Adverse Impact of Pre‐Transplant Liver Dysfunction in Allogeneic Hematopoietic Cell Transplantation

医学 内科学 肝移植 胃肠病学 造血细胞 丙型肝炎 不利影响 多元分析 移植 造血 干细胞 生物 遗传学
作者
Yukiko Misaki,Masaharu Tamaki,Ryu Yanagisawa,Noriko Doki,Naoyuki Uchida,Masatsugu Tanaka,Tetsuya Nishida,Masashi Sawa,Yuta Hasegawa,Shuichi Ota,Makoto Onizuka,Mamiko Sakata‐Yanagimoto,Yuta Katayama,Noboru Asada,Junya Kanda,Takahiro Fukuda,Yoshiko Atsuta,Yoshinobu Kanda,Kimikazu Yakushijin,Hideki Nakasone
出处
期刊:American Journal of Hematology [Wiley]
标识
DOI:10.1002/ajh.27652
摘要

Although the hematopoietic cell transplantation (HCT)-comorbidity index (HCT-CI) score is associated with an increased risk of mortality after allogeneic HCT, it remains unclear how pre-HCT liver dysfunction affects clinical outcomes. We retrospectively compared clinical HCT outcomes among four groups stratified according to the presence of HCT-CI liver and other organ scores, using a Japan transplant registry database between 2010 and 2020. Of the 14235 recipients, 1527 tested positive for an HCT-CI liver score including HBV or HCV hepatitis (n = 503). The 5-year overall survival (OS) was significantly lower in the HCT-CI liver(+) other(+) and HCT-CI liver(-) other(+) groups compared to the HCT-CI liver(+) other(-) and HCT-CI liver(-) other(-) groups [49.9% vs. 59% vs. 66.5% vs. 68.3%, p < 0.001]. A multivariate analysis showed that both the HCT-CI liver(+) other(+) [HR 1.62, p < 0.001] and HCT-CI liver(-) other(+) groups [HR 1.21, p < 0.001] were significantly associated with inferior OS. Similarly, both the HCT-CI liver(+) other(+) [HR 1.89, p < 0.001] and liver(-) other(+) groups [HR 1.26, p < 0.001] were significantly associated with an increased risk of NRM. On the other hand, the HCT-CI liver(+) other(-) group was not associated with either OS or NRM. Separately analyzing the subcohorts with or without HCT-CI other scores, the presence of an HCT-CI liver score alone did not affect survival, while the co-presence of pretransplant liver dysfunction seemed to synergistically increase the adverse impact on OS and NRM among recipients with other organ comorbidities. Further studies will be needed to identify optimal strategies for recipients with pretransplant liver dysfunction.
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