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
Toshiki Terao,
Takumi Kondo,
Makoto Nakamura,
Hiroki Takasuka,
Hideaki Fujiwara,
Noboru Asada,
Daisuke Ennishi,
Hisakazu Nishimori,
Keiko Fujii,
Nobuharu Fujii,
Yoshinobu Maeda,
Ken‐ichi Matsuoka
Affiliations
Toshiki Terao
Department of Hematology and Oncology Okayama University Hospital Okayama Okayama Japan
Takumi Kondo
Department of Hematology and Oncology Okayama University Hospital Okayama Okayama Japan
Makoto Nakamura
Department of Hematology and Oncology Okayama University Hospital Okayama Okayama Japan
Hiroki Takasuka
Department of Hematology and Oncology Okayama University Hospital Okayama Okayama Japan
Hideaki Fujiwara
Department of Hematology and Oncology Okayama University Hospital Okayama Okayama Japan
Noboru Asada
Department of Hematology and Oncology Okayama University Hospital Okayama Okayama Japan
Daisuke Ennishi
Department of Hematology and Oncology Okayama University Hospital Okayama Okayama Japan
Hisakazu Nishimori
Department of Hematology and Oncology Okayama University Hospital Okayama Okayama Japan
Keiko Fujii
Department of Hematology and Oncology Okayama University Hospital Okayama Okayama Japan
Nobuharu Fujii
Department of Hematology and Oncology Okayama University Hospital Okayama Okayama Japan
Yoshinobu Maeda
Department of Hematology and Oncology Okayama University Hospital Okayama Okayama Japan
Ken‐ichi Matsuoka
Department of Hematology and Oncology Okayama University Hospital Okayama Okayama Japan
Abstract We 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.