Cell Transplantation (Aug 2023)

Mild Acute Graft-Versus-Host Disease Improves Outcomes After HLA-Haploidentical-Related Donor Transplantation Using Posttransplant Cyclophosphamide and Cord Blood Transplantation

  • Fumiya Wada,
  • Junya Kanda,
  • Kimimori Kamijo,
  • Masashi Nishikubo,
  • Satoshi Yoshioka,
  • Takayuki Ishikawa,
  • Yasunori Ueda,
  • Takashi Akasaka,
  • Yasuyuki Arai,
  • Kiyotaka Izumi,
  • Hirokazu Hirata,
  • Takashi Ikeda,
  • Akihito Yonezawa,
  • Naoyuki Anzai,
  • Mitsumasa Watanabe,
  • Kazunori Imada,
  • Kazuhiro Yago,
  • Naoki Tamura,
  • Mitsuru Itoh,
  • Yuki Masuo,
  • Akane Kunitomi,
  • Tomoharu Takeoka,
  • Toshiyuki Kitano,
  • Nobuyoshi Arima,
  • Masakatsu Hishizawa,
  • Kohsuke Asagoe,
  • Tadakazu Kondo,
  • Akifumi Takaori-Kondo

DOI
https://doi.org/10.1177/09636897231194497
Journal volume & issue
Vol. 32

Abstract

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Haploidentical-related donor transplantation using posttransplant cyclophosphamide (PTCy-haplo) and cord blood transplantation (CBT) are valid alternatives for patients with hematological malignancies when HLA-matched donor transplantation (MDT) is unavailable. However, the effects of graft-versus-host disease (GVHD) on outcomes after these transplants have not been fully elucidated. Therefore, we evaluated the effects of acute and chronic GVHD on transplant outcomes after PTCy-haplo transplants and compared them with CBT and MDT. We included a total of 914 adult patients with hematological malignancies in the Kyoto Stem Cell Transplantation Group registry who received PTCy-haplo (N = 120), CBT (N = 402), and MDT (N = 392), and achieved neutrophil engraftment. A multivariate analysis revealed that grade I–II acute GVHD improved of overall survival (OS) after PTCy-haplo [hazard ratio (HR) = 0.39, P = 0.018] and CBT (HR = 0.48, P < 0.001), but not after MDT (HR = 0.80, P = 0.267) compared with patients without acute GVHD. Grade I–II acute GVHD had a trend toward reducing the risk of nonrelapse mortality (NRM) after PTCy-haplo (HR = 0.13, P = 0.060) and this positive effect was significant after CBT (HR = 0.39, P = 0.003). A negative impact of grade III–IV acute GVHD on NRM was observed after CBT and MDT, but not after PTCy-haplo. Limited chronic GVHD had a positive impact on OS after CBT and MDT, but not after PTCy-haplo. In conclusion, mild acute GVHD improved outcomes after PTCy-haplo and CBT, and limited chronic GVHD improved outcomes after CBT and MDT. These data indicated that the effects of GVHD on transplant outcomes depended on transplant platforms.