Combination of reduced post‐transplant cyclophosphamide and early tacrolimus initiation increases the incidence of chronic graft‐versus‐host disease in human leukocyte antigen‐haploidentical peripheral blood stem‐cell transplantation

Author:

Terao Toshiki1ORCID,Kondo Takumi1,Nakamura Makoto1,Takasuka Hiroki1,Fujiwara Hideaki1,Asada Noboru1ORCID,Ennishi Daisuke1,Nishimori Hisakazu1,Fujii Keiko12,Fujii Nobuharu13,Maeda Yoshinobu1,Matsuoka Ken‐ichi1ORCID

Affiliation:

1. Department of Hematology and Oncology Okayama University Hospital Okayama Okayama Japan

2. Division of Clinical Laboratory Okayama University Hospital Okayama Okayama Japan

3. Division of Blood Transfusion Okayama University Hospital Okayama Okayama Japan

Abstract

AbstractWe evaluated the clinical impacts of the concurrent modification of post‐transplant cyclophosphamide (PTCy) dose and tacrolimus (Tac)‐initiation timing in 61 patients with human leukocyte antigen‐haploidentical transplantation. Reduced‐dose PTCy (80 mg/kg) was associated with a higher incidence of moderate‐to‐severe chronic graft‐versus‐host disease (GVHD) than standard‐dose PTCy (100 mg/kg) (35.0% vs. 26.6%, p = 0.053). Notably, early‐initiation Tac (day ‐1) increased moderate‐to‐severe chronic GVHD than standard‐initiation Tac (day 5) in the reduced‐dose PTCy group (p = 0.032), whereas Tac‐initiation timing did not impact chronic GVHD in the standard‐dose PTCy group. These data indicate that the combination of reduced‐dose PTCy and early‐initiation Tac can amplify chronic GVHD.

Publisher

Wiley

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