Literature DB >> 28052467

The combination of cyclosporine and mycophenolate mofetil is less effective than cyclosporine and methotrexate in the prevention of acute graft-versus host disease after stem-cell transplantation from unrelated donors.

Ronit Yerushalmi1, Noga Shem-Tov1, Ivetta Danylesko1, Roni Shouval1, Arnon Nagler1, Avichai Shimoni1.   

Abstract

Acute graft-versus-host disease (GVHD) is the major treatment-related complication after stem-cell transplantation (SCT) from unrelated-donors. Several GVHD prophylaxis regimens have been explored, but no regimen has shown superiority. We analyzed transplantation outcomes in 472 consecutive unrelated-donor SCT recipients, using cyclosporine/methotrexate (MTX, n = 314) or cyclosporine/mycophenolate-mofetil (MMF, n = 158) for GVHD prophylaxis. Neutrophil engraftment was faster after MMF, days 11 and 14, respectively (P = .001). Acute GVHD grade II-IV and III-IV occurred in 47% and 28% after MMF compared to 27% and 12% after MTX, respectively (P < .001). Nonrelapse mortality (NRM) was 44% and 24%, respectively (P < .001). Death associated with GVHD occurred in 25% and 8% (P < .0001), while other NRM causes occurred in 19% and 16%, respectively (P = .39). Relapse mortality was similar. Overall survival was better after MTX, 40% and 29%, respectively (P = .006). However, this difference had only borderline significance when adjusting for differences in patient characteristics (HR, 1.3, P = .08). To minimize potential selection bias we analyzed outcomes on the basis of an intention-to-treat like analysis. During the years 2008-2009, the leading GVHD prophylaxis regimen for unrelated-donor SCT included MMF (89% of transplants). During the other periods, MTX was used predominantly (82% of transplants). The two periods were otherwise well-matched. Acute GVHD occurred more often in 2008-2009. Death associated with GVHD occurred more often, while other NRM causes occurred less often resulting in similar NRM and overall survival. In conclusion, cyclosporine/MMF is associated with faster engraftment and possibly with less organ toxicity than cyclosporine/MTX. However, it is associated with increased rates of acute GVHD and GVHD-associated deaths.
© 2017 Wiley Periodicals, Inc.

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Year:  2017        PMID: 28052467     DOI: 10.1002/ajh.24631

Source DB:  PubMed          Journal:  Am J Hematol        ISSN: 0361-8609            Impact factor:   10.047


  4 in total

Review 1.  Clinical potential of mesenchymal stem/stromal cell-derived extracellular vesicles.

Authors:  Bernd Giebel; Lambros Kordelas; Verena Börger
Journal:  Stem Cell Investig       Date:  2017-10-24

2.  A prospective single-center study on CNI-free GVHD prophylaxis with everolimus plus mycophenolate mofetil in allogeneic HCT.

Authors:  Henning Schäfer; Jacqueline Blümel-Lehmann; Gabriele Ihorst; Hartmut Bertz; Ralph Wäsch; Robert Zeiser; Jürgen Finke; Reinhard Marks
Journal:  Ann Hematol       Date:  2021-03-23       Impact factor: 3.673

3.  Cytomegalovirus gastroenteritis in patients with acute graft-versus-host disease.

Authors:  Yu Akahoshi; Shun-Ichi Kimura; Yuma Tada; Toshihiro Matsukawa; Masaharu Tamaki; Noriko Doki; Naoyuki Uchida; Masatsugu Tanaka; Hirohisa Nakamae; Takuro Kuriyama; Ken-Ichi Matsuoka; Takashi Ikeda; Takafumi Kimura; Takahiro Fukuda; Yoshinobu Kanda; Yoshiko Atsuta; Makoto Murata; Seitaro Terakura; Hideki Nakasone
Journal:  Blood Adv       Date:  2022-01-25

4.  [Impact of mycophenolate mofetil prophylaxis duration on acute graft-versus-host disease after haploidentical stem cell transplantation].

Authors:  Y Q Sun; X J Huang; L P Xu; X H Zhang; C H Yan; K Y Liu; Y Wang
Journal:  Zhonghua Xue Ye Xue Za Zhi       Date:  2018-04-14
  4 in total

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