TY - JOUR
T1 - Comparison of reduced-intensity/toxicity conditioning regimens for umbilical cord blood transplantation for lymphoid malignancies
AU - for the Donor/Source Working Group of the Japan Society for Hematopoietic Cell Transplantation
AU - Imahashi, Nobuhiko
AU - Terakura, Seitaro
AU - Kondo, Eisei
AU - Kako, Shinichi
AU - Uchida, Naoyuki
AU - Kobayashi, Hikaru
AU - Inamoto, Yoshihiro
AU - Sakai, Hitoshi
AU - Tanaka, Masatsugu
AU - Ishikawa, Jun
AU - Kozai, Yasuji
AU - Matsuoka, Ken ichi
AU - Kimura, Takafumi
AU - Fukuda, Takahiro
AU - Atsuta, Yoshiko
AU - Kanda, Junya
AU - Kanda, Junya
AU - Ago, Hiroatsu
AU - Atsuta, Yoshiko
AU - Imai, Kiyotoshi
AU - Uchida, Naoyuki
AU - Kato, Koji
AU - Kato, Shunichi
AU - Kanda, Yoshinobu
AU - Kuwatsuka, Yachiyo
AU - Kobayashi, Takeshi
AU - Sawa, Masashi
AU - Sunami, Kazutaka
AU - Seo, Sachiko
AU - Tanaka, Masatsugu
AU - Taniguchi, Shuichi
AU - Tabuchi, Ken
AU - Tsukada, Nobuhiro
AU - Terakura, Seitaro
AU - Nagata, Yasuyuki
AU - Nishiwaki, Satoshi
AU - Fujita, Naoto
AU - Matsuno, Ryosuke
AU - Matsumoto, Kimikazu
AU - Mitamura, Shin
AU - Mihara, Hidetsugu
AU - Miyamura, Koichi
AU - Morishima, Yasuo
AU - Yakushijin, Kimikazu
AU - Watanabe, Nobuhiro
AU - Ishiyama, Ken
AU - Kimura, Fumihiko
AU - Nagafuji, Koji
AU - Yabe, Toshio
AU - Imahashi, Nobuhiko
N1 - Funding Information:
Acknowledgements We thank all staff members of the collaborating institutions of the Japan Society for Hematopoietic Cell Transplantation (JSHCT) and all the members of the data management committees of the JSHCT. This work was supported in part by the Practical Research Project for Allergic Diseases and Immunology (Research Technology of Medical Transplantation) from the Japan Agency for Medical Research and Development, AMED, under grant number 19ek0510023h0002.
Publisher Copyright:
© 2020, The Author(s), under exclusive licence to Springer Nature Limited.
PY - 2020/11/1
Y1 - 2020/11/1
N2 - To investigate which reduced-intensity conditioning (RIC)/reduced-toxicity conditioning (RTC) is superior for umbilical cord blood transplantation (UCBT) for lymphoid malignancies, we retrospectively compared three widely used RIC/RTC regimens: fludarabine/melphalan/total body irradiation (FM-TBI, n = 524), fludarabine/cyclophosphamide/total body irradiation (FC-TBI, n = 96), and fludarabine/busulfan/total body irradiation or melphalan (FB-based, n = 159). Among patients with acute lymphoblastic leukemia (ALL) (n = 314), there were no differences in overall survival (OS) by conditioning regimen. Among patients with malignant lymphoma (ML) (n = 465), FM-TBI and FC-TBI regimens had similar OS, whereas FB-based regimen had lower OS (hazard ratio [HR], 1.73; P < 0.01) than did FM-TBI regimen due to higher non-relapse mortality (HR, 1.72; P = 0.02). In addition, mycophenolate mofetil-containing GVHD prophylaxis was associated with better OS than methotrexate-containing GVHD prophylaxis among patients who received FM-TBI (HR, 0.65; P = 0.03) and FC-TBI (HR, 0.25; P < 0.01) regimens due to a decreased relapse risk. In summary, our results suggest that all three RIC/RTC regimens have comparable clinical outcomes in ALL, while the FM-TBI or FC-TBI regimens combined with mycophenolate mofetil-containing GVHD prophylaxis is preferable in RIC/RTC-UCBT for ML. Large prospective studies are warranted to confirm these results.
AB - To investigate which reduced-intensity conditioning (RIC)/reduced-toxicity conditioning (RTC) is superior for umbilical cord blood transplantation (UCBT) for lymphoid malignancies, we retrospectively compared three widely used RIC/RTC regimens: fludarabine/melphalan/total body irradiation (FM-TBI, n = 524), fludarabine/cyclophosphamide/total body irradiation (FC-TBI, n = 96), and fludarabine/busulfan/total body irradiation or melphalan (FB-based, n = 159). Among patients with acute lymphoblastic leukemia (ALL) (n = 314), there were no differences in overall survival (OS) by conditioning regimen. Among patients with malignant lymphoma (ML) (n = 465), FM-TBI and FC-TBI regimens had similar OS, whereas FB-based regimen had lower OS (hazard ratio [HR], 1.73; P < 0.01) than did FM-TBI regimen due to higher non-relapse mortality (HR, 1.72; P = 0.02). In addition, mycophenolate mofetil-containing GVHD prophylaxis was associated with better OS than methotrexate-containing GVHD prophylaxis among patients who received FM-TBI (HR, 0.65; P = 0.03) and FC-TBI (HR, 0.25; P < 0.01) regimens due to a decreased relapse risk. In summary, our results suggest that all three RIC/RTC regimens have comparable clinical outcomes in ALL, while the FM-TBI or FC-TBI regimens combined with mycophenolate mofetil-containing GVHD prophylaxis is preferable in RIC/RTC-UCBT for ML. Large prospective studies are warranted to confirm these results.
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U2 - 10.1038/s41409-020-0905-6
DO - 10.1038/s41409-020-0905-6
M3 - Article
C2 - 32440015
AN - SCOPUS:85085030119
SN - 0268-3369
VL - 55
SP - 2098
EP - 2108
JO - Bone Marrow Transplantation
JF - Bone Marrow Transplantation
IS - 11
ER -