Danaparoid as the Prophylaxis for Hepatic Veno-Occlusive Disease After Allogeneic Hematopoietic Stem Cell Transplantation in Childhood Hematological Malignancy
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作者:
Sakaguchi, Hirotoshi
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Japanese Red Cross Nagoya First Hosp, Div Haematol & Oncol, Childrens Med Ctr, Nakamura Ku, Nagoya, Aichi 4538511, JapanJapanese Red Cross Nagoya First Hosp, Div Haematol & Oncol, Childrens Med Ctr, Nakamura Ku, Nagoya, Aichi 4538511, Japan
Sakaguchi, Hirotoshi
[1
]
Watanabe, Nobuhiro
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Natl Nagoya Hosp, Dept Pediat, Nagoya, Aichi, JapanJapanese Red Cross Nagoya First Hosp, Div Haematol & Oncol, Childrens Med Ctr, Nakamura Ku, Nagoya, Aichi 4538511, Japan
Watanabe, Nobuhiro
[2
]
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Muramatsu, Hideki
[3
]
Doisaki, Sayoko
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Natl Nagoya Hosp, Dept Pediat, Nagoya, Aichi, JapanJapanese Red Cross Nagoya First Hosp, Div Haematol & Oncol, Childrens Med Ctr, Nakamura Ku, Nagoya, Aichi 4538511, Japan
Doisaki, Sayoko
[2
]
Yoshida, Nao
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机构:Japanese Red Cross Nagoya First Hosp, Div Haematol & Oncol, Childrens Med Ctr, Nakamura Ku, Nagoya, Aichi 4538511, Japan
Yoshida, Nao
Matsumoto, Kimikazu
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机构:Japanese Red Cross Nagoya First Hosp, Div Haematol & Oncol, Childrens Med Ctr, Nakamura Ku, Nagoya, Aichi 4538511, Japan
Matsumoto, Kimikazu
Kato, Koji
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机构:Japanese Red Cross Nagoya First Hosp, Div Haematol & Oncol, Childrens Med Ctr, Nakamura Ku, Nagoya, Aichi 4538511, Japan
Kato, Koji
机构:
[1] Japanese Red Cross Nagoya First Hosp, Div Haematol & Oncol, Childrens Med Ctr, Nakamura Ku, Nagoya, Aichi 4538511, Japan
[2] Natl Nagoya Hosp, Dept Pediat, Nagoya, Aichi, Japan
[3] Nagoya Univ, Grad Sch Med, Dept Pediat, Nagoya, Aichi 4648601, Japan
Background. Veno-occlusive disease (VOD) is a regimen-related toxicity that occurs in the early phase of hematopoietic stern cell transplantation (HSCT). Therapeutic modalities for established VOD are limited, and severe VOD characterized by multiple organ failure is associated with a fatal prognosis despite intensive supportive care. Procedure. We analyzed the data of 95 consecutive allogeneic HSCT for childhood hematological malignancies, and assessed the efficacy of our VOD prophylaxis regimen based on danaparoid (n = 48), comparing with historical control regimen based on dalteparin (n = 47). Results. Eight patients (danaparoid cohort in one; dalteparin cohort in seven) developed VOD on day +30 (median onset, day +22; range, day +11 to day +28) after HSCT. The probability of developing VOD for the danaparoid cohort was 2% (95% CI, 0-6%) and that of the dalteparin cohort was 15% (95% CI, 5-26%). In the Cox hazard proportional model, the danaparoid cohort had a significant advantage over the dalteparin cohort for the prophylaxis of VOD (hazard ratio (HR), 0.0; 95% CI, 0.0-0.3; P < 0.01) without increasing hemorrhagic events. Conclusions. Our findings suggest that danaparoid may have promise for the prophylaxis of VOD after allogeneic HSCT and further randomized studies are warranted. Pediatr Blood Cancer. 2010;55:1118-1125. (C) 2010 Wiley-Liss, Inc.
机构:
Univ Hong Kong, Dept Pediat & Adolescent Med, Queen Mary Hosp, Hong Kong, Hong Kong, Peoples R ChinaUniv Hong Kong, Dept Pediat & Adolescent Med, Queen Mary Hosp, Hong Kong, Hong Kong, Peoples R China
Cheuk, D. K. L.
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Wang, P.
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Univ Hong Kong, Dept Pediat & Adolescent Med, Queen Mary Hosp, Hong Kong, Hong Kong, Peoples R ChinaUniv Hong Kong, Dept Pediat & Adolescent Med, Queen Mary Hosp, Hong Kong, Hong Kong, Peoples R China
Wang, P.
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Lee, T. L.
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Univ Hong Kong, Dept Pediat & Adolescent Med, Queen Mary Hosp, Hong Kong, Hong Kong, Peoples R ChinaUniv Hong Kong, Dept Pediat & Adolescent Med, Queen Mary Hosp, Hong Kong, Hong Kong, Peoples R China
Lee, T. L.
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Chiang, A. K. S.
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Univ Hong Kong, Dept Pediat & Adolescent Med, Queen Mary Hosp, Hong Kong, Hong Kong, Peoples R ChinaUniv Hong Kong, Dept Pediat & Adolescent Med, Queen Mary Hosp, Hong Kong, Hong Kong, Peoples R China
Chiang, A. K. S.
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Ha, S. Y.
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Univ Hong Kong, Dept Pediat & Adolescent Med, Queen Mary Hosp, Hong Kong, Hong Kong, Peoples R ChinaUniv Hong Kong, Dept Pediat & Adolescent Med, Queen Mary Hosp, Hong Kong, Hong Kong, Peoples R China
Ha, S. Y.
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Lau, Y. L.
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Univ Hong Kong, Dept Pediat & Adolescent Med, Queen Mary Hosp, Hong Kong, Hong Kong, Peoples R ChinaUniv Hong Kong, Dept Pediat & Adolescent Med, Queen Mary Hosp, Hong Kong, Hong Kong, Peoples R China
Lau, Y. L.
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Chan, G. C. F.
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Univ Hong Kong, Dept Pediat & Adolescent Med, Queen Mary Hosp, Hong Kong, Hong Kong, Peoples R ChinaUniv Hong Kong, Dept Pediat & Adolescent Med, Queen Mary Hosp, Hong Kong, Hong Kong, Peoples R China
机构:
Univ Hong Kong, Dept Pediat & Adolescent Med, Queen Mary Hosp, Hong Kong, Hong Kong, Peoples R ChinaUniv Hong Kong, Dept Pediat & Adolescent Med, Queen Mary Hosp, Hong Kong, Hong Kong, Peoples R China
Cheuk, D. K. L.
;
Wang, P.
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Univ Hong Kong, Dept Pediat & Adolescent Med, Queen Mary Hosp, Hong Kong, Hong Kong, Peoples R ChinaUniv Hong Kong, Dept Pediat & Adolescent Med, Queen Mary Hosp, Hong Kong, Hong Kong, Peoples R China
Wang, P.
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Lee, T. L.
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Univ Hong Kong, Dept Pediat & Adolescent Med, Queen Mary Hosp, Hong Kong, Hong Kong, Peoples R ChinaUniv Hong Kong, Dept Pediat & Adolescent Med, Queen Mary Hosp, Hong Kong, Hong Kong, Peoples R China
Lee, T. L.
;
Chiang, A. K. S.
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Univ Hong Kong, Dept Pediat & Adolescent Med, Queen Mary Hosp, Hong Kong, Hong Kong, Peoples R ChinaUniv Hong Kong, Dept Pediat & Adolescent Med, Queen Mary Hosp, Hong Kong, Hong Kong, Peoples R China
Chiang, A. K. S.
;
Ha, S. Y.
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Univ Hong Kong, Dept Pediat & Adolescent Med, Queen Mary Hosp, Hong Kong, Hong Kong, Peoples R ChinaUniv Hong Kong, Dept Pediat & Adolescent Med, Queen Mary Hosp, Hong Kong, Hong Kong, Peoples R China
Ha, S. Y.
;
Lau, Y. L.
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Univ Hong Kong, Dept Pediat & Adolescent Med, Queen Mary Hosp, Hong Kong, Hong Kong, Peoples R ChinaUniv Hong Kong, Dept Pediat & Adolescent Med, Queen Mary Hosp, Hong Kong, Hong Kong, Peoples R China
Lau, Y. L.
;
Chan, G. C. F.
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Univ Hong Kong, Dept Pediat & Adolescent Med, Queen Mary Hosp, Hong Kong, Hong Kong, Peoples R ChinaUniv Hong Kong, Dept Pediat & Adolescent Med, Queen Mary Hosp, Hong Kong, Hong Kong, Peoples R China