Chromosomal analysis of myelodysplastic syndromes among atomic bomb survivors in Nagasaki

Summary The myelodysplastic syndromes (MDS) are clonal haematopoietic disorders that develop de novo and also secondary to chemotherapy and/or radiation therapy. We previously demonstrated that the risk of MDS is increased among atomic bomb survivors with significant correlation to radiation dose; h...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:British journal of haematology 2018-02, Vol.180 (3), p.381-390
Hauptverfasser: Horai, Makiko, Satoh, Shinya, Matsuo, Masatoshi, Iwanaga, Masako, Horio, Kensuke, Jo, Tatsuro, Takasaki, Yumi, Kawaguchi, Yasuhisa, Tsushima, Hideki, Yoshida, Shinichiro, Taguchi, Masataka, Itonaga, Hidehiro, Sawayama, Yasushi, Taguchi, Jun, Imaizumi, Yoshitaka, Hata, Tomoko, Moriuchi, Yukiyoshi, Haase, Detlef, Yoshiura, Koh‐Ichiro, Miyazaki, Yasushi
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Summary The myelodysplastic syndromes (MDS) are clonal haematopoietic disorders that develop de novo and also secondary to chemotherapy and/or radiation therapy. We previously demonstrated that the risk of MDS is increased among atomic bomb survivors with significant correlation to radiation dose; however, the clinical characteristics of these survivors have not been well analysed. In this study, we investigated chromosomal abnormalities of MDS among survivors. The frequency of abnormal karyotypes was significantly higher, with more very poor risk karyotypes, according to the revised International Prognostic Scoring System, among those exposed close to the hypocentre compared with unexposed cases. However, abnormal karyotype frequency did not reflect the prognosis of exposed cases with respect to distance from the hypocentre. In addition, there was no difference in prognosis between exposed and unexposed cases. Among proximally exposed cases (
ISSN:0007-1048
1365-2141
DOI:10.1111/bjh.15050