2019
article
OpenAlex
Koji Nagafuji, Toshihiro Miyamoto, Tetsuya Eto, Ryosuke Ogawa et autres
OBJECTIVE: We investigated whether minimal residual disease (MRD) status in adult patients with Philadelphia chromosome (Ph)-negative acute lymphoblastic leukemia (ALL) is useful for decision on clinical indications for allogeneic hematopoietic stem cell transplantation (HSCT). METHODS: We prospectively monitored MRD after induction and …
jp
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2018
conference-abstract
OpenAlex
Koji Nagafuji, Toshihiro Miyamoto, Tetsuya Eto, Ryosuke Ogawa et autres
Abstract Introduction A clinical indication for allogeneic hematopoietic stem cell transplantation (HSCT) in adult Philadelphia-chromosome negative [Ph (-)] acute lymphoblastic leukemia (ALL) patients in complete remission 1 (CR1) remains to be clarified. Minimal residual disease (MRD) status has been reported to be …
jp
(code pays fourni par la source)
2015
article
OpenAlex
Arata Watanabe, Toshinori Hori, Yasuto Shimomura, Chihaya Imai et autres
Abstract BACKGROUND: Minimal residual disease (MRD) level after induction (Time Point1:TP1) and before consolidation therapy (Time Point2:TP2) has a strong impact in prediction of outcome for childhood acute lymphoblastic leukemia and it has clinical utility of a prognostic factor to stratify the …
jp
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Accès ouvert
2015
article
OpenAlex
Hiroto Kaneko, Yasuhiko Tsutsumi, Takahiro Fujino, Saeko Kuwahara et autres
High-dose chemotherapy followed by autologous stem cell transplantation (ASCT) has been applied to patients with diffuse large Bcell lymphoma (DLBCL); it is well established that ASCT shows significant survival benefits for chemosensitive relapse. However, half of relapsed patients are resistant to salvage …
jp
(code pays fourni par la source)
Accès ouvert
2014
article
OpenAlex
Hiroto Kaneko, Kazuho Shimura, Saeko Kuwahara, Muneo Ohshiro et autres
INTRODUCTION: Deletions of chromosome 7 are often detected in myelodysplastic syndrome. The most commonly deleted segments are clustered at band 7q22. A critical gene is therefore suggested to be located in this region. We report a patient with myelodysplastic syndrome whose marrow …
jp
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Accès ouvert
2013
article
OpenAlex
Koji Nagafuji, Toshihiro Miyamoto, Tetsuya Eto, Tomohiko Kamimura et autres
BACKGROUND: Allogeneic hematopoietic stem cell transplantation (HSCT) for patients with Philadelphia chromosome (Ph)-negative acute lymphoblastic leukemia (ALL) in first complete remission (CR1) is much more intensive than multi-agent combined chemotherapy, although allogeneic HSCT is associated with increased morbidity and mortality when compared …
jp
(code pays fourni par la source)
2011
article
OpenAlex
Koji Nagafuji, Toshihiro Miyamoto, Tetsuya Eto, Tomohiko Kamimura et autres
Abstract Abstract 2581 Introduction A clinical indication for allogeneic hematopoietic stem cell transplantation (HSCT) in adult Philadelphia-chromosome negative [Ph (−)] acute lymphoblastic leukemia (ALL) patients in complete remission 1 (CR1) remains to be clarified. An international study showed that matched related donors …
jp
(code pays fourni par la source)
2010
article
OpenAlex
Hiroto Kaneko, Kazuho Shimura, Koichi Nishida, Yasuo Ohkawara et autres
jp
(code pays fourni par la source)
2009
article
OpenAlex
Tsukasa Okuda, Shouhei Yokota, Taira Maekawa, Yoshiaki Sonoda et autres
To investigate the clonal origin of refractory anaemia, we carried out cytogenetic studies on single haematopoietic colonies derived from granulocyte-macrophage precursors (CFU-GM) and erythroid precursors (BFU-E). Marrow cells from a patient with refractory anaemia revealed the coexistence of a normal and an …
jp
(code pays fourni par la source)
Accès ouvert
2008
article
OpenAlex
Hiroto Kaneko, Mihoko Yamashita, Muneo Ohshiro, Yasuo Ohkawara et autres
Protein-losing enteropathy (PLE) is characterized by gastrointestinal loss of serum protein. It is usually caused by hypersecretion from a tumor, ulcer, or long standing lymphangiectasia. However, we report a 47-year-old man of peritoneal nodal follicular lymphoma who developed PLE with none of …
jp
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2006
article
OpenAlex
Hiroto Kaneko, Yasuo Ohkawara, Kouichi Taniguchi, Yousuke Matsumoto et autres
We report a 72-year-old female case of IgG-kappa type multiple myeloma (MM) simultaneously complicated with Sjögren syndrome (SS). She also presented marked hyperamylasemia of salivary-type isozyme. Although she had received sequential chemotherapy completed with high-dose therapy with autologous hematopoietic stem cell transplantation, …
jp
(code pays fourni par la source)
2005
article
OpenAlex
Takeshi Inukai, Shouhei Yokota, Tomomi Okamoto, Atsushi Nemoto et autres
jp
(code pays fourni par la source)