eJHaem (Jun 2025)

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

  • Yasuyuki Arai,
  • Ruta Brazauskas,
  • Naya He,
  • A. Samer Al‐Homsi,
  • Saurabh Chhabra,
  • Minoo Battiwalla,
  • Masamitsu Yanada,
  • Amir Steinberg,
  • Miguel Angel Diaz Perez,
  • Sanghee Hong,
  • Junya Kanda,
  • Asad Bashey,
  • Haydar A. Frangoul,
  • Sherif M. Badawy,
  • Leo F. Verdonck,
  • Hillard M. Lazarus,
  • Jean A. Yared,
  • Hasan Hashem,
  • Akshay Sharma,
  • Mahmoud Aljurf,
  • Ajoy L. Dias,
  • Muhammad Bilal Abid,
  • Baldeep Wirk,
  • César O. Freytes,
  • Amer M. Zeidan,
  • Usama Gergis,
  • Amer Beitinjaneh,
  • Medhat Askar,
  • Jeffrey J. Pu,
  • Leslie E. Lehmann,
  • Hemalatha G. Rangarajan,
  • William A. Wood,
  • Shahrukh Hashmi,
  • Shingo Yano,
  • Shinichi Kako,
  • Yukiyasu Ozawa,
  • Noriko Doki,
  • Yoshinobu Kanda,
  • Takahiro Fukuda,
  • Yuta Katayama,
  • Tatsuo Ichinohe,
  • Junji Tanaka,
  • Takanori Teshima,
  • Shinichiro Okamoto,
  • Yoshiko Atsuta,
  • Wael Saber

DOI
https://doi.org/10.1002/jha2.70061
Journal volume & issue
Vol. 6, no. 3
pp. n/a – n/a

Abstract

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ABSTRACT Background 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). Methods 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. Results The acute myeloid leukemia (AML) cohort (N = 480, 38.8%) indicated that overall survival (OS) was poorer in CY/TBI+AraC (hazard ratio [HR] 1.46, p < 0.001) and CY/TBI+VP16 (HR 1.39, p = 0.059) compared to CY/TBI. Relapse was not suppressed, while treatment‐related mortality (TRM) was significantly higher (HR 1.78 and 1.74, p < 0.001 and 0.018, respectively). In the acute lymphoblastic leukemia (ALL) cohort (N = 3901, 61.2%), OS was comparable among these regimens. With intensified regimens, relapse was significantly suppressed in CY/TBI+VP16 (HR 0.74, p = 0.005), while TRM was higher (HR 1.21, p = 0.077). No interactions were observed regarding the country. Conclusion 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. Clinical Trial Registration The authors have confirmed clinical trial registration is not needed for this submission.

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