論文

査読有り 国際誌
2020年6月

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

BONE MARROW TRANSPLANTATION
  • Kato, Motohiro
  • Nakasone, Hideki
  • Nakano, Nobuaki
  • Fuji, Shigeo
  • Shinohara, Akihito
  • Yokoyama, Hisayuki
  • Sakashita, Kazuo
  • Hori, Tsukasa
  • Takahashi, Satoshi
  • Nara, Miho
  • Kanda, Yoshinobu
  • Mori, Takehiko
  • Takita, Junko
  • Kawaguchi, Hiroshi
  • Kawakita, Toshiro
  • Ichinohe, Tatsuo
  • Fukuda, Takahiro
  • Atsuta, Yoshiko
  • Ogata, Masao
  • 全て表示

55
6
開始ページ
1023
終了ページ
1028
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1038/s41409-019-0765-0
出版者・発行元
NATURE PUBLISHING GROUP

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.

リンク情報
DOI
https://doi.org/10.1038/s41409-019-0765-0
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/31819152
ID情報
  • DOI : 10.1038/s41409-019-0765-0
  • ISSN : 0268-3369
  • PubMed ID : 31819152

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