TY - JOUR
T1 - Use of mycophenolate mofetil and a calcineurin inhibitor in allogeneic hematopoietic stem-cell transplantation from HLA-matched siblings or unrelated volunteer donors
T2 - Japanese multicenter phase II trials
AU - Nakane, Takahiko
AU - Nakamae, Hirohisa
AU - Yamaguchi, Takuhiro
AU - Kurosawa, Saiko
AU - Okamura, Atsuo
AU - Hidaka, Michihiro
AU - Fuji, Shigeo
AU - Kohno, Akio
AU - Saito, Takeshi
AU - Aoyama, Yasutaka
AU - Hatanaka, Kazuo
AU - Katayama, Yoshio
AU - Yakushijin, Kimikazu
AU - Matsui, Toshimitsu
AU - Yamamori, Motohiro
AU - Takami, Akiyoshi
AU - Hino, Masayuki
AU - Fukuda, Takahiro
N1 - Funding Information:
This work was supported in part by grants from the National Cancer Research and Development Fund (26-A-26) and Health and Labour Sciences Research Grants (Gan Rinsho) from the Ministry of Health, Labour and Welfare, Japan. HN and MH received grants and personal fees from CHUGAI PHARMACEUTICAL CO.,LTD., outside the submitted work. AT received grant from CHUGAI PHARMACEUTICAL CO.,LTD., outside the submitted work. All other authors have no conflicts of interest to disclose.
Publisher Copyright:
© 2016, The Japanese Society of Hematology.
PY - 2017/4/1
Y1 - 2017/4/1
N2 - To test the feasibility of mycophenolate mofetil (MMF) for graft-versus-host disease (GVHD) prophylaxis in Japanese patients, we conducted two multicenter prospective phase II trials of allogeneic hematopoietic stem-cell transplantation (HSCT) from HLA-matched related donors (MRD group) with MMF and cyclosporine or HLA 7–8/8 allele-matched unrelated bone-marrow donors (URD group) with MMF and tacrolimus. The cumulative incidences of grade II–IV acute GVHD on day 100, which was the primary endpoint in these trials, were 45.0% (90% CI 25.8–62.5) and 25.8% (90% CI 13.9–39.5) in the MRD (n = 20) and URD (n = 31) groups, respectively. The rates of 3-year overall survival and non-relapse mortality were 80.0 and 15.0% in the MRD group and 74.2 and 6.5% in the URD group, respectively. GVHD prophylaxis with MMF may lead to a lower incidence of severe mucositis and faster neutrophil engraftment compared to that with methotrexate. A pharmacokinetics study of mycophenolic acid (MPA) showed that a relatively higher plasma concentration of MPA was associated with a lower incidence of acute GVHD. In conclusion, the results of these studies suggest that GVHD prophylaxis with MMF may be useful as an alternative in Japanese patients who may benefit from faster engraftment or less severe mucositis after allogeneic HSCT.
AB - To test the feasibility of mycophenolate mofetil (MMF) for graft-versus-host disease (GVHD) prophylaxis in Japanese patients, we conducted two multicenter prospective phase II trials of allogeneic hematopoietic stem-cell transplantation (HSCT) from HLA-matched related donors (MRD group) with MMF and cyclosporine or HLA 7–8/8 allele-matched unrelated bone-marrow donors (URD group) with MMF and tacrolimus. The cumulative incidences of grade II–IV acute GVHD on day 100, which was the primary endpoint in these trials, were 45.0% (90% CI 25.8–62.5) and 25.8% (90% CI 13.9–39.5) in the MRD (n = 20) and URD (n = 31) groups, respectively. The rates of 3-year overall survival and non-relapse mortality were 80.0 and 15.0% in the MRD group and 74.2 and 6.5% in the URD group, respectively. GVHD prophylaxis with MMF may lead to a lower incidence of severe mucositis and faster neutrophil engraftment compared to that with methotrexate. A pharmacokinetics study of mycophenolic acid (MPA) showed that a relatively higher plasma concentration of MPA was associated with a lower incidence of acute GVHD. In conclusion, the results of these studies suggest that GVHD prophylaxis with MMF may be useful as an alternative in Japanese patients who may benefit from faster engraftment or less severe mucositis after allogeneic HSCT.
KW - Allogeneic hematopoietic stem-cell transplantation
KW - Graft-versus-host disease prophylaxis
KW - Mycophenolate mofetil
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U2 - 10.1007/s12185-016-2154-4
DO - 10.1007/s12185-016-2154-4
M3 - Article
C2 - 27943166
AN - SCOPUS:85004190427
SN - 0925-5710
VL - 105
SP - 485
EP - 496
JO - International Journal of Hematology
JF - International Journal of Hematology
IS - 4
ER -