Role of alternative donor allogeneic hematopoietic stem cell transplantation in patients with intermediate- or poor-risk acute myeloid leukemia in first complete remission.


Journal

Bone marrow transplantation
ISSN: 1476-5365
Titre abrégé: Bone Marrow Transplant
Pays: England
ID NLM: 8702459

Informations de publication

Date de publication:
12 2019
Historique:
received: 30 08 2018
accepted: 30 04 2019
revised: 29 04 2019
pubmed: 4 6 2019
medline: 18 9 2020
entrez: 2 6 2019
Statut: ppublish

Résumé

Allogeneic hematopoietic stem cell transplantation (HCT) offers the most effective prevention of relapse and has significant overall survival (OS) benefits for patients with acute myeloid leukemia (AML) in first complete remission (CR1). We conducted a retrospective analysis of a cohort of patients with intermediate- or poor-risk AML. The purpose of the present study was to investigate the role of alternative donors for AML in CR1. We analyzed 1561 patients who underwent HCT from an HLA-matched related donor (MRD), HLA 8/8-matched unrelated donor (MUD), or umbilical cord blood (UCB). The results of a multivariate analysis showed that HCT from UCB (HR = 1.28, 95% CI: 1.07-1.52), age ≥50 years (HR = 1.36, 95% CI: 1.14-1.62), male (HR = 1.42, 95% CI: 1.21-1.66), PS > 1 (HR = 1.68, 95% CI: 1.17-2.42), and poor-risk cytogenetics (HR = 1.53, 95% CI: 1.29-1.81) had an inferior prognostic impact on OS. We conclude that an MUD is the best alternative to an HLA identical MRD for patients with AML in CR1. UCB is an alternative option if neither MRD nor MUD are available, or when patients need to receive urgent HCT for poor-risk AML in CR1.

Identifiants

pubmed: 31152148
doi: 10.1038/s41409-019-0571-8
pii: 10.1038/s41409-019-0571-8
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2004-2012

Références

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Auteurs

Shingo Yano (S)

Division of Clinical Oncology and Hematology, Department of Internal Medicine, The Jikei University School of Medicine, Tokyo, Japan. yano@jikei.ac.jp.

Hiroki Yokoyama (H)

Division of Clinical Oncology and Hematology, Department of Internal Medicine, The Jikei University School of Medicine, Tokyo, Japan.

Masamitsu Yanada (M)

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

Jinichi Mori (J)

Division of Hematology, Jyoban Hospital Tokiwa Foundation, Fukushima, Japan.

Jun Aoki (J)

Department of Hematology, Yokohama City University Medical Center, Yokohama, Japan.

Kazuteru Ohashi (K)

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

Heiwa Kanomori (H)

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

Yuichiro Ozawa (Y)

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

Masashi Sawa (M)

Department of Hematology and Oncology, Anjo Kosei Hospital, Anjo, Japan.

Hiroshisa Nakamae (H)

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

Tetsuya Eto (T)

Department of Hematology, Hamanomachi Hospital, Fukuoka, Japan.

Shuichi Ohta (S)

Department of Hematology, Sapporo Hokuyu Hospital, Sapporo, Japan.

Junji Tanaka (J)

Department of Hematology, Tokyo Women's Medical University, Tokyo, Japan.

Tatsuo Ichinohe (T)

Department of Hematology and Oncology, Research Institute for Radiation Biology and Medicine, Hiroshima University, Hiroshima, Japan.

Yoshiko Atsuta (Y)

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

Akiyoshi Takami (A)

Division of Hematology, Department of Internal Medicine, School of Medicine, Aichi Medical University, Nagakute, Japan.

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