A Prospective, Longitudinal Observation of the Incidence, Treatment, and Survival of Late Acute and Chronic Graft-versus-Host Disease by National Institutes of Health Criteria in a Japanese Cohort.


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:
01 2020
Historique:
received: 02 08 2019
revised: 13 09 2019
accepted: 13 09 2019
pubmed: 20 9 2019
medline: 22 1 2021
entrez: 20 9 2019
Statut: ppublish

Résumé

To prospectively validate the incidence, manifestations, and outcomes of graft-versus-host disease (GVHD) by National Institutes of Health criteria, we recruited 406 hematopoietic stem cell transplantation recipients at 16 transplant centers in Japan from May 2012 to June 2014. The 2-year cumulative incidence of late acute and chronic GVHD was 3.2% (n = 13) and 35.4% (n = 145), with a median onset of 3.6 and 4.7 months after transplant, respectively. The global severity at onset was mild in 30.3%, moderate in 43.5%, and severe in 26.2%. Eighty-two patients were followed up for 2 years, with 79.3% still manifesting GVHD symptoms, and 80.6% (n = 117) of the patients received systemic immunosuppressive treatment (IST), with a 2-year cumulative incidence of IST termination of 33.1%. Severe patients showed a significantly lower rate of IST termination than those with mild and moderate severities (mild, 38.5%; moderate, 40.9%; and severe, 17.2%). The 2-year incidence of nonrelapse mortality (NRM) and relapse was not significantly different according to the severity at onset (NRM: mild [16.6%] versus moderate [8.7%] versus severe [16.1%]; relapse: mild [14.9%] versus moderate [14.7%] versus severe [5.3%]). As a result, 2-year overall survival (OS) and GVHD-specific survival (GSS) were equivalent according to the severity at onset (mild: OS = 81.0%, GSS = 85.7%; moderate: OS = 84.2%, GSS = 92.5%; severe: OS = 83.9%, GSS = 89.2%). Our study helped identify the characteristics of late acute and chronic GVHD in Japanese patients. Further investigation is needed to identify an optimal endpoint for survival prediction.

Identifiants

pubmed: 31536824
pii: S1083-8791(19)30627-5
doi: 10.1016/j.bbmt.2019.09.016
pii:
doi:

Types de publication

Clinical Trial Journal Article Multicenter Study Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

162-170

Informations de copyright

Copyright © 2019 American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. All rights reserved.

Auteurs

Chikako Ohwada (C)

Department of Hematology, Chiba University Hospital, Chiba, Japan. Electronic address: chikako_ohwada@faculty.chiba-u.jp.

Emiko Sakaida (E)

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

Aiko Igarashi (A)

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

Takeshi Kobayashi (T)

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

Noriko Doki (N)

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

Takehiko Mori (T)

Division of Hematology, Department of Medicine, Keio University School of Medicine, Tokyo, Japan.

Jun Kato (J)

Division of Hematology, Department of Medicine, Keio University School of Medicine, Tokyo, Japan.

Yuya Koda (Y)

Division of Hematology, Department of Medicine, Keio University School of Medicine, Tokyo, Japan.

Heiwa Kanamori (H)

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

Masatsugu Tanaka (M)

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

Takayoshi Tachibana (T)

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

Shin Fujisawa (S)

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

Yuki Nakajima (Y)

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

Ayumi Numata (A)

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

Masako Toyosaki (M)

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

Yasuyuki Aoyama (Y)

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

Makoto Onizuka (M)

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

Maki Hagihara (M)

Department of Hematology and Clinical Immunology, Yokohama City University School of Medicine, Kanagawa, Japan.

Satoshi Koyama (S)

Department of Hematology and Clinical Immunology, Yokohama City University School of Medicine, Kanagawa, Japan.

Yoshinobu Kanda (Y)

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

Hideki Nakasone (H)

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

Hiroaki Shimizu (H)

Department of Hematology, Gunma University Graduate School of Medicine, Gunma, Japan.

Seiko Kato (S)

Department of Hematology/Oncology, The Institute of Medical Science, University of Tokyo, Tokyo, Japan.

Reiko Watanabe (R)

Department of Hematology, Saitama Medical Center, Saitama Medical University, Saitama, Japan.

Katsuhiro Shono (K)

Department of Hematology, Chiba Aoba Municipal Hospital, Chiba, Japan.

Rika Sakai (R)

Department of Medical Oncology, Kanagawa Cancer Center, Kanagawa, Japan.

Takeshi Saito (T)

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

Chiaki Nakaseko (C)

Department of Hematology, International University of Health and Welfare School of Medicine, Chiba, Japan.

Shinichiro Okamoto (S)

The Kanto Study Group for Cell Therapy (KSGCT).

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