Reducing Mortality of Single-Unit Unrelated Cord Blood Transplantation for Relapsed Acute Myeloid Leukemia after a Previous Allogeneic Transplantation: A Real-World Retrospective Study Over the Past 19 Years in Japan.


Journal

Transplantation and cellular therapy
ISSN: 2666-6367
Titre abrégé: Transplant Cell Ther
Pays: United States
ID NLM: 101774629

Informations de publication

Date de publication:
11 2022
Historique:
received: 06 07 2022
revised: 02 08 2022
accepted: 04 08 2022
pubmed: 15 8 2022
medline: 8 11 2022
entrez: 14 8 2022
Statut: ppublish

Résumé

Relapse is the most common cause of treatment failure after allogeneic hematopoietic cell transplantation (HCT) for acute myeloid leukemia (AML). Second or subsequent allogeneic HCT using unrelated cord blood has been performed for adult patients with AML who have relapsed after a previous allogeneic HCT. Although outcomes after unrelated cord blood transplantation (CBT) as the first allogeneic HCT have significantly improved in recent years, it is unclear whether survival and engraftment improve after CBT as the second or subsequent allogeneic HCT for adult AML patients relapsing after a previous allogeneic HCT. The objective of this retrospective study was to evaluate trends of survival and other transplantation outcomes after single-unit unrelated CBT as a second or subsequent allogeneic HCT in adult patients with relapsed AML after a previous allogeneic HCT over the past 19 years in Japan. We retrospectively assessed survival trends and other outcomes of single-unit unrelated CBT as a second or subsequent allogeneic HCT in adult patients with relapsed AML after a previous allogeneic HCT according to the time period of CBT (2001-2007, 2008-2013, or 2014-2019) using a nationwide Japanese database. The median age was 45 years among 1109 CBTs, and 844 (78.6%) patients were not in complete remission at the time of CBT. Over the 3 time periods, there was a progressive increase in higher cryopreserved cord blood total nucleated cell dose and myeloablative conditioning regimens. The 2-year overall survival was 14.0% in 2001-2007, 19.9% in 2008-2013, and 24.4% in 2014-2019 (P <.001 by log-rank trend test). The 2-year relapse-related mortality was 54.0% in 2001-2007, 44.4% in 2008-2013, and 39.1% in 2014-2019 (P < 0.001 by Gray's test), but nonrelapse mortality was not significantly different across the time periods (P = 0.557 by Gray's test). The 42-day neutrophil engraftment also significantly improved (62.9% in 2001-2007, 69.7% in 2008-2013, and 79.9% in 2014-2019; P < 0.001 by Gray's test). Our data demonstrate significant improvements in overall and relapse-related mortality, as well as neutrophil engraftment, after single-unit unrelated CBT as a second or subsequent allogeneic HCT for adult patients with AML relapsed after previous allogeneic HCT over the past 19 years.

Identifiants

pubmed: 35964936
pii: S2666-6367(22)01544-5
doi: 10.1016/j.jtct.2022.08.006
pii:
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

777.e1-777.e11

Informations de copyright

Copyright © 2022 The American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest There are no conflicts of interest to report.

Auteurs

Takaaki Konuma (T)

Department of Hematology/Oncology, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan. Electronic address: tkonuma@ims.u-tokyo.ac.jp.

Shohei Mizuno (S)

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

Kaito Harada (K)

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

Naoyuki Uchida (N)

Department of Hematology, Toranomon Hospital, Tokyo, Japan.

Satoshi Takahashi (S)

Division of Clinical Precision Research Platform, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.

Tetsuya Eto (T)

Department of Hematology, Hamanomachi Hospital, Fukuoka, Japan.

Shuichi Ota (S)

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

Hikaru Kobayashi (H)

Department of Hematology, Nagano Red Cross Hospital, Nagano, Japan.

Yuta Katayama (Y)

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

Yasuo Mori (Y)

Hematology, Oncology & Cardiovascular medicine, Kyushu University Hospital, Fukuoka, Japan.

Yumiko Maruyama (Y)

Department of Hematology, University of Tsukuba Hospital, Tsukuba, Japan.

Makoto Onizuka (M)

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

Akihito Yonezawa (A)

Department of Hematology, Kokura Memorial Hospital, Fukuoka, Japan.

Toshiro Kawakita (T)

Department of Hematology, National Hospital Organisation Kumamoto Medical Center, Kumamoto, Japan.

Takafumi Kimura (T)

Preparation Department, Japanese Red Cross Kinki Block Blood Center, Osaka, Japan.

Yoshinobu Kanda (Y)

Division of Hematology, Jichi Medical University, Tochigi, Japan.

Takahiro Fukuda (T)

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

Yoshiko Atsuta (Y)

Japanese Data Center for Hematopoietic Cell Transplantation, Nagoya, Japan; Department of Registry Science for Transplant and Cellular Therapy, Aichi Medical University School of Medicine, Nagakute, Japan.

Masamitsu Yanada (M)

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

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