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降低所有人群的慢性移植物抗宿主病发生率。

Decreasing chronic graft-versus-host disease rates in all populations.

机构信息

Clinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA.

Department of Pediatrics, University of Washington Medical Center, Seattle, WA.

出版信息

Blood Adv. 2024 Nov 26;8(22):5829-5837. doi: 10.1182/bloodadvances.2024012722.

DOI:10.1182/bloodadvances.2024012722
PMID:39167805
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11609357/
Abstract

Since 2005, there has been a steady decline in chronic graft-versus-host disease (cGVHD) at the Fred Hutchinson Cancer Center. To better understand this phenomenon, we studied the risk of cGVHD requiring systemic immunosuppression (cGVHD-IS) as a function of hematopoietic cell transplantation (HCT) date in 3066 survivors from 2005 through 2019. Cox regression models were fit to assess associations of HCT date (as a continuous linear variable) with cause-specific hazards of cGVHD using unadjusted and adjusted models. Median follow-up for study subjects was 7.0 years (range, 1.0-17.2). Two-year probabilities of cGVHD-IS declined among all survivors from 45% to 52% (2005-2007) to ∼40% (2008-2012) and then further to ∼26% by 2017. A decline was also observed when the analysis was restricted to 502 pediatric survivors, with cGVHD-IS probabilities <10% since 2013. Among 305 adult and pediatric survivors who underwent transplantation for nonmalignant diseases, cGVHD rates showed greater fluctuation but remained <20% after 2016. Each 5-year increase in HCT date was associated with a 27% decrease in the cause-specific hazard of cGVHD (unadjusted hazard ratio [HR], 0.73; 95% confidence interval [CI], 0.68-0.78; P < .0001); the HR was 0.81 (95% CI, 0.75-0.87; P < .0001) even after adjusting for various factors (age, donor/stem-cell source, race, sex, conditioning intensity, GVHD prophylaxis, among others) that could lead to cGVHD reduction. The decline in cGVHD was not fully explained by demographic shifts and greater use of HCT approaches that are generally associated with lower cGVHD rates. This observation underscores that single-cohort cGVHD prevention studies should use contemporaneous and not historical controls for comparison.

摘要

自 2005 年以来,弗雷德·哈钦森癌症研究中心的慢性移植物抗宿主病(cGVHD)一直在稳步下降。为了更好地了解这一现象,我们研究了造血细胞移植(HCT)日期与 2005 年至 2019 年间 3066 名幸存者中需要系统性免疫抑制的 cGVHD(cGVHD-IS)风险之间的关系。使用未调整和调整后的模型,通过 Cox 回归模型评估 HCT 日期(作为连续线性变量)与 cGVHD 特定原因危害之间的关联。研究对象的中位随访时间为 7.0 年(范围,1.0-17.2)。所有幸存者的 cGVHD-IS 两年概率从 2005-2007 年的 45%降至 2008-2012 年的 40%左右,随后到 2017 年进一步降至约 26%。当分析仅限于 502 名儿科幸存者时,也观察到了下降,自 2013 年以来,cGVHD-IS 概率<10%。在 305 名接受非恶性疾病移植的成人和儿科幸存者中,cGVHD 发生率波动较大,但 2016 年后仍<20%。HCT 日期每增加 5 年,cGVHD 的特定原因危害降低 27%(未调整的危害比[HR],0.73;95%置信区间[CI],0.68-0.78;P<0.0001);即使在调整了可能导致 cGVHD 减少的各种因素(年龄、供体/干细胞来源、种族、性别、预处理强度、GVHD 预防等)后,HR 仍为 0.81(95%CI,0.75-0.87;P<.0001)。cGVHD 的下降不能完全用人口统计学的变化和更广泛使用通常与较低 cGVHD 率相关的 HCT 方法来解释。这一观察结果强调,单队列 cGVHD 预防研究应使用同期而不是历史对照进行比较。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/892f/11609357/38fa33a64c67/BLOODA_ADV-2024-012722-gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/892f/11609357/470840e0165e/BLOODA_ADV-2024-012722-ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/892f/11609357/1a4a6cd055b1/BLOODA_ADV-2024-012722-gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/892f/11609357/272c516b95dd/BLOODA_ADV-2024-012722-gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/892f/11609357/9031fe519770/BLOODA_ADV-2024-012722-gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/892f/11609357/38fa33a64c67/BLOODA_ADV-2024-012722-gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/892f/11609357/470840e0165e/BLOODA_ADV-2024-012722-ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/892f/11609357/1a4a6cd055b1/BLOODA_ADV-2024-012722-gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/892f/11609357/272c516b95dd/BLOODA_ADV-2024-012722-gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/892f/11609357/9031fe519770/BLOODA_ADV-2024-012722-gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/892f/11609357/38fa33a64c67/BLOODA_ADV-2024-012722-gr4.jpg

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