研究概要
这些治疗联合使用显示出良好的疗效。
中文摘要
对于不适合移植的高危骨髓增生异常综合征(MDS)患者,唯一治疗选择是持续使用去甲基化药物(HMA)。近年来虽开发了一些新的 HMA 联合方案及作用机制不同的其他药物,但尚未取得突破。在临床实践中,作者逐步探索了多种新方法:诱导治疗采用改良 VIALE-A(VA)方案,巩固期交替使用改良 VA 和 VHAG 方案。对微小残留病(MRD)持续阳性的部分患者给予 HLA 不匹配脐带血;对造血恢复不佳的患者则额外输注间充质干细胞。上述治疗取得了较好疗效。本文介绍一名典型患者的完整治疗过程,并回顾相关文献。
展开英文摘要原文
The only treatment option for high-risk MDS patients unfit for transplantation is continuous treatment with a hypomethylating agent (HMA). In this context, some new combination HMA regimens and other drugs with different mechanisms of action have been developed recently; however, no breakthroughs have been made. In our clinical practice, we have gradually explored various new methods-induction therapy with a modified VIALE-A (VA) regimen and an alternating regimen of modified VA and VHAG for the consolidation period. Some patients who were persistently positive for MRD were treated with HLA-mismatched umbilical cord blood, and patients with poor hematopoietic recovery additionally received mesenchymal stem cells infusion. Together, these treatments showed good efficacy. Here, the total treatment process for a typical patient is described, and a review of the literature is provided.
论文信息
- 作者
- Sun Q、Wen Z、Ling Y、Kuang J、Chen G、Zhu Z、Wang H、Li K
- 单位
- Department of Geriatric Hematology and Oncology, Guangzhou First People's Hospital, Guangzhou, Guangdong, China.China
- 文献类型
- 病例报告
- 期刊
- Frontiers in oncology2026