Hematopoietic cell infusion-related adverse events in pediatric/small recipients in a prospective/multicenter study.


Journal

Transfusion
ISSN: 1537-2995
Titre abrégé: Transfusion
Pays: United States
ID NLM: 0417360

Informations de publication

Date de publication:
05 2020
Historique:
received: 14 08 2019
revised: 02 02 2020
accepted: 03 03 2020
pubmed: 20 4 2020
medline: 9 9 2020
entrez: 20 4 2020
Statut: ppublish

Résumé

Hematopoietic cell infusion-related adverse events (HCI-AEs) in hematopoietic stem cell transplantations (HSCTs) have been largely attributed to toxicity of dimethyl sulfoxide (DMSO) for cryopreservation, but HSC products also contain various cells and plasma components. Our recent prospective study of 1125 HSCT recipients revealed the highest overall HCI-AE rate in bone marrow transplantation (BMT) using fresh/noncryopreserved products, although products of peripheral blood stem cell transplantation and cord blood transplantation (CBT) are generally cryopreserved with DMSO containing smaller plasma volumes. We aimed to clarify if product volume and component effects are more substantial in small recipients including children. We performed subgroup analysis on 219 recipients of 45 kg or less body weight (whole small recipients), including 90 children (pediatric recipients), from the original cohort (general recipients). Whereas overall HCI-AE rates did not differ among hematopoietic stem cell sources in the general recipients, bradycardia most often occurred after CBT in whole small recipients. Conversely, whole small and general recipients shared the same trend of having the highest rate of hypertension in BMT. The overall HCI-AE rate was higher in allogeneic HSCT compared with autologous HSCT. Notably, pediatric recipients showed a 10-fold higher incidence of nausea and vomiting in allogeneic HSCT compared with autologous HSCT, suggesting a possible role of allogeneic antigens. Multivariate analysis identified a relatively large infusion volume per body weight as a significant factor correlating with HCI-AE in whole small recipients. We should be aware of product volume and specific HCI-AEs such as nausea and vomiting in small patients including children.

Sections du résumé

BACKGROUND
Hematopoietic cell infusion-related adverse events (HCI-AEs) in hematopoietic stem cell transplantations (HSCTs) have been largely attributed to toxicity of dimethyl sulfoxide (DMSO) for cryopreservation, but HSC products also contain various cells and plasma components. Our recent prospective study of 1125 HSCT recipients revealed the highest overall HCI-AE rate in bone marrow transplantation (BMT) using fresh/noncryopreserved products, although products of peripheral blood stem cell transplantation and cord blood transplantation (CBT) are generally cryopreserved with DMSO containing smaller plasma volumes. We aimed to clarify if product volume and component effects are more substantial in small recipients including children.
STUDY DESIGN AND METHODS
We performed subgroup analysis on 219 recipients of 45 kg or less body weight (whole small recipients), including 90 children (pediatric recipients), from the original cohort (general recipients).
RESULTS
Whereas overall HCI-AE rates did not differ among hematopoietic stem cell sources in the general recipients, bradycardia most often occurred after CBT in whole small recipients. Conversely, whole small and general recipients shared the same trend of having the highest rate of hypertension in BMT. The overall HCI-AE rate was higher in allogeneic HSCT compared with autologous HSCT. Notably, pediatric recipients showed a 10-fold higher incidence of nausea and vomiting in allogeneic HSCT compared with autologous HSCT, suggesting a possible role of allogeneic antigens. Multivariate analysis identified a relatively large infusion volume per body weight as a significant factor correlating with HCI-AE in whole small recipients.
CONCLUSIONS
We should be aware of product volume and specific HCI-AEs such as nausea and vomiting in small patients including children.

Identifiants

pubmed: 32306410
doi: 10.1111/trf.15786
doi:

Substances chimiques

Cryoprotective Agents 0
Dimethyl Sulfoxide YOW8V9698H

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1015-1023

Subventions

Organisme : Japan Society of Transfusion and Cell Therapy
Pays : International
Organisme : Ministry of Health, Labour and Welfare
Pays : International

Informations de copyright

© 2020 AABB.

Références

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Auteurs

Kazuhiko Ikeda (K)

Cell Therapy Committee, Japan Society of Transfusion Medicine and Cell Therapy, Tokyo, Japan.
Department of Blood Transfusion and Transplantation Immunology, Fukushima Medical University, Fukushima, Japan.

Hitoshi Ohto (H)

Cell Therapy Committee, Japan Society of Transfusion Medicine and Cell Therapy, Tokyo, Japan.
Department of Blood Transfusion and Transplantation Immunology, Fukushima Medical University, Fukushima, Japan.

Minami Yamada-Fujiwara (M)

Cell Therapy Committee, Japan Society of Transfusion Medicine and Cell Therapy, Tokyo, Japan.
Division of Blood Transfusion and Cell Therapy, Tohoku University Hospital, Sendai, Japan.

Yoshiki Okuyama (Y)

Cell Therapy Committee, Japan Society of Transfusion Medicine and Cell Therapy, Tokyo, Japan.
Division of Transfusion and Cell Therapy, Tokyo Metropolitan Komagome Hospital, Tokyo, Japan.

Shin-Ichiro Fujiwara (SI)

Cell Therapy Committee, Japan Society of Transfusion Medicine and Cell Therapy, Tokyo, Japan.
Division of Hematology, Department of Medicine, Jichi Medical University, Shimotsuke, Japan.

Kazuo Muroi (K)

Cell Therapy Committee, Japan Society of Transfusion Medicine and Cell Therapy, Tokyo, Japan.
Cell Transplantation and Transfusion, Jichi Medical University, Tochigi, Japan.

Takehiko Mori (T)

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

Kinuyo Kasama (K)

Department of Transfusion Medicine, Tokyo Jikei University Hospital, Tokyo, Japan.

Heiwa Kanamori (H)

Cell Therapy Committee, Japan Society of Transfusion Medicine and Cell Therapy, Tokyo, Japan.
Department of Hematology, Kanagawa Cancer Center, Yokohama, Japan.

Tohru Iseki (T)

Cell Therapy Committee, Japan Society of Transfusion Medicine and Cell Therapy, Tokyo, Japan.
Department of Transfusion Medicine and Cell Therapy, Chiba University Hospital, Chiba, Japan.

Tokiko Nagamura-Inoue (T)

Cell Therapy Committee, Japan Society of Transfusion Medicine and Cell Therapy, Tokyo, Japan.
Institution of Medical Science, University of Tokyo, Tokyo, Japan.

Kazuaki Kameda (K)

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

Junya Kanda (J)

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

Kazuhiro Nagai (K)

Transfusion and Cell Therapy Unit, Nagasaki University Hospital, Nagasaki, Japan.

Nobuharu Fujii (N)

Department of Transfusion Medicine, Okayama University Hospital, Okayama-shi, Japan.

Takashi Ashida (T)

Center for Transfusion and Cell Therapy, Kindai University Hospital, Osakasayama, Japan.

Asao Hirose (A)

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

Tsutomu Takahashi (T)

Department of Oncology/Hematology, Shimane University Hospital, Shimane, Japan.

Keiji Minakawa (K)

Department of Blood Transfusion and Transplantation Immunology, Fukushima Medical University, Fukushima, Japan.

Ryuji Tanosaki (R)

Cell Therapy Committee, Japan Society of Transfusion Medicine and Cell Therapy, Tokyo, Japan.

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