with a median FFS of 4.9 months. There were no observable side effects of MSC therapy. Conclusions: MSC therapy appears to be an effective and safe treatment for pediatric SR-aGVHD, with a steroid-sparing effect and satisfactory efficacy upon re-administration. Further studies are needed to determine its appropriate combination with additional treatments and the optimal use of re-administration of MSCs.

Indexed as

mesenchymal stem cellpediatric hematopoietic stem cell transplantationsteroid-refractory acute graft-versus-host diseasetemcell

Identifiers

PMID38486829
PMCPMC10937086

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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.