Evidence map›Paper›PMID 32444864›Full record

ArticleBone marrow transplantation2020

Conditioning regimen for allogeneic bone marrow transplantation in children with acquired bone marrow failure: fludarabine/melphalan vs. fludarabine/cyclophosphamide.

Nao Yoshida, Yoshiyuki Takahashi, Hiromasa Yabe, Ryoji Kobayashi, Kenichiro Watanabe, Kazuko Kudo, Miharu Yabe, Takako Miyamura, Katsuyoshi Koh, Hiroshi Kawaguchi and 10 more

Abstract read
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In one paragraph

Article 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 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 26% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

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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 at 12 institutions in 1 country.

Nao YoshidaDepartment of Hematology and Oncology, Children's Medical Center, Japanese Red Cross Nagoya First Hospital, Nagoya, Japan. nao-y@med.nagoya-u.ac.jp.ORCID http://orcid.org/0000-0002-3783-2121
Yoshiyuki TakahashiDepartment of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Hiromasa YabeDepartment of Innovative Medical Science, Tokai University School of Medicine, Isehara, Japan.ORCID http://orcid.org/0000-0001-6508-5496
Ryoji KobayashiDepartment of Pediatrics, Sapporo Hokuyu Hospital, Sapporo, Japan.ORCID http://orcid.org/0000-0002-3937-0856
Kenichiro WatanabeDepartment of Hematology and Oncology, Shizuoka Children's Hospital, Shizuoka, Japan.
Kazuko KudoDepartment of Pediatrics, Fujita Health University School of Medicine, Toyoake, Japan.
Miharu YabeDepartment of Innovative Medical Science, Tokai University School of Medicine, Isehara, Japan.ORCID http://orcid.org/0000-0003-0697-5506
Takako MiyamuraDepartment of Pediatrics, Osaka University Graduate School of Medicine, Osaka, Japan.
Katsuyoshi KohDepartment of Hematology/Oncology, Saitama Children's Medical Center, Saitama, Japan.
Hiroshi KawaguchiDepartment of Pediatrics, Hiroshima University Graduate School of Biomedical Sciences, Hiroshima, Japan.ORCID http://orcid.org/0000-0003-0036-451X
Hiroaki GotoDivision of Hematology/Oncology, Kanagawa Children's Medical Center, Yokohama, Japan.
Naoto FujitaDepartment of Pediatrics, Hiroshima Red Cross Hospital and Atomic-bomb Survivors Hospital, Hiroshima, Japan.
Keiko OkadaDepartment of Pediatric Hematology/Oncology, Osaka City General Hospital, Osaka, Japan.
Yasuhiro OkamotoDepartment of Pediatrics, Kagoshima University Hospital, Kagoshima, Japan.
Koji KatoCentral Japan Cord Blood Bank, Seto, Japan.
Masami InoueDepartment of Hematology/Oncology, Osaka Women's and Children's Hospital, Izumi, Japan.
Ritsuro SuzukiDepartment of HSCT Data Management & Biostatistics, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Yoshiko AtsutaJapanese Data Center for Hematopoietic Cell Transplantation, Nagoya, Japan.
Seiji KojimaDepartment of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Pediatric Aplastic Anemia Working Group of the Japan Society for Hematopoietic Cell Transplantation
Tokai University · JPHiroshima University · JPOsaka City General Hospital · JPOsaka Women's and Children's Hospital · JPThe Japanese Data Center for Hematopoietic Cell Transplantation · JPFujita Health University · JPHiroshima Red Cross Hospital & Atomic-bomb Survivors Hospital · JPJapanese Red Cross Nagoya Daiichi Hospital · JPKagoshima University Hospital · JPNagoya University · JPSaitama Children's Medical Center · JPSapporo Hokuyu Hospital · JP

Funding

Japan Agency for Medical Research and Development (AMED) 19ek0510023h0002
6 · The paper itself

Abstract

Fludarabine/cyclophosphamide-based conditioning regimens are standard in bone marrow transplantation (BMT) for acquired bone marrow failure in children, however, graft failure may occur. Using the data from a nationwide transplantation registry, we compared the outcomes of children aged <16 years with acquired aplastic anemia and refractory cytopenia of childhood who underwent allogeneic BMT with either fludarabine/melphalan (n = 71) or fludarabine/cyclophosphamide (n = 296) between 2000 and 2016. The fludarabine/melphalan regimen provided excellent outcomes, with 3-year overall survival and failure-free survival rates of 98% and 97%, respectively. The 83% 3-year failure-free survival in the fludarabine/cyclophosphamide group was significantly inferior (P = 0.002), whereas the overall survival did not differ between the two groups. Late graft failure was the most common cause of treatment failure in the fludarabine/cyclophosphamide group, which experienced a significantly higher incidence of late graft failure than the fludarabine/melphalan group (11% vs. 3%; P = 0.035). Multivariate analyses showed that the fludarabine/melphalan regimen was associated with a better failure-free survival (hazard ratio [HR] 0.12; P = 0.005) and lower risk of late graft failure (HR 0.16; P = 0.037). Fludarabine/melphalan-based conditioning regimen can be a promising option for children with acquired bone marrow failure receiving BMT.

Indexed as

Anemia, AplasticGraft vs Host DiseaseHematopoietic Stem Cell TransplantationBone Marrow TransplantationChildCyclophosphamideHumansMelphalanTransplantation ConditioningVidarabineCyclophosphamidefludarabineMelphalanVidarabine

Identifiers

PMID32444864
OpenAlexW3026184039

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.