Suppr超能文献

异基因干细胞移植后急性髓系白血病复发的新型治疗方法

Novel Approaches to Treatment of Acute Myeloid Leukemia Relapse Post Allogeneic Stem Cell Transplantation.

作者信息

Liberatore Carmine, Di Ianni Mauro

机构信息

Hematology Unit, Department of Oncology and Hematology, Santo Spirito Hospital, 65124 Pescara, Italy.

Department of Medicine and Sciences of Aging, "G. d'Annunzio" University of Chieti-Pescara, 66100 Chieti, Italy.

出版信息

Int J Mol Sci. 2023 Oct 9;24(19):15019. doi: 10.3390/ijms241915019.

Abstract

The management of patients with acute myeloid leukemia (AML) relapsed post allogeneic hematopoietic stem cell transplantation (HSCT) remains a clinical challenge. Intensive treatment approaches are limited by severe toxicities in the early post-transplantation period. Therefore, hypomethylating agents (HMAs) have become the standard therapeutic approach due to favorable tolerability. Moreover, HMAs serve as a backbone for additional anti-leukemic agents. Despite discordant results, the addition of donor lymphocytes infusions (DLI) generally granted improved outcomes with manageable GvHD incidence. The recent introduction of novel targeted drugs in AML gives the opportunity to add a third element to salvage regimens. Those patients harboring targetable mutations might benefit from IDH1/2 inhibitors Ivosidenib and Enasidenib as well as FLT3 inhibitors Sorafenib and Gilteritinib in combination with HMA and DLI. Conversely, patients lacking targetable mutations actually benefit from the addition of Venetoclax. A second HSCT remains a valid option, especially for fit patients and for those who achieve a complete disease response with salvage regimens. Overall, across studies, higher response rates and longer survival were observed in cases of pre-emptive intervention for molecular relapse. Future perspectives currently rely on the development of adoptive immunotherapeutic strategies mainly represented by CAR-T cells.

摘要

异基因造血干细胞移植(HSCT)后复发的急性髓系白血病(AML)患者的管理仍然是一项临床挑战。强化治疗方法受到移植后早期严重毒性的限制。因此,由于耐受性良好,去甲基化药物(HMA)已成为标准治疗方法。此外,HMA是其他抗白血病药物的基础。尽管结果不一致,但添加供体淋巴细胞输注(DLI)通常能改善预后,且移植物抗宿主病(GvHD)发生率可控。AML中新型靶向药物的近期引入为挽救方案增加了第三个要素提供了机会。那些携带可靶向突变的患者可能受益于IDH1/2抑制剂艾伏尼布和恩西地平以及FLT3抑制剂索拉非尼和吉瑞替尼,它们可与HMA和DLI联合使用。相反,缺乏可靶向突变的患者实际上受益于添加维奈克拉。第二次HSCT仍然是一个有效的选择,特别是对于身体状况良好的患者以及那些通过挽救方案实现完全疾病缓解的患者。总体而言,在各项研究中,对分子复发进行抢先干预的病例观察到更高的缓解率和更长的生存期。目前,未来的前景依赖于主要以嵌合抗原受体T细胞(CAR-T细胞)为代表的过继性免疫治疗策略的发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f063/10573608/f4da0e8dced4/ijms-24-15019-g001.jpg

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