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The stability of initial tacrolimus concentration following allogeneic hematopoietic stem cell transplantation reduces the risk of acute GVHD
Author(s) -
Okabe Motohito,
Morishita Takanobu,
Ichiki Tomoe,
Kawaguchi Yuka,
Lee Yoonha,
Ohbiki Marie,
Goto Miyo,
Osaki Masahide,
Araie Hiroaki,
Goto Tatsunori,
Ozawa Yukiyasu,
Miyamura Koichi
Publication year - 2020
Publication title -
clinical transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.918
H-Index - 76
eISSN - 1399-0012
pISSN - 0902-0063
DOI - 10.1111/ctr.14052
Subject(s) - medicine , tacrolimus , cumulative incidence , hematopoietic stem cell transplantation , methotrexate , confidence interval , odds ratio , gastroenterology , incidence (geometry) , transplantation , physics , optics
Background Early tacrolimus (TAC) concentrations correlate with the risk of acute graft‐versus‐host disease (aGVHD); however, whether the variability of early TAC concentrations after allo‐HSCT governs the occurrence of aGVHD remains unknown. Here, we evaluate the correlation between the intrapatient variability (IPV) of initial TAC concentrations and the development of aGVHD. Methods We retrospectively assessed 202 patients who underwent allo‐HSCT and received standard GVHD prophylaxis by continuous intravenous (iv) infusion of TAC and iv methotrexate. IPV was calculated by using the % coefficient of variation in the initial 4 weeks. Results With median follow‐up duration of 20.7 months, 24 patients were diagnosed with grades II‐IV aGVHD. Overall survival (OS) and relapse at 12 months after allo‐HSCT were 70.6% (95% confidence interval [CI], 63.7%‐76.4%) and 18.9% (95% CI, 13.0%‐24.4%), respectively. When IPV was categorized into two groups (high: ≥9.5%; low: <9.5%), the cumulative incidence of grades II‐IV aGVHD was greater in the IPV‐high group at week 3 (odds ratio: 4.15; 95% CI, 1.37%‐12.6%, P = .01). No significant differences were observed in OS and relapse between the two groups. Conclusion We concluded that adjusting early TAC concentration stable may reduce aGVHD after allo‐HSCT without affecting the relapse rate.