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  1. No Access

    Article

    KRAS G12 mutations as adverse prognostic factors in KMT2A-rearranged acute myeloid leukemia

    Shinju Iyoda, Kenichi Yoshida, Kota Shoji, Nana Ito, Miu Tanaka in Leukemia (2024)

  2. Article

    Open Access

    Cellular and humoral immunogenicity against SARS-CoV-2 vaccination or infection is associated with the memory phenotype of T- and B-lymphocytes in adult allogeneic hematopoietic cell transplant recipients

    We conducted a cross-sectional study to evaluate cellular and humoral immunogenicity against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccination or infection and examine how lymphocyte sub...

    Takaaki Konuma, Megumi Hamatani-Asakura in International Journal of Hematology (2024)

  3. No Access

    Article

    Sustained remission after cord blood transplantation for breast cancer with lung metastases and myelodysplastic syndrome

    Allogenic hematopoietic stem cell transplantation (allo-HSCT) is not a standard therapy for solid cancer because of its high toxicity and insufficient evidence levels. However, the potential graft-versus-solid...

    Naokazu Nakamura, Nao Yamamoto, Tadakazu Kondo in International Journal of Hematology (2024)

  4. Article

    Open Access

    Feasibility and safety of the discontinuation of systemic immunosuppressive treatment after single-unit cord blood transplantation in adults

    We retrospectively evaluated the incidence, factors, and clinical outcomes of the discontinuation of immunosuppressive treatment (IST) after single-unit unrelated cord blood transplantation (CBT) in adults rec...

    Takaaki Konuma, Maki Monna-Oiwa, Seiko Kato, Masamichi Isobe in Bone Marrow Transplantation (2024)

  5. No Access

    Article

    First report of familial mixed phenotype acute leukemia: shared clinical characteristics, Philadelphia translocation, and germline variants

    While our understanding of the molecular basis of mixed phenotype acute leukemia (MPAL) has progressed over the decades, our knowledge is limited and the prognosis remains poor. Investigating cases of familial...

    Yuka Shiozawa, Shinya Fujita, Yasuhito Nannya in International Journal of Hematology (2024)

  6. No Access

    Article

    Donor NKG2D rs1049174 polymorphism predicts hematopoietic recovery and event-free survival after single-unit cord blood transplantation in adults

    Takaaki Konuma, Megumi Hamatani-Asakura, Maki Monna-Oiwa in Bone Marrow Transplantation (2024)

  7. Article

    Open Access

    Clinical implications of augmented renal clearance after unrelated single cord blood transplantation in adults

    Augmented renal clearance (ARC) is a phenomenon characterized by increased renal functionality, which can impact the pharmacokinetics and pharmacodynamics of antimicrobial drugs eliminated by the kidneys. It i...

    Takaaki Konuma, Kosuke Takano, Maki Monna-Oiwa in International Journal of Hematology (2023)

  8. Article

    Open Access

    Progression to B acute lymphoblastic leukemia in 8p11 myeloproliferative syndrome with t(6;8)(q27;p12)

    8p11 myeloproliferative syndrome is a rare hematological malignancy caused by the translocation of FGFR1. Patients present with a myeloproliferative neoplasm that frequently transforms into acute myeloid leuke...

    Fumi Nakamura, Sachiko Seo, Yasuhito Nannya in International Journal of Hematology (2023)

  9. No Access

    Article

    Unrelated hematopoietic stem cell transplantation for familial platelet disorder/acute myeloid leukemia with germline RUNX1 mutations

    Germline mutations in RUNX1 result in rare autosomal-dominant familial platelet disorder with predisposition to acute myeloid leukemia (FPD/AML). As genetic analysis is becoming increasingly prevalent, the diagno...

    Kazunori Toratani, Mizuki Watanabe, Junya Kanda in International Journal of Hematology (2023)

  10. No Access

    Article

    Successful azacitidine therapy for myelodysplastic syndrome associated with VEXAS syndrome

    VEXAS (vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic) syndrome is caused by UBA1 somatic mutations and is characterized by late-onset systemic autoimmune inflammation and blood abnormalities such as cy...

    Asami Kataoka, Chisaki Mizumoto, Junya Kanda in International Journal of Hematology (2023)

  11. No Access

    Article

    Thyrotoxicosis after unrelated cord blood transplantation for adults

    Takaaki Konuma, Akira Tomonari, Jun Ooi, Hitomi Nagayama in Annals of Hematology (2023)

  12. No Access

    Article

    Genetic deletion and pharmacologic inhibition of E3 ubiquitin ligase HOIP impairs the propagation of myeloid leukemia

    We investigated the role of Hoip, a catalytic subunit of linear ubiquitin chain assembly complex (LUBAC), in adult hematopoiesis and myeloid leukemia by using both conditional deletion of Hoip and small-molecule ...

    Koji Jimbo, Ayuna Hattori, Shuhei Koide, Takahiro Ito, Katsuhiro Sasaki in Leukemia (2023)

  13. Article

    Open Access

    ASXL1 mutations with serum EPO levels predict poor response to darbepoetin alfa in lower-risk MDS: W-JHS MDS01 trial

    Darbepoetin alfa (DA) is used to treat anemia in lower-risk (IPSS low or int-1) myelodysplastic syndromes (MDS). However, whether mutations can predict the effectiveness of DA has not been examined. The presen...

    Yasuyoshi Morita, Yasuhito Nannya, Motoshi Ichikawa in International Journal of Hematology (2022)

  14. No Access

    Article

    Prognostic impact of switching from cyclosporine to corticosteroids early after single cord blood transplantation

    Kosuke Takano, Takaaki Konuma, Maki Monna-Oiwa, Masamichi Isobe in Annals of Hematology (2022)

  15. No Access

    Article

    Immunoglobulin superfamily member 8 maintains myeloid leukemia stem cells through inhibition of β-catenin degradation

    The identification of characteristic differences between cancer stem cells and their normal counterparts remains a key challenge for cancer treatment. Here, we investigated the role of immunoglobulin superfami...

    Koji Jimbo, Yaeko Nakajima-Takagi, Takahiro Ito, Shuhei Koide, Yasuhito Nannya in Leukemia (2022)

  16. No Access

    Article

    Identification of an asymptomatic Shwachman–Bodian–Diamond syndrome mutation in a patient with acute myeloid leukemia

    Shwachman–Diamond syndrome (SDS) is an autosomal recessive inherited disorder characterized by bone marrow failure, exocrine pancreatic dysfunction, and skeletal abnormalities. SDS is typically caused by a pat...

    Sho Shibata, Shojiro Inano, Mizuki Watanabe in International Journal of Hematology (2022)

  17. No Access

    Article

    Germline RUNX1 translocation in familial platelet disorder with propensity to myeloid malignancies

    Masatoshi Sakurai, Yasuhito Nannya, Rie Yamazaki, Kentaro Yamaguchi in Annals of Hematology (2022)

  18. No Access

    Article

    Hematological effects on peri-transplant use of linezolid in adults undergoing single-unit cord blood transplantation

    Takeo Yasu, Takaaki Konuma, Maki Oiwa-Monna, Satoshi Takahashi in Annals of Hematology (2021)

  19. No Access

    Article

    Paroxysmal nocturnal hemoglobinuria complicated with essential thrombocythemia harboring concomitant PIGA, CALR, and ASXL1 mutations

    Haruya Okamoto, Nobuhiko Uoshima, Yuri Kamitsuji, Eri Kawata in Annals of Hematology (2021)

  20. No Access

    Article

    Co-mutation pattern, clonal hierarchy, and clone size concur to determine disease phenotype of SRSF2P95-mutated neoplasms

    Somatic mutations in splicing factor genes frequently occur in myeloid neoplasms. While SF3B1 mutations are associated with myelodysplastic syndromes (MDS) with ring sideroblasts, SRSF2P95 mutations are found in ...

    Gabriele Todisco, Maria Creignou, Anna Gallì, Paola Guglielmelli, Elisa Rumi in Leukemia (2021)

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