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Comparison of continuous and twice-daily infusions of cyclosporine A for graft-versus-host-disease prophylaxis in pediatric hematopoietic stem cell transplantation.
Umeda, Katsutsugu; Adachi, Souichi; Tanaka, Shiro; Ogawa, Atsushi; Hatakeyama, Naoki; Kudo, Kazuko; Sakata, Naoki; Igarashi, Shunji; Ohshima, Kumi; Hyakuna, Nobuyuki; Chin, Motoaki; Goto, Hiroaki; Takahashi, Yoshiyuki; Azuma, Eiichi; Koh, Katsuyoshi; Sawada, Akihisa; Kato, Koji; Inoue, Masami; Atsuta, Yoshiko; Takami, Akiyoshi; Murata, Makoto.
Afiliação
  • Umeda K; Department of Pediatrics, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
  • Adachi S; Human Health Sciences, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
  • Tanaka S; Department of Pharmacoepidemiology, Graduate School of Medicine and Public Health, Kyoto University, Kyoto, Japan.
  • Ogawa A; Department of Pediatrics, Niigata Cancer Center Hospital, Niigata, Japan.
  • Hatakeyama N; Department of Pediatrics, Sapporo Medical University Hospital, Sapporo, Japan.
  • Kudo K; Division of Hematology and Oncology, Shizuoka Children's Hospital, Shizuoka, Japan.
  • Sakata N; Department of Pediatrics, Kinki University, Faculty of Medicine, Osaka, Japan.
  • Igarashi S; Division of Pediatrics, Japanese Red Cross Narita Hospital, Narita, Japan.
  • Ohshima K; Division of Hematology, Saitama Medical Center, Jichi Medical University, Saitama, Japan.
  • Hyakuna N; Center of Bone Marrow Transplantation, Ryukyu University Hospital, Okinawa, Japan.
  • Chin M; Department of Pediatrics and Child Health, Nihon University Itabashi Hospital, Tokyo, Japan.
  • Goto H; Division of Hemato-oncology/Regeneration Medicine, Kanagawa Children's Medical Center, Kanagawa, Japan.
  • Takahashi Y; Department of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Azuma E; Department of Pediatrics and Cell Transplantation, Mie University Graduate School of Medicine, Mie, Japan.
  • Koh K; Department of Hematology/Oncology, Saitama Children's Medical Center, Saitama, Japan.
  • Sawada A; Department of Hematology/Oncology, Osaka Medical Center and Research Institute for Maternal and Child Health, Osaka, Japan.
  • Kato K; Department of Hematology and Oncology, Children's Medical Center, Japanese Red Cross Nagoya First Hospital, Nagoya, Japan.
  • Inoue M; Department of Hematology/Oncology, Osaka Medical Center and Research Institute for Maternal and Child Health, Osaka, Japan.
  • Atsuta Y; Japanese Data Center for Hematopoietic Cell Transplantation, Nagoya, Japan.
  • Takami A; Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Murata M; Department of Hematology and Oncology, Kanazawa University Hospital, Kanazawa, Japan.
Pediatr Blood Cancer ; 62(2): 291-298, 2015 02.
Article em En | MEDLINE | ID: mdl-25307105
BACKGROUND: Cyclosporine A (CsA) is used widely for graft-versus-host disease (GVHD) prophylaxis in hematopoietic stem cell transplantation (HSCT); however, the optimal schedule of its administration has not been established. Although comparative studies of adult patients undergoing HSCT have demonstrated enhanced efficacy and safety of twice-daily infusion (TD) compared with continuous infusion (CIF) of CsA, to our knowledge, similar studies have not yet been performed in pediatric groups. PROCEDURE: A self-administered questionnaire was used to retrospectively compare the clinical outcome and incidence of CsA-associated adverse events of 70 pediatric acute myelogenous leukemia patients who were receiving CsA by TD (n = 36) or CIF (n = 34) as GVHD prophylaxis for their first allogeneic HSCT. RESULTS: The cumulative incidences of grade II-IV acute GVHD and chronic GVHD, as well as the overall survival and event-free survival rates, did not differ significantly between the TD and CIF groups; however, the incidence of severe hypertension was significantly higher in the CIF group than the TD group. CONCLUSIONS: The analysis presented here indicates that TD and CIF administration of CsA have similar prophylactic effect on pediatric GVHD and suggest that TD is associated with a lower rate of toxicity than CIF in pediatric patients undergoing HSCT. Pediatr Blood Cancer 2015;62:291-298. © 2014 Wiley Periodicals, Inc.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Leucemia Mielogênica Crônica BCR-ABL Positiva / Ciclosporina / Transplante de Células-Tronco Hematopoéticas / Doença Enxerto-Hospedeiro / Imunossupressores Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Leucemia Mielogênica Crônica BCR-ABL Positiva / Ciclosporina / Transplante de Células-Tronco Hematopoéticas / Doença Enxerto-Hospedeiro / Imunossupressores Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Ano de publicação: 2015 Tipo de documento: Article