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

View/ Open
Date
2025-06Author
Arai, YasuyukiBrazauskas, 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
...show more authors ...show less authors
Metadata
Show full item recordAbstract
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.
Collections
- Medicine Research [1932 items ]

