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急性移植物抗宿主病的疾病进展、治疗、住院和临床结局:一项多中心图表回顾。

Disease progression, treatments, hospitalization, and clinical outcomes in acute GVHD: a multicenter chart review.

机构信息

Univeristy of Minnesota, Minneapolis, MN, USA.

Incyte Corporation, Wilmington, DE, USA.

出版信息

Bone Marrow Transplant. 2022 Oct;57(10):1581-1585. doi: 10.1038/s41409-022-01764-w. Epub 2022 Jul 30.

DOI:10.1038/s41409-022-01764-w
PMID:35908108
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9576589/
Abstract

Acute graft-versus-host disease (GVHD) remains a barrier to successful allogeneic hematopoietic cell transplantation (HCT) outcomes. This multicenter, retrospective chart review describes disease progression, treatment patterns, hospitalizations, and clinical outcomes among 475 patients (≥12 years old) who developed grades II-IV acute GVHD after their first HCT (January 2014-June 2016). Median (interquartile range) age at HCT was 55 (44-63) years. From the date of acute GVHD diagnosis, 190 patients (40.0%) experienced progression to more severe disease and/or developed new organ involvement. Among 431 patients with grades II-IV acute GVHD at diagnosis, 73.1% received first-line systemic corticosteroids. During follow-up (median 524 days since acute GVHD diagnosis), 23.4% of patients had an increase in steroid dose and 44.4% were unable to taper below 10 mg/day. Over half of patients (54.9%) required ≥1 hospital readmission within 100 days post-HCT (≥2 readmissions in 22.3%); mean inpatient length of stay upon readmission was 27.5 days. Approximately half of patients (52.8%) died during follow-up; 1-year overall mortality from date of acute GVHD diagnosis and nonrelapse mortality rates were 35.2% and 25.5%, respectively. Overall, patients who developed acute GVHD following HCT had poor clinical outcomes, highlighting the unmet need for early and effective treatment strategies.

摘要

急性移植物抗宿主病(GVHD)仍然是异体造血细胞移植(HCT)成功的障碍。这项多中心回顾性图表研究描述了 475 名(年龄≥12 岁)首次 HCT 后发生 II-IV 级急性 GVHD 的患者的疾病进展、治疗模式、住院和临床结局。HCT 时的中位(四分位距)年龄为 55(44-63)岁。从急性 GVHD 诊断之日起,190 名患者(40.0%)病情进展为更严重的疾病和/或发生新的器官受累。在 431 名诊断为 II-IV 级急性 GVHD 的患者中,73.1%接受了一线全身性皮质类固醇治疗。在随访期间(从急性 GVHD 诊断之日起中位数为 524 天),23.4%的患者增加了类固醇剂量,44.4%的患者无法将剂量降至 10mg/天以下。超过一半的患者(54.9%)在 HCT 后 100 天内需要至少 1 次住院(22.3%需要 2 次以上住院);再次入院时的平均住院时间为 27.5 天。大约一半的患者(52.8%)在随访期间死亡;从急性 GVHD 诊断之日起的 1 年总死亡率和非复发死亡率分别为 35.2%和 25.5%。总体而言,接受 HCT 后发生急性 GVHD 的患者临床结局较差,突出表明需要早期和有效的治疗策略。

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