Search Results - "Hidefumi, Hiramatsu"
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Current status of CAR-T cell therapy for pediatric hematologic malignancies
Published in International journal of clinical oncology (01-06-2023)“…Acute lymphoblastic leukemia (ALL) is the most common cancer in the pediatric population, and the long-term survival can reach 90%. However, approximately, 20%…”
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Genetic mechanisms of target antigen loss in CAR19 therapy of acute lymphoblastic leukemia
Published in Nature medicine (01-10-2018)“…We identified genetic mutations in CD19 and loss of heterozygosity at the time of CD19 – relapse to chimeric antigen receptor (CAR) therapy. The mutations are…”
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3
Attenuation of miR-126 Activity Expands HSC In Vivo without Exhaustion
Published in Cell stem cell (07-12-2012)“…Lifelong blood cell production is governed through the poorly understood integration of cell-intrinsic and -extrinsic control of hematopoietic stem cell (HSC)…”
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Adverse prognostic impact of KIT exon 17 mutations despite negative flow cytometric measurable residual disease in pediatric acute myeloid leukemia with RUNX1::RUNX1T1
Published in Haematologica (Roma) (05-09-2024)“…Not available.Not available…”
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Efficacy and safety of tisagenlecleucel in Japanese pediatric and young adult patients with relapsed/refractory B cell acute lymphoblastic leukemia
Published in International journal of hematology (01-02-2020)“…Tisagenlecleucel is an autologous T cell genetically modified ex vivo using a lentiviral vector encoding an anti-CD19 chimeric antigen receptor. Here, we…”
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Identification of hematopoietic stem cell-specific miRNAs enables gene therapy of globoid cell leukodystrophy
Published in Science translational medicine (17-11-2010)“…Globoid cell leukodystrophy (GLD; also known as Krabbe disease) is an invariably fatal lysosomal storage disorder caused by mutations in the…”
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7
Successful re‐administration of all‐trans retinoic acid after acute pancreatitis
Published in Pediatrics international (01-08-2021)Get full text
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8
CD146 is a potential immunotarget for neuroblastoma
Published in Cancer science (01-11-2021)“…Neuroblastoma, the most common extracranial solid tumor of childhood, is thought to arise from neural crest‐derived immature cells. The prognosis of patients…”
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Temozolomide and etoposide combination for the treatment of relapsed osteosarcoma
Published in Japanese journal of clinical oncology (01-08-2020)“…The prognosis of patients with relapsed osteosarcoma is extremely poor and the optimal treatment remains to be identified. Here, we retrospectively analysed…”
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Ponatinib in pediatric patients with Philadelphia chromosome-positive leukemia: a retrospective survey of the Japan Children’s Cancer Group
Published in International journal of hematology (01-07-2022)“…Ponatinib is effective in adults with Philadelphia chromosome-positive (Ph+) leukemia, resistant or intolerant to second-generation tyrosine kinase inhibitors,…”
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11
Post‐transplant Lymphoproliferative Disorders After Liver Transplantation: A Retrospective Cohort Study Including 1954 Transplants
Published in Liver transplantation (01-08-2021)“…Post‐transplant lymphoproliferative disorders (PTLDs) are life‐threatening neoplasms after organ transplantation. Because of their rarity and multiple grades…”
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Pluripotent stem cell model of Shwachman–Diamond syndrome reveals apoptotic predisposition of hemoangiogenic progenitors
Published in Scientific reports (09-09-2020)“…Shwachman–Diamond syndrome (SDS), an autosomal recessive disorder characterized by bone marrow failure, exocrine pancreatic insufficiency, and skeletal…”
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Influence of post-transplant mucosal-associated invariant T cell recovery on the development of acute graft-versus-host disease in allogeneic bone marrow transplantation
Published in International journal of hematology (01-07-2018)“…Mucosal-associated invariant T (MAIT) and invariant natural killer T (iNKT) cells are T cell subpopulations that possess innate-like properties. We examined…”
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Post-induction MRD by FCM and GATA1-PCR are significant prognostic factors for myeloid leukemia of Down syndrome
Published in Leukemia (01-09-2021)“…Myeloid leukemia of Down syndrome (ML-DS) is associated with good response to chemotherapy, resulting in favorable outcomes. However, no universal prognostic…”
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Outcome and growth of lobar graft after pediatric living-donor lobar lung transplantation
Published in The Journal of heart and lung transplantation (01-05-2023)“…Living-donor lobar lung transplantation (LDLLT) remains a life-saving option for pediatric patients with respiratory failure. However, the long-term survival…”
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Author Correction: Pluripotent stem cell model of Shwachman–Diamond syndrome reveals apoptotic predisposition of hemoangiogenic progenitors
Published in Scientific reports (18-01-2021)“…An amendment to this paper has been published and can be accessed via a link at the top of the paper…”
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A phase III clinical trial evaluating efficacy and safety of minimal residual disease-based risk stratification for children with acute myeloid leukemia, incorporating a randomized study of gemtuzumab ozogamicin in combination with post-induction chemotherapy for non-low-risk patients (JPLSG-AML-20)
Published in Japanese journal of clinical oncology (06-10-2022)“…The purpose of this study is to establish a treatment with appropriate intensity for children (<16 years old at diagnosis) with de novo acute myeloid leukemia…”
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PAX5 alterations in an infant case of KMT2A‐rearranged leukemia with lineage switch
Published in Cancer science (01-07-2022)“…Lineage switch is a rare event at leukemic relapse. While mostly known to occur in KMT2A‐rearranged infant leukemia, the underlying mechanism is yet to be…”
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Correction to: Post-induction MRD by FCM and GATA1-PCR are significant prognostic factors for myeloid leukemia of Down syndrome
Published in Leukemia (01-12-2021)Get full text
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Reduced-intensity conditioning is effective for hematopoietic stem cell transplantation in young pediatric patients with Diamond–Blackfan anemia
Published in Bone marrow transplantation (Basingstoke) (01-05-2021)“…Allogeneic hematopoietic stem cell transplantation (HSCT) is the only curative therapy for the hematologic manifestations of Diamond–Blackfan anemia (DBA)…”
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