Suppr超能文献

多中心生物制剂分配试验:比较降低强度的异基因造血细胞移植与低甲基化疗法或最佳支持治疗,用于年龄在50至75岁、患有中危2和高危骨髓增生异常综合征的患者:血液和骨髓移植临床试验网络#1102研究原理、设计和方法

Multicenter biologic assignment trial comparing reduced-intensity allogeneic hematopoietic cell transplant to hypomethylating therapy or best supportive care in patients aged 50 to 75 with intermediate-2 and high-risk myelodysplastic syndrome: Blood and Marrow Transplant Clinical Trials Network #1102 study rationale, design, and methods.

作者信息

Saber Wael, Le Rademacher Jennifer, Sekeres Mikkael, Logan Brent, Lewis Moira, Mendizabal Adam, Leifer Eric, Appelbaum Frederick R, Horowitz Mary M, Nakamura Ryotaro, Cutler Corey S

机构信息

Center for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, Wisconsin.

Center for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, Wisconsin.

出版信息

Biol Blood Marrow Transplant. 2014 Oct;20(10):1566-72. doi: 10.1016/j.bbmt.2014.06.010. Epub 2014 Jun 24.

Abstract

The introduction of reduced-intensity conditioning (RIC) regimens made it possible to offer allogeneic hematopoietic cell transplantation (alloHCT) to older patients with myelodysplastic syndromes (MDS). However, the relative risks and benefits of alloHCT compared with novel nontransplant therapies continue to be the source of considerable uncertainty. We will perform a prospective biologic assignment trial to compare RIC alloHCT with nontransplant therapies based on donor availability. Primary outcome is 3-year overall survival. Secondary outcomes include leukemia-free survival, quality of life, and cost-effectiveness. Four hundred patients will be enrolled over roughly 3 years. Planned subgroup analyses will evaluate key biologic questions, such as the impact of age and response to hypomethylating agents on treatment effects. Findings from this study potentially may set a new standard of care for older MDS patients who are considered candidates for alloHCT.

摘要

减低强度预处理(RIC)方案的引入使得为老年骨髓增生异常综合征(MDS)患者提供异基因造血细胞移植(alloHCT)成为可能。然而,与新型非移植疗法相比,alloHCT的相对风险和益处仍然存在很大的不确定性。我们将进行一项前瞻性生物学分配试验,根据供体可用性比较RIC alloHCT与非移植疗法。主要结局是3年总生存率。次要结局包括无白血病生存率、生活质量和成本效益。大约3年内将招募400名患者。计划的亚组分析将评估关键的生物学问题,如年龄和对去甲基化药物的反应对治疗效果的影响。这项研究的结果可能会为被认为适合alloHCT的老年MDS患者设定新的护理标准。

相似文献

引用本文的文献

4
Existing agents, novel agents, or transplantation for high-risk MDS.高危 MDS 的现有药物、新型药物或移植。
Hematology Am Soc Hematol Educ Program. 2020 Dec 4;2020(1):411-417. doi: 10.1182/hematology.2020000125.
7
Outcomes after Umbilical Cord Blood Transplantation for Myelodysplastic Syndromes.脐带血移植治疗骨髓增生异常综合征后的疗效
Biol Blood Marrow Transplant. 2017 Jun;23(6):971-979. doi: 10.1016/j.bbmt.2017.03.014. Epub 2017 Mar 10.

本文引用的文献

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