Evidence map›Paper›PMID 34508178›Full record

ArticleBone marrow transplantation2021

Prognostic value of the revised International Prognostic Scoring System five-group cytogenetic abnormality classification for the outcome prediction of hematopoietic stem cell transplantation in pediatric myelodysplastic syndrome.

Shohei Yamamoto, Motohiro Kato, Kenichiro Watanabe, Sae Ishimaru, Daisuke Hasegawa, Maiko Noguchi, Asahito Hama, Maho Sato, Takashi Koike, Fuminori Iwasaki and 8 more

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Article in Bone marrow transplantation, 2021. 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
0.6field-weighted citation impact, top 32% 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, 5 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

18 authors at 13 institutions in 1 country.

Shohei YamamotoDepartment of Cell Transplantation and Regenerative Medicine, Tokai University School of Medicine, Kanagawa, Japan. shohei-y@tsc.u-tokai.ac.jp.
Motohiro KatoChildren's Cancer Center, National Center for Child Health and Development, Tokyo, Japan.
Kenichiro WatanabeDepartment of Hematology and Oncology, Shizuoka Children's Hospital, Shizuoka, Japan.
Sae IshimaruDepartment of Pediatric Oncology, National Cancer Center Hospital, Tokyo, Japan.ORCID http://orcid.org/0000-0002-5437-8821
Daisuke HasegawaDepartment of Pediatrics, St Luke's International Hospital, Tokyo, Japan.ORCID http://orcid.org/0000-0002-9446-9568
Maiko NoguchiDepartment of Pediatrics, National Hospital Organization Kyushu Cancer Center, Fukuoka, Japan.
Asahito HamaDepartment of Hematology and Oncology, Children's Medical Center, Japanese Red Cross Nagoya First Hospital, Aichi, Japan.
Maho SatoDepartment of Hematology/Oncology, Osaka Women's and Children's Hospital, Osaka, Japan.
Takashi KoikeDivision of Cell Transplantation, Tokai University School of Medicine, Kanagawa, Japan.
Fuminori IwasakiDivision of Hemato-Oncology/Regenerative Medicine, Kanagawa Children's Medical Center, Kanagawa, Japan.
Hiroshi YagasakiDepartment of Pediatrics and Child Health, Nihon University Itabashi Hospital, Tokyo, Japan.
Yoshiyuki TakahashiDepartment of Pediatrics, Nagoya University Graduate School of Medicine, Aichi, Japan.
Yoshiyuki KosakaDepartment of Hematology and Oncology, Center of Childhood Cancer, Hyogo Prefectural Kobe Children's Hospital, Hyogo, Japan.
Yoshiko HashiiCancer Immunotherapy/Pediatrics, Osaka University Graduate School of Medicine, Osaka, Japan.
Akira MorimotoDepartment of Pediatrics, Jichi Medical University School of Medicine, Tochigi, Japan.
Yoshiko AtsutaDepartment of Healthcare Administration, Nagoya University Graduate School of Medicine, Japanese Data Center for Hematopoietic Cell Transplantation, Aichi, Japan.ORCID http://orcid.org/0000-0003-4404-2870
Daiichiro HasegawaDepartment of Hematology and Oncology, Center of Childhood Cancer, Hyogo Prefectural Kobe Children's Hospital, Hyogo, Japan.
Nao YoshidaDepartment of Hematology and Oncology, Children's Medical Center, Japanese Red Cross Nagoya First Hospital, Aichi, Japan.ORCID http://orcid.org/0000-0002-3783-2121
St. Luke's International Hospital · JPTokai University · JPJichi Medical University · JPKanagawa Children's Medical Center · JPKobe Children's Hospital · JPNagoya University · JPNational Center For Child Health and Development · JPNational Hospital Organization Kyushu Cancer Center · JPNihon University Itabashi Hospital · JPOsaka Women's and Children's Hospital · JPShizuoka Children's Hospital · JPThe Japanese Data Center for Hematopoietic Cell Transplantation · JPThe University of Osaka · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cytogenetic abnormalities are a major risk factor for relapse after hematopoietic stem cell transplantation (HSCT) for myelodysplastic syndrome (MDS). We aimed to evaluate the value of the five-group cytogenetic classification according to the revised International Prognostic Scoring System (R-IPSS) for predicting the outcome after HSCT in pediatric patients with MDS. We retrospectively analyzed the Japanese registration data of 242 pediatric patients with MDS. According to the R-IPSS classification, 112 (45.5%) patients had good, 55 (22.7%) had intermediate, 64 (26.4%) had poor, and 11 (4.6%) had very poor cytogenetics. The 5-year overall survival (5yOS) was 72%, 69%, 59%, and 30% in the good, intermediate, poor, and very poor cytogenetic subgroups (p = 0.026), respectively. The very good, good, and intermediate subgroups were grouped into a "standard" subgroup and reclassified into three subgroups (standard, poor, and very poor). Patients with very poor risk had worse 5yOS (hazard ratio 2.17, 95% confidence interval (CI) 1.02-4.61; p = 0.04) and a much higher 5yCIR (hazard ratio 2.52, 95% CI 1.05-6.04; p = 0.04) than those of patients in the standard group in the multivariate analysis, indicating that very poor risk cytogenetic characteristics independently predicted worse outcome after HSCT in pediatric patients with MDS.

Indexed as

Hematopoietic Stem Cell TransplantationMyelodysplastic SyndromesChildChromosome AberrationsHumansPrognosisRetrospective Studies

Identifiers

PMID34508178
OpenAlexW3198145801

What OpenQuestion holds

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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.