Publications by authors named "Keino D"

Eltrombopag is used with first-line immunosuppressive therapy for adult aplastic anemia, although its practical utility in childhood remains unclear. We retrospectively analyzed the outcomes of pediatric patients who received eltrombopag in Japan. Of the 27 eligible patients, 23 (85%) were previously treated, and 15 (56%) had severe or very-severe disease.

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Objective: Chimerism analysis is an important post-transplant assessment for allogeneic hematopoietic stem cell transplant (HCT) recipients. Although various chimerism analysis techniques are already established, they are limited in terms of sensitivity, versatility, and turnaround time. Our objective was to develop a digital droplet polymerase chain reaction (ddPCR) assay for chimerism analysis using ABO gene polymorphisms as markers.

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  • * A novel FBXW7 variant was found in a patient with intellectual disability who also developed Wilms tumor, indicating a potential genetic link.
  • * The study suggests that the tumor's development may follow a two-hit model, highlighting the need for further research to improve management and monitoring strategies.
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  • Silent inactivation (SI) of L-asparaginase (ASP) is a process where antibodies decrease ASP activity in patients without allergic reactions, affecting those with acute lymphoblastic leukemia (ALL) negatively.
  • A clinical trial in Japan, named ALL-ASP19, measured ASP activity (ASA) to identify SI in newly diagnosed ALL patients, enrolling 110 participants but analyzing 66 after exclusions.
  • The study found that the incidence of SI was low (4.5%) in Japan compared to other countries, and while all SI patients had antibodies, not all with antibodies experienced SI, indicating the importance of measuring ASA levels for effective treatment.
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  • IL10RA deficiency is a serious genetic disease that causes gut inflammation in babies and can be fatal, but a special type of treatment called hematopoietic cell transplantation (HCT) can help.
  • In Japan, researchers looked at seven patients with this deficiency, including both new and previously known cases.
  • All five patients who had HCT survived and got better, showing that this treatment should be done early for the best chance of recovery.
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Alemtuzumab is used with reduced-toxicity conditioning (RTC) in allogeneic hematopoietic cell transplantation (HCT), demonstrating efficacy and feasibility for patients with inborn errors of immunity (IEI) in Western countries; however, the clinical experience in Asian patients with IEI is limited. We retrospectively analyzed patients with IEI who underwent the first allogeneic HCT with alemtuzumab combined with RTC regimens in Japan. A total of 19 patients were included and followed up for a median of 18 months.

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Metronomic chemotherapy (MC) is based on chronic administration of chemotherapeutic agents at minimally toxic doses without prolonged drug-free breaks, that inhibits tumor angiogenesis and induces tumor dormancy. This study aimed to determine the efficacy of MC for pediatric refractory solid tumors. We retrospectively analyzed the data of pediatric patients with relapsed/refractory solid tumors who received treatment, including low-dose continuous administration of anticancer drugs, at our institute.

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Survival rates of patients with Philadelphia chromosome-positive ALL (Ph+ALL) have improved considerably with the introduction of tyrosine kinase inhibitors (TKI); however, hematopoietic stem cell transplantation (HSCT) continues to play an important role. Reduced-intensity conditioning (RIC) regimens have been widely applied particularly for older patients, but their validity for children and adolescents with Ph+ALL has not been investigated. In this study, data from patients receiving HSCT for de novo Ph+ALL in first or second remission at ages younger than 25 years and with a history of pre-HSCT TKI therapy were retrospectively collected through the nationwide registry in Japan.

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Background: One of the most significant challenges in patients with medulloblastoma is reducing the dose of craniospinal irradiation (CSI) to minimize neurological sequelae in survivors. Molecular characterization of patients receiving lower than standard dose of CSI therapy is important to facilitate further reduction of treatment burden.

Methods: We conducted DNA methylation analysis using an Illumina Methylation EPIC array to investigate molecular prognostic markers in 38 patients with medulloblastoma who were registered in the Japan Pediatric Molecular Neuro-Oncology Group and treated with reduced-dose CSI.

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  • - Recent shifts in communication with children about cancer highlight a lack of understanding regarding discussions on future infertility risks due to cancer therapy; a study compared practices in Japan and the U.S. to clarify these patterns.
  • - An online survey conducted in 2019 and 2020 collected responses from pediatric oncologists in both countries, leading to the creation of educational videos tailored for different age groups regarding cancer and fertility concerns.
  • - Results indicated that while U.S. physicians consistently inform patients of their diagnosis regardless of age, a lower percentage of Japanese physicians engage in direct discussions about fertility risks; 85% of physicians surveyed expressed a preference for using the developed educational videos in their practice.
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  • Germline genetic variants play a significant role in the development of pediatric B cell acute lymphoblastic leukemia (B-ALL), with genome-wide association studies identifying specific susceptibility loci.
  • The study focused on rare variants of a key transcription factor involved in B cell development and involved sequencing saliva DNA from 527 pediatric B-ALL patients in remission.
  • The analyses found a strong association between rare deleterious variants and pediatric B-ALL, particularly highlighting the variant rs372168347, which may influence B cell maturation and increase leukemia risk.
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We herein report a case of hepatitis-associated aplastic anemia (HAAA) that occurred after severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccination. In this patient, progressive pancytopenia observed two months after acute hepatitis following the second dose of the SARS-CoV-2 vaccine indicated the development of HAAA. Although some reports have suggested that SARS-CoV-2 vaccination may be involved in the development of autoimmune diseases, no cases of HAAA developing after SARS-CoV-2 vaccination have been reported.

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  • Minimal residual disease (MRD) refers to the few cancer cells that persist in the body after treatment, which is particularly important in managing blood cancers like acute lymphoblastic leukemia (ALL).
  • This study introduces a new method for detecting MRD using droplet digital PCR (ddPCR) to identify specific genetic mutations, demonstrating a sensitivity level of 1E-4, which outperformed traditional PCR in some cases.
  • The ddPCR-MRD method showed promising results across various cancer types, as it could also detect low levels of cancer cells in stored ovarian tissue from pediatric patients, suggesting its potential as a versatile tool for MRD detection beyond just ALL.
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Objective: To verify understanding and awareness of fertility preservation (FP) in pediatric patients undergoing FP treatments.

Methods: A questionnaire survey was conducted before and after explanation of fertility issues and FP treatments for patients 6-17 years old who visited or were hospitalized for the purpose of ovarian tissue cryopreservation (OTC) or oocyte cryopreservation (OC), or sperm cryopreservation between October 2018 and April 2022. This study was approved by the institutional review board at St.

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Inherited genetic variation is associated with 6-mercaptopurine (6-MP) dose reduction and frequent toxicities induced by 6-MP. However, the tolerable dose for 6-MP is not fully predicted by the known variation in NUDT15 and TPMT among Asian children with acute lymphoblastic leukaemia (ALL). We performed a genome-wide association study (GWAS) related to 6-MP dose among Japanese children with ALL.

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  • The study investigates the adequacy of revised patient selection criteria for fertility preservation in children and adolescents, focusing on their characteristics and the consultation process at a university hospital.
  • Out of 74 patients referred for consultation, more than half had hematological diseases, with 41.9% successfully undergoing ovarian tissue cryopreservation; complications were minimal.
  • The results showed that most patients over 12 experienced primary ovarian insufficiency post-treatment, suggesting that while the selection criteria may be appropriate, some long-term challenges remain.
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IKAROS and CTLA4 deficiencies are inborn errors of immunity and show similar clinical phenotypes, including hypogammaglobulinemia and autoimmune diseases (ADs). However, the differences in clinical features and pathogenesis of these are not fully understood. Therefore, we performed systematic literature reviews for IKAROS and CTLA4 deficiencies.

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  • * Researchers conducted in vitro drug sensitivity testing on blood samples from eight TAM patients to explore new treatment options, screening a total of 41 different drugs.
  • * The study found that TAM cells are particularly sensitive to glucocorticoids, the MAP2K inhibitor trametinib, and cytarabine, indicating these could be potential therapeutic approaches for TAM.
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Background: Cerebrospinal fluid (CSF) cytology and spinal MR imaging are routinely performed for staging before treatment of intracranial germinoma. However, the interpretation of the results of CSF cytology poses 2 unresolved clinical questions: (1) Does positive CSF cytology correlate with the presence of spinal lesion before treatment? and (2) Is craniospinal irradiation (CSI) necessary for patients with positive CSF cytology in the absence of spinal lesion?

Methods: Multicenter retrospective analyses were performed based on a questionnaire on clinical features, spinal MR imaging finding, results of CSF cytology, treatments, and outcomes which was sent to 86 neurosurgical and 35 pediatrics departments in Japan. Pretreatment frequencies of spinal lesion on MR imaging were compared between the patients with positive and negative cytology.

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  • * The majority of patients (79.6%) received information about fertility preservation before starting treatment, but many hospitals lacked reproductive departments and specific materials to support these discussions.
  • * Findings highlight the need for better educational resources for oncologists and nurses, as well as improved collaboration between pediatric and reproductive specialists to enhance fertility preservation services.
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  • Fertility preservation for children, specifically through ovarian tissue cryopreservation (OTC), is under-researched, particularly regarding its surgical methods.
  • A study analyzed 25 girls who had OTC from November 2015 to May 2020, focusing on their preoperative management and medical backgrounds, which included various health conditions like leukemia and brain tumors.
  • The findings indicate that OTC can be safely performed in children, even those with severe medical issues, and that monitoring white blood cell and C-reactive protein levels post-surgery can help detect potential infections.
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Background: Deficiency of adenosine deaminase 2 (DADA2) is an autosomal recessive inflammatory disease caused by loss-of-function mutations in both alleles of the ADA2 gene. Most patients with DADA2 exhibit systemic vasculopathy consistent with polyarteritis nodosa, but large phenotypic variability has been reported, and the pathogenesis of DADA2 remains unclear.

Objectives: This study sought to assess the clinical and genetic characteristics of Japanese patients with DADA2 and to gain insight into the pathogenesis of DADA2 by multi-omics analysis.

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