TY - JOUR
T1 - Prognostic Impact of the Fractionation of Total Body Irradiation for Patients with Acute Myeloid Leukemia Undergoing Myeloablative Allogeneic Hematopoietic Cell Transplantation
AU - Ueda, Norihiro
AU - Konuma, Takaaki
AU - Aoki, Jun
AU - Takahashi, Satoshi
AU - Ozawa, Yukiyasu
AU - Mori, Takehiko
AU - Ota, Shuichi
AU - Eto, Tetsuya
AU - Takada, Satoru
AU - Yoshioka, Satoshi
AU - Shiratori, Souichi
AU - Kako, Shinichi
AU - Onizuka, Makoto
AU - Fukuda, Takahiro
AU - Kanda, Yoshinobu
AU - Atsuta, Yoshiko
AU - Yanada, Masamitsu
N1 - Funding Information:
Financial disclosure: This work was supported in part by a grant from the Practical Research Project for Allergic Diseases and Immunology (Research Technology of Medical Transplantation) from the Japan Agency for Medical Research and Development (grant 18ek0510023h0002) and a grant from the Aichi Cancer Research Foundation (grant 2020-1-11).
Publisher Copyright:
© 2020 The American Society for Transplantation and Cellular Therapy
PY - 2021/2
Y1 - 2021/2
N2 - Fractionated total body irradiation (TBI) at a total dose of 12 Gy is widely used for patients with acute myeloid leukemia (AML) undergoing allogeneic hematopoietic cell transplantation (HCT); however, there is limited information regarding the optimal number of fractions. To address this issue, Japanese nationwide transplantation registry data were analyzed. Because it was found that TBI was delivered almost exclusively in 4 (n = 1215, 30%) or 6 fractions (n = 2697, 67%), we focused on comparing 4- versus 6-fraction TBI. Compared to 6-fraction TBI, the 4-fraction version was associated with reduced risk of overall mortality (P = .002) and relapse (P = .018), while there was no difference in the risk of nonrelapse mortality (P = .422). The 4-fraction version did not aggravate acute graft-versus-host disease (GVHD), interstitial pneumonia, or sinusoidal obstruction syndrome of the liver. Chronic GVHD developed more frequently with the use of 4-fraction TBI, although the incidence of extensive chronic GVHD was similar. Subgroup analyses revealed that the 4-fraction version provided benefits for patients in non-complete remission (non-CR) but not for those in CR at transplantation. These findings suggest the advantage of 4-fraction over 6-fraction TBI for patients with AML undergoing allogeneic HCT in non-CR.
AB - Fractionated total body irradiation (TBI) at a total dose of 12 Gy is widely used for patients with acute myeloid leukemia (AML) undergoing allogeneic hematopoietic cell transplantation (HCT); however, there is limited information regarding the optimal number of fractions. To address this issue, Japanese nationwide transplantation registry data were analyzed. Because it was found that TBI was delivered almost exclusively in 4 (n = 1215, 30%) or 6 fractions (n = 2697, 67%), we focused on comparing 4- versus 6-fraction TBI. Compared to 6-fraction TBI, the 4-fraction version was associated with reduced risk of overall mortality (P = .002) and relapse (P = .018), while there was no difference in the risk of nonrelapse mortality (P = .422). The 4-fraction version did not aggravate acute graft-versus-host disease (GVHD), interstitial pneumonia, or sinusoidal obstruction syndrome of the liver. Chronic GVHD developed more frequently with the use of 4-fraction TBI, although the incidence of extensive chronic GVHD was similar. Subgroup analyses revealed that the 4-fraction version provided benefits for patients in non-complete remission (non-CR) but not for those in CR at transplantation. These findings suggest the advantage of 4-fraction over 6-fraction TBI for patients with AML undergoing allogeneic HCT in non-CR.
KW - Acute myeloid leukemia
KW - Allogeneic hematopoietic cell transplantation
KW - Fractionation
KW - Total body irradiation
UR - http://www.scopus.com/inward/record.url?scp=85101157224&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85101157224&partnerID=8YFLogxK
U2 - 10.1016/j.jtct.2020.10.018
DO - 10.1016/j.jtct.2020.10.018
M3 - Article
AN - SCOPUS:85101157224
SN - 2666-6375
VL - 27
SP - 185.e1-185.e6
JO - Transplantation and Cellular Therapy
JF - Transplantation and Cellular Therapy
IS - 2
ER -