Impact of Donor Source on Allogeneic Hematopoietic Stem Cell Transplantation for Mature T Cell and Natural Killer Cell Neoplasms in the Kyoto Stem Cell Transplantation Group.

Allogenic hematopoietic stem cell transplantation Cord blood transplantation Donor source Mature T and NK cell neoplasms NK cell lymphomas/leukemia T cell lymphomas

Journal

Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation
ISSN: 1523-6536
Titre abrégé: Biol Blood Marrow Transplant
Pays: United States
ID NLM: 9600628

Informations de publication

Date de publication:
12 2020
Historique:
received: 06 04 2020
revised: 18 07 2020
accepted: 25 07 2020
pubmed: 2 8 2020
medline: 24 6 2021
entrez: 2 8 2020
Statut: ppublish

Résumé

Although allogeneic hematopoietic stem cell transplantation (allo-HSCT) is the key strategy to cure patients with mature T and natural killer (NK) cell lymphomas/leukemia, especially those with relapsed/refractory diseases, there is no consensus strategy for donor selection. We retrospectively analyzed the outcomes of allo-HSCT in 111 patients in 15 Japanese institutions as a multi-institutional joint research project. Thirty-nine patients received bone marrow or peripheral blood stem cell transplantation from related donors (rBMT/rPBSCT), 37 received BMT/PBSCT from unrelated donors (uBMT/uPBSCT), and 35 received cord blood transplantation (CBT). Overall survival (OS) and progression-free survival (PFS) at 4 years were 42% and 34%, respectively. The cumulative incidences of relapse and nonrelapse mortality were 43% and 25%. In multivariate analysis, CBT showed comparable OS with rBMT/rPBSCT (rBMT/rPBSCT versus CBT: hazard ratio [HR], 1.63; P = .264) and better OS compared with uBMT/uPBSCT (HR, 2.99; P = .010), with a trend toward a lower relapse rate (rBMT/rPBSCT versus CBT: HR, 2.60; P = .010; uBMT/uPBSCT versus CBT: HR, 2.05; P = .082). This superiority of CBT was more definite in on-disease patients (OS: rBMT/rPBSCT versus CBT: HR, 5.52; P = .021; uBMT/uPBSCT versus CBT: HR, 6.80; P = .007). Better disease control was also strongly associated with better OS and PFS with lower relapse rate. In conclusion, allo-HSCT is beneficial for the survival of patients with mature T and NK cell lymphomas/leukemia if performed in a timely fashion. Since CBT showed favorable survival with a lower relapse risk, it could be a preferred alternative, especially in on-disease patients.

Identifiants

pubmed: 32738500
pii: S1083-8791(20)30464-X
doi: 10.1016/j.bbmt.2020.07.032
pii:
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

2346-2358

Informations de copyright

Copyright © 2020 American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. All rights reserved.

Auteurs

Mizuki Watanabe (M)

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

Junya Kanda (J)

Department of Hematology and Oncology, Graduate School of Medicine, Kyoto University, Kyoto, Japan. Electronic address: jkanda16@kuhp.kyoto-u.ac.jp.

Yasuyuki Arai (Y)

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

Masakatsu Hishizawa (M)

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

Momoko Nishikori (M)

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

Takayuki Ishikawa (T)

Department of Hematology, Kobe City Medical Center General Hospital, Kobe, Japan.

Kazunori Imada (K)

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

Yasunori Ueda (Y)

Department of Hematology, Kurashiki Central Hospital, Kurashiki, Japan.

Takashi Akasaka (T)

Department of Hematology, Tenri Hospital, Tenri, Japan.

Akihito Yonezawa (A)

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

Masaharu Nohgawa (M)

Department of Hematology, Japanese Red Cross Wakayama Medical Center, Wakayama, Japan.

Toshiyuki Kitano (T)

Department of Hematology, Medical Research Institute Kitano Hospital, Osaka, Japan.

Mitsuru Itoh (M)

Department of Hematology, Kyoto City Hospital, Kyoto, Japan.

Tomoharu Takeoka (T)

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

Toshinori Moriguchi (T)

Department of Hematology, Kyoto-Katsura Hospital, Kyoto, Japan.

Kazuhiro Yago (K)

Department of Hematology, Shizuoka General Hospital, Shizuoka, Japan.

Nobuyoshi Arima (N)

Department of Hematology, Shinko Hospital, Kobe, Japan.

Naoyuki Anzai (N)

Department of Hematology and Oncology, Takatsuki Red Cross Hospital, Takatsuki, Japan.

Mitsumasa Watanabe (M)

Department of Hematology, Hyogo Prefectural Amagasaki General Medical Center, Amagasaki, Japan.

Tadakazu Kondo (T)

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

Akifumi Takaori-Kondo (A)

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

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