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    Efficacy of Total-Body Irradiation-based Intensified Myeloablative Regimens for Acute Leukemia-An International Collaborative Study.

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    JHA2-6-e70061.pdf (724.6Kb)
    Date
    2025-06
    Author
    Arai, Yasuyuki
    Brazauskas, Ruta
    He, Naya
    Al-Homsi, A Samer
    Chhabra, Saurabh
    Battiwalla, Minoo
    Yanada, Masamitsu
    Steinberg, Amir
    Diaz Perez, Miguel Angel
    Hong, Sanghee
    Kanda, Junya
    Bashey, Asad
    Frangoul, Haydar A
    Badawy, Sherif M
    Verdonck, Leo F
    Lazarus, Hillard M
    Yared, Jean A
    Hashem, Hasan
    Sharma, Akshay
    Aljurf, Mahmoud
    Dias, Ajoy L
    Abid, Muhammad Bilal
    Wirk, Baldeep
    Freytes, César O
    Zeidan, Amer M
    Gergis, Usama
    Beitinjaneh, Amer
    Askar, Medhat
    Pu, Jeffrey J
    Lehmann, Leslie E
    Rangarajan, Hemalatha G
    Wood, William A
    Hashmi, Shahrukh
    Yano, Shingo
    Kako, Shinichi
    Ozawa, Yukiyasu
    Doki, Noriko
    Kanda, Yoshinobu
    Fukuda, Takahiro
    Katayama, Yuta
    Ichinohe, Tatsuo
    Tanaka, Junji
    Teshima, Takanori
    Okamoto, Shinichiro
    Atsuta, Yoshiko
    Saber, Wael
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    Abstract
    In this study, we compared outcomes of intensified myeloablative conditioning regimens using large registry data from Japan (Japanese Society for Transplantation and Cellular Therapy) and the United States (Center for International Blood and Marrow Transplant Research). Adult patients who underwent their first myeloablative allogeneic hematopoietic stem cell transplantation (HSCT) for acute leukemia in remission between 2010 and 2018 using conditioning regimens of cyclophosphamide plus total-body irradiation (CY/TBI), CY/TBI+cytarabine (AraC), or CY/TBI+etoposide (VP16) were included. The acute myeloid leukemia (AML) cohort ( = 480, 38.8%) indicated that overall survival (OS) was poorer in CY/TBI+AraC (hazard ratio [HR] 1.46, < 0.001) and CY/TBI+VP16 (HR 1.39, = 0.059) compared to CY/TBI. Relapse was not suppressed, while treatment-related mortality (TRM) was significantly higher (HR 1.78 and 1.74, < 0.001 and 0.018, respectively). In the acute lymphoblastic leukemia (ALL) cohort ( = 3901, 61.2%), OS was comparable among these regimens. With intensified regimens, relapse was significantly suppressed in CY/TBI+VP16 (HR 0.74, = 0.005), while TRM was higher (HR 1.21, = 0.077). No interactions were observed regarding the country. In AML adding AraC and VP16 to CY/TBI had an adverse effect on OS. Conversely, in ALL, adding VP16 or AraC to CY/TBI did not affect survival, but the addition of VP16 reduced the risk of relapse. The authors have confirmed clinical trial registration is not needed for this submission.
    DOI/handle
    http://dx.doi.org/10.1002/jha2.70061
    http://hdl.handle.net/10576/68262
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