Evidence map›Paper›PMID 31819152›Full record

ArticleBone marrow transplantation2020

Clinical course of autologous recovery with chromosomal abnormalities after allogeneic hematopoietic stem cell transplantation.

Motohiro Kato, Hideki Nakasone, Nobuaki Nakano, Shigeo Fuji, Akihito Shinohara, Hisayuki Yokoyama, Kazuo Sakashita, Tsukasa Hori, Satoshi Takahashi, Miho Nara 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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.1field-weighted citation impact, top 20% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
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.

Motohiro KatoChildren's Cancer Center, National Center for Child Health and Development, Tokyo, Japan. katom-tky@umin.ac.jp.ORCID http://orcid.org/0000-0001-5145-1774
Hideki NakasoneDivision of Hematology, Jichi Medical University Saitama Medical Center, Saitama, Japan.
Nobuaki NakanoDepartment of Hematology, Imamura General Hospital, Kagoshima, Japan.
Shigeo FujiDepartment of Hematology, Osaka International Cancer Center, Osaka, Japan.ORCID http://orcid.org/0000-0001-5118-7950
Akihito ShinoharaDepartment of Hematology, Tokyo Women's Medical University, Tokyo, Japan.
Hisayuki YokoyamaDepartment of Hematology, National Hospital Organization Sendai Medical Center, Sendai, Japan.
Kazuo SakashitaDepartment of Hematology/Oncology, Nagano Children's Hospital, Nagano, Japan.
Tsukasa HoriDepartment of Pediatrics, Sapporo Medical University Hospital, Sapporo, Japan.
Satoshi TakahashiDivision of Molecular Therapy, the Advanced Clinical Research Center, the Institute of Medical Science, the University of Tokyo, Tokyo, Japan.
Miho NaraDivision of Hematology, Nephrology and Rheumatology, Akita University Hospital, Akita, Japan.
Yoshinobu KandaDivision of Hematology, Jichi Medical University Saitama Medical Center, Saitama, Japan.
Takehiko MoriDivision of Hematology, Department of Medicine, Keio University School of Medicine, Tokyo, Japan.ORCID http://orcid.org/0000-0002-8176-4760
Junko TakitaDepartment of Pediatrics, Kyoto University Hospital, Kyoto, Japan.
Hiroshi KawaguchiDepartment of Pediatrics, Hiroshima University Graduate School of Biomedical & Health Sciences, Hiroshima, Japan.ORCID http://orcid.org/0000-0003-0036-451X
Toshiro KawakitaDepartment of Hematology, National Hospital Organization Kumamoto Medical Center, Kumamoto, Japan.
Tatsuo IchinoheDepartment of Hematology and Oncology, Research Institute for Radiation Biology and Medicine, Hiroshima, Japan.
Takahiro FukudaHematopoietic Stem Cell Transplantation Division, National Cancer Center Hospital, Tokyo, Japan.
Yoshiko AtsutaJapanese Data Center for Hematopoietic Cell Transplantation, Nagoya, Japan.
Masao OgataDepartment of Hematology, Oita University Hospital, Oita, Japan.ORCID http://orcid.org/0000-0002-4896-5878
Transplantation Complication Working Group of the Japan Society for Hematopoietic Cell Transplantation
Jichi Medical University · JPHiroshima University · JPOita University Hospital · JPSapporo Medical University Hospital · JPSendai Medical Center · JPAkita University Hospital · JPImamura Hospital · JPKeio University · JPKumamoto Medical Center · JPNational Center For Child Health and Development · JPThe Japanese Data Center for Hematopoietic Cell Transplantation · JPTokyo Women's Medical University · JP

Funding

National Center for Child Health and Development (NCCHD) 28-5B
6 · The paper itself

Abstract

After primary graft failure following allogeneic hematopoietic stem cell transplantation, some patients experience autologous recovery of hematopoiesis without salvage transplantation. However, clinicians occasionally encounter unusual chromosomal abnormalities in recipient cells, not related to the original underlying diseases. In this study, through a survey based on data from the nationwide registry at the Japan Society for Hematopoietic Cell Transplantation, 42 patients were identified as having chromosomal abnormalities after autologous recovery. The complex chromosomal abnormalities were not consistent and randomly changed at each testing. Of the 42 patients, seven experienced disappearance of chromosome abnormalities without any treatment, and the probability was estimated as 17.4% (95% CI: 7.5-30.7%) at the 5-year observation. On the other hand, two patients developed hematologic malignancy at 1447 and 6202 days. Ten patients were alive without relapse or development of hematologic disorders, even though chromosomal abnormalities were continuously detected at a median of 3192 (103-4710) days. In conclusion, chromosomal abnormalities can persist for more than 10 years, and may eventually contribute to hematologic malignancy development in a small fraction of cases. Although oncogenic effects of the chromosomal abnormalities are still unclear, these findings may provide supporting evidence for late occurrence of secondary malignant neoplasms after cancer treatment.

Indexed as

Hematopoietic Stem Cell TransplantationNeoplasm Recurrence, LocalChromosome AberrationsHumansJapanTransplantation, AutologousTransplantation, Homologous

Identifiers

PMID31819152
OpenAlexW2992594891

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.