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Publication
Featured researches published by Miwa Sakai.
International Journal of Hematology | 2011
Chiaki Nakaseko; Shinichi Ozawa; Emiko Sakaida; Miwa Sakai; Yoshinobu Kanda; Kumi Oshima; Mineo Kurokawa; Satoshi Takahashi; Jun Ooi; Takayuki Shimizu; Akira Yokota; Fumiaki Yoshiba; Katsumichi Fujimaki; Heiwa Kanamori; Rika Sakai; Takayuki Saitoh; Tohru Sakura; Atsuo Maruta; Hisashi Sakamaki; Shinichiro Okamoto
Bronchiolitis obliterans (BO) after allogeneic stem cell transplantation (allo-SCT) is a late-onset, life-threatening respiratory complication that significantly reduces a patient’s quality of life. We retrospectively analysed the incidence of and risk factors for BO in allo-SCT recipients. In 2087 patients who underwent allo-SCT between January 1994 and June 2005 and survived >90 days after transplantation, 57 patients developed BO with a 5-year cumulative incidence of 2.8%. The median time interval from transplantation to BO diagnosis was 335 days (range 83–907 days). The 5-year cumulative incidence of BO was 1.62% in bone marrow transplantation (BMT) from related donors, 3.83% in peripheral blood stem cell transplantation (PBSCT) from related donors (R-PBSCT), 2.91% in BMT from unrelated donors and 2.65% in unrelated cord blood transplantation. The incidence of BO after R-PBSCT was significantly higher than that after any other type of allo-SCT (p = 0.02). R-PBSCT (p = 0.019) and preceding chronic graft-versus-host disease (GVHD) (p < 0.001) were BO-associated risk factors. Overall 5-year survival of patients with BO from the time of diagnosis was 45.4%, significantly less than those without (77.5% from day 335, p < 0.001). R-PBSCT recipients with existent chronic GVHD have a high risk of developing BO, and need extensive care and repeated pulmonary function tests.
Pathology & Oncology Research | 2004
Aiko Kida; Kazuteru Ohashi; Takeshi Kobayashii; Miwa Sakai; Takuya Yamashita; Hideki Akiyama; Shuji Kishida; Hisashi Sakamaki
Calcineurin-inhibitor induced pain syndrome (CIPS) is a newly described entity with a characteristic feature of sudden onset of severe lower limb pain, and high levels of cyclosporine or tacrolimus may be involved in the pathogenesis. This syndrome is rarely seen in recipients of hematopoietic stem cell transplantation (HSCT) compared with other organ transplant recipients, however, heightened awareness of this complication after HSCT may be needed for hematologists, as misdiagnosis can result in catastrophic consequences. We report herein two cases of lower limb pain syndrome, with some clinical features resembling CIPS, occurring during the early phase of cord blood stem cell transplantation for hematological malignancy.
International Journal of Hematology | 2006
Miwa Sakai; Kazuteru Ohashi; Keiko Ohta; Takuya Yamashita; Hideki Akiyama; Shuji Kisida; Noriko Kamata; Hisashi Sakamaki
We report a case of immune-mediated myelopathy occurring 4 months after unrelated bone marrow transplantation for myelodysplastic syndrome. After the tapering of cyclosporine for graft-versus-host disease prophylaxis, the patient developed several neurological symptoms mimicking the clinical features of multiple sclerosis (MS).Although neurological exacerbation was well stabilized with a bulk dose of corticosteroid, sustained improvement of neurological deficits occurred after the patient developed hematopoietic mixed chimerism (HMC).This experience may provide clinical evidence supporting the current therapeutic concept, in which HMC induction can potentially cure several immune diseases, including MS.
Biology of Blood and Marrow Transplantation | 2005
Rie Kojima; Ukihide Tateishi; Masahiro Kami; Naoko Murashige; Yasuhito Nannya; Eiji Kusumi; Miwa Sakai; Yuji Tanaka; Yoshinobu Kanda; Shin-ichiro Mori; Shigeru Chiba; Masahiko Kusumoto; Shigesaburo Miyakoshi; Hisamaru Hirai; Shuichi Taniguchi; Hisashi Sakamaki; Yoichi Takaue
Biology of Blood and Marrow Transplantation | 2004
Rie Kojima; Masahiro Kami; Yasuhito Nannya; Eiji Kusumi; Miwa Sakai; Yuji Tanaka; Yoshinobu Kanda; Shin-ichiro Mori; Shigeru Chiba; Shigesaburo Miyakoshi; Kinuko Tajima; Hisamaru Hirai; Shuichi Taniguchi; Hisashi Sakamaki; Yoichi Takaue
American Journal of Hematology | 2006
Yoshinobu Kanda; Rie Hyo; Takuya Yamashita; Katsumichi Fujimaki; Kumi Oshima; Masahiro Onoda; Takehiko Mori; Toru Sakura; Masatsugu Tanaka; Miwa Sakai; Jun Taguchi; Mineo Kurakawa; Atsuo Maruta; Shinichiro Okamoto; Hisashi Sakamaki
Internal Medicine | 2001
Miwa Sakai; Naoto Egawa; Hisashi Sakamaki; Masaki Sanaka; Tu Yuyang; Terami Kamisawa; Nobuhiro Sakaki; Nobuaki Funata; Yuichi Nakazawa; Toshihiko Ikegami; Yasuhiko Hashikura; Seiji Kawasaki
American Journal of Hematology | 2005
Miwa Sakai; Kazuteru Ohashi; Takeshi Kobayashi; Takuya Yamashita; Hideki Akiyama; Tetuo Nemoto; Shuji Kishida; Noriko Kamata; Hisashi Sakamaki
The Japanese journal of clinical hematology | 2010
Maki Hagihara; Heiwa Kanamori; Miwa Sakai; Takehiko Mori; Chiaki Nakaseko; Nobuyuki Aotsuka; Taeko Uehara; Tohru Sakura; Fumio Yoshiba; Nobutaka Kawai; Masatsugu Tanaka; Shin Fujisawa; Chikako Ohwada; Hisashi Wakita; Akira Yokota; Toshihide Kawamura; Atsuo Maruta; Hisashi Sakamaki; Shinichiro Okamoto
The Japanese journal of clinical hematology | 2007
Katsumichi Fujimaki; Chiaki Nakaseko; Oshima K; Miwa Sakai; Chou R; Yoshinobu Kanda; Miki Nishimura; Heiwa Kanamori; Hisashi Sakamaki