Effect of allogeneic HCT from unrelated donors in AML patients with intermediate- or poor-risk cytogenetics: a retrospective study from the Japanese Society for HCT.


Journal

Annals of hematology
ISSN: 1432-0584
Titre abrégé: Ann Hematol
Pays: Germany
ID NLM: 9107334

Informations de publication

Date de publication:
Dec 2020
Historique:
received: 05 07 2020
accepted: 07 09 2020
pubmed: 18 9 2020
medline: 15 12 2020
entrez: 17 9 2020
Statut: ppublish

Résumé

This study aimed to analyze the factors associated with outcomes of bone marrow transplantation (UR-BMT) or cord blood stem cell transplantation from unrelated donors (UR-CBT). We assessed the time from diagnosis to transplantation among acute myeloid leukemia (AML) patients with intermediate- or poor-risk cytogenetics to identify the potential clinical efficacy of transplantation. We retrospectively analyzed 5331 patients who received UR-BMT or UR-CBT between 2008 and 2017. Patients were divided into four groups according to time from diagnosis to transplantation: (1) UR-BMT and > 5 months (n = 2353), (2) UR-BMT and ≤ 5 months (n = 379), (3) UR-CBT and > 5 months (n = 1494), and (4) UR-CBT and ≤ 5 months (n = 1106). There was no difference in overall survival (OS) for transplantation at ≤5 months and > 5 months in patients with first complete remission for both UR-BMT and UR-CBT, but OS in patients with primary induction failure (PIF) and transplantation at ≤ 5 months was significantly higher in the UR-CBT group compared with that at >5 months (P < 0.001). Multivariate Cox regression analysis also showed that transplantation at >5 months in patients with PIF was an independent predictor of poorer OS. Therefore, UR-CBT at ≤ 5 months after diagnosis is an alternative option for AML patients with PIF.

Identifiants

pubmed: 32940726
doi: 10.1007/s00277-020-04261-6
pii: 10.1007/s00277-020-04261-6
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2927-2937

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Auteurs

Satoshi Yamasaki (S)

Department of Hematology and Clinical Research Institute, National Hospital Organization Kyushu Medical Center, Fukuoka, Japan. yamas009@gmail.com.

Jinichi Mori (J)

Department of Hematology, Jyoban Hospital, Iwaki, Japan.

Junya Kanda (J)

Department of Hematology and Oncology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

Nobuhiko Imahashi (N)

Department of Hematology, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.

Naoyuki Uchida (N)

Department of Hematology, Federation of National Public Service Personnel Mutual Aid Associations Toranomon Hospital, Tokyo, Japan.

Noriko Doki (N)

Hematology Division, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital, Tokyo, Japan.

Masatsugu Tanaka (M)

Department of Hematology, Kanagawa Cancer Center, Yokohama, Japan.

Yuta Katayama (Y)

Department of Hematology, Hiroshima Red Cross Hospital & Atomic-bomb Survivors Hospital, Hiroshima, Japan.

Tetsuya Eto (T)

Department of Hematology, Hamanomachi Hospital, Fukuoka, Japan.

Yukiyasu Ozawa (Y)

Department of Hematology, Japanese Red Cross Nagoya First Hospital, Nagoya, Japan.

Satoru Takada (S)

Leukemia Research Center, Saiseikai Maebashi Hospital, Maebashi, Japan.

Makoto Onizuka (M)

Department of Hematology and Oncology, Tokai University School of Medicine, Isehara, Japan.

Masayuki Hino (M)

Department of Hematology, Osaka City University, Osaka, Japan.

Yoshinobu Kanda (Y)

Division of Hematology, Jichi Medical University Saitama Medical Center, Saitama, Japan.

Takahiro Fukuda (T)

Division of Hematopoietic Stem Cell Transplantation, National Cancer Center Hospital, Tokyo, Japan.

Yoshiko Atsuta (Y)

Department of Healthcare Administration, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Japanese Data Center for Hematopoietic Cell Transplantation, Nagoya, Japan.

Masamitsu Yanada (M)

Department of Hematology and Cell Therapy, Aichi Cancer Center, Nagoya, Japan.

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