TY - JOUR
T1 - Hematopoietic Cell Transplantation for Inborn Errors of Immunity Other than Severe Combined Immunodeficiency in Japan
T2 - Retrospective Analysis for 1985–2016
AU - Miyamoto, Satoshi
AU - Umeda, Katsutsugu
AU - Kurata, Mio
AU - Yanagimachi, Masakatsu
AU - Iguchi, Akihiro
AU - Sasahara, Yoji
AU - Okada, Keiko
AU - Koike, Takashi
AU - Tanoshima, Reo
AU - Ishimura, Masataka
AU - Yamada, Masafumi
AU - Sato, Maho
AU - Takahashi, Yoshiyuki
AU - Kajiwara, Michiko
AU - Kawaguchi, Hiroshi
AU - Inoue, Masami
AU - Hashii, Yoshiko
AU - Yabe, Hiromasa
AU - Kato, Koji
AU - Atsuta, Yoshiko
AU - Imai, Kohsuke
AU - Morio, Tomohiro
N1 - Funding Information:
This work was supported by the Japanese Ministry of Health, Labor, and Welfare [grant number 20FC1053], and Japan Agency for Medical Research and Development [grant numbers JP19lk0201100 and JP19gk0110041].
Funding Information:
We thank the Japan Marrow Donor Program, the cord blood banks in Japan, and the staff at the participating hospitals who attended to the patients and provided information for the TRUMP registry. We also thank Soichi Adachi, Shunichi Kato, Yasuo Horikoshi, Miharu Yabe, Nao Yoshida, Hiromitsu Takakura, Sae Ishimaru, Shinya Osone, Hidetoshi Takada, Nozomu Kawashima, Shinobu Tamura, Ayako Yamamori, Koji Kawaguchi, Akira Nishimura, Risa Matsumura, and Takako Miyamura, who supported this study as members of the Hereditary Disorder Working Group of the Japanese Society for Transplantation and Cellular Therapy. We would also like to thank Kay Tanita for her support in preparing the figures.
Publisher Copyright:
© 2022, The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.
PY - 2022/4
Y1 - 2022/4
N2 - Purpose: Hematopoietic cell transplantation (HCT) is a curative therapy for most patients with inborn errors of immunity (IEI). We conducted a nationwide study on HCT for patients with IEI other than severe combined immunodeficiency (non-SCID) in Japan. Methods: Data from the Japanese national database (Transplant Registry Unified Management Program, TRUMP) for 566 patients with non-SCID IEI, who underwent their first HCT between 1985 and 2016, were retrospectively analyzed. Results: The 10-year overall survival (OS) and event-free survival (EFS) were 74% and 64%, respectively. The 10-year OS for HCT from unrelated bone marrow (URBM), accounting for 39% of HCTs, was comparable to that for HCT from matched sibling donor (MSD), 79% and 81%, respectively. HCT from unrelated cord blood (URCB), accounting for 28% of HCTs, was also common, with a 10-year OS of 69% but less robust engraftment. The intensity of conditioning was not associated with OS or neutrophil recovery; however, myeloablative conditioning was more frequently associated with infection-related death. Patients who received myeloablative irradiation showed poor OS. Multivariate analyses revealed that HCT in 1985–1995 (hazard ratio [HR], 2.0; P = 0.03), URCB (HR, 2.0; P = 0.01), and related donor other than MSD (ORD) (HR, 2.9; P < 0.001) were associated with poor OS, and URCB (HR, 3.6; P < 0.001) and ORD (HR, 2.7; P = 0.02) showed a higher incidence of retransplantation. Conclusions: We present the 1985–2016 status of HCT for non-SCID IEI in Japan with sufficient statistical power, highlighting the potential of URBM as an alternative donor and the feasibility of reduced intensity conditioning.
AB - Purpose: Hematopoietic cell transplantation (HCT) is a curative therapy for most patients with inborn errors of immunity (IEI). We conducted a nationwide study on HCT for patients with IEI other than severe combined immunodeficiency (non-SCID) in Japan. Methods: Data from the Japanese national database (Transplant Registry Unified Management Program, TRUMP) for 566 patients with non-SCID IEI, who underwent their first HCT between 1985 and 2016, were retrospectively analyzed. Results: The 10-year overall survival (OS) and event-free survival (EFS) were 74% and 64%, respectively. The 10-year OS for HCT from unrelated bone marrow (URBM), accounting for 39% of HCTs, was comparable to that for HCT from matched sibling donor (MSD), 79% and 81%, respectively. HCT from unrelated cord blood (URCB), accounting for 28% of HCTs, was also common, with a 10-year OS of 69% but less robust engraftment. The intensity of conditioning was not associated with OS or neutrophil recovery; however, myeloablative conditioning was more frequently associated with infection-related death. Patients who received myeloablative irradiation showed poor OS. Multivariate analyses revealed that HCT in 1985–1995 (hazard ratio [HR], 2.0; P = 0.03), URCB (HR, 2.0; P = 0.01), and related donor other than MSD (ORD) (HR, 2.9; P < 0.001) were associated with poor OS, and URCB (HR, 3.6; P < 0.001) and ORD (HR, 2.7; P = 0.02) showed a higher incidence of retransplantation. Conclusions: We present the 1985–2016 status of HCT for non-SCID IEI in Japan with sufficient statistical power, highlighting the potential of URBM as an alternative donor and the feasibility of reduced intensity conditioning.
KW - Inborn errors of immunity
KW - Japan
KW - hematopoietic cell transplantation
KW - retrospective study
KW - umbilical cord blood transplantation
UR - http://www.scopus.com/inward/record.url?scp=85122242762&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85122242762&partnerID=8YFLogxK
U2 - 10.1007/s10875-021-01199-w
DO - 10.1007/s10875-021-01199-w
M3 - Article
C2 - 34981329
AN - SCOPUS:85122242762
SN - 0271-9142
VL - 42
SP - 529
EP - 545
JO - Journal of Clinical Immunology
JF - Journal of Clinical Immunology
IS - 3
ER -