Suppr超能文献

儿童白血病或骨髓增生异常综合征(MDS)经造血细胞移植(HCT)治疗后复发的预后。

Prognosis of relapse after hematopoietic cell transplant (HCT) for treatment of leukemia or myelodysplastic syndrome (MDS) in children.

机构信息

Fred Hutchinson Cancer Research Center and University of Washington, Seattle, WA, USA.

出版信息

Bone Marrow Transplant. 2019 Aug;54(8):1337-1345. doi: 10.1038/s41409-019-0438-z. Epub 2019 Jan 22.

Abstract

We studied 232 consecutive children transplanted between 1990 and 2011 with relapse after first hematopoietic cell transplant (HCT). Kaplan-Meier survival and hazard ratios for mortality were calculated for factors known at time of relapse using Cox proportional hazards models. The median (range) age at time of first HCT was 10.9 (0.5-20.9) years, time to relapse was 6.1 (0.2-89.5) months after HCT, and age at relapse was 11.7 (0.7-23.6) years. The 3-year overall survival (OS) after relapse was 13% (95% confidence interval (CI): 9%, 18%).The median (range) follow-up for the 18 surviving patients was 7.2 (3.0-24.4) years after relapse. The remaining 214 died after a median of 3 months (0.02-190.4). OS was not significantly different for patients with ALL as compared to AML. Fifty-one patients proceeded to second transplant of whom nine survive. Factors associated with improved survival included late relapse (>12 months), ALL in first CR at the time of first transplant and chemotherapy-based first conditioning regimens. These results can be used to counsel patients at the time of relapse after first transplant and as a baseline for comparison as to the effectiveness of newer therapies which are greatly needed for treatment of post-transplant relapse.

摘要

我们研究了 1990 年至 2011 年间接受过造血细胞移植(HCT)后首次复发的 232 例连续儿童。使用 Cox 比例风险模型,根据复发时已知的因素,计算Kaplan-Meier 生存和死亡率的风险比。首次 HCT 时的中位(范围)年龄为 10.9(0.5-20.9)岁,HCT 后复发的时间为 6.1(0.2-89.5)个月,复发时的年龄为 11.7(0.7-23.6)岁。复发后 3 年总生存率(OS)为 13%(95%置信区间(CI):9%,18%)。18 例存活患者的中位(范围)随访时间为复发后 7.2(3.0-24.4)年。其余 214 例患者在中位时间 3 个月(0.02-190.4)后死亡。与 AML 相比,ALL 患者的 OS 无显著差异。51 例患者接受了第二次移植,其中 9 例存活。与生存相关的因素包括晚期复发(>12 个月)、首次移植时首次完全缓解(CR)中的 ALL 和基于化疗的首次预处理方案。这些结果可用于在首次移植后复发时为患者提供咨询,并作为比较新疗法有效性的基线,新疗法对于治疗移植后复发非常必要。

相似文献

引用本文的文献

本文引用的文献

1
New developments in immunotherapy for pediatric leukemia.小儿白血病免疫治疗的新进展。
Curr Opin Pediatr. 2018 Feb;30(1):25-29. doi: 10.1097/MOP.0000000000000572.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验